135,968 results on '"GENE expression"'
Search Results
2. Methods to Study the Structure and Catalytic Activity of cis-Splicing Inteins.
- Author
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Zhao J, Du Z, Wang C, and Mills KV
- Subjects
- Aspartic Acid chemistry, Carbon Isotopes, Cysteine chemistry, Electrophoresis, Polyacrylamide Gel methods, Escherichia coli chemistry, Escherichia coli genetics, Escherichia coli metabolism, Exteins, Gene Expression, Genetic Vectors genetics, Histidine chemistry, Hydrogen-Ion Concentration, Maltose-Binding Proteins chemistry, Maltose-Binding Proteins genetics, Nitrogen Isotopes, Nuclear Magnetic Resonance, Biomolecular methods, Recombinant Fusion Proteins biosynthesis, Biocatalysis, Biochemistry methods, Inteins, Protein Splicing, Recombinant Fusion Proteins chemistry, Recombinant Fusion Proteins genetics
- Abstract
The autocatalytic process of protein splicing is facilitated by an intein, which interrupts flanking polypeptides called exteins. The mechanism of protein splicing has been studied by overexpression in E. coli of intein fusion proteins with nonnative exteins. Inteins can be used to generate reactive α-thioesters, as well as proteins with N-terminal Cys residues, to facilitate expressed protein ligation. As such, a more detailed understanding of the function of inteins can have significant impact for biotechnology applications. Here, we provide biochemical methods to study splicing activity and NMR methods to study intein structure and the catalytic mechanism.
- Published
- 2020
- Full Text
- View/download PDF
3. Stressing Escherichia coli to educate students about research: A CURE to investigate multiple levels of gene regulation.
- Author
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McDonough J, Goudsouzian LK, Papaj A, Maceli AR, Klepac-Ceraj V, and Peterson CN
- Subjects
- Educational Measurement, Escherichia coli metabolism, Humans, Laboratories, Biochemistry education, Curriculum, Escherichia coli genetics, Gene Expression Regulation, Bacterial, Research education, Stress, Physiological genetics, Students psychology
- Abstract
Course-based undergraduate research experiences (CUREs) have been shown to increase student retention and learning in the biological sciences. Most CURES cover only one aspect of gene regulation, such as transcriptional control. Here we present a new inquiry-based lab that engages understanding of gene expression from multiple perspectives. Students carry out a forward genetic screen to identify regulators of the stationary phase master regulator RpoS in the model organism Escherichia coli and then use a series of reporter fusions to determine if the regulation is at the level of transcription or the post-transcription level. This easy-to-implement course has been run both as a 9-week long project and a condensed 5-6 week version in three different schools and types of courses. A majority of the genes found in the screen are novel, thus giving students the opportunity to contribute to original findings to the field. Assessments of this CURE show student gains in learning in many knowledge areas. In addition, attitudinal surveys suggest the students are enthusiastic about the screen and their learning about gene regulation. In summary, this lab would be an appropriate addition to an intermediate or advanced level Molecular Biology, Genetics, or Microbiology curriculum. © 2017 by The International Union of Biochemistry and Molecular Biology, 45(5):449-458, 2017., (© 2017 The International Union of Biochemistry and Molecular Biology.)
- Published
- 2017
- Full Text
- View/download PDF
4. An investigative graduate laboratory course for teaching modern DNA techniques.
- Author
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de Lencastre A, Thomas Torello A, and Keller LC
- Subjects
- Animals, Cell Line, Curriculum, Drosophila melanogaster genetics, Education, Graduate methods, Educational Measurement statistics & numerical data, Humans, Reverse Transcriptase Polymerase Chain Reaction methods, Sequence Analysis, DNA, Students, Transformation, Bacterial, Biochemistry education, Cloning, Molecular methods, DNA-Binding Proteins genetics, Drosophila Proteins genetics, Gene Expression, Molecular Biology education, Phosphoproteins genetics
- Abstract
This graduate-level DNA methods laboratory course is designed to model a discovery-based research project and engages students in both traditional DNA analysis methods and modern recombinant DNA cloning techniques. In the first part of the course, students clone the Drosophila ortholog of a human disease gene of their choosing using Gateway
® cloning. In the second part of the course, students examine the expression of their gene of interest in human cell lines by reverse transcription PCR and learn how to analyze data from quantitative reverse transcription PCR (qRT-PCR) experiments. The adaptability of the Gateway® cloning system is ideally suited for students to design and create different types of expression constructs to achieve a particular experimental goal (e.g., protein purification, expression in cell culture, and/or subcellular localization), and the genes chosen can be aligned to the research interests of the instructor and/or ongoing research in a department. Student evaluations indicate that the course fostered a genuine excitement for research and in depth knowledge of both the techniques performed and the theory behind them. Our long-term goal is to incorporate this DNA methods laboratory as the foundation for an integrated laboratory sequence for the Master of Science degree program in Molecular and Cellular Biology at Quinnipiac University, where students use the reagents and concepts they developed in this course in subsequent laboratory courses, including a protein methods and cell culture laboratory. © 2017 by The International Union of Biochemistry and Molecular Biology, 45(4):351-359, 2017., (© 2017 The International Union of Biochemistry and Molecular Biology.)- Published
- 2017
- Full Text
- View/download PDF
5. A model system for the study of gene expression in the undergraduate laboratory.
- Author
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Hargadon KM
- Subjects
- Curriculum, Education, Medical, Undergraduate, Educational Measurement, Humans, Melanoma, Experimental genetics, Melanoma, Experimental pathology, RNA, Messenger genetics, Real-Time Polymerase Chain Reaction methods, Reverse Transcriptase Polymerase Chain Reaction methods, Students psychology, Transforming Growth Factor beta1 analysis, Tumor Cells, Cultured, Biochemistry education, Biomedical Research education, Gene Expression Regulation, Neoplastic, Laboratories, Models, Biological, Problem-Based Learning methods, Transforming Growth Factor beta1 genetics
- Abstract
The flow of genetic information from DNA to RNA to protein, otherwise known as the "central dogma" of biology, is one of the most basic and overarching concepts in the biological sciences. Nevertheless, numerous studies have reported student misconceptions at the undergraduate level of this fundamental process of gene expression. This study reports on the efficacy of a model system for teaching gene expression in the undergraduate laboratory. A student-centered investigation of Tgfb1 gene expression in two murine melanoma cell lines was used to emphasize not only the process of gene expression but also various research methods for studying this phenomenon. Traditional RT-PCR, quantitative real-time RT-PCR, and flow cytometry-based in situ hybridization assays were employed to study expression of this immunosuppressive cytokine gene in the highly tumorigenic B16-F1 melanoma cell line and the poorly tumorigenic D5.1G4 melanoma cell line, both at the population and single-cell levels. A pre- and post-laboratory assessment instrument demonstrated the utility of this model system in enhancing student learning both of content related to gene expression and of research methods and data analysis skills. The pedagogical approach described in this study is therefore an effective way to improve the teaching and learning of gene expression at the undergraduate level. © 2016 by The International Union of Biochemistry and Molecular Biology, 44(4):397-404, 2016., (© 2016 The International Union of Biochemistry and Molecular Biology.)
- Published
- 2016
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6. Expression, purification, and characterization of a carbohydrate-active enzyme: A research-inspired methods optimization experiment for the biochemistry laboratory.
- Author
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Willbur JF, Vail JD, Mitchell LN, Jakeman DL, and Timmons SC
- Subjects
- Curriculum, DNA, Recombinant genetics, Escherichia coli genetics, Biochemistry education, Carbohydrate Metabolism, Enzymes metabolism
- Abstract
The development and implementation of research-inspired, discovery-based experiences into science laboratory curricula is a proven strategy for increasing student engagement and ownership of experiments. In the novel laboratory module described herein, students learn to express, purify, and characterize a carbohydrate-active enzyme using modern techniques and instrumentation commonly found in a research laboratory. Unlike in a traditional cookbook-style experiment, students generate their own hypotheses regarding expression conditions and quantify the amount of protein isolated using their selected variables. Over the course of three 3-hour laboratory periods, students learn to use sterile technique to express a protein using recombinant DNA in E. coli, purify the resulting enzyme via affinity chromatography and dialysis, analyze the success of their purification scheme via SDS-PAGE, assess the activity of the enzyme via an HPLC-based assay, and quantify the amount of protein isolated via a Bradford assay. Following the completion of this experiment, students were asked to evaluate their experience via an optional survey. All students strongly agreed that this laboratory module was more interesting to them than traditional experiments because of its lack of a pre-determined outcome and desired additional opportunities to participate in the experimental design process. This experiment serves as an example of how research-inspired, discovery-based experiences can benefit both the students and instructor; students learned important skills necessary for real-world biochemistry research and a more concrete understanding of the research process, while generating new knowledge to enhance the scholarly endeavors of the instructor., (© 2015 The International Union of Biochemistry and Molecular Biology.)
- Published
- 2016
- Full Text
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7. Production and Purification of Recombinant SUMOylated Proteins Using Engineered Bacteria.
- Author
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Brockly F, Piechaczyk M, and Bossis G
- Subjects
- Cell Engineering methods, Cloning, Molecular, Escherichia coli genetics, Escherichia coli metabolism, Gene Expression, Genetic Vectors chemistry, Genetic Vectors metabolism, Histidine genetics, Histidine metabolism, Humans, JNK Mitogen-Activated Protein Kinases genetics, JNK Mitogen-Activated Protein Kinases isolation & purification, Mannose-Binding Lectin genetics, Mannose-Binding Lectin metabolism, Oligopeptides genetics, Oligopeptides metabolism, Protein Binding, Recombinant Fusion Proteins genetics, Recombinant Fusion Proteins isolation & purification, SUMO-1 Protein genetics, Sumoylation, Ubiquitins genetics, Biochemistry methods, JNK Mitogen-Activated Protein Kinases metabolism, Protein Processing, Post-Translational, Recombinant Fusion Proteins metabolism, SUMO-1 Protein metabolism, Ubiquitins metabolism
- Abstract
SUMO is a ubiquitin-like protein that is covalently conjugated to numerous cellular proteins to modify their function and fate. Although large progresses have been made in the identification of SUMOylated proteins, the molecular consequences of their SUMOylation are generally unknown. This is, most often, due to the low abundance of SUMOylated proteins in the cell, usually less than 1 % of a given protein being modified at steady state. To gain insights into the role of specific SUMOylation targets, SUMO conjugation can be reconstituted in vitro using purified proteins. However, for most substrates, the efficiency of in vitro SUMOylation is too low to obtain sufficient amounts of their SUMOylated forms for biochemical studies. Here, we describe a detailed protocol to purify large amounts of recombinant SUMOylated proteins using bacteria modified to express His-tagged SUMO as well as the SUMO-activating and -conjugating enzymes.
- Published
- 2016
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8. qPCR for second year undergraduates: A short, structured inquiry to illustrate differential gene expression.
- Author
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McCauslin CS, Gunn KE, Pirone D, and Staiger J
- Subjects
- Curriculum, Gene Expression, Humans, Laboratories, Biochemistry education, Molecular Biology education, Real-Time Polymerase Chain Reaction methods, Teaching methods
- Abstract
We describe a structured inquiry laboratory exercise that examines transcriptional regulation of the NOS2 gene under conditions that simulate the inflammatory response in macrophages. Using quantitative PCR and the comparative CT method, students are able determine whether transcriptional activation of NOS2 occurs and to what degree. The exercise is aimed at second year undergraduates who possess basic knowledge of gene expression events. It requires only 4-5 hr of dedicated laboratory time and focuses on use of the primary literature, data analysis, and interpretation. Importantly, this exercise provides a mechanism to introduce the concept of differential gene expression and provides a starting point for development of more complex guided or open inquiry projects for students moving into upper level molecular biology, immunology, and biochemistry course work., (© 2015 The International Union of Biochemistry and Molecular Biology.)
