44 results on '"Sawazaki, T."'
Search Results
2. Development of 50 gene-associated microsatellite markers using BAC clones and the construction of a linkage map of swine chromosome 4
- Author
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Fujishima-Kanaya, N., Toki, D., Suzuki, K., Sawazaki, T., Hiraiwa, H., Iida, M., Hayashi, T., Uenishi, H., Wada, Y., Ito, Y., and Awata, T.
- Published
- 2003
3. Physical assignment of markers, SJ017, SJ042, and SJ065 to swine chromosome X
- Author
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Sugai, N, Sawazaki, T, Itoh, T, Mikawa, S, Wada, Y, and Yasue, H
- Published
- 2000
4. New synthesis of alpha-acyl imines by radical-mediated group-transfer imidoylation of acyl tellurides with isonitriles
- Author
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Yamago, S, Miyazoe, H, Sawazaki, T, Goto, R, and Yoshida, J
- Subjects
isocyanides ,radicals and radical reactions ,imidic acids and derivatives ,carbonylation - Published
- 2000
5. Genomic organization and assignment of the interleukin 7 gene (IL7) to porcine chromosome 4q11→q13 by FISH and by analysis of radiation hybrid panels.
- Author
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Uenishi, H., Hiraiwa, H., Sawazaki, T., Kiuchi, S., and Yasue, H.
- Subjects
GENETICS ,GENES ,CHROMOSOMES ,IN situ hybridization ,CYTOKINES ,AMINO acids - Abstract
Interleukin 7 (IL7) is a cytokine that has many immunological functions, including regulation of hematopoiesis and peripheral lymphocytes. cDNA and a genomic DNA segment containing the porcine IL7 gene were isolated and sequenced, showing that porcine IL7 consists of 176 amino acids and that its gene spans over about 13 kb of genomic DNA. Porcine IL7 has 85% and 73% homology with human IL7 in terms of the nucleotide and amino acid sequences, respectively. Whereas the murine IL7 gene does not have an exon corresponding to human exon 5 (Lupton et al., 1990), the porcine IL7 gene was found to contain the same exon-intron structure as the human gene. These findings, together with the upstream structure of the cDNA elucidated in the present study, indicate that the relationship between swine and human IL7 is closer than that between mouse and human IL7. The IL7 gene was mapped to swine chromosome 4q11→q13 by fluorescence in situ hybridization and, using a radiation hybrid panel, was localized between microsatellite markers Sw1336 and Sw1073 on the same chromosome. Copyright © 2001 S. Karger AG, Basel [ABSTRACT FROM AUTHOR]
- Published
- 2001
- Full Text
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6. The pig aminoacylase 1 (ACY1) and ribosomal protein L29 (RPL29)/heparin/heparan sulfate interacting protein (HIP) genes are located together at 13q21→q22, corresponding to human 3p21.1.
- Author
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Sawazaki, T. and Minezawa, M.
- Subjects
- *
AMINOACYL-tRNA , *HEPARIN , *ANIMAL genetic engineering , *FLUORESCENCE in situ hybridization , *AMINO acids , *TUMOR suppressor genes - Abstract
The pig aminoacylase 1 (ACY1; N -acylamino acid aminohydrolase) gene was isolated from a pig cosmid library and characterized. The gene spans about 4.7 kb and consists of 15 exons. Fluorescence in situ hybridization found ACY1 to be located on pig chromosome 13 in the region q21→q22. This result and previous reports show that a large part of pig chromosome 13 corresponds to human chromosome 3. BLAST search results reveal that chromosome 13 contains a transcript similar to human ribosomal protein L29 (RPL29)/heparan sulfate/heparin-interacting protein (HIP). The transcript lies near the 3′-flanking region of the pig ACY1 gene; the 2 genes are linked tail-to-tail. The deduced amino acid sequence shows distinct homology to human RPL29/HIP, 96% identical in the N-terminal region. In the corresponding human 3p21.1 region, a deletion closely linked to the ACY1 locus has been observed in carcinoma cells. This suggests that a tumor suppressor gene is located in this region. Comparative mapping suggests also that the human RPL29/HIP gene may be near ACY1. Because many growth factors and cytokines interact with cells via heparin/heparan sulfate–proteoglycan, RPL29/HIP may play an important role on the cell surface by modulating interactions between cells and extracellular molecules. [ABSTRACT FROM AUTHOR]
- Published
- 1999
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7. The porcine homologues of six genes located on human chromosome 8 (RAB2,CA3,PTDSS1,MATN2,FZD6andSQLE) assigned to porcine chromosome 4 by fluorescencein situhybridization.
- Author
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Fujishima-Kanaya, N., Ito, Y., Suzuki, K., Sawazaki, T., Hiraiwa, H., Uenishi, H., and Awata, T.
- Subjects
SWINE breeding ,ANIMAL genetics ,ANIMAL genome mapping ,GENE mapping ,CHROMOSOMES ,FLUORESCENCE in situ hybridization - Abstract
Discusses a research about the assignment of homologues of six genes located on human chromosome 8 to porcine chromosome 4 by fluorescence in situ hybridization. Suggestion that SSC4 gene encompasses several quantitative trait loci which are important in pig breeding for economic benefit; Claim that half of the SSC4 gene which are proximal to p-ter shares homology with human chromosome 8.
- Published
- 2004
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8. Catalysis driven by an amyloid-substrate complex.
- Author
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Sawazaki T, Sasaki D, and Sohma Y
- Subjects
- Catalysis, Amines chemistry, Amines metabolism, Hydrogen Bonding, Islet Amyloid Polypeptide chemistry, Islet Amyloid Polypeptide metabolism, Hydrogen-Ion Concentration, Humans, Amyloid chemistry, Amyloid metabolism
- Abstract
Amine modification through nucleophilic attack of the amine functionality is a very common chemical transformation. Under biorelevant conditions using acidic-to-neutral pH buffer, however, the nucleophilic reaction of alkyl amines (pKa ≈ 10) is not facile due to the generation of ammonium ions lacking nucleophilicity. Here, we disclose a unique molecular transformation system, c atalysis driven by a myloid- s ubstrate comp l ex (CASL), that promotes amine modifications in acidic buffer. Ammonium ions attached to molecules with amyloid-binding capability were activated through deprotonation due to the close proximity to the amyloid catalyst formed by Ac-Asn-Phe-Gly-Ala-Ile-Leu-NH
2 ( NL6 ), derived from islet amyloid polypeptide (IAPP). Under the CASL conditions, alkyl amines underwent various modifications, i.e., acylation, arylation, cyclization, and alkylation, in acidic buffer. Crystallographic analysis and chemical modification studies of the amyloid catalysts suggested that the carbonyl oxygen of the Phe-Gly amide bond of NL6 plays a key role in activating the substrate amine by forming a hydrogen bond. Using CASL, selective conversion of substrates possessing equivalently reactive amine functionalities was achieved in catalytic reactions using amyloids. CASL provides a unique method for applying nucleophilic conversion reactions of amines in diverse fields of chemistry and biology., Competing Interests: Competing interests statement:The authors declare no competing interest.- Published
- 2024
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9. Modular synthetic strategy for N/C-terminal protected amyloidogenic peptides.
