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Transfer RNA-derived fragments (tRFs) are noncoding RNAs that arise from either mature transfer RNAs (tRNAs) or their precursors. One important category of tRFs comprises the tRNA halves, which are generated through cleavage at the anticodon. A given tRNA typically gives rise to several co-expressed 5'-tRNA halves (5′-tRHs) that differ in the location of their 3′ ends. These 5′-tRHs, even though distinct, have traditionally been treated as indistinguishable from one another due to their near-identical sequences and lengths. We focused on co-expressed 5′-tRHs that arise from the same tRNA and systematically examined their exact sequences and abundances across 10 different human tissues. To this end, we manually curated and analyzed several hundred human RNA-seq datasets from NCBI's Sequence Run Archive (SRA). We grouped datasets from the same tissue into their own collection and examined each group separately. We found that a given tRNA produces different groups of co-expressed 5′-tRHs in different tissues, different cell lines, and different diseases. Importantly, the co-expressed 5′-tRHs differ in their sequences, absolute abundances, and relative abundances, even among tRNAs with near-identical sequences from the same isodecoder or isoacceptor group. The findings suggest that co-expressed 5′-tRHs that are produced from the same tRNA or closely related tRNAs have distinct, context-dependent roles. Moreover, our analyses show that cell lines modeling the same tissue type and disease may not be interchangeable when it comes to experimenting with tRFs. [ABSTRACT FROM AUTHOR]

Alternative splicing is an important means of generating the protein diversity necessary for cellular functions. Hence, there is a growing interest in assessing the structural and functional impact of alternative protein isoforms. Typically, experimental studies are used to determine the structures of the canonical proteins ignoring the other isoforms. Therefore, there is still a large gap between abundant sequence information and meager structural data on these isoforms. During the last decade, significant progress has been achieved in the development of bioinformatics tools for structural and functional annotations of proteins. Moreover, the appearance of the AlphaFold program opened up the possibility to model a large number of high-confidence structures of the isoforms. In this study, using state-of-the-art tools, we performed in silico analysis of 58 eukaryotic proteomes. The evaluated structural states included structured domains, intrinsically disordered regions, aggregation-prone regions, and tandem repeats. Among other things, we found that the isoforms have fewer signal peptides, transmembrane regions, or tandem repeat regions in comparison with their canonical counterparts. This could change protein function and/or cellular localization. The AlphaFold modeling demonstrated that frequently isoforms, having differences with the canonical sequences, still can fold in similar structures though with significant structural rearrangements which can lead to changes of their functions. Based on the modeling, we suggested classification of the structural differences between canonical proteins and isoforms. Altogether, we can conclude that a majority of isoforms, similarly to the canonical proteins are under selective pressure for the functional roles. [ABSTRACT FROM AUTHOR]

Glycans are involved in many fundamental cellular processes such as growth, differentiation, and morphogenesis. However, their broad structural diversity makes analysis difficult. Glycomics via mass spectrometry has focused on the composition of glycans, but informatics analysis has not kept pace with the development of instrumentation and measurement techniques. We developed Toolbox Accelerating Glycomics (TAG), in which glycans can be added manually to the glycan list that can be freely designed with labels and sialic acid modifications, and fast processing is possible. In the present work, we improved TAG for large-scale analysis such as cohort analysis of serum samples. The sialic acid linkage-specific alkylamidation (SALSA) method converts differences in linkages such as α2,3- and α2,6-linkages of sialic acids into differences in mass. Glycans modified by SALSA and several structures discovered in recent years were added to the glycan list. A routine to generate calibration curves has been implemented to explore quantitation. These improvements are based on redefinitions of residues and glycans in the TAG List to incorporate information on glycans that could not be attributed because it was not assumed in the previous version of TAG. These functions were verified through analysis of purchased sera and 74 spectra with linearity at the level of R2 > 0.8 with 81 estimated glycan structures obtained including some candidate of rare glycans such as those with the N,N'-diacetyllactosediamine structure, suggesting they can be applied to large-scale analyses. [ABSTRACT FROM AUTHOR]

X chromosome inactivation is a mammalian dosage compensation mechanism, where one of two X chromosomes is randomly inactivated in female cells. Previous studies have suggested that primed human embryonic stem cells (hESCs) maintain an eroded state of the X chromosome and do not express XIST, while in naïve transition, both XIST and the eroded X chromosome are reactivated. However, the pattern of chromosome X reactivation in naïve hESCs remains mainly unknown. In this study, we examine the variations in the status of X chromosome between primed and naïve hESCs by analyzing RNA sequencing samples from different studies. We show that most samples of naïve hESCs indeed reactivate XIST and there is an increase in gene expression levels on chromosome X. However, most of the naïve samples do not fully activate chromosome X in a uniform manner and present a distinct eroded pattern, probably as a result of XIST reactivation and initiation of re-inactivation of chromosome X. This large-scale analysis provides a higher-resolution description of the changes occurring in chromosome X during primed-to-naïve transition and emphasizes the importance of taking these variations into consideration when studying X inactivation in embryonic development. [ABSTRACT FROM AUTHOR]