- Published
- 2015
- Full Text
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9. Heterologous expression, purification and biochemical characterization of endochitinase ChiA74 from Bacillus thuringiensis.
- Author
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Casados-Vázquez LE, Avila-Cabrera S, Bideshi DK, and Barboza-Corona JE
- Subjects
- Blotting, Western, Cations, Divalent pharmacology, Chitin metabolism, Chromatography, Thin Layer, Hydrogen-Ion Concentration, Kinetics, Models, Molecular, Recombinant Fusion Proteins isolation & purification, Temperature, Bacillus thuringiensis enzymology, Biochemistry methods, Chitinases isolation & purification, Chitinases metabolism, Gene Expression
- Abstract
ChiA74 is a secreted endochitinase produced by Bacillus thuringiensis. Previously we have partially characterized the physical parameters that affect enzymatic activity of ChiA74 in crude preparations of bacterial secretomes. In the present study, we cloned the chiA74 open reading frame (ORF) lacking the 5' sequence coding for its secretion signal peptide (chiA74Δsp) into a cold shock expression vector (pColdI) for production of the enzyme in Escherichia coli BL21-Rosetta 2. As a result, the N-terminal end of ChiA74Δsp ORF was fused to an artificial sequence of 28 amino acid, including a 6× histidine tag for purification of recombinant 6×His tagged-ChiA74Δsp (rChiA74, ∼74kDa). Along with a protein of ∼74kDa, we co-purified its ∼55kDa processed form which was confirmed by Western blot analysis. Optimal endochitinase activity of purified rChiA74 occurred at pH 7 and 40°C. Most divalent cations (e.g. Ba(+2), Ca(+2), Mn(+2), Mg(+2), Zn(+2) and Cu(+2)) at concentration of 10mM reduced chitinase activity by ∼30%, and Hg(+2) (10mM) drastically inhibited ChiA74 activity by ∼75-100%. The Vmax, Km and kcat for rChiA74 were 0.11±0.01nmol/min, 2.15μM±0.45 and 3.81s(-1), respectively, using 4-MU-GlcNAc3 as substrate. Using purified rChiA74 and colloidal chitin as substrate, chitin-derived oligosaccharides with degree of polymerization of 2 and 1 were detected., (Copyright © 2014 Elsevier Inc. All rights reserved.)
- Published
- 2015
- Full Text
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10. A method for isolating high quality RNA from mouse cortical and cancellous bone.
- Author
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Kelly NH, Schimenti JC, Patrick Ross F, and van der Meulen MC
- Subjects
- Animals, Bone Marrow metabolism, Bone and Bones cytology, Centrifugation, Gene Expression Regulation, Male, Mice, Inbred C57BL, Biochemistry methods, Bone and Bones metabolism, RNA isolation & purification
- Abstract
The high incidence of fragility fractures in cortico-cancellous bone locations, plus the fact that individual skeletal sites exhibit different responsiveness to load and disease, emphasizes the need to document separately gene expression in cortical and cancellous bone. A further confounding factor is marrow contamination since its high cellularity may effect gene expression measurements. We isolated RNA from cortical and cancellous bone of intact mouse tibiae, and also after marrow removal by flushing or centrifugation. RNA isolated from cancellous bone by each method was sufficient for gene expression analysis. Centrifugation removed contaminating cells more efficiently than flushing, as indexed by histology and decreased expression of Icam4, a highly expressed erythroid gene. In contrast, centrifuged cortical bone had 12- and 13- fold higher expression of the bone-related genes Col1a1 and Bglap, while levels in marrow-free cancellous bone were 30- and 31-fold higher when compared to bone where marrow was left intact. Furthermore, cortical bone had higher expression of Col1a1 and Bglap than cancellous bone. Thus, RNA isolated by this novel approach can reveal site-specific changes in gene expression in cortical and cancellous bone sites., (Copyright © 2014 Elsevier Inc. All rights reserved.)
- Published
- 2014
- Full Text
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11. Isolation of high-quality RNA from grains of different maize varieties.
- Author
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Messias Rda S, Galli V, Buss JH, Borowski JM, Nora L, e Silva SD, Margis R, and Rombaldi CV
- Subjects
- Cetrimonium, Cetrimonium Compounds chemistry, Mixed Function Oxygenases genetics, Real-Time Polymerase Chain Reaction, Seeds genetics, Biochemistry methods, RNA, Plant isolation & purification, Zea mays genetics
- Abstract
The study of gene expression in maize varieties represents a powerful tool aiming to increase vitamin A precursors. However, the isolation of RNA from different maize varieties is challenging because these varieties show different levels of polysaccharides, and most methods available for RNA isolation are inappropriate for grain samples. The polysaccharides co-purify and co-precipitate with RNA during isolation, resulting in low-quality RNA, compromising the use of RNA in subsequent applications. Thus, a cetyltrimethylammonium bromide (CTAB)-based method was adapted in this study and compared with six methods for RNA isolation, including commercial reagents and RNA and DNA isolation kits, in order to identify the most appropriate for maize grains from different varieties. Most of the methods evaluated were considered inadequate due to limitations in terms of purity and/or quantity of the isolated RNA, which affected the efficiency of subsequent RT-qPCR analysis, resulting in nonamplification of β-carotene hydroxylase gene (HYD3) or high deviation among replicates. However, the CTAB modified method allowed the study to obtain intact RNA, with high quality and quantity, from 25 maize varieties. Furthermore, this RNA was successfully used to evaluate the expression of HYD3 gene by real-time qualitative polymerase chain reaction (RT-qPCR), and thus represents a simple, efficient, and low-cost strategy.
- Published
- 2014
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12. Method of conditional moments (MCM) for the Chemical Master Equation: a unified framework for the method of moments and hybrid stochastic-deterministic models.
- Author
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Hasenauer J, Wolf V, Kazeroonian A, and Theis FJ
- Subjects
- Gene Expression, Proteins genetics, Stochastic Processes, Biochemistry methods, Data Interpretation, Statistical, Models, Chemical
- Abstract
The time-evolution of continuous-time discrete-state biochemical processes is governed by the Chemical Master Equation (CME), which describes the probability of the molecular counts of each chemical species. As the corresponding number of discrete states is, for most processes, large, a direct numerical simulation of the CME is in general infeasible. In this paper we introduce the method of conditional moments (MCM), a novel approximation method for the solution of the CME. The MCM employs a discrete stochastic description for low-copy number species and a moment-based description for medium/high-copy number species. The moments of the medium/high-copy number species are conditioned on the state of the low abundance species, which allows us to capture complex correlation structures arising, e.g., for multi-attractor and oscillatory systems. We prove that the MCM provides a generalization of previous approximations of the CME based on hybrid modeling and moment-based methods. Furthermore, it improves upon these existing methods, as we illustrate using a model for the dynamics of stochastic single-gene expression. This application example shows that due to the more general structure, the MCM allows for the approximation of multi-modal distributions.
- Published
- 2014
- Full Text
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13. Environmental regulation of plant gene expression: an RT-qPCR laboratory project for an upper-level undergraduate biochemistry or molecular biology course.
- Author
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Eickelberg GJ and Fisher AJ
- Subjects
- Arabidopsis genetics, Arabidopsis Proteins genetics, Curriculum, Gene Expression Profiling, MADS Domain Proteins genetics, Students, Biochemistry education, Environment, Gene Expression Regulation, Plant, Laboratories, Molecular Biology education, Real-Time Polymerase Chain Reaction, Universities
- Abstract
We present a novel laboratory project employing "real-time" RT-qPCR to measure the effect of environment on the expression of the FLOWERING LOCUS C gene, a key regulator of floral timing in Arabidopsis thaliana plants. The project requires four 3-hr laboratory sessions and is aimed at upper-level undergraduate students in biochemistry or molecular biology courses. The project provides students with hands-on experience with RT-qPCR, the current "gold standard" for gene expression analysis, including detailed data analysis using the common 2-ΔΔCT method. Moreover, it provides a convenient starting point for many inquiry-driven projects addressing diverse questions concerning ecological biochemistry, naturally occurring genetic variation, developmental biology, and the regulation of gene expression in nature., (Copyright © 2013 Wiley Periodicals, Inc.)
- Published
- 2013
- Full Text
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14. PEGylation-aided refolding of globular adiponectin.
- Author
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Gao M, Tong Y, Gao X, and Yao W
- Subjects
- Adiponectin genetics, Adiponectin metabolism, Adiponectin pharmacology, Animals, Escherichia coli metabolism, Gene Expression, Glucose Tolerance Test, Humans, Hypoglycemic Agents metabolism, Hypoglycemic Agents pharmacology, Inclusion Bodies genetics, Inclusion Bodies metabolism, Male, Mice, Recombinant Fusion Proteins biosynthesis, Recombinant Fusion Proteins chemistry, Recombinant Fusion Proteins genetics, Recombinant Fusion Proteins pharmacology, Adiponectin chemistry, Biochemistry methods, Escherichia coli genetics, Hypoglycemic Agents chemistry, Polyethylene Glycols chemistry, Protein Refolding
- Abstract
Globular adiponectin (GAD) as the active domain of adiponectin is a promising candidate for anti-diabetic drug development. The recombinant production of GAD in Escherichia coli, however, is difficult because it is mainly expressed as inclusion bodies which need to be refolded to regain function. In this study we developed a novel method for refolding of GAD with a high efficiency by using polyethylene glycol (PEG) conjugation. An artificially designed DNA sequence encoding for GAD was synthesized and inserted into the pET28a vector to construct an expression plasmid which was thereafter transformed into E. coli BL21 (DE3) host cells for heterologous expression. After bacterial cell culture employing auto-induction medium, the inclusion bodies were collected, washed and dissolved in guanidine hydrochloride before PEG conjugation. Then the PEG-conjugated GAD was refolded by dialysis and purified by two steps of chromatography. The refolded conjugate showed a marked glucose-lowering activity in mice, demonstrating that it had been successfully refolded. As a convenient method, PEGylation-aided refolding could also be tested on other proteins to explore its suitability.
- Published
- 2013
- Full Text
- View/download PDF
15. Synchronizing protein transport in the secretory pathway.
- Author
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Boncompain G and Perez F
- Subjects
- Animals, Fluorescent Dyes metabolism, Gene Expression, Genes, Reporter, Humans, Streptavidin metabolism, Temperature, Biochemistry methods, Cell Membrane metabolism, Endoplasmic Reticulum metabolism, Eukaryota metabolism, Golgi Apparatus metabolism, Protein Transport, Secretory Pathway
- Abstract
To be secreted or transported to their target compartments, newly synthesized proteins leave the endoplasmic reticulum to reach the Golgi apparatus, where they are processed and sorted toward their final destinations along the secretory pathway. It is now clear that many Golgi-intersecting and non-intersecting pathways exist in cells to carry out proper transport, modification, and addressing. To analyze and visualize the intracellular trafficking of any secretory protein, we developed the retention using selective hooks (RUSH) system. This assay allows the simultaneous release of a pool of particular secretory proteins from the endoplasmic reticulum and the monitoring of their anterograde trafficking. The use of the RUSH system is detailed in these protocols, from sub-cloning the sequence coding for the protein of interest into RUSH plasmids to visualization of its trafficking.