- Author
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Sawazaki T and Sohma Y
- Subjects
- Chromatography, High Pressure Liquid, Solid-Phase Synthesis Techniques, Peptides chemistry, Biocompatible Materials
- Abstract
N/C-terminal protected amyloidogenic peptides are valuable biomaterials. Optimization of the protective structures at both termini is, however, synthetically laborious because a linear sequence of solid-phase peptide synthesis protocol (on-resin peptide assembly/peptide removal from resin/high-performance liquid chromatography purification) is required for the peptides each time the protective group is modified. In this study, we demonstrate a modular synthetic strategy for the purpose of rapidly deriving the N/C-terminal structures of amyloidogenic peptides. The precursor sequences that can be easily synthesized due to a non-amyloidogenic property were stocked as the synthetic intermediates. Condensation of the intermediates with N/C-terminal units in a liquid phase followed by high-performance liquid chromatography purification gave the desired peptides P1-P8. The amyloidogenic peptides that have various N/C-terminal protective structures were therefore synthesized in a labor-effective manner. This method is suggested to be useful for synthesizing amyloidogenic peptides possessing divergent protective structures at the N/C-terminus., (© 2023 European Peptide Society and John Wiley & Sons, Ltd.)
- Published
- 2024
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10. Quantitative Assays for Catalytic Photo-Oxygenation of Alzheimer Disease-Related Tau Proteins.
- Author
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Umeda H, Sawazaki T, Furuta M, Suzuki T, Kawashima SA, Mitsunuma H, Hori Y, Tomita T, Sohma Y, and Kanai M
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- Humans, tau Proteins metabolism, Chromatography, Liquid, Histidine, Tandem Mass Spectrometry, Alzheimer Disease metabolism, Tauopathies metabolism
- Abstract
Catalytic photo-oxygenation of tau amyloid is a potential therapeutic approach to tauopathies, including Alzheimer disease (AD). However, tau is a complex target containing great molecular size and heterogeneous isoforms/proteoforms. Although catalytic photo-oxygenation has been confirmed when using catalyst 1 and recombinant tau pretreated with heparin, its effects on tau from human patients have not yet been clarified. In this study, focusing on the histidine residues being oxygenated, we have constructed two assay systems capable of quantitatively evaluating the catalytic activity when used on human patient tau: (1) fluorescence labeling at oxygenated histidine sites and (2) LC-MS/MS analysis of histidine-containing fragments. Using these assays, we identified 2 as a promising catalyst for oxygenation of human tau. In addition, our results suggest that aggregated tau induced by heparin is different from actual AD patient tau in developing effective photo-oxygenation catalysts.
- Published
- 2023
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11. Tetrathienyl Corannulene Compounds with Highly Sensitive Photochromism.
- Author
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Yamada M, Sawazaki T, Fujita M, Asanoma F, Nishikawa Y, and Kawai T
- Abstract
We have designed and synthesized photochromic tetrathienyl corannulene compounds, 1,2,7,8-tetrakis(2-methyl-5-phenylthiophen-3-yl)corannulene (1) and 1,2,7,8-tetrakis(2,4-dimethyl-5-phenylthiophen-3-yl)corannulene (2), by fusing two units of photochromic terarylene with a curved aromatic corannulene with a promising antenna effect. Compound 1 exhibited highly sensitive photoreactivity, with a large molar absorption coefficient of 8.2×10
4 M-1 cm-1 and practically photon-quantitative photocyclization. On the other hand, a terarylene derivative with a planar aromatic phenanthrene, 9,10-bis(2,4-dimethyl-5-phenylthiophen-3-yl)phenanthrene (4) showed no photoreactivity. The reason for such a difference was attributed to the predominance of the photoreactive atropisomers amplified by energy migration, and the shortened distance between reactive carbons induced by the curved structure., (© 2022 Wiley-VCH GmbH.)- Published
- 2022
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12. Knoevenagel Condensation between 2-Methyl-thiazolo[4,5-b]pyrazines and Aldehydes.
- Author
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Sawazaki T, Sohma Y, and Kanai M
- Subjects
- Alkenes chemistry, Molecular Structure, Aldehydes chemistry, Alkenes chemical synthesis, Pyrazines chemistry
- Abstract
Knoevenagel condensation, an olefin-forming reaction from active methyl/methylene-containing compounds and aldehydes, is a fundamental and useful synthetic method. Benzothiazoles are, however, out of the scope of Knoevenagel condensation. Here, we report that Knoevenagel condensation between aldehydes and 2-methyl-thiazolo[4,5-b]pyrazines (MeTPy), a fused ring structure comprising pyrazine and thiazole, proceeded smoothly, despite minor structural differences from benzothiazoles. This finding will be useful for short synthesis of MeTPy-containing functional molecules, such as a tau probe analog 1.
- Published
- 2022
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13. Chemical catalyst-promoted photooxygenation of amyloid proteins.
- Author
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Sohma Y, Sawazaki T, and Kanai M
- Subjects
- Animals, Catalysis, Humans, Amyloidogenic Proteins chemistry, Oxygen chemistry, Photochemical Processes
- Abstract
Misfolded proteins produce aberrant fibrillar aggregates, called amyloids, which contain cross-β-sheet higher order structures. The species generated in the aggregation process ( i.e. , oligomers, protofibrils, and fibrils) are cytotoxic and can cause various diseases. Interfering with the amyloid formation of proteins could be a drug development target for treating diseases caused by aberrant protein aggregation. In this review, we introduce a variety of chemical catalysts that oxygenate amyloid proteins under light irradiation using molecular oxygen as the oxygen atom donor ( i.e. , photooxygenation catalysts). Catalytic photooxygenation strongly inhibits the aggregation of amyloid proteins due to covalent installation of hydrophilic oxygen atoms and attenuates the neurotoxicity of the amyloid proteins. Recent in vivo studies in disease model animals using photooxygenation catalysts showed promising therapeutic effects, such as memory improvement and lifespan extension. Moreover, photooxygenation catalysts with new modes of action, including interference with the propagation of amyloid core seeds and enhancement in the metabolic clearance of amyloids in the brain, have begun to be identified. Manipulation of catalytic photooxygenation with secured amyloid selectivity is indispensable for minimizing the side effects in clinical application. Here we describe several strategies for designing catalysts that selectively photooxygenate amyloids without reacting with other non-amyloid biomolecules.
- Published
- 2021
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14. Evaluation of rehabilitation exercise effects by using gradation-based skeletal muscle echo intensity in older individuals: a one-group before-and-after trial study.