In recent decades, the Rocky Mountains (RM) have undergone significant changes associated with anthropogenic activities and natural disturbances. These changes have the potential to alter primary productivity and biomass carbon storage. In particular, dissolved organic carbon (DOC) in RM streams can affect heterotrophic processes, act as a source for the nutrient cycle, absorb sunlight radiation, alter metal transport, and can promote the production of carcinogenic byproducts during water treatment. Recent studies have focused on the relationship between bark beetle infestations and stream organic matter but have reached conflicting conclusions. Consequently, here we compile and process multiple datasets representing features of the RM for the period 1983–2012 with the purpose of assessing their relative influence on stream DOC concentrations using spatial statistical modeling. Features representing climate, land cover, forest disturbances, topography, soil types, and anthropogenic activities are included. We focus on DOC during base-flow conditions in RM streams because base-flow concentrations are more representative of the longer-term (annual to decadal) impacts and are less dependent on episodic, short-term storm and runoff/erosion events. To predict DOC throughout the network, we use a stream network model in a 56,550 km2 area to address the intrinsic connectivity and hydrologic directionality of the stream network. Natural forest disturbances are positively correlated with increased DOC concentrations; however, the effect of urbanization is far greater. Similarly, higher maximum temperatures, which can be exacerbated by climate change, are also associated with elevated DOC concentrations. Overall, DOC concentrations present an increasing trend over time in the RM region. [ABSTRACT FROM AUTHOR]

Scientific literature about energy retrofit focuses on single buildings, but the investigation of whole building stocks is particularly worthy because it can yield substantial energy, environmental and economic benefits. Hence, how to address large-scale energy retrofit of existing building stocks? The paper handles this issue by employing a methodology that provides a robust energy analysis of building categories. This is denoted as SLABE, "Simulation-based Large-scale uncertainty/sensitivity Analysis of Building Energy performance". It was presented by the same authors and is here enhanced to investigate a whole and heterogeneous building stock that includes various categories. Each category is represented via a Representative Building Sample (RBS), which is defined through Latin hypercube sampling and uncertainty analysis. Hence, optimal retrofit packages are found in function of building location, intended use and construction type. Two families of optimal solutions are achieved. The first one collects the most energy-efficient (and thus sustainable) solutions, among the ones that produce global cost savings, thereby addressing the public perspective. The second one collects cost-optimal solutions thereby addressing the private perspective. EnergyPlus is employed as a simulation tool and coupled with MATLAB® for data analysis and processing. The methodology is applied to a significant share of the Italian public administration building stock, which includes several building categories depending on location, use destination and construction type. The outcomes show huge potential energy and economic savings, and could support a deep energy renovation of the Italian building stock. [ABSTRACT FROM AUTHOR]

We propose a numerical method to learn maximum entropy (MaxEnt) distributions with spatio-temporal constraints from experimental spike trains. This is an extension of two papers, [10] and [4], which proposed the estimation of parameters where only spatial constraints were taken into account. The extension we propose allows one to properly handle memory effects in spike statistics, for large-sized neural networks. [ABSTRACT FROM AUTHOR]

Simple Summary: The current classification of central nervous system tumors has incorporated molecular changes that have clarified biological behavior and categorized gliomas into different types and malignancy grades. The most malignant type—glioblastoma, represents one of the most therapeutically challenging tumors, with a median survival of only 12–14 months despite trimodal therapy. In our integrative large-scale study, we used genomics, transcriptomics, epigenomics, and proteomics to investigate and make sense of the molecular changes that activate or inhibit the EGFR-PI3K-AKT-mTOR signaling pathway. Different pathohistological types of diffuse brain gliomas harbored distinct changes. A better understanding of signaling pathway regulation helps to the discovery of new targets for glioma therapies. Our results have potential for diagnostics improvement and tailored therapies. Diffuse gliomas are a heterogeneous group of tumors with aggressive biological behavior and a lack of effective treatment methods. Despite new molecular findings, the differences between pathohistological types still require better understanding. In this in silico analysis, we investigated AKT1, AKT2, AKT3, CHUK, GSK3β, EGFR, PTEN, and PIK3AP1 as participants of EGFR-PI3K-AKT-mTOR signaling using data from the publicly available cBioPortal platform. Integrative large-scale analyses investigated changes in copy number aberrations (CNA), methylation, mRNA transcription and protein expression within 751 samples of diffuse astrocytomas, anaplastic astrocytomas and glioblastomas. The study showed a significant percentage of CNA in PTEN (76%), PIK3AP1 and CHUK (75% each), EGFR (74%), AKT2 (39%), AKT1 (32%), AKT3 (19%) and GSK3β (18%) in the total sample. Comprehensive statistical analyses show how genomics and epigenomics affect the expression of examined genes differently across various pathohistological types and grades, suggesting that genes AKT3, CHUK and PTEN behave like tumor suppressors, while AKT1, AKT2, EGFR, and PIK3AP1 show oncogenic behavior and are involved in enhanced activity of the EGFR-PI3K-AKT-mTOR signaling pathway. Our findings contribute to the knowledge of the molecular differences between pathohistological types and ultimately offer the possibility of new treatment targets and personalized therapies in patients with diffuse gliomas. [ABSTRACT FROM AUTHOR]