- Published
- 2012
- Full Text
- View/download PDF
16. Protein pyrophosphorylation by diphosphoinositol pentakisphosphate (InsP7).
- Author
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Werner JK Jr, Speed T, and Bhandari R
- Subjects
- Amino Acid Sequence, Autoradiography methods, Blotting, Western methods, Diphosphates metabolism, Escherichia coli genetics, Gene Expression, Inositol Phosphates metabolism, Molecular Sequence Data, Phosphorylation, Proteins genetics, Proteins isolation & purification, Recombinant Fusion Proteins chemistry, Recombinant Fusion Proteins genetics, Recombinant Fusion Proteins isolation & purification, Recombinant Fusion Proteins metabolism, Saccharomyces cerevisiae genetics, Biochemistry methods, Diphosphates analysis, Inositol Phosphates analysis, Proteins chemistry, Proteins metabolism
- Abstract
Diphosphoinositol polyphosphates, also known as inositol pyrophosphates, are a family of water soluble inositol phosphates that possess diphosphate or pyrophosphate moieties. In the presence of divalent cations such as Mg(2+), the "high energy" beta phosphate can be transferred from the inositol pyrophosphates, InsP(7) and InsP(8), to prephosphorylated serine residues on proteins, to form pyrophosphoserine. This chapter provides detailed methods to identify proteins that are substrates for pyrophosphorylation by InsP(7), conduct phosphorylation assays on purified protein, and detect protein pyrophosphorylation.
- Published
- 2010
- Full Text
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17. Matrix metalloproteinases.
- Author
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Birkedal-Hansen H, Yamada S, Windsor J, Pollard AH, Lyons G, Stetler-Stevenson W, and Birkedal-Hansen B
- Subjects
- Animals, Collagen metabolism, Gene Expression, Humans, Matrix Metalloproteinase Inhibitors, Matrix Metalloproteinases genetics, Rats, Staining and Labeling, Tendons metabolism, Tissue Inhibitor of Metalloproteinases metabolism, alpha-Macroglobulins metabolism, Biochemistry methods, Matrix Metalloproteinases metabolism
- Abstract
Matrix metalloproteinases are a class of enzymes that play an important role in the remodeling of the extracellular matrix in development and cancer metastasis. This unit describes a set of methods--cell-mediated dissolution of type-1 collagen fibrils, direct and reverse zymography, enzyme capture based on alpha2-macroglobulin and TIMP-1 and -2, and demonstration of cryptic thiol groups in metalloproteinase precursors--that are used to characterize the functions of matrix metalloproteinases and their inhibitors., (Copyright 2008 by John Wiley & Sons, Inc.)
- Published
- 2008
- Full Text
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18. Biochemistry. A postgenomic visual icon.
- Author
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Weinstein JN
- Subjects
- Biochemical Phenomena, Cluster Analysis, Color, Computer Graphics, Genomics, Biochemistry, Computational Biology, Data Display, Gene Expression
- Published
- 2008
- Full Text
- View/download PDF
19. Towards synthesis of a minimal cell.
- Author
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Forster AC and Church GM
- Subjects
- Biochemistry trends, Biomimetics trends, Cell-Free System, Gene Expression, Genome genetics, Biochemistry methods, Biomimetics methods, Cells metabolism
- Abstract
Construction of a chemical system capable of replication and evolution, fed only by small molecule nutrients, is now conceivable. This could be achieved by stepwise integration of decades of work on the reconstitution of DNA, RNA and protein syntheses from pure components. Such a minimal cell project would initially define the components sufficient for each subsystem, allow detailed kinetic analyses and lead to improved in vitro methods for synthesis of biopolymers, therapeutics and biosensors. Completion would yield a functionally and structurally understood self-replicating biosystem. Safety concerns for synthetic life will be alleviated by extreme dependence on elaborate laboratory reagents and conditions for viability. Our proposed minimal genome is 113 kbp long and contains 151 genes. We detail building blocks already in place and major hurdles to overcome for completion.
- Published
- 2006
- Full Text
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20. Integration of metabolic networks and gene expression in virtual reality.
- Author
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Yang Y, Engin L, Wurtele ES, Cruz-Neira C, and Dickerson JA
- Subjects
- Algorithms, Arabidopsis genetics, Computer Graphics, Computer Simulation, Gene Expression, Gene Expression Regulation, Genes, Plant, Genome, Plant, Internet, Models, Biological, Multigene Family, Proteomics, Software, Software Design, Transcription, Genetic, User-Computer Interface, Biochemistry methods, Metabolism
- Abstract
Motivation: Metabolic networks combine metabolism and regulation. These complex networks are difficult to understand and visualize due to the amount and diverse types of information that need to be represented. For example, pathway information gives indications of interactions. Experimental data, such as transcriptomics, proteomics and metabolomics data, give snapshots of the system state. Stereoscopic virtual environments provide a true three-dimensional representation of metabolic networks, which can be intuitively manipulated, and may help to manage the data complexity., Results: MetNet3D, a 3D virtual reality system, allows a user to explore gene expression and metabolic pathway data simultaneously. Normalized gene expression data are processed in R and visualized as a 3D plot. Users can find a particular gene of interest or a cluster of genes that behave similarly and see how these genes function in metabolic networks from MetNetDB, a database of Arabidopsis metabolic networks, using animated network graphs. Interactive virtual reality, with its enhanced ability to display more information, makes such integration more effective by abstracting key relationships., Availability: MetNet3D and some sample datasets are available at http://www.vrac.iastate.edu/research/sites/metnet/Download/Download.htm., Supplementary Information: Color snapshots and movies are available at http://www.vrac.iastate.edu/research/sites/metnet/Bioinformatics/SupplementaryInformation.htm.
- Published
- 2005
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21. Biography of Erin K. O'Shea.
- Author
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Marino M
- Subjects
- Gene Expression, History, 20th Century, History, 21st Century, Leucine Zippers, Nucleosomes genetics, Proteomics history, San Francisco, Biochemistry history
- Published
- 2004
- Full Text
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22. Analysis of nuclear receptor function in the mouse auditory system.
- Author
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Kelley MW, Lanford PJ, Jones I, Amma L, Ng L, and Forrest D
- Subjects
- Animals, Cochlea physiology, Gene Expression, Hearing Tests instrumentation, Mice, Plasmids metabolism, RNA, Messenger metabolism, Species Specificity, Time Factors, Biochemistry methods, Cell Nucleus metabolism, Evoked Potentials, Auditory physiology, Receptors, Cytoplasmic and Nuclear metabolism
- Published
- 2003
- Full Text
- View/download PDF
23. Chemical approaches to the investigation of cellular systems.
- Author
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Cook BN and Bertozzi CR
- Subjects
- Animals, Cytological Techniques, Diagnostic Imaging methods, Gene Expression, Humans, Membrane Glycoproteins, Molecular Probes, Signal Transduction, Biochemistry methods, Cell Physiological Phenomena, Cells chemistry
- Abstract
Biochemistry in the context of a living cell or organism is complicated by many variables such as supramolecular organization, cytoplasmic viscosity, and substrate heterogeneity. While these variables are easily excluded or avoided in reconstituted systems, they must be dealt with in cellular environments. New developments have allowed researchers to begin probing the inner workings of the cell to gain new insight into cell function and metabolism. Advances in cellular imaging and in small molecule-controlled gene expression, signal transduction and cell surface modification are discussed in this review. These techniques have permitted the study of molecular components within the context of living cells.
- Published
- 2002
- Full Text
- View/download PDF
24. Molecular imaging: new applications for biochemistry.
- Author
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Mountz JD, Hsu HC, Wu Q, Liu HG, Zhang HG, and Mountz JM
- Subjects
- Animals, Antibodies analysis, Cells cytology, Gene Expression, Humans, Ligands, Biochemistry instrumentation, Biochemistry methods, Cells metabolism, Diagnostic Imaging instrumentation, Diagnostic Imaging methods
- Abstract
Molecular imaging can reveal in vivo analysis and quantification of biochemical reactions. To enable cell-surface imaging of receptors, novel ligands have been developed which can be radiolabeled or imaged by bioluminescence. Specific examples include somatostatin receptors, estrogen and progesterone receptors, receptors involved in adhesion and externalization of phosphatidyl serine as an indicator of apoptosis. Central nervous system imaging can be carried out using ligands for receptors including dopamine, serotonin and Gamma amino butyric acid (GABA). In addition, tumor and metabolic imaging can be carried out with the Na-K ATPase pump using the tracer thallium-201 for SPECT or F-18 FDG for PET imaging. Finally, novel receptors or endogenous metabolic pathways can be analyzed combining cell-gene therapy to create specific tracer targets in cells that can be studied by molecular imaging. The challenge of molecular imaging is to first identify key pathways that are unique for a specific disease processes, such as atherosclerosis, cancer, CNS disorders, immunologic and arthritis disorders and next to devise a high-affinity specific small molecular ligand that can be adapted to be a radiolabeled tracer to study this pathway. Advances in genomics and proteomics combine with new peptide-chemistry approaches should provide a large number of targets and tracers in the near future to achieve these imaging objectives., (Copyright 2002 Wiley-Liss, Inc.)
- Published
- 2002
- Full Text
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25. High resolution spatial analysis of plant systems.
- Author
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Kehr J
- Subjects
- Biochemistry instrumentation, Cell Separation, Plant Physiological Phenomena, Plants chemistry, Plants genetics, Biochemistry methods, Gene Expression, Plant Cells, Plant Proteins analysis
- Abstract
Analysis of organisms using techniques that provide high spatial and temporal resolution is of increasing interest in many disciplines of biomedical research. Although the examination of animal tissues has been the main focus to date, the recent development and improvement of methods for the sampling and handling of single cells and for their biochemical analysis now provide tools for investigating plant as well as animal cells.
- Published
- 2001
- Full Text
- View/download PDF
26. Seeing the machinery of live cells.
- Author
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Tsien RY and Miyawaki A
- Subjects
- Animals, Flow Cytometry, Gene Expression, Green Fluorescent Proteins, Proteins analysis, Recombinant Fusion Proteins, Biochemistry methods, Cell Physiological Phenomena, Fluorescent Dyes, Indicators and Reagents, Luminescent Proteins
- Published
- 1998
- Full Text
- View/download PDF
27. Identification of cross-talk pathways and PANoptosis-related genes in periodontitis and Alzheimer's disease by bioinformatics analysis and machine learning.
- Author
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Xiantao Chen, Yifei Dai, Yushen Li, Jiajun Xin, Jiatong Zou, Rui Wang, Hao Zhang, and Zhihui Liu
- Subjects
ALZHEIMER'S disease risk factors ,GENETICS of Alzheimer's disease ,STATISTICAL correlation ,PEARSON correlation (Statistics) ,DOWNLOADING ,ALZHEIMER'S disease ,RECEIVER operating characteristic curves ,RESEARCH funding ,PHENOMENOLOGICAL biology ,APOPTOSIS ,GENETIC markers ,DESCRIPTIVE statistics ,INFORMATION storage & retrieval systems ,CELLULAR signal transduction ,BIOCHEMISTRY ,TRANSCRIPTION factors ,IMMUNE system ,BIOINFORMATICS ,GENE expression ,GENE expression profiling ,METABOLISM ,RESEARCH ,CELL death ,MACHINE learning ,DATA analysis software ,GENETIC techniques ,PERIODONTITIS ,ALGORITHMS ,INTERLEUKINS ,DISEASE complications - Abstract
Background and objectives: Periodontitis (PD), a chronic inflammatory disease, is a serious threat to oral health and is one of the risk factors for Alzheimer's disease (AD). A growing body of evidence suggests that the two diseases are closely related. However, current studies have not provided a comprehensive understanding of the common genes and common mechanisms between PD and AD. This study aimed to screen the crosstalk genes of PD and AD and the potential relationship between cross-talk and PANoptosis-related genes. The relationship between core genes and immune cells will be analyzed to provide new targets for clinical treatment. Materials and methods: The PD and AD datasets were downloaded from the GEO database and differential expression analysis was performed to obtain DEGs. Overlapping DEGs had cross-talk genes linking PD and OP, and PANoptosis-related genes were obtained from a literature review. Pearson coefficients were used to compute cross-talk and PANoptosis-related gene correlations in the PD and AD datasets. Cross-talk genes were obtained from the intersection of PD and AD-related genes, protein-protein interaction (PPI) networks were constructed and cross-talk genes were identified using the STRING database. The intersection of cross-talk and PANoptosis-related genes was defined as cross-talk-PANoptosis genes. Core genes were screened using ROC analysis and XGBoost. PPI subnetwork, gene-biological process, and gene-pathway networks were constructed based on the core genes. In addition, immune infiltration on the PD and AD datasets was analyzed using the CIBERSORT algorithm. Results: 366 cross-talk genes were overlapping between PD DEGs and AD DEGs. The intersection of cross-talk genes with 109 PANoptosis-related genes was defined as cross-talk-PANoptosis genes. ROC and XGBoost showed that MLKL, DCN, IL1B, and IL18 were more accurate than the other cross-talk-PANoptosis genes in predicting the disease, as well as better in overall characterization. GO and KEGG analyses showed that the four core genes were involved in immunity and inflammation in the organism. Immune infiltration analysis showed that B cells naive, Plasma cells, and T cells gamma delta were significantly differentially expressed in patients with PD and AD compared with the normal group. Finally, 10 drugs associated with core genes were retrieved from the DGIDB database. Conclusion: This study reveals the joint mechanism between PD and AD associated with PANoptosis. Analyzing the four core genes and immune cells may provide new therapeutic directions for the pathogenesis of PD combined with AD. [ABSTRACT FROM AUTHOR]
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- 2024
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28. Genetic changes from type I interferons and JAK inhibitors: clues to drivers of juvenile dermatomyositis.