- Author
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Yoshiko A, Kaji T, Kozuka T, Sawazaki T, and Akima H
- Subjects
- Aged, Aged, 80 and over, Exercise Therapy, Female, Humans, Male, Muscle Strength, Ultrasonography, Activities of Daily Living, Muscle, Skeletal diagnostic imaging
- Abstract
Background: Higher muscle echo intensity (EI) reflects higher content of fat and/or connective tissue within skeletal muscle, eventually inducing lower muscle strength, physical dysfunction, and metabolic impairment. Continuous exercise decreases muscle EI in older individuals; however, it is not well understood how several months' rehabilitation exercise affects gradation-based EI. The purpose of this study was to investigate the effects of 6 months of rehabilitation exercise on gradation-based higher and lower EI in older men and women., Methods: Twenty-seven men and women (7 men, 20 women; age, 75.6 ± 6.4 years; height, 154.3 ± 8.5 cm; weight, 55.8 ± 9.7 kg) participated in this study. This study was a one-group before-and-after trial. They needed long-term care for activities of daily living. They performed rehabilitation exercises consisting of resistance exercises using a hydraulic resistance machine, stretching, and aerobic exercises using a recumbent bicycle once or twice a week for 6 months. B-mode ultrasonographic transverse image was taken from thigh muscles, e.g., rectus femoris, vastus lateralis, and biceps femoris. We calculated gradation-based cross-sectional area (CSA) from thigh muscles by dividing 256 greyscale level to 10 different components levels (e.g., 0-24, 25-49, 50-74, …, 200-224 and 225-249 a.u.)., Results: Lowest EI (e.g., 0-24 a.u.) CSA of thigh muscle was significantly increased after the exercise (0.3 ± 0.3 to 1.0 ± 0.8 cm
2 ; P < 0.05). Middle to higher EI (e.g., 50-74, 75-99, 100-124, 125-149, 150-174, 175-199 and 200-224 a.u.) CSAs were significantly decreased from 23.0 to 68.7% after the exercise (P < 0.05)., Conclusions: Several months' rehabilitation exercise affected both lower and higher EI in older men and women. This result suggests that rehabilitation exercise changes muscle composition by increasing contractile muscle tissue and decreasing fat and connective tissues., (© 2021. The Author(s).)- Published
- 2021
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15. Influences of lower limb edema on daily lives of elderly individuals in an elderly day care center.
- Author
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Tsuchiya S, Sawazaki T, Osawa S, Fujiu M, Okuwa M, and Sugama J
- Subjects
- Aged, Aged, 80 and over, Edema, Humans, Lower Extremity, Walking, Day Care, Medical, Quality of Life
- Abstract
Aim: The purpose of this study is to describe the influences of lower limb edema on the daily lives of elderly individuals in elderly day care to describe the necessity of care for lower limb edema., Methods: Semi-structured interviews based on a quality of life questionnaire for limb lymphedema were conducted. Two types of text mining analysis methods were used: a frequent word analysis and a content analysis. The edema severity was graded on a scale of 0 to 3, and the sum of the numerical values of the grades for each person was defined as the pitting score., Results: The seven participants had a mean age of 83.4 ± 4.6 years (mean ± SD). The pitting scores ranged from 1 to 25 in the participants. The words "think" (389 times), "walk" (136 times), and "put on" (135 times) were extracted frequently. The content analysis focused on the words "walk" and "put on." The participants complained of difficulty walking, pain, and numbness when walking, weakness of their lower limbs, difficulty putting on shoes, restrictions on shoe types, and difficulty finding shoes., Conclusions: These results demonstrate that elderly individuals experienced troubles during their daily lives caused by lower limb edema, which highlights the necessity of symptom management. Active interventions for edema by nurses are necessary to improve quality of life in elderly individuals., (© 2020 Japan Academy of Nursing Science.)
- Published
- 2021
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16. Gravity magnetic resonance imaging measurement of muscle pump change accompanied by aging and posture.
- Author
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Fujii T, Ohno N, Sawazaki T, Ogura K, Miyati T, and Sugama J
- Abstract
Aim: To date no age-comparative study has been reported about effect of exercise on muscle pump action change, while its effect is suggested to differ in ages. This study aims to clarify the changes in muscle pump action with aging by measuring the muscle and vein area, and blood flow in lower legs., Methods: Subjects were healthy volunteers and consisted of three groups: young age group (N = 20), middle age group (N = 20) and old age group (N = 16). The lower leg flexor muscle area and popliteal vein area were measured by using T1-weighed magnetic resonance imaging at the condition pre- and post-ankle exercise in three positions. Moreover, popliteal blood flow velocity was also measured using phase contrast magnetic resonance imaging., Results: The elderly had the highest number of individuals who had exercise habits (p < .001). In a multiple linear regression analysis, sitting posture, leg muscle volume, and rate of change in the soleus muscle were significantly related to blood flow velocity change., Conclusions: No difference was found in the changes in muscle pump action with age. The study results suggested that elderly people with exercise habits might be able to maintain the muscle pump action., (© 2021 The Authors. Japan Journal of Nursing Science published by John Wiley & Sons Australia, Ltd on behalf of Japan Academy of Nursing Science.)
- Published
- 2021
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17. Nanoscale View of Amyloid Photodynamic Damage.
- Author
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Bondia P, Torra J, Tone CM, Sawazaki T, Del Valle A, Sot B, Nonell S, Kanai M, Sohma Y, and Flors C
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- Benzothiazoles chemistry, Lactoglobulins chemistry, Microscopy, Fluorescence methods, Reactive Oxygen Species chemistry, Singlet Oxygen chemistry, Spectroscopy, Near-Infrared methods, Amyloid chemistry, Light adverse effects, Microscopy, Atomic Force methods, alpha-Synuclein chemistry
- Abstract
A combination of time-resolved optical spectroscopy and nanoscale imaging has been used to study the complex binding to amyloids of a photocatalyst that selectively photo-oxygenates pathogenic aggregates, as well as the consequences of its irradiation. Correlative atomic force microscopy (AFM) and fluorescence microscopy reveals topography-dependent binding of the dye to model β-lactoglobulin fibers, which may also explain the observed difference in their response to photodegradation. We provide direct evidence of the photosensitization of singlet oxygen by the photocatalyst bound to amyloid fibers by direct detection of its NIR phosphorescence. The effect of singlet oxygen at the molecular level brings about nanoscale morphological changes that can be observed with AFM at the single-fiber level. We also find differential response of two α-synuclein mutants to photodamage, which can be rationalized by the presence of amino acids susceptible to photo-oxygenation. Overall, our results help to unravel some of the complexity associated with highly heterogeneous amyloid populations and contribute to the development of improved phototherapeutic strategies for amyloid-related disorders.
- Published
- 2020
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18. Photo-oxygenation inhibits tau amyloid formation.
- Author
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Suzuki T, Hori Y, Sawazaki T, Shimizu Y, Nemoto Y, Taniguchi A, Ozawa S, Sohma Y, Kanai M, and Tomita T
- Subjects
- Alzheimer Disease metabolism, Alzheimer Disease pathology, Amyloidogenic Proteins metabolism, Brain metabolism, Brain pathology, Catalysis, Cycloaddition Reaction, HEK293 Cells, Humans, Oxygen metabolism, Photochemical Processes, tau Proteins antagonists & inhibitors, tau Proteins biosynthesis
- Abstract
Tau amyloid formation and deposition are responsible for the onset of Alzheimer's disease. In particular, the seeding activity of the tau protein plays an important role in the spreading of tau pathology via its propagation in the human brain. Here we demonstrate that catalytic photo-oxygenation markedly suppresses tau seeding activity, resulting in the inhibition of amyloid formation, both in vitro and in cultured cells.
- Published
- 2019
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19. Photophysical properties and application in live cell imaging of B,B-fluoro-perfluoroalkyl BODIPYs.