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Covert, Lauren T, Prinz, Joseph A, Swain-Lenz, Devjanee, Dvergsten, Jeffrey, and Truskey, George A
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DERMATOMYOSITIS , *SKELETAL muscle , *PHENOMENOLOGICAL biology , *TREATMENT effectiveness , *CELLULAR signal transduction , *BIOCHEMISTRY , *INTERFERONS , *JANUS kinases , *GENE expression , *GENE expression profiling , *NEUROTRANSMITTER uptake inhibitors , *CYTOKINES , *MUSCLES , *SEQUENCE analysis - Abstract
Objective To better understand the pathogenesis of juvenile dermatomyositis (JDM), we examined the effect of the cytokines type I interferons (IFN I) and JAK inhibitor drugs (JAKi) on gene expression in bioengineered pediatric skeletal muscle. Methods Myoblasts from three healthy pediatric donors were used to create three-dimensional skeletal muscle units termed myobundles. Myobundles were treated with IFN I, either IFNα or IFNβ. A subset of IFNβ-exposed myobundles was treated with JAKi tofacitinib or baricitinib. RNA sequencing analysis was performed on all myobundles. Results Seventy-six myobundles were analysed. Principal component analysis showed donor-specific clusters of gene expression across IFNα and IFNβ-exposed myobundles in a dose-dependent manner. Both cytokines upregulated interferon response and proinflammatory genes; however, IFNβ led to more significant upregulation. Key downregulated pathways involved oxidative phosphorylation, fatty acid metabolism and myogenesis genes. Addition of tofacitinib or baricitinib moderated the gene expression induced by IFNβ, with partial reversal of upregulated inflammatory and downregulated myogenesis pathways. Baricitinib altered genetic profiles more than tofacitinib. Conclusion IFNβ leads to more pro-inflammatory gene upregulation than IFNα, correlating to greater decrease in contractile protein gene expression and reduced contractile force. JAK inhibitors, baricitinib more so than tofacitinib, partially reverse IFN I-induced genetic changes. Increased IFN I exposure in healthy bioengineered skeletal muscle leads to IFN-inducible gene expression, inflammatory pathway enrichment, and myogenesis gene downregulation, consistent with what is observed in JDM. [ABSTRACT FROM AUTHOR]
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- 2024
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29. Bone marrow mesenchymal stem cell‐derived exosomal miR‐221‐3p promotes angiogenesis and wound healing in diabetes via the downregulation of forkhead box P1.
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Qiu, Zhi‐Yang, Xu, Wei‐cheng, and Liang, Zun‐Hong
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PROTEIN metabolism , *WOUND healing , *IN vitro studies , *PHENOMENOLOGICAL biology , *RESEARCH funding , *MESENCHYMAL stem cells , *MICRORNA , *ELECTRON microscopy , *POLYMERASE chain reaction , *BIOCHEMISTRY , *CELL motility , *GENE expression , *MICE , *ANIMAL experimentation , *WESTERN immunoblotting , *MICROSCOPY , *CELL survival , *EXOSOMES , *NEOVASCULARIZATION , *DIABETES - Abstract
Aim: Impaired wound healing in patients with diabetes can develop into nonhealing ulcerations. Because bone marrow mesenchymal stem cells (BMSCs) exosomes can promote wound healing, this study aims to investigate the mechanism of BMSCs‐isolated exosomal miR‐221‐3p in angiogenesis and diabetic wound healing. Methods: To mimic diabetes in vitro, human umbilical vein endothelial cells (HUVECs) were subjected to high glucose (HG). Exosomes were derived from BMSCs and identified by transmission electron microscopy (TEM), western blot analysis and dynamic light scattering (DLS). The ability to differentiate BMSCs was assessed via Oil red O staining, alkaline phosphatase (ALP) staining and alizarin red staining. The ability to internalise PKH26‐labelled exosomes was assessed using confocal microscopy. Migration, cell viability and angiogenesis were tested by scratch, MTT and tube formation assays separately. The miRNA and protein levels were analysed by quantitative reverse transcriptase polymerase chain reaction (qRT‐PCR) or western blotting. The relationship among miR‐221‐3p, FOXP1 and SPRY1 was determined using the dual‐luciferase reporter, ChIP and RIP assays. Results: Exosomal miR‐221‐3p was successfully isolated from BMSCs and delivered into HUVECs. HG was found to suppress the angiogenesis, cell viability and migration of HUVECs and exosomal miR‐221‐3p separated from BMSCs inhibited the above phenomenon. FOXP1 could transcriptionally upregulate SPRY1, and the silencing of FOXP1 reversed the HG‐stimulated angiogenesis inhibition, cell viability and migration in HUVECs via the downregulation of SPRY1. Meanwhile, miR‐221‐3p directly targeted FOXP1 and the overexpression of FOXP1 reversed the positive effect of exosomal miR‐221‐3p on HUVEC angiogenesis. Conclusion: Exosomal miR‐221‐3p isolated from BMSCs promoted angiogenesis in diabetic wounds through the mediation of the FOXP1/SPRY1 axis. Furthermore, the findings of this study can provide new insights into probing strategies against diabetes. [ABSTRACT FROM AUTHOR]
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- 2024
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30. Comparative mathematical modeling reveals the differential effects of high-fat diet and ketogenic diet on the PI3K-Akt signaling pathway in heart.
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Tseng, Yu-Yao
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HEART physiology , *STATISTICAL models , *CARDIOVASCULAR diseases , *KETOGENIC diet , *RESEARCH funding , *NUTRITIONAL assessment , *APOPTOSIS , *DIETARY fats , *BIOCHEMISTRY , *CELLULAR signal transduction , *DESCRIPTIVE statistics , *MICE , *GENE expression , *ANIMAL experimentation , *COMPARATIVE studies - Abstract
Background: Obesity is a global health concern associated with increased risk of diseases like cardiovascular conditions including ischemic heart disease, a leading cause of mortality. The ketogenic diet (KD) has potential therapeutic applications in managing obesity and related disorders. However, the intricate effects of KD on diverse physiological conditions remain incompletely understood. The PI3K-Akt signaling pathway is critical for heart health, and its dysregulation implicates numerous cardiac diseases. Methods: We developed comprehensive mathematical models of the PI3K-Akt signaling pathway under high-fat diet (HFD) and KD conditions to elucidate their differential impacts and quantify apoptosis. Simulations and sensitivity analysis were performed. Results: Simulations demonstrate that KD can reduce the activation of key molecules like Erk and Trp53 to mitigate apoptosis compared to HFD. Findings align with experimental data, highlighting the potential cardiac benefits of KD. Sensitivity analysis identifies regulators like Trp53 and Bcl2l1 that critically influence apoptosis under HFD. Conclusions: Mathematical modeling provides quantitative insights into the contrasting effects of HFD and KD on cardiac PI3K-Akt signaling and apoptosis. Findings have implications for precision nutrition and developing novel therapeutic strategies to address obesity-related cardiovascular diseases. [ABSTRACT FROM AUTHOR]
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- 2024
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31. Coix Sprouts Affect Triglyceride Metabolism in Huh7 Cells and High-Fat Diet-Induced Obese Mice.
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Shin, Mi-Rae, Kim, Min Ju, Lee, Jin A., Lee, Eun Song, Park, Hae-Jin, and Roh, Seong-Soo
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PREVENTION of obesity , *PLANT anatomy , *IN vitro studies , *LIPID metabolism disorders , *PHENOMENOLOGICAL biology , *RESEARCH funding , *DIETARY fats , *BIOCHEMISTRY , *IN vivo studies , *CELL lines , *MICE , *MESSENGER RNA , *GENE expression , *MEDICINAL plants , *METABOLISM , *GENETIC disorders , *ANTIOBESITY agents , *ANIMAL experimentation , *TRIGLYCERIDES , *FATTY acids , *GENETIC mutation , *OBESITY , *PHARMACODYNAMICS - Abstract
Lipolysis is the hydrolysis of triglycerides (TGs), commonly known as fats. Intracellular lipolysis of TG is associated with adipose triglyceride lipase (ATGL), which provides fatty acids during times of metabolic need. The aim of this study was to determine whether Coix lacryma-jobi L. var. ma-yuen Stapf (Coix) sprouts (CS) can alleviate obesity through lipolysis. Overall, we investigated the potential of CS under in vitro and in vivo conditions and confirmed the underlying mechanisms. Huh7 cells were exposed to free fatty acids (FFAs), and C57BL/6J mice were fed a 60% high-fat diet. When FFA were introduced into Huh7 cells, the intracellular TG levels increased within the Huh7 cells. However, CS treatment significantly reduced intracellular TG levels. Furthermore, CS decreased the expression of Pparγ and Srebp1c mRNA and downregulated the mutant Pnpla3 (I148M) mRNA. Notably, CS significantly upregulated ATGL expression. CS treatment at a dose of 200 mg/kg/day resulted in a significant and dose-dependent decrease in body weight gain and epididymal adipose tissue weight. Specifically, the group treated with CS (200 mg/kg/day) exhibited a significant modulation of serum lipid biomarkers. In addition, CS ameliorated histological alterations in both the liver and adipose tissues. In summary, CS efficiently inhibited lipid accumulation through the activation of the lipolytic enzyme ATGL coupled with the suppression of enzymes involved in TG synthesis. Consequently, CS show promise as a potential anti-obesity agent. [ABSTRACT FROM AUTHOR]
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- 2024
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32. Posttranscriptional regulation of the T-box gene midline via the 3′UTR in Drosophila is complex and cell- and tissue-dependent.
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Makhijani, Kalpana, Mar, Jordan, Gaziova, Ivana, and Bhat, Krishna Moorthi
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AMINO acid metabolism , *RNA metabolism , *DNA metabolism , *CARRIER proteins , *RESEARCH funding , *PHENOMENOLOGICAL biology , *CELL physiology , *BIOCHEMISTRY , *GENE expression , *MESSENGER RNA , *CELL culture , *CELL lines , *ANIMAL experimentation , *INSECTS , *IMMUNITY - Abstract
The T-box (Tbx) proteins have a 180–230 amino acid DNA-binding domain, first reported in the Brachyury (T) protein. They are highly conserved among metazoans. They regulate a multitude of cellular functions in development and disease. Here, we report posttranscriptional and translational regulation of midline (mid), a Tbx member in Drosophila. We found that the 3′UTR of mid has mRNA degradation elements and AT-rich sequences. In Schneider S2 cells, mid- mRNA could be detected only when the transgene was without the 3′UTR. Similarly, the 3′UTR linked to the Renilla luciferase reporter significantly reduced the activity of the Luciferase, whereas deleting only the degradation elements from the 3′UTR resulted in reduced activity, but not as much. Overexpression of mid in MP2, an embryonic neuroblast, showed no significant difference in the levels of mid- mRNA between the 2 transgenes, with and without the 3′UTR, indicating the absence of posttranscriptional regulation of mid in MP2. Moreover, while elevated mid- RNA was detected in MP2 in nearly all hemisegments, only a fifth of those hemisegments had elevated levels of the protein. Overexpression of the 2 transgenes resulted in MP2-lineage defects at about the same frequency. These results indicate a translational/posttranslational regulation of mid in MP2. The regulation of ectopically expressed mid in the wing imaginal disc was complex. In the wing disc, where mid is not expressed, the ectopic expression of the transgene lacking the 3′UTR had a higher level of mid- RNA and the protein had a stronger phenotypic effect. These results indicate that the 3′UTR can subject mid -mRNA to degradation in a cell- and tissue-specific manner. We further report a balancer-mediated transgenerational modifier effect on the expression and gain of function effects of the 2 transgenes. [ABSTRACT FROM AUTHOR]
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- 2024
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33. Recombinant Human TSH Fails to Induce the Proliferation and Migration of Papillary Thyroid Carcinoma Cell Lines.
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Kalampounias, Georgios, Varemmenou, Athina, Aronis, Christos, Mamali, Irene, Shaukat, Athanasios-Nasir, Chartoumpekis, Dionysios V., Katsoris, Panagiotis, and Michalaki, Marina
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CELL migration inhibition , *THYROID gland tumors , *PHENOMENOLOGICAL biology , *RESEARCH funding , *CELL proliferation , *PAPILLARY carcinoma , *BIOCHEMISTRY , *DESCRIPTIVE statistics , *TREATMENT effectiveness , *CELL lines , *GENE expression , *RECOMBINANT proteins , *THYROTROPIN - Abstract
Simple Summary: Serum TSH suppression in the management of PTC patients will inevitably cause iatrogenic thyrotoxicosis. Our study challenges, for the first time, the role of human recombinant thyrotropin (rh-TSH) as a mitogen on PTC cell lines. For this study, both K1 and TPC-1 cells were treated with clinically relevant rh-TSH under various conditions. The expression levels of TSHR and thyroglobulin (Tg) were determined and, subsequently, the proliferation and migration were assessed. Additionally, cells were engineered to overexpress TSHR in order to multiply TSH signal transduction. Under the conditions employed, rh-TSH was inadequate for inducing either the proliferation or the migration rate of both transformed and non-transformed cells, while Tg expression was increased. We report that, clinically speaking, rh-TSH doses cannot induce proliferation and migration in PTC cell lines, thus questioning TSH suppression in PTC patients. Further research is warranted to dissect the underlying mechanisms. These results could translate into better PTC patient management. Thyrotropin (TSH) suppression is required in the management of patients with papillary thyroid carcinoma (PTC) to improve their outcomes, inevitably causing iatrogenic thyrotoxicosis. Nevertheless, the evidence supporting this practice remains limited and weak, and in vitro studies examining the mitogenic effects of TSH in cancerous cells used supraphysiological doses of bovine TSH, which produced conflicting results. Our study explores, for the first time, the impact of human recombinant thyrotropin (rh-TSH) on human PTC cell lines (K1 and TPC-1) that were transformed to overexpress the thyrotropin receptor (TSHR). The cells were treated with escalating doses of rh-TSH under various conditions, such as the presence or absence of insulin. The expression levels of TSHR and thyroglobulin (Tg) were determined, and subsequently, the proliferation and migration of both transformed and non-transformed cells were assessed. Under the conditions employed, rh-TSH was not adequate to induce either the proliferation or the migration rate of the cells, while Tg expression was increased. Our experiments indicate that clinically relevant concentrations of rh-TSH cannot induce proliferation and migration in PTC cell lines, even after the overexpression of TSHR. Further research is warranted to dissect the underlying molecular mechanisms, and these results could translate into better management of treatment for PTC patients. [ABSTRACT FROM AUTHOR]
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- 2024
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34. A Novel Human Interleukin‐23A Overexpressing Mouse Model of Systemic Lupus Erythematosus.
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Christodoulou‐Vafeiadou, Eleni, Geka, Christina, Iliopoulou, Lida, Ntari, Lydia, Denis, Maria C., Karagianni, Niki, and Kollias, George
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THERAPEUTIC use of monoclonal antibodies , *BIOLOGICAL models , *PROTEINS , *RESEARCH funding , *PHENOMENOLOGICAL biology , *SYSTEMIC lupus erythematosus , *BIOCHEMISTRY , *FLUORESCENT antibody technique , *GENE expression , *MICE , *MONOCLONAL antibodies , *DRUG efficacy , *ANIMAL experimentation , *HISTOLOGICAL techniques , *CYTOKINES , *INTERLEUKINS , *SEQUENCE analysis , *EVALUATION - Abstract
Objective: Interleukin‐23 (IL‐23) is a crucial cytokine implicated in chronic inflammation and autoimmunity, associated with various diseases such as psoriasis, psoriatic arthritis, and systemic lupus erythematosus (SLE). This study aimed to create and characterize a transgenic mouse model overexpressing human IL‐23A (TghIL‐23A), providing a valuable tool for investigating the pathogenic role of human IL‐23A and evaluating the efficacy of anti–human IL‐23A therapeutics. Methods: TghIL‐23A mice were generated via microinjection of CBA × C57BL/6 zygotes with a fragment of the human IL23A gene, flanked by its 5′‐regulatory sequences and the 3′ untranslated region of human β‐globin. The TghIL‐23A pathology was assessed through hematologic and biochemic analyses, cytokine and antinuclear antibody detection, and histopathologic examination of skin and renal tissues. The response to the anti–human IL‐23A therapeutic agent guselkumab was evaluated in groups of eight mixed‐sex mice receiving subcutaneous treatment twice weekly for 10 weeks using clinical, biomarker, and histopathologic readouts. Results: TghIL‐23A mice exhibited interactions between human IL‐23A and mouse IL‐23/IL‐12p40 and developed a chronic multiorgan autoimmune disease marked by proteinuria, anti–double‐stranded DNA antibodies, severe inflammatory lesions in the skin, and milder phenotypes in the kidneys and lungs. The TghIL‐23A pathologic features exhibited significant similarities to those observed in human patients with SLE, and they were reversed following guselkumab treatment. Conclusion: We have generated and characterized a novel genetic mouse model of SLE, providing proof‐of‐concept for the etiopathogenic role of human IL‐23A. This new model has a normal life span and integrates several characteristics of the human disease's complexity and chronicity, making it an attractive preclinical tool for studying IL‐23–dependent pathogenic mechanisms and assessing the efficacy of anti–human IL‐23A or modeled disease‐related therapeutics. [ABSTRACT FROM AUTHOR]
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- 2024
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35. Regulation of the Lewis Blood Group Antigen Expression: A Literature Review Supplemented with Computational Analysis.
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Wipplinger, Martin, Mink, Sylvia, Bublitz, Maike, and Gassner, Christoph
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ANTIGEN analysis , *RNA-binding proteins , *EPITHELIAL cells , *PHENOMENOLOGICAL biology , *NEOPLASTIC cell transformation , *MICRORNA , *EPIGENOMICS , *BLOOD groups , *TRANSCRIPTION factors , *BIOCHEMISTRY , *HUMAN microbiota , *GENE expression , *BIOINFORMATICS , *GENETIC polymorphisms , *INFLAMMATORY bowel diseases , *DIGESTIVE organs , *VIRUS diseases , *TUMORS , *GENOTYPES - Abstract
Background: The Lewis (Le) blood group system, unlike most other blood groups, is not defined by antigens produced internally to the erythrocytes and their precursors but rather by glycan antigens adsorbed on to the erythrocyte membrane from the plasma. These oligosaccharides are synthesized by the two fucosyltransferases FUT2 and FUT3 mainly in epithelial cells of the digestive tract and transferred to the plasma. At their place of synthesis, some Lewis blood group carbohydrate antigen variants also seem to be involved in various gastrointestinal malignancies. However, relatively little is known about the transcriptional regulation of FUT2 and FUT3. Summary: To address this question, we screened existing literature and additionally used in silico prediction tools to identify novel candidate regulators for FUT2 and FUT3 and combine these findings with already known data on their regulation. With this approach, we were able to describe a variety of transcription factors, RNA binding proteins and microRNAs, which increase FUT2 and FUT3 transcription and translation upon interaction. Key Messages: Understanding the regulation of FUT2 and FUT3 is crucial to fully understand the blood group system Lewis (ISBT 007 LE) phenotypes, to shed light on the role of the different Lewis antigens in various pathologies, and to identify potential new diagnostic targets for these diseases. Plain Language Summary: The Lewis (Le) blood group system, in contrast to the majority of blood groups, is not able to synthesize its antigens itself. It depends on the attachment of different oligosaccharides to the erythrocyte membrane, which are adsorbed from the plasma. These glycans are modified by the fucosyltransferases 2 and 3 enzymes (FUT2/3). Beside their role in defining the Lewis blood group, FUT2 and FUT3 are also known to be involved in the susceptibility and progression of various gastrointestinal pathologies, like inflammatory bowel diseases (IBD) or colorectal cancer (CRC). Even though different expression levels of FUT2 and FUT3 have been described in these malignancies, relatively little is known about the mechanisms behind their transcriptional regulation. In this review, we aim to shed light on transcription factors (TFs) responsible for FUT2 and FUT3 expression as well as on post-transcriptional regulators by the means of RNA binding proteins (RBPs) and microRNAs (miRNAs). To achieve our goal, we combined previous knowledge on FUT2 and FUT3 expression regulation with a computational analysis to predict additional novel regulators. On this way, we are able to broaden our knowledge on FUT2 and FUT3 expression regulation and consequently might be able to transfer our findings into diagnostics or therapeutics in the future. [ABSTRACT FROM AUTHOR]
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- 2024
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36. Targeting BRD4 attenuates the stemness and aggressiveness of ameloblastoma.