- Author
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Taniguchi A, Sawazaki T, Shimizu Y, Sohma Y, and Kanai M
- Abstract
The photophysical properties of newly identified B,B-fluoro-perfluoroalkyl BODIPYs ( 2 and 3 ), which possess a fluoro group and a trifluoromethyl or pentafluoroethyl group at the boron center, were investigated. B,B-Fluoro-perfluoroalkyl BODIPYs 2 and 3 exhibited better photophysical/chemical properties than B,B-difluoro-BODIPY 1 , as follows: (1) higher photostability both in methanol solvent and in a live cell environment, (2) higher stability against acid degradation, and (3) improved fluorescence signal-to-noise ratios in a cell system. These favorable properties of B,B-fluoro-perfluoroalkyl BODIPYs are likely due to the highly electron-withdrawing nature of the perfluoroalkyl groups on the boron atom, which reduces the reactivity to
1 O2 and strengthens the complexation of the dipyrromethene ligands to the boron atom. Thus, B,B-fluoro perfluoroalkyl BODIPYs may be useful functional molecules for various applications.- Published
- 2019
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20. Convergent and Functional-Group-Tolerant Synthesis of B-Organo BODIPYs.
- Author
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Sawazaki T, Shimizu Y, Oisaki K, Sohma Y, and Kanai M
- Abstract
Boron-dipyrromethenes (BODIPYs) are one of the most important fluorescent materials. Despite their potential unique properties, however, B,B-fluoro-organo BODIPYs (BFR-BODIPYs) possessing an organo group (R) on the boron center have not been studied in detail, due in part to challenges related to their synthesis. In this paper, a convergent synthesis of BFR-BODIPYs operative under mild conditions is reported. Conversions of the thus-synthesized functionalized BFR-BODIPYs by cross-coupling, condensation, and S
N 2 reactions at the R group are also demonstrated.- Published
- 2018
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21. Hydroxy Group Directed Catalytic Hydrosilylation of Amides.
- Author
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Ni J, Oguro T, Sawazaki T, Sohma Y, and Kanai M
- Abstract
Chemo- and site-selective hydrosilylation of α- or β-hydroxy amides using organocatalyst B(C
6 F5 )3 and commercially available hydrosilanes is described. This transformation is operative under mild conditions and tolerates a wide range of functional groups. The reaction was applied for selective reduction of a specific amide group of the therapeutically important cyclic peptide cyclosporin A, demonstrating the potential usefulness of this catalytic method in late-stage structural transformations of drug lead molecules.- Published
- 2018
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22. Efficacy of Honeydew Honey and Blossom Honey on Full-thickness Wound Healing in Mice.
- Author
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Sawazaki T, Nakajima Y, Urai T, Mukai K, Ohta M, Kato I, Kawaguchi A, Kinoshita Y, Kumagai Y, Sakashita A, Yamazaki A, and Nakatani T
- Subjects
- Administration, Cutaneous, Animals, Disease Models, Animal, Male, Mice, Mice, Inbred BALB C, Re-Epithelialization drug effects, Wounds and Injuries therapy, Anti-Infective Agents, Local pharmacology, Honey, Re-Epithelialization physiology, Wound Healing physiology, Wounds and Injuries pathology
- Abstract
Introduction: The wound healing properties of honey, including blossom honey, are well known; however, the effects of honeydew honey during the wound healing process have not yet been investigated and thus remain unclear., Objective: This study compares the effects of honeydew honey with those of blossom honey., Materials and Methods: A total of 140 mice were divided into 2 control groups, which received either a hydrocolloid dressing (HCD; n = 22) or gauze (n = 22), and 4 experimental groups: honeydew honey (n = 23), Acacia honey (n = 23), Manuka honey (n = 22), and Japanese Pharmacopoeia honey (n = 28). Two circular full-thickness wounds were made and measured for 14 days. Each wound in the experimental groups was treated with 0.1 mL of honey and covered with gauze. Dressings in the control and experimental groups were changed daily., Results: The wounds in all of the honey groups and the HCD group were moist by day 14, while those in the gauze group were dry. The ratio of wound area to initial wound area and the number of inflammatory cells decreased during the inflammatory phase in all honey groups. However, the honey groups exhibited reepithelialization rates of < 40%, numerous neutrophils, weak wound contraction, and impaired collagen deposition in wounds after day 11., Conclusions: These results suggest honeydew honey and blossom honey both exert anti-inflammatory effects during the inflammatory phase. However, all of the honeys examined were less effective at promoting full-thickness wound healing than the controls. Further studies are warranted.
- Published
- 2018
23. Objective assessment of leg edema using ultrasonography with a gel pad.
- Author
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Iuchi T, Kobayashi M, Tsuchiya S, Ohno N, Dai M, Matsumoto M, Ogai K, Sato A, Sawazaki T, Miyati T, Tanaka S, and Sugama J
- Subjects
- Adult, Aged, Aged, 80 and over, Body Weights and Measures methods, Diagnostic Errors, Edema diagnosis, Female, Humans, Male, Young Adult, Edema diagnostic imaging, Subcutaneous Fat diagnostic imaging, Subcutaneous Tissue diagnostic imaging, Ultrasonography methods
- Abstract
Ultrasonography (US) is useful for visual detection of edematous tissues to assess subcutaneous echogenicity. However, visualization of subcutaneous echogenicity is interpreted differently among operators because the evaluation is subjective and individual operators have unique knowledge. This study objectively assessed leg edema using US with a gel pad including fat for normalization of echogenicity in subcutaneous tissue. Five younger adults and four elderly people with leg edema were recruited. We compared assessments of US and limb circumference before and after the intervention of vibration to decrease edema in younger adults, and edema prior to going to sleep and reduced edema in the early morning in elderly people. These assessments were performed twice in elderly people by three operators and reliability, interrater differences, and bias were assessed. For US assessment, echogenicity in subcutaneous tissue was normalized to that of the gel pad by dividing the mean echogenicity of subcutaneous tissue by the mean echogenicity of the gel pad. In younger adults, the normalized subcutaneous echogenicity before the intervention was significantly higher than that after the intervention. In elderly people, echogenicity indicating edema was significantly higher than that after edema reduction. Edema was detected with accuracy rates of 76.9% in younger adults and 75.0% in elderly people. Meanwhile, limb circumference could be used to detect edema in 50.0% of healthy adults and 87.8% of elderly people. The intra-reliability was excellent (intraclass correlation coefficient > 0.9, p < 0.01), and the inter-reliability was good (intraclass correlation coefficient > 0.7, p < 0.01) for normalized subcutaneous echogenicity. Bland-Altman plots revealed that inter-rater differences and systematic bias were small. Normalized subcutaneous echogenicity with the pad can sensitively and objectively assess leg edema with high reliability. Therefore, this method has the potential to become a new gold standard for objective assessment of leg edema in clinical practice.
- Published
- 2017
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24. Direct chemical vapor deposition growth of WS2 atomic layers on hexagonal boron nitride.
- Author
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Okada M, Sawazaki T, Watanabe K, Taniguch T, Hibino H, Shinohara H, and Kitaura R
- Abstract
Atomically thin transition metal dichalcogenides (TMDCs) have attracted considerable interest owing to the spin-valley coupled electronic structure and possibility in next-generation devices. Substrates are one of the most important factors to limit physical properties of atomic-layer materials, and among various substrates so far investigated, hexagonal boron nitride (hBN) is the best substrate to explore the intrinsic properties of atomic layers. Here we report direct chemical vapor deposition (CVD) growth of WS2 onto high-quality hBN using a 3-furnace CVD setup. Triangular-shaped WS2 grown on hBN have shown limited crystallographic orientation that is related to that of the underlying hBN. Photoluminescence spectra of the WS2 show an intense emission peak at 2.01 eV with a quite small fwhm of 26 meV. The sharp emission peak indicates the high quality of the present WS2 atomic layers with high crystallinity and clean interface.