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Xie, Jiaxiang, Zhang, Jingqi, Xiong, Gan, Ouyang, Shengqi, Yun, Bokai, Xu, Xiuyun, Wang, Wenjin, Zhang, Ming, Xie, Nan, Chen, Demeng, and Wang, Cheng
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CELL migration , *PEARSON correlation (Statistics) , *BROMODOMAIN-containing proteins , *PHENOMENOLOGICAL biology , *T-test (Statistics) , *RESEARCH funding , *BIOCHEMISTRY , *GENE expression , *IMMUNOHISTOCHEMISTRY , *RNA , *BIOINFORMATICS , *MICROBIOLOGICAL assay , *DRUG efficacy , *ANALYSIS of variance , *ONE-way analysis of variance , *STEM cells , *CARCINOGENESIS , *AMELOBLASTOMA , *SEQUENCE analysis , *DISEASE progression , *WNT proteins , *EVALUATION - Abstract
Background: BRD4, belonging to the bromodomain extra‐terminal (BET) protein family, plays a unique role in tumor progression. However, the potential impact of BRD4 in ameloblastoma (AM) remains largely unknown. Herein, we aimed to assess the expression and functional role of BRD4 in AM. Methods: The expression level of BRD4 was assessed by immunohistochemistry. The proliferation, migration, invasion, and tumorigenic abilities of AM cells were assessed by a series of assays. To explore the molecular expression profile of BRD4‐depleted AM cells, RNA sequencing (RNA‐seq) was performed. Bioinformatic analysis was performed on AM expression matrices obtained from the Gene Expression Omnibus (GEO). The therapeutic efficacy of BET‐inhibitors (BETi) was assessed with AM patient‐derived organoids. Results: Upregulation of BRD4 was observed in conventional AMs, recurrent AMs, and ameloblastic carcinomas. Depletion of BRD4 inhibited proliferation, invasion, migration, and tumorigenesis in AM. Administration of BETi attenuated the aggressiveness of AM and the growth of AM patient‐derived organoids. Bioinformatic analysis indicated that BRD4 may promote AM progression by regulating the Wnt pathway and stemness‐associated pathways. Conclusion: BRD4 increases the aggressiveness and promotes the recurrence of ameloblastoma by regulating the Wnt pathway and stemness‐associated pathways. These findings highlight BRD4 as a promising therapeutic target in AM management. [ABSTRACT FROM AUTHOR]
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- 2024
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37. Unveiling the hidden players: noncoding RNAs orchestrating polyamine metabolism in disease
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Marianna Nicoletta Rossi, Cristian Fiorucci, Paolo Mariottini, and Manuela Cervelli
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Polyamines ,Noncoding RNA ,Gene expression ,Polyamine metabolism ,Biotechnology ,TP248.13-248.65 ,Biology (General) ,QH301-705.5 ,Biochemistry ,QD415-436 - Abstract
Abstract Polyamines (PA) are polycations with pleiotropic functions in cellular physiology and pathology. In particular, PA have been involved in the regulation of cell homeostasis and proliferation participating in the control of fundamental processes like DNA transcription, RNA translation, protein hypusination, autophagy and modulation of ion channels. Indeed, their dysregulation has been associated to inflammation, oxidative stress, neurodegeneration and cancer progression. Accordingly, PA intracellular levels, derived from the balance between uptake, biosynthesis, and catabolism, need to be tightly regulated. Among the mechanisms that fine-tune PA metabolic enzymes, emerging findings highlight the importance of noncoding RNAs (ncRNAs). Among the ncRNAs, microRNA, long noncoding RNA and circRNA are the most studied as regulators of gene expression and mRNA metabolism and their alteration have been frequently reported in pathological conditions, such as cancer progression and brain diseases. In this review, we will discuss the role of ncRNAs in the regulation of PA genes, with a particular emphasis on the changes of this modulation observed in health disorders.
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- 2024
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38. Bradykinin promotes immune responses in differentiated embryonic neurospheres carrying APPswe and PS1dE9 mutations
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Guilherme Juvenal, Carine Meinerz, Ana Carolina Ayupe, Henrique Correia Campos, Eduardo Moraes Reis, Beatriz Monteiro Longo, Micheli Mainardi Pillat, and Henning Ulrich
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Alzheimer’s disease ,Immune response ,Stem cells ,Gene expression ,Biological system ,Biotechnology ,TP248.13-248.65 ,Biology (General) ,QH301-705.5 ,Biochemistry ,QD415-436 - Abstract
Abstract Background Neural progenitor cells (NPCs) can be cultivated from developing brains, reproducing many of the processes that occur during neural development. They can be isolated from a variety of animal models, such as transgenic mice carrying mutations in amyloid precursor protein (APP) and presenilin 1 and 2 (PSEN 1 and 2), characteristic of familial Alzheimer’s disease (fAD). Modulating the development of these cells with inflammation-related peptides, such as bradykinin (BK) and its antagonist HOE-140, enables the understanding of the impact of such molecules in a relevant AD model. Results We performed a global gene expression analysis on transgenic neurospheres treated with BK and HOE-140. To validate the microarray data, quantitative real-time reverse-transcription polymerase chain reaction (RT-PCR) was performed on 8 important genes related to the immune response in AD such as CCL12, CCL5, CCL3, C3, CX3CR1, TLR2 and TNF alpha and Iba-1. Furthermore, comparative analysis of the transcriptional profiles was performed between treatments, including gene ontology and reactome enrichment, construction and analysis of protein-protein interaction networks and, finally, comparison of our data with human dataset from AD patients. The treatments affected the expression levels of genes mainly related to microglia-mediated neuroinflammatory responses, with BK promoting an increase in the expression of genes that enrich processes, biological pathways, and cellular components related to immune dysfunction, neurodegeneration and cell cycle. B2 receptor inhibition by HOE-140 resulted in the reduction of AD-related anomalies caused in this system. Conclusions BK is an important immunomodulatory agent and enhances the immunological changes identified in transgenic neurospheres carrying the genetic load of AD. Bradykinin treatments modulate the expression rates of genes related to microglia-mediated neuroinflammation. Inhibiting bradykinin activity in Alzheimer’s disease may slow disease progression.
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- 2024
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39. P-hydroxybenzaldehyde protects Caenorhabditis elegans from oxidative stress and β-amyloid toxicity*.
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Xingzhi Yu, Jie Tao, Tian Xiao, and Xiaohua Duan
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BIOLOGICAL models ,GLUCOSE ,ALZHEIMER'S disease ,RESEARCH funding ,PHENOMENOLOGICAL biology ,T-test (Statistics) ,POLYMERASE chain reaction ,OXIDATIVE stress ,IN vivo studies ,CELLULAR signal transduction ,BIOCHEMISTRY ,DESCRIPTIVE statistics ,PLANT extracts ,ANTI-infective agents ,REACTIVE oxygen species ,RNA ,GENE expression ,LOG-rank test ,ANTIOXIDANTS ,ANIMAL experimentation ,MOLECULAR structure ,MEDICINAL plants ,ONE-way analysis of variance ,CAENORHABDITIS elegans ,PHYSIOLOGICAL stress ,STAINS & staining (Microscopy) ,SURVIVAL analysis (Biometry) ,COMPARATIVE studies ,DATA analysis software ,AMYLOID beta-protein precursor ,BIOMARKERS ,LONGEVITY ,PARALYSIS ,SEQUENCE analysis ,PHARMACODYNAMICS - Abstract
Introduction: Gastrodia elata is the dried tuber of the orchid Gastrodia elata Bl. It is considered a food consisting of a source of precious medicinal herbs, whose chemical composition is relatively rich. Gastrodia elata and its extracted fractions have been shown to have neuroprotective effects. P-hydroxybenzaldehyde (p-HBA), as one of the main active components of Gastrodia elata, has antiinflammatory, antioxidative stress, and cerebral protective effects, which has potential for the treatment of Alzheimer's disease (AD). The aim of this study was to verify the role of p-HBA in AD treatment and to investigate its mechanism of action in depth based using the Caenorhabditis elegans (C. elegans) model. Methods: In this study, we used paralysis, lifespan, behavioral and antistress experiments to investigate the effects of p-HBA on AD and aging. Furthermore, we performed reactive oxygen species (ROS) assay, thioflavin S staining, RNA-seq analysis, qPCR validation, PCR Array, and GFP reporter gene worm experiment to determine the anti-AD effects of p-HBA, as well as in-depth studies on its mechanisms. Results: p-HBA was able to delay paralysis, improve mobility and resistance to stress, and delay aging in the AD nematode model. Further mechanistic studies showed that ROS and lipofuscin levels, Aβ aggregation, and toxicity were reduced after p-HBA treatment, suggesting that p-HBA ameliorated Aβ-induced toxicity by enhancing antioxidant and anti-aging activity and inhibiting Aβ aggregation. p-HBA had a therapeutic effect on AD by improving stress resistance, as indicated by the down-regulation of NLP-29 and UCR-11 expression and up-regulation of PQN-75 and LYS-3 expression. In addition, the gene microarray showed that p-HBA treatment played a positive role in genes related to AD, anti-aging, ribosomal protein pathway, and glucose metabolism, which were collectively involved in the anti-AD mechanism of p-HBA. Finally, we also found that p-HBA promoted nuclear localization of DAF-16 and increased the expression of SKN-1, SOD-3, and GST-4, which contributed significantly to inhibition of Aβ toxicity and enhancement of antioxidative stress. Conclusion: Our work suggests that p-HBA has some antioxidant and antiaging activities. It may be a viable candidate for the treatment and prevention of Alzheimer's disease. [ABSTRACT FROM AUTHOR]
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- 2024
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40. Prolonged Cadmium Exposure and Osteoclastogenesis: A Mechanistic Mouse and in Vitro Study.
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Zhiyuan Liu, Jinzhi Wu, Zhe Dong, Yanshuai Wang, Gang Wang, Chengjie Chen, Huihui Wang, Yang Yang, Yongxin Sun, Maowei Yang, Jingqi Fu, Jiliang Li, Qiang Zhang, Yuanyuan Xu, and Jingbo Pi
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PROTEIN metabolism , *BONE resorption , *IN vitro studies , *RESEARCH funding , *PHENOMENOLOGICAL biology , *T-test (Statistics) , *DATA analysis , *CADMIUM , *COMPUTED tomography , *KRUSKAL-Wallis Test , *BIOCHEMISTRY , *CELLULAR signal transduction , *REVERSE transcriptase polymerase chain reaction , *DESCRIPTIVE statistics , *MICE , *CELL culture , *RNA , *GENE expression , *HISTOLOGICAL techniques , *WESTERN immunoblotting , *ONE-way analysis of variance , *STATISTICS , *HEMATOPOIETIC stem cells , *NUCLEAR factor E2 related factor , *GENETIC testing , *GENOTYPES , *BIOMARKERS ,BONE marrow examination - Abstract
BACKGROUND: Cadmium (Cd) is a highly toxic and widespread environmental oxidative stressor that causes a myriad of health problems, including osteoporosis and bone damage. Although nuclear factor erythroid 2-related factor 2 (NRF2) and its Cap ‘n’ Collar and basic region Leucine Zipper (CNC-bZIP) family member nuclear factor erythroid 2-related factor 1 (NRF1) coordinate various stress responses by regulating the transcription of a variety of antioxidant and cytoprotective genes, they play distinct roles in bone metabolism and remodeling. However, the precise roles of both transcription factors in bone loss induced by prolonged Cd exposure remain unclear. OBJECTIVES: We aimed to understand the molecular mechanisms underlying Cd-induced bone loss, focusing mainly on the roles of NRF2 and NRF1 in osteoclastogenesis provoked by Cd. METHODS: Male wild-type (WT), global Nrf2-knockout (Nrf2-/-) and myeloid-specific Nrf2 knockout [Nrf2(M)-KO] mice were administered Cd (50 or 100 ppm) via drinking water for 8 or 16 wk, followed by micro-computed tomography, histological analyses, and plasma biochemical testing. Osteoclastogenesis was evaluated using bone marrow-derived osteoclast progenitor cells (BM-OPCs) and RAW 264.7 cells in the presence of Cd (10 or 20 nM) with a combination of genetic and chemical modulations targeting NRF2 and NRF1. RESULTS: Compared with relevant control mice, global Nrf2-/- or Nrf2(M)-KO mice showed exacerbated bone loss and augmented osteoclast activity following exposure to 100 ppm Cd in drinking water for up to 16 wk. In vitro osteoclastogenic analyses suggested that Nrf2-deficient BM-OPCs and RAW 264.7 cells responded more robustly to low levels of Cd (up to 20 nM) with regard to osteoclast differentiation compared with WT cells. Further mechanistic studies supported a compensatory up-regulation of long isoform of NRF1 (L-NRF1) and subsequent induction of nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1 (NFATc1) as the key molecular events in the Nrf2 deficiency-worsened and Cd-provoked osteoclastogenesis. L-Nrf1 silenced (via lentiviral means) Nrf2-knockdown (KD) RAW cells exposed to Cd showed dramatically different NFATc1 and subsequent osteoclastogenesis outcomes compared with the cells of Nrf2-KD alone exposed to Cd, suggesting a mitigating effect of the Nrf1 silencing. In addition, suppression of reactive oxygen species by exogenous antioxidants N-acetyl-L-cysteine (2 mM) and mitoquinone mesylate (MitoQ; 0.2 μM) mitigated the L-NRF1-associated effects on NFATc1-driven osteoclastogenesis outcomes in Cd-exposed Nrf2-KD cells. CONCLUSIONS: This in vivo and in vitro study supported the authors’ hypothesis that Cd exposure caused bone loss, in which NRF2 and L-NRF1 responded to Cd and osteoclastogenic stimuli in a cooperative, but contradictive, manner to coordinate Nfatc1 expression, osteoclastogenesis and thus bone homeostasis. Our study suggests a novel strategy targeting NRF2 and L-NRF1 to prevent and treat the bone toxicity of Cd. [ABSTRACT FROM AUTHOR]
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- 2024
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41. Modest effect of differential dietary vitamin A intake on the pathogenesis of alcohol‐associated liver disease.
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Ferdouse, Afroza and Clugston, Robin D.
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VITAMIN A metabolism , *LIPID metabolism , *HIGH performance liquid chromatography , *FOOD consumption , *FATTY liver , *T-test (Statistics) , *DATA analysis , *RESEARCH funding , *VITAMIN A , *POLYMERASE chain reaction , *ALCOHOLIC liver diseases , *BIOCHEMISTRY , *VITAMIN A deficiency , *MICE , *GENE expression , *ANIMAL experimentation , *WESTERN immunoblotting , *ANALYSIS of variance , *STATISTICS , *INFLAMMATION , *COLLECTION & preservation of biological specimens , *ALCOHOLS (Chemical class) , *DATA analysis software , *DIETARY supplements , *HISTOLOGY , *BIOMARKERS - Abstract
Background: Chronic alcohol consumption is a major public health issue. The primary organ damaged by alcohol abuse is the liver, leading to alcohol‐associated liver disease (ALD). ALD begins with hepatic steatosis and can progress to fibrosis and cirrhosis; however, we have an incomplete understanding of ALD pathogenesis. Interestingly, the liver is also the major organ for vitamin A metabolism and storage, and ALD has previously been linked with altered hepatic vitamin A homeostasis. We hypothesize that alcohol‐induced vitamin A depletion disrupts its normal function in the liver, contributing to the pathogenesis of ALD. To test this hypothesis, we postulated that adding copious vitamin A to the diet might alleviate ALD, and conversely, that a vitamin A deficient diet would worsen ALD. Methods: We conducted two dietary intervention studies in mice comparing deficient (0 IU/g diet) and copious (25 IU/g diet) dietary vitamin A intake versus control (4 IU/g diet), using the NIAAA chronic‐binge model of ALD. Hepatic steatosis was assessed using histopathological and biochemical approaches. Tissue Vitamin A levels were measured using high‐performance liquid chromatography. Markers of ALD, hepatic inflammation and lipid metabolism were analyzed by the quantitative polymerase chain reaction and western blotting. Results: As expected, a 0 IU/g Vitamin A diet decreased, and a 25 IU/g Vitamin A diet increased hepatic Vitamin A stores. However, alcohol induced changes in hepatic triglyceride levels, markers of hepatic lipid metabolism, inflammation and fibrosis were not significantly different in mice consuming a copious or deficient vitamin A diet compared to control. Conclusions: Altered vitamin A intake and hepatic vitamin A storage have a minor effect on the pathogenesis of ALD. Thus, given the known link between altered retinoic acid signaling and ALD, future studies that further explore this linkage are warranted. [ABSTRACT FROM AUTHOR]
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- 2024
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42. Relationship between GTSE1 and Cell Cycle and Potential Regulatory Mechanisms in Lung Cancer Cells.
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Chuanlin WANG, Jiali XU, Mingzhu LIU, Jiayu LIU, Yunchao HUANG, and Lan ZHOU
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PROTEIN kinase inhibitors ,CELL cycle proteins ,PHENOMENOLOGICAL biology ,RESEARCH funding ,CELL proliferation ,APOPTOSIS ,CELL cycle ,CELLULAR signal transduction ,BIOCHEMISTRY ,CELL lines ,GENE expression ,LUNG tumors - Abstract
The regulation of the cell cycle is essential for maintaining normal cellular function, especially in the development of diseases such as lung cancer. The cell cycle consists of four major phases (G1, S, G2 and M phases), which are characterized by a series of precise molecular events to ensure proper cell proliferation and division. In lung cancer cells, cell cycle dysregulation can lead to disordered proliferation and increased invasiveness of cancer cells. G2 and S-phase expressed 1 (GTSE1) is a regulatory protein found in the cytoplasm of the cell, which plays a key role in the cell cycle distribution of a wide range of cancer cells and is involved in life processes such as cell proliferation and apoptosis. GTSE1 affects cell cycle progression by interacting with cyclin-dependent kinase inhibitor 1A (p21) and maintaining the stability of p21, which in turn inhibits the activity of cyclin-dependent kinase 1/2 (CDK1/2). In addition, GTSE1 is also involved in the regulation of tumor protein 53 (p53) signaling pathway. With the assistance of mouse double minute 2 homolog (MDM2), GTSE1 is able to transport p53 from the nucleus to the cytoplasm and promote its ubiquitination and degradation, thus affecting cell cycle and cell deathrelated signaling pathways. This paper reviews the expression of GTSE1 in lung cancer cells and its effects on lung cancer, as well as its potential mechanisms involved in cell cycle regulation. [ABSTRACT FROM AUTHOR]
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- 2024
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43. Pien Tze Huang Inhibits Proliferation of Colorectal Cancer Cells through Suppressing PNO1 Expression and Activating p53/p21 Signaling Pathway.
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Cao, Liu-jing, Liu, Li-ya, Chen, You-qin, Han, Yu-ying, Wei, Li-hui, Yao, Meng-ying, Fang, Yi, Wu, Mei-zhu, Cheng, Ying, Sferra, Thomas J., Liu, Hui-xin, Li, Li, Peng, Jun, and Shen, A.-ling
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CHINESE medicine ,IN vitro studies ,PHENOMENOLOGICAL biology ,HERBAL medicine ,CELL proliferation ,POLYMERASE chain reaction ,APOPTOSIS ,COLORECTAL cancer ,CELLULAR signal transduction ,QUANTITATIVE research ,IN vivo studies ,BIOCHEMISTRY ,GENE expression ,MICE ,ANIMAL experimentation ,WESTERN immunoblotting ,CELL survival ,GENETIC techniques - Abstract
Objective: To explore the regulatory effect of Pien Tze Huang (PZH) on targeting partner of NOB1 (PNO1) and it's down-stream mediators in colorectal cancer (CRC) cells. Methods: Quantitative polymerase chain reaction was performed to determine mRNA levels of PNO1, TP53, and CDKN1A. Western blotting was performed to determine protein levels of PNO1, p53, and p21. HCT-8 cells were transduced with a lentivirus over-expressing PNO1. Colony formation assay was used to detect cell survival in PNO1 overexpression of HCT-8 cells after PZH treatment. Cell-cycle distribution, cell viability and cell apoptosis were performed to identify the effect of PNO1 overexpression on cell proliferation and apoptosis of HCT-8 cells after PZH treatment. Xenograft BALB/c nude mice bearing HCT116 cells transduced with sh-PNO1 or sh-Ctrl lentivirus were evaluated. Western blot assay was performed to detect PNO1, p53, p21 and PCNA expression in tumor sections. Terminal deoxynucleotidyl transferase dUTP nick end labling (TUNEL) assay was used to determine the apoptotic cells in tissues. Results: PZH treatment decreased cell viability, down-regulated PNO1 expression, and up-regulated p53 and p21 expressions in HCT-8 cells (P<0.05). PNO1 overexpression attenuated the effects of PZH treatment, including the expression of p53 and p21, cell growth, cell viability, cell cycle arrest and cell apoptosis in vitro (P<0.05). PNO1 knockdown eliminated the effects of PZH treatment on tumor growth, inhibiting cell proliferation inhibition and apoptosis induction in vivo (P<0.05). Similarly, PNO1 knockdown attenuated the effects of PZH treatment on the down-regulation of PNO1 and up-regulation of p53 and p21 in vivo (P<0.05). Conclusion: The mechanism by which PZH induces its CRC anti-proliferative effect is at least in part by regulating the expression of PNO1 and its downstream targets p53 and p21. [ABSTRACT FROM AUTHOR]
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- 2024
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44. Serum stromal cell-derived factor-1 concentrations are increased and associated with nonalcoholic fatty liver disease in children with obesity.
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Liu, Yuesheng, Hao, Lijun, Wang, Linhao, Lu, Mengnan, Yin, Chunyan, and Xiao, Yanfeng
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BLOOD serum analysis , *NON-alcoholic fatty liver disease , *CHEMOKINES , *STATISTICAL correlation , *BASAL metabolism , *DOPPLER ultrasonography , *BODY mass index , *ADIPOSE tissues , *HOMEOSTASIS , *RESEARCH funding , *ENZYME-linked immunosorbent assay , *ASPARTATE aminotransferase , *MULTIPLE regression analysis , *BIOCHEMISTRY , *GENE expression , *STROMAL cells , *RESEARCH , *WAIST-hip ratio , *ALANINE aminotransferase , *CHOLESTEROL , *CHILDHOOD obesity , *SYSTOLIC blood pressure , *TRIGLYCERIDES , *BIOMARKERS , *CHILDREN - Abstract
Introduction: Stromal cell-derived factor-1 (SDF-1) is a newly discovered small molecule adipocytokine, and research has shown that it is closely related to the occurrence and development of obesity. However, there are currently few research reports on SDF-1 in childhood obesity and nonalcoholic fatty liver disease (NAFLD), and this study aims to explore the relationship between SDF-1 and obesity related indicators in obese children. Methods: Serum SDF-1 concentrations were measured using enzyme-linked immunosorbent assay (ELISA). Clinical and biochemical data were collected, such as body mass index (BMI), waist and hip circumference, blood pressure, liver enzymes, cholesterol, and fasting insulin. Children with NAFLD or not were evaluated through Color Doppler Ultrasound. Results: Serum SDF-1 concentrations were significantly higher in obese subjects than in non-obese subjects (P < 0.05), and were elevated in the NAFLD obese subjects than in the non-NAFLD obese subjects (P < 0.05). SDF-1 was positively correlated with BMI, waist-to-hip ratio, systolic blood pressure, body fat percentage (BFP), basal metabolic rate (BMR), alanine transaminase (ALT), aspartate transaminase (AST), glutyltranspeptidase (GT), and homoeostasis model of HOMA-IR, independent of their uric acid (UA), total cholesterol (TC), triglycerides (TG), high-density lipoprotein (HDL), low-density lipoprotein (LDL), very-low-density lipoprotein (VLDL), gender and age. BFP and BMR were associated with the serum SDF-1 concentrations in multivariable linear regression analysis. Conclusion: These results suggest that SDF-1 levels are elevated in obese children and are associated with NAFLD, indicating that SDF-1 may play a role in the development of childhood obesity and metabolic disorders. [ABSTRACT FROM AUTHOR]
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- 2024
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45. Dietary Protein Optimization for Growth and Immune Enhancement in Juvenile Hybrid Sturgeon (Acipenser baerii × A. schrenckii): Balancing Growth Performance, Serum Biochemistry, and Expression of Immune-Related Genes.