- Published
- 2014
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25. Calcitonin gene-related peptide is an important regulator of cutaneous immunity: effect on dendritic cell and T cell functions.
- Author
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Mikami N, Matsushita H, Kato T, Kawasaki R, Sawazaki T, Kishimoto T, Ogitani Y, Watanabe K, Miyagi Y, Sueda K, Fukada S, Yamamoto H, and Tsujikawa K
- Subjects
- Animals, Calcitonin Gene-Related Peptide physiology, Dermatitis, Contact immunology, Immunity, Mice, Mice, Knockout, Calcitonin Gene-Related Peptide immunology, Dendritic Cells immunology, Skin immunology, T-Lymphocytes immunology
- Abstract
Some cutaneous inflammations are induced by percutaneous exposure to foreign Ags, and many chemical mediators regulate this inflammation process. One of these mediators, calcitonin gene-related peptide (CGRP), is a neuropeptide released from nerve endings in the skin. CGRP binds to its receptors composed of receptor activity-modifying protein 1 and calcitonin receptor-like receptor to modulate immune cell function. We show that CGRP regulates skin inflammation under physiological conditions, using contact hypersensitivity (CHS) models of receptor activity-modifying protein 1-deficient mice. CGRP has different functions in CHS responses mediated by Th1 or Th2 cells; it inhibits Th1-type CHS, such as 2,4,6-trinitrochlorobenzene-induced CHS, but promotes Th2-type CHS, such as FITC-induced CHS. CGRP inhibits the migration of Langerin(+) dermal dendritic cells to the lymph nodes in 2,4,6-trinitrochlorobenzene-induced CHS, and upregulates IL-4 production of T cells in the draining lymph nodes in FITC-CHS. These findings suggest that CGRP regulates several types of CHS reactions under physiological conditions and plays an important role in cutaneous immunity.
- Published
- 2011
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26. Detection of autoantibody to aldolase B in sera from patients with troglitazone-induced liver dysfunction.
- Author
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Maniratanachote R, Shibata A, Kaneko S, Yamamori I, Wakasugi T, Sawazaki T, Katoh K, Tokudome S, Nakajima M, and Yokoi T
- Subjects
- Aged, Alanine Transaminase blood, Autoantibodies immunology, Chromans therapeutic use, Diabetes Mellitus, Type 2 drug therapy, Electrophoresis, Gel, Two-Dimensional, Electrophoresis, Polyacrylamide Gel, Enzyme-Linked Immunosorbent Assay, Female, Humans, Hypoglycemic Agents therapeutic use, Immunoblotting, Liver enzymology, Liver immunology, Liver Cirrhosis blood, Liver Cirrhosis chemically induced, Liver Cirrhosis enzymology, Liver Cirrhosis immunology, Liver Diseases blood, Liver Diseases enzymology, Liver Diseases immunology, Male, Middle Aged, Subcellular Fractions drug effects, Subcellular Fractions enzymology, Subcellular Fractions immunology, Thiazolidinediones therapeutic use, Troglitazone, Autoantibodies blood, Chemical and Drug Induced Liver Injury blood, Chemical and Drug Induced Liver Injury enzymology, Chemical and Drug Induced Liver Injury etiology, Chemical and Drug Induced Liver Injury immunology, Chromans adverse effects, Fructose-Bisphosphate Aldolase immunology, Hypoglycemic Agents adverse effects, Liver drug effects, Thiazolidinediones adverse effects
- Abstract
Troglitazone is a thiazolidinedione antidiabetic agent with insulin-sensitizing activities that was withdrawn from the market in 2000 due to its association with idiosyncratic hepatotoxicity. To address the suspected autoantibody production associated with troglitazone, we investigated autoantibodies in sera from patients with type II diabetes mellitus with troglitazone-induced liver dysfunction. Two female patients (47- and 70-year-old) ceased taking troglitazone (400 mg/day) after 23.5 and 16 weeks, respectively, due to increased serum ALT. Using two-dimensional electrophoresis and amino acid sequence analyses, aldolase B was identified as an autoantigen that reacted with antibodies in sera from both patients. The titer of anti-aldolase B remained high for several weeks after stopping troglitazone administration. The mean reactivity of autoantibodies to aldolase B determined by ELISA with sera of patients with chronic hepatitis (n = 40) and liver cirrhosis (n = 40) was significantly higher (p < 0.05 and p < 0.001, respectively) than with sera of healthy subjects (n = 80). These findings suggest that liver injury may cause the appearance of autoantibodies to aldolase B which may then aggravate the hepatitis. In addition, the anti-aldolase B titer might indicate the severity of liver dysfunction.
- Published
- 2005
- Full Text
- View/download PDF
27. PEDE (Pig EST Data Explorer): construction of a database for ESTs derived from porcine full-length cDNA libraries.
- Author
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Uenishi H, Eguchi T, Suzuki K, Sawazaki T, Toki D, Shinkai H, Okumura N, Hamasima N, and Awata T
- Subjects
- Animals, Base Sequence, Computational Biology, Genomics, Information Storage and Retrieval, Internet, Molecular Sequence Data, Organ Specificity, User-Computer Interface, DNA, Complementary genetics, Databases, Genetic, Expressed Sequence Tags, Gene Library, Swine genetics
- Abstract
We generated the PEDE (Pig EST Data Explorer; http://pede.dna.affrc.go.jp/) database using sequences assembled from porcine 5' ESTs from oligo-capped full-length cDNA libraries. Thus far we have performed EST analysis of various organs (thymus, spleen, uterus, lung, liver, ovary and peripheral blood mononuclear cells) and assembled 68,076 high-quality sequences into 5546 contigs and 28,461 singlets. PEDE provides a search interface for getting results of homology searches and enables users to obtain information on sequence data and cDNA clones of interest. Single-nucleotide polymorphisms detected through comparison of the EST sequences are classified by origin (western and oriental breeds) and are searchable in the database. This database system can accelerate analyses of livestock traits and yields information that can lead to new applications in pigs as model systems for medical research.
- Published
- 2004
- Full Text
- View/download PDF
28. Elucidation of correspondence between swine chromosome 4 and human chromosome 1 by assigning 27 genes to the ImpRH map, and development of microsatellites in the proximity of 14 genes.
- Author
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Hiraiwa H, Sawazaki T, Suzuki K, Fujishima-Kanaya N, Toki D, Ito Y, Uenishi H, Hayashi T, Awata T, and Yasue H
- Subjects
- Animals, Chromosomes, Artificial, Bacterial genetics, Genomic Library, Humans, Radiation Hybrid Mapping, Synteny, Chromosome Mapping methods, Chromosomes, Human, Pair 1 genetics, Chromosomes, Mammalian genetics, Microsatellite Repeats genetics, Swine genetics
- Abstract
Loci affecting swine intramuscular fat content, backfat thickness, carcass weight, and daily weight gain were assigned to regions of swine chromosome (SSC) 4, which were shown to correspond to human chromosome (HSA) 1p22--> q25 by ZOO-FISH, bidirectional chromosome painting, as well as by the linkage map of genes. In order to select candidate genes responsible for the above traits from the human genome database, precise correspondence between SSC4 and HSA1 is a prerequisite. In the present study, 27 genes, PTGFR, GBP1, GBP2, GFI1, GCLM, ABCD3, EXTL2, KCNA3, ADORA3, KCND3, WNT2B, NRAS, SYCP1, PTGFRN, IGSF2, NOTCH2, S100A10, SHC1, SSR2, LMNA, CCT3, CD5L, PEA15, FCER1G, EAT2, DDR2, and LAMB3, located in the HSA1 region corresponding to SSC4 or possibly SSC4, were assigned to the IMpRH map. The alignment of genes from centromere to telomere in the SSC4 q arm is basically conserved in HSA1p22-->q25 with the direction from the q arm to the p arm, which is in good agreement with results from linkage mapping. In addition, the present study first demonstrated that WNT2B residing in the middle of the HSA1 region was assigned to SSC18 with a high lod score (> 5), and that at least three intrachromosomal rearrangements occurred in the region in the process of swine and human evolution. PTGFR, and LAMB3 localized at both ends of the HSA1 region were assigned to SSC6 and SSC9, respectively, which is consistent with regional correspondence reported earlier. In the course of the above analysis, microsatellite markers were developed in the proximity of eleven genes localized on SSC4, and three genes on other swine chromosomes., (Copyright 2003 S. Karger AG, Basel)
- Published
- 2003
- Full Text
- View/download PDF
29. Determination of antigenic proteins of housedust mites in 90 dogs suffering from atopic dermatitis.
- Author
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Yamashita K, Fujiwara C, Azuma R, Sawazaki T, Nakao Y, and Hasegawa A
- Subjects
- Animals, Antigens, Dermatophagoides chemistry, Antigens, Dermatophagoides classification, Antigens, Dermatophagoides immunology, Dermatitis, Atopic immunology, Dogs, Dust, Electrophoresis, Polyacrylamide Gel veterinary, Enzyme-Linked Immunosorbent Assay veterinary, Female, Immunoblotting veterinary, Immunoglobulin E immunology, Male, Molecular Weight, Antigens, Dermatophagoides analysis, Dermatitis, Atopic veterinary, Dog Diseases immunology, Immunoglobulin E blood, Pyroglyphidae immunology
- Abstract
Housedust mites, Dermatophagoides pteronyssinus (D. pteronyssinus) and Dermatophagoides farinae (D. farinae), are the important causative agents of allergic diseases in human and animals. By using 165 dogs suffering from atopic dermatitis (AD), serum levels of immunogloblin E (IgE) antibody against 25 kinds of allergen including housedust mites were determined. Housedust mites were the most frequent allergen against which 90 of the 165 allergic dogs (54.5%) by IMMUNODOT assay. With the further analysis of immunoblotting assay in the 90 dogs sensitized with housedust mites, antigenic proteins of housedust mites recognized by IgE antibodies were with the apparent molecular masses of 15, 76, 90, 98, and 170-kD. Among them, the 15-kD protein that might be identical to Group 2 antigens (Der f2, Der p2) was prominently observed (52/90). This study indicates that about a half of dogs with AD were sensitized to housedust mites, suggesting that Group 2 antigens of housedust mites may be a major allergen in canine AD.
- Published
- 2002
- Full Text
- View/download PDF
30. Synthetic and theoretical studies on group-transfer imidoylation of organotellurium compounds. remarkable reactivity of isonitriles in comparison with carbon monoxide in radical-mediated reactions.
- Author
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Yamago S, Miyazoe H, Goto R, Hashidume M, Sawazaki T, and Yoshida J
- Abstract
Imidoylation of organotellurium compounds with isonitriles has been investigated in conjunction with the radical-mediated C1 homologation reaction by using CO and isonitriles. Carbon-centered radicals generated photochemically or thermally from organotellurium compounds react with isonitriles in a group-transfer manner to give the corresponding imidoylated products. Organotellurium compounds have been found to serve as effective precursors of a wide variety of stabilized radicals, namely benzyl, alpha-alkoxy, alpha-amino, and acyl radicals, which take part in the imidoylation with high efficiency. The reactions are compatible with various functional groups, and can be carried out in various solvents including environmentally benign water. The reactivity of isonitriles has been compared with that of CO through competition experiments, and the results indicate that isonitriles are superior to CO as radical acceptors in reactions with stabilized radicals. The origin of the differences has been addressed in theoretical studies with density functional theory calculations using the B3LYP hybrid functional. The calculations suggest that both carbonylation and imidoylation proceed with low activation energies, and that there are virtually no differences in the kinetic sense. Instead, it indicates that thermodynamic effects, namely differences in the stability of the acyl and the imidoyl radicals, control the overall course of the reactions.
- Published
- 2001
- Full Text
- View/download PDF
31. Genomic organization and assignment of the interleukin 7 gene (IL7) to porcine chromosome 4q11-->q13 by FISH and by analysis of radiation hybrid panels.
- Author
-
Uenishi H, Hiraiwa H, Sawazaki T, Kiuchi S, and Yasue H
- Subjects
- Amino Acid Sequence, Animals, Base Sequence, Cloning, Molecular, DNA, Complementary genetics, Humans, Interleukin-7 chemistry, Mice, Molecular Sequence Data, Sequence Alignment, Chromosomes genetics, Exons genetics, In Situ Hybridization, Fluorescence, Interleukin-7 genetics, Introns genetics, Radiation Hybrid Mapping, Swine genetics
- Abstract
Interleukin 7 (IL7) is a cytokine that has many immunological functions, including regulation of hematopoiesis and peripheral lymphocytes. cDNA and a genomic DNA segment containing the porcine IL7 gene were isolated and sequenced, showing that porcine IL7 consists of 176 amino acids and that its gene spans over about 13 kb of genomic DNA. Porcine IL7 has 85% and 73% homology with human IL7 in terms of the nucleotide and amino acid sequences, respectively. Whereas the murine IL7 gene does not have an exon corresponding to human exon 5 (Lupton et al., 1990), the porcine IL7 gene was found to contain the same exon-intron structure as the human gene. These findings, together with the upstream structure of the cDNA elucidated in the present study, indicate that the relationship between swine and human IL7 is closer than that between mouse and human IL7. The IL7 gene was mapped to swine chromosome 4q11-->q13 by fluorescence in situ hybridization and, using a radiation hybrid panel, was localized between microsatellite markers Sw1336 and Sw1073 on the same chromosome., (Copyright 2001 S. Karger AG, Basel)
- Published
- 2001
- Full Text
- View/download PDF
32. A novel variant of translation elongation factor-1beta: isolation and characterization of the rice gene encoding EF-1beta2.
- Author
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Terui Y, Tsutsumi K, Kidou S, Sawazaki T, Kuroiwa Y, Yamaki M, and Ejiri S
- Subjects
- Amino Acid Sequence, Animals, Artemia genetics, Genes, Plant, Genomic Library, Molecular Sequence Data, Molecular Weight, Peptide Elongation Factor 1, Peptide Elongation Factors biosynthesis, Peptide Elongation Factors chemistry, Sequence Alignment, Sequence Homology, Amino Acid, Genetic Variation, Oryza genetics, Peptide Elongation Factors genetics
- Abstract
A rice gene encoding a novel isoform of translation elongation factor-1beta subunit (termed EF-1beta2) was isolated and characterized. The gene comprises of eight exons, and encodes a 226-amino-acid protein. Expression of EF-1beta2 mRNA is abundant in seeds and cultured cells, but is considerably low in the tissues of the rice seedling. Antiserum raised against an EF-1beta2 synthetic peptide detected a protein with a relative molecular mass of about 32 kDa, indicating the EF-1beta2 gene is actually expressed in rice tissues. EF-1beta2 showed a close similarity to the cognate subunits from plant (beta and beta').