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Wang, Chang'an, Liu, Entong, Zhang, Hui, Shi, Honghe, Qiu, Guangwen, Lu, Shaoxia, Han, Shicheng, Jiang, Haibo, and Liu, Hongbai
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DIETARY proteins , *LEUCINE , *ACIPENSER , *GLUTAMIC acid , *IMMUNOGLOBULIN M , *ESSENTIAL amino acids , *BIOCHEMISTRY , *STURGEONS - Abstract
Simple Summary: This research assessed the effects of dietary protein levels on juvenile hybrid sturgeon growth and health over 12 weeks, with protein levels varying from 30% to 45%. It identified an optimal protein range of 35.9% to 38.3%, which maximized weight gain, improved protein efficiency, and enhanced serum health indicators, including essential amino acid content. Immune system performance also peaked within this range, correlating with increased activity of growth and immune-related genes in the intestine, indicating diet–gene interaction. Exceeding this range showed no additional benefits and could harm the fish. These findings underline the necessity of fine-tuning dietary protein for optimal aquaculture outcomes in hybrid sturgeon. This study aimed to evaluate the effects of dietary protein levels on growth performance, serum indices, body amino acid composition, and intestinal gene expression in juvenile hybrid sturgeon (Acipenser baerii × A. schrenckii). Hybrid sturgeons (initial weight 29.21 ± 2.04 g) were fed isolipidic diets containing 30%, 33%, 36%, 39%, 42% or 45% crude protein for 12 weeks (n = 18 tanks, 30 fish/tank). Results showed significant differences between treatments, where weight gain and protein efficiency ratio peaked optimally between 35.9% and 38.3% dietary protein. Serum parameters such as glucose, alanine aminotransferase, aspartate aminotransferase, superoxide dismutase, and lipid peroxidation levels varied significantly with changes in dietary protein levels. Specifically, the highest enzymatic activities and growth parameters were observed in groups fed with 33% to 39% protein, enhancing whole-body concentrations of lysine, leucine, phenylalanine, proline, and glutamic acid. Immune parameters such as immunoglobulin M and lysozyme activity also showed peak levels at higher protein concentrations, particularly notable at 42% for lysozyme and 36% for both component 3 and immunoglobulin M. Gene expression related to immune and growth pathways, including MyD88, TLR1, IL-8, IL-6, NF-κB, and IL1β, was significantly upregulated at protein levels of 33% to 36%, with a noted peak in expression at 39% for TLR1, IL-10, and TOR signaling genes, before diminishing at higher protein levels. Overall, the dietary protein requirement for juvenile hybrid sturgeon ranges from 35.9% to 38.3% crude protein. [ABSTRACT FROM AUTHOR]
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- 2024
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46. Gene of the month: the uroplakins.
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Sivakumaar, Krithicck, Griffin, Jon, Schofield, Ella, Catto, James W. F., and Jubber, Ibrahim
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UROTHELIUM ,BIOCHEMISTRY ,MOLECULAR biology ,URODYNAMICS ,TRANSITIONAL cell carcinoma ,BREAST ,GENES ,GENE expression - Published
- 2024
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47. Association of DOK3 and infiltrated tumor-associated macrophages with risk for the prognosis of Porphyromonas gingivalis-infected oral cancer: a 12-year data analysis of 200 patients from a tertiary teaching hospital, Urumqi, China.
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Li, Chenxi, Li, Muqiu, Wei, Wei, Wang, Zhengye, Yu, Jingwen, and Gong, Zhongcheng
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SURVIVAL rate , *ORAL cancer , *TEACHING hospitals , *PROGNOSIS , *GENE expression - Abstract
Background: While there is an understanding of the association between the expression of Porphyromonas gingivalis (P. gingivalis) and prognosis of oral squamous cell carcinoma (OSCC), significance specially to address the relevance between different immunohistochemical intensities of P. gingivalis and tumor-associated macrophages (TAMs) in OSCC tissue and related clinicopathologic characteristics has not been well investigated. The present study aimed to investigate the pathological features related to M2-TAM in P. gingivalis-infected OSCC and ascertain its clinical relevance with patients' prognosis. Methods: A prospective cohort study was designed to comparatively analyze 200 patients from June 2008 to June 2020. Bioinformatics analyses were implemented to identify DOK3 as a key molecule and to appraise immunocyte infiltration using Gene Expression Omnibus and The Cancer Genome Atlas databases. Immunohistochemical evaluation was performed to analyze the association between the expression levels of P. gingivalis, DOK3, and M2-TAM and clinicopathological variables using Fisher's exact test or Pearson's chi-square test. Cox analysis was used to calculate hazard ratios (HR) with corresponding 95% confidence interval (CI) for various clinicopathological features. The Kaplan–Meier approach and log-rank test were used to plot the survival curves. Results: The expression level of P. gingivalis was positively associated with DOK3 and M2-TAMs expression level (P < 0.001). Parameters, including body mass index, clinical stage, recurrence, tumor differentiation, and P. gingivalis, DOK3, and M2-TAM immunoexpression levels, affected the prognosis of patients with OSCC (all P < 0.05). In addition, P. gingivalis (HR = 1.674, 95%CI 1.216–4.142, P = 0.012), DOK3 (HR = 1.881, 95%CI 1.433–3.457, P = 0.042), and M2-TAM (HR = 1.649, 95%CI 0.824–3.082, P = 0.034) were significantly associated with the 10-year cumulative survival rate. Conclusions: Elevated expression of P. gingivalis and DOK3 indicates M2-TAM infiltration and unfavorable prognosis of OSCC, and could be considered as three novel independent risk factors for predicting the prognosis of OSCC. [ABSTRACT FROM AUTHOR]
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- 2024
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48. Biochemistry and transcriptomic analyses of Phthorimaeaabsoluta (Lepidoptera: Gelechiidae) response to insecticides.
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Karanu, Samantha W., Ajene, Inusa J., Lelmen, Elijah K., Ong'onge, Maureen A., Akutse, Komivi S., and Khamis, Fathiya M.
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INSECTICIDES , *GELECHIIDAE , *BIOCHEMISTRY , *METABOLIC detoxification , *GENE expression , *TRANSCRIPTOMES - Abstract
Phthorimaeaabsoluta is an invasive solanaceous plant pest with highly devastating effects on tomato plant. Heavy reliance on insecticide use to tackle the pest has been linked to insecticide resistance selection in P.absoluta populations. To underline insights on P.absoluta insecticide resistance mechanisms to diamides and avermectins, we evaluated the transcriptomic profile of parental (field-collected) and F8 (lab-reared) populations. Furthermore, to screen for the presence of organophosphate and pyrethroid resistance, we assessed the gene expression levels of acetylcholinesterase (ace1) and para-type voltage-gated sodium channel (VGSG) genes in the F1 to F8 lab-reared progeny of diamide and avermectin exposed P.absoluta field-collected populations. The VGSG gene showed up-regulation in 12.5% and down-regulation in 87.5% of the screened populations, while ace1 gene showed up-regulation in 37.5% and down-regulation in 62.5% of the screened populations. Gene ontology of the differentially expressed genes from both parental and eighth generations of diamide-sprayed P.absoluta populations revealed three genes involved in the metabolic detoxification of diamides in P.absoluta. Therefore, our study showed that the detoxification enzymes found could be responsible for P.absoluta diamide-based resistance, while behavioural resistance, which is stimulus-dependent, could be attributed to P.absoluta avermectin resistance. [ABSTRACT FROM AUTHOR]
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- 2024
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49. Distinct genomic contexts predict gene presence–absence variation in different pathotypes of Magnaporthe oryzae.
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Joubert, Pierre M and Krasileva, Ksenia V
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ANTIFUNGAL agents , *GENOMICS , *RESEARCH funding , *PHENOMENOLOGICAL biology , *WHEAT , *RICE , *EPIGENOMICS , *FUNGI , *DESCRIPTIVE statistics , *BIOCHEMISTRY , *DNA , *GENE expression , *GENETIC variation , *PLANT extracts , *HISTONES , *PLANT diseases - Abstract
Fungi use the accessory gene content of their pangenomes to adapt to their environments. While gene presence–absence variation contributes to shaping accessory gene reservoirs, the genomic contexts that shape these events remain unclear. Since pangenome studies are typically species-wide and do not analyze different populations separately, it is yet to be uncovered whether presence–absence variation patterns and mechanisms are consistent across populations. Fungal plant pathogens are useful models for studying presence–absence variation because they rely on it to adapt to their hosts, and members of a species often infect distinct hosts. We analyzed gene presence–absence variation in the blast fungus, Magnaporthe oryzae (syn. Pyricularia oryzae), and found that presence–absence variation genes involved in host–pathogen and microbe–microbe interactions may drive the adaptation of the fungus to its environment. We then analyzed genomic and epigenomic features of presence–absence variation and observed that proximity to transposable elements, gene GC content, gene length, expression level in the host, and histone H3K27me3 marks were different between presence–absence variation genes and conserved genes. We used these features to construct a model that was able to predict whether a gene is likely to experience presence–absence variation with high precision (86.06%) and recall (92.88%) in M. oryzae. Finally, we found that presence–absence variation genes in the rice and wheat pathotypes of M. oryzae differed in their number and their genomic context. Our results suggest that genomic and epigenomic features of gene presence–absence variation can be used to better understand and predict fungal pangenome evolution. We also show that substantial intra-species variation can exist in these features. [ABSTRACT FROM AUTHOR]
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- 2024
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50. Role of the Atypical MAPK ERK3 in Cancer Growth and Progression.
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Elkhadragy, Lobna, Myers, Amanda, and Long, Weiwen
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MITOGEN-activated protein kinases , *PHENOMENOLOGICAL biology , *CANCER invasiveness , *DRUG resistance in cancer cells , *CHALONES , *CELL proliferation , *BIOCHEMISTRY , *CELL motility , *CELLULAR signal transduction , *GENE expression , *CANCER chemotherapy , *ONCOGENES , *TUMORS , *TRANSFERASES , *MOLECULAR biology , *DISEASE progression - Abstract
Simple Summary: Extracellular signal-regulated kinase 3 (ERK3) is a member of the atypical mitogen-activated protein kinase (MAPK) subfamily. While it remains largely unknown regarding the upstream stimuli and regulators for its kinase activation, ERK3 has been shown to play important roles in physiological processes and cancers. This review discusses the growing body of work that unveils the roles for ERK3 in regulating cell growth, migration and invasion, as well as cancer growth and progression. In addition, it provides important insights on the molecular regulation of ERK3 expression and activity and its implications in different signaling pathways in cancers. Extracellular signal-regulated kinase 3 (ERK3) is an atypical mitogen-activated protein kinase (MAPK) whose structural and regulatory features are distinct from those of conventional MAPKs, such as ERK1/2. Since its identification in 1991, the regulation, substrates and functions of ERK3 have remained largely unknown. However, recent years have witnessed a wealth of new findings about ERK3 signaling. Several important biological functions for ERK3 have been revealed, including its role in neuronal morphogenesis, inflammation, metabolism, endothelial cell tube formation and epithelial architecture. In addition, ERK3 has been recently shown to play important roles in cancer cell proliferation, migration, invasion and chemoresistance in multiple types of cancers. Furthermore, accumulating studies have uncovered various molecular mechanisms by which the expression level, protein stability and activity of ERK3 are regulated. In particular, several post-translational modifications (PTMs), including ubiquitination, hydroxylation and phosphorylation, have been shown to regulate the stability and activity of ERK3 protein. In this review, we discuss recent findings regarding biochemical and cellular functions of ERK3, with a main focus on its roles in cancers, as well as the molecular mechanisms of regulating its expression and activity. [ABSTRACT FROM AUTHOR]
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- 2024
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