- Published
- 1998
- Full Text
- View/download PDF
33. A unique exon-intron organization of a porcine S100C gene: close evolutionary relationship to calmodulin genes.
- Author
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Nakamura T, Hayashi M, Kato A, Sawazaki T, Yasue H, Nakano T, and Tanaka T
- Subjects
- Animals, Base Sequence, Blotting, Southern, DNA, Complementary chemistry, Exons, Humans, Introns, Molecular Sequence Data, Sequence Alignment, Calcium-Binding Proteins genetics, Calmodulin genetics, Evolution, Molecular, S100 Proteins genetics, Swine genetics
- Abstract
We found a unique exon-intron structure of the porcine S100C gene, a member of the S100 family, in which all other genes characterized to date have common exon-intron organization. The genomic DNA encoding the porcine S100C was cloned and the entire nucleotide sequence of the gene was analyzed. The gene is present as a single copy and consists of three exons and two introns with a total size of 5.3 kb. The first intron is located after the ATG translation initiation codon. Such an intron has never been found in other S100 genes, but is found in almost all calmodulin genes. The gene structural similarity suggests a close evolutionary relationship between the S100C gene and calmodulin genes.
- Published
- 1998
- Full Text
- View/download PDF
34. Anti-oncogene product p53 binds DNA helicase.
- Author
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Sakurai T, Suzuki M, Sawazaki T, Ishii S, and Yoshida S
- Subjects
- Chromatography, Affinity, Chromatography, DEAE-Cellulose, DNA Helicases isolation & purification, DNA, Single-Stranded metabolism, Deoxyribonucleotides metabolism, Electrophoresis, Polyacrylamide Gel, Female, Glutathione Transferase isolation & purification, Glutathione Transferase metabolism, HeLa Cells, Humans, Placenta metabolism, Pregnancy, Protein Binding, Recombinant Fusion Proteins isolation & purification, Recombinant Fusion Proteins metabolism, Restriction Mapping, Tumor Suppressor Protein p53 isolation & purification, DNA Helicases metabolism, Genes, p53, Tumor Suppressor Protein p53 metabolism
- Abstract
An oncogene product, p53, interacts with a simian virus 40-encoded T-antigen, which is an initiation protein for the viral DNA replication and also works as DNA helicase during elongation. Here we examine the interaction of p53 with cellular DNA helicase. A recombinant human wild type p53 fused with glutathione S-transferase was immobilized on glutathione-agarose as a ligand for affinity column. Hela cell extract was applied to the p53 column and the adsorbed proteins were eluted with buffers containing salt, 50% ethylene glycol, and glutathione. The ethylene glycol fraction contained a number of p53 binding proteins, and this fraction showed a DNA helicase activity measured by the displacement of DNA fragment from partially duplexed M13 DNA. The DNA helicase translocated in a 5'-to-3' direction on the single-stranded DNA using ATP as an energy source. The glutathione fraction that contained the p53 glutathione S-transferase fused protein also showed the same activity. The corresponding fractions from a control column carrying glutathione S-transferase showed only a trace amount of activity of DNA helicase. Therefore, the binding may be specific. Furthermore, an anti-p53 antibody column retained a p53-DNA helicase complex when the crude extracts of human placenta and of osteosarcoma cells were applied. These results indicate that p53 physically interacts with DNA helicase in vitro as well as in vivo.
- Published
- 1994
- Full Text
- View/download PDF
35. Independent control of transcription initiations from two sites by an initiator-like element and TATA box in the human c-erbB-2 promoter.
- Author
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Mizuguchi G, Kanei-Ishii C, Sawazaki T, Horikoshi M, Roeder RG, Yamamoto T, and Ishii S
- Subjects
- Base Sequence, DNA, HeLa Cells, Humans, Molecular Sequence Data, Proto-Oncogene Mas, Receptor, ErbB-2, Transcription Factor TFIID, Transcription Factors metabolism, Transcription, Genetic, ErbB Receptors genetics, Gene Expression Regulation, Proto-Oncogene Proteins genetics, TATA Box
- Abstract
Transcription of the human c-erbB-2-proto-oncogene starts mainly at two sites, nucleotide positions +1 and -69. The present studies have identified an initiator-like element that specifies the position of transcription initiation at position -69. This initiator-like element contains six GGA repeats and is located just downstream from the transcription start site between positions -68 and -45. In addition, both in vitro and in vivo studies indicated that transcription initiation at position +1 is specified by a TATA box 25 bp upstream from the transcription startpoint. Thus, initiation at two sites in the c-erbB-2 promoter is controlled independently by the initiator-like element and the TATA box.
- Published
- 1994
- Full Text
- View/download PDF
36. Placental and plasma cystine aminopeptidase in pregnant animals.
- Author
-
Ikenaga H, Mizuta Y, Ono K, Sawazaki T, Suzuki N, and Tomoda I
- Subjects
- Animals, Callithrix, Cattle, Cystinyl Aminopeptidase analysis, Cystinyl Aminopeptidase blood, Dogs, Edetic Acid pharmacology, Enzyme Stability, Female, Goats, Horses, Humans, Kinetics, Macaca fascicularis, Methionine pharmacology, Pregnancy, Species Specificity, Swine, Cystinyl Aminopeptidase metabolism, Placenta enzymology, Pregnancy, Animal metabolism
- Abstract
The placental and plasma cystine aminopeptidase (CAP) in pregnant animals was examined on stability after the treatment with L-methionine, ethylene diamine tetra-acetic acid (EDTA) and heat. Inhibitory effects of these treatments on enzyme activities were different among CAPs from the animal species, however, significant correlation in those effects between placental and plasma CAPs was observed. These results suggested that plasma CAP might reflect placental CAP and seemed to be available for estimating maternal gestational conditions.
- Published
- 1993
- Full Text
- View/download PDF
37. Transcriptional control by myb oncogene product.
- Author
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Ishii S, Nomura T, Kanei-Ishii C, Nakagoshi H, Sudo T, and Sawazaki T
- Subjects
- Animals, Cell Line, Genes, Regulator, HeLa Cells, Humans, Magnetic Resonance Spectroscopy, Models, Chemical, Nucleic Acid Conformation, Oncogene Proteins v-myb, Solubility, Tryptophan chemistry, Water chemistry, DNA-Binding Proteins genetics, Leucine Zippers genetics, Retroviridae Proteins, Oncogenic genetics, Transcription, Genetic, Tryptophan analysis
- Abstract
Structure and function of two domains of c-Myb were analyzed. We show that a leucine zipper structure is a component of the negative regulatory domain, because its disruption markedly increases both the transactivating and transforming capacities of c-Myb. Our results suggest that an inhibitor which suppresses transactivation binds to c-Myb through the leucine zipper, and that c-Myb can be oncogenically activated by mis-sense mutation. We also proposed a model, the "tryptophan cluster", for the structure of the Myb DNA-binding domain, in which the three tryptophans form a cluster in the hydrophobic core in each repeat. The results of NMR analysis of repeat 3 revealed that the conserved tryptophans play a key role to make the hydrophobic core.
- Published
- 1992
- Full Text
- View/download PDF
38. Overlap of the p53-responsive element and cAMP-responsive element in the enhancer of human T-cell leukemia virus type I.
- Author
-
Aoyama N, Nagase T, Sawazaki T, Mizuguchi G, Nakagoshi H, Fujisawa JI, Yoshida M, and Ishii S
- Subjects
- Animals, Base Sequence, Cell Line, Chloramphenicol O-Acetyltransferase genetics, Chloramphenicol O-Acetyltransferase metabolism, Chromosome Deletion, Cyclic AMP Response Element-Binding Protein, DNA-Binding Proteins genetics, Genes, ras, Humans, Molecular Sequence Data, Oligodeoxyribonucleotides, Promoter Regions, Genetic, Transfection, Tumor Suppressor Protein p53 genetics, DNA-Binding Proteins metabolism, Enhancer Elements, Genetic, Genes, p53, Human T-lymphotropic virus 1 genetics, Mutagenesis, Site-Directed, Transcriptional Activation, Tumor Suppressor Protein p53 metabolism
- Abstract
The wild-type p53 protein suppresses transformation, but certain missense mutants of p53 can transform cells. Although the wild-type p53 protein contains a transcriptional activation domain, no p53-responsive element has been identified. Here, we identified the p53-responsive element within the Tax-responsive element [21-base-pair (bp) enhancer] of human T-cell leukemia virus type I. Mutation analysis of the 21-bp enhancer indicated that the 16-bp sequence containing the cAMP-responsive element and its surrounding sequence was responsible for p53-induced transactivation. This 16-bp sequence was demonstrated to bind specifically to wild-type human p53 protein in vitro. Using a series of deletion mutants of p53, we showed that almost the entire region of p53 is needed for the transactivating capacity. Furthermore, the transforming mutants of p53 were unable to act as transcriptional activators. The p53-responsive element identified here should be useful to analyze the mechanism by which p53 regulates expression of a set of genes with a negative effect on cellular growth.
- Published
- 1992
- Full Text
- View/download PDF
39. Transcriptional activation of the c-myc gene by the c-myb and B-myb gene products.
- Author
-
Nakagoshi H, Kanei-Ishii C, Sawazaki T, Mizuguchi G, and Ishii S
- Subjects
- Animals, Base Sequence, Cell Line, Chloramphenicol O-Acetyltransferase genetics, Chloramphenicol O-Acetyltransferase metabolism, Chromosome Deletion, DNA-Binding Proteins genetics, Humans, Molecular Sequence Data, Oligodeoxyribonucleotides, Proto-Oncogene Proteins genetics, Proto-Oncogene Proteins c-myb, Recombinant Fusion Proteins metabolism, Sequence Homology, Nucleic Acid, Transfection, DNA-Binding Proteins metabolism, Genes, myc, Oncogenes, Promoter Regions, Genetic, Proto-Oncogene Proteins metabolism, Transcription, Genetic, Transcriptional Activation
- Abstract
To identify the target genes modulated by the myb gene product (Myb), a co-transfection assay with a Myb expression plasmid was performed. Both c-Myb and B-Myb, another member of the myb gene family, trans-activated the human c-myc promoter. DNAase I footprint analysis using the bacterially expressed c-Myb, identified multiple c-Myb binding sites in the c-myc promoter region. Deletion analysis of the c-myc promoter suggested that some number of Myb binding sites, not a specific Myb binding site, is important for the c-Myb-induced trans-activation of the c-myc promoter. Using the c-myc-chloramphenicol acetyltransferase (CAT) construct as a reporter in a co-transfection assay, the domains of c-Myb required for trans-activation were examined. The functional domains of c-Myb identified using the c-myc promoter were almost the same as those identified previously with the artificial target gene containing Myb binding sites, but unlike the case with the artificial target gene the N-terminal half of the previously identified negative regulatory domains and the C-terminal 136 amino acids were required for the maximal trans-activation of the c-myc promoter. These results indicate that there are some differences in the regulation of Myb-dependent trans-activation in different target genes.
- Published
- 1992
40. The tryptophan cluster: a hypothetical structure of the DNA-binding domain of the myb protooncogene product.
- Author
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Kanei-Ishii C, Sarai A, Sawazaki T, Nakagoshi H, He DN, Ogata K, Nishimura Y, and Ishii S
- Subjects
- Animals, Binding Sites, Escherichia coli genetics, Mice, Molecular Structure, Mutagenesis, Site-Directed, Phosphorylation, Plasmids, Protein Conformation, Proto-Oncogene Proteins genetics, Proto-Oncogene Proteins metabolism, Proto-Oncogene Proteins c-myb, Repetitive Sequences, Nucleic Acid, Spectrum Analysis, Raman, Transcription, Genetic, Transfection, DNA metabolism, Proto-Oncogene Proteins chemistry, Tryptophan
- Abstract
In the DNA-binding domain of the c-myb protooncogene product (c-Myb) which consists of three repeats of 51-52 amino acids, there are 3 perfectly conserved tryptophans in each repeat. Site-directed mutagenesis of these tryptophans showed that any single or multiple mutations of tryptophan to hydrophilic residues or alanine abolished or greatly reduced the sequence-specific DNA-binding activity, but mutations to hydrophobic amino acids retained considerable activity. Raman spectroscopic study showed that these tryptophans were buried in the protein core. These 3 tryptophans are proposed to form a cluster in the hydrophobic core in each repeat. This hypothetical structure is referred to as the "tryptophan cluster," and it may represent a characteristic property of a group of DNA-binding proteins including the myb- and ets-related proteins.
- Published
- 1990
41. A new antibiotic, grisamine.
- Author
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SAWAZAKI T, NAKAMURA G, KAWASAKI M, YAMASHITA S, ISONO K, ANZAI K, SERIZAWA Y, SEKIYAMA Y, and SUZUKI S
- Subjects
- Anti-Bacterial Agents, Streptomyces
- Published
- 1955
42. Streptomycin production by a new strain. Streptomyces mashuensis.
- Author
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SAWAZAKI T, SUZUKI S, NAKAMURA G, KAWASAKI M, YAMASHITA S, ISONO K, ANZAI K, SERIZAWA Y, and SEKIYAMA Y
- Subjects
- Streptomyces, Streptomycin, Yeasts drug effects
- Published
- 1955
43. An antibiotic produced by Streptomyces chromogenus sp.
- Author
-
ISONO K, SUZUKI S, SAWAZAKI T, NAKAMURA G, KAWASAKI M, YAMASHITA T, ANZAI K, SERIZAWA Y, and SEKIYAMA Y
- Subjects
- Humans, Anti-Bacterial Agents, Streptomyces
- Published
- 1955
44. A new antiyeast substance, cerevioccidin, produced by streptomycete.
- Author
-
YAMASHITA S, SAWAZAKI T, KAWASAKI M, NAKAMURA G, ANZAI K, ISONO K, SERIZAWA Y, SEKIYAMA Y, and SUZUKI S
- Subjects
- Humans, Anti-Bacterial Agents pharmacology, Streptomyces, Yeasts drug effects
- Published
- 1955
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