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dc.contributor.authorShukunami, Chisaen
dc.contributor.authorTakimoto, Akien
dc.contributor.authorNishizaki, Yurikoen
dc.contributor.authorYoshimoto, Yukien
dc.contributor.authorTanaka, Seimaen
dc.contributor.authorMiura, Shigenorien
dc.contributor.authorWatanabe, Hitomien
dc.contributor.authorSakuma, Tetsushien
dc.contributor.authorYamamoto, Takashien
dc.contributor.authorKondoh, Genen
dc.contributor.authorHiraki, Yujien
dc.contributor.alternative宿南, 知佐ja
dc.contributor.alternative滝本, 晶ja
dc.contributor.alternative西崎, 有利子ja
dc.contributor.alternative三浦, 重徳ja
dc.contributor.alternative渡邊, 仁美ja
dc.contributor.alternative近藤, 玄ja
dc.contributor.alternative開, 祐司ja
dc.date.accessioned2018-09-14T07:53:10Z-
dc.date.available2018-09-14T07:53:10Z-
dc.date.issued2018-02-16-
dc.identifier.issn2045-2322-
dc.identifier.urihttp://hdl.handle.net/2433/234567-
dc.description.abstractTenomodulin (Tnmd) is a type II transmembrane glycoprotein predominantly expressed in tendons and ligaments. We found that scleraxis (Scx), a member of the Twist-family of basic helix-loop-helix transcription factors, is a transcriptional activator of Tnmd expression in tenocytes. During embryonic development, Scx expression preceded that of Tnmd. Tnmd expression was nearly absent in tendons and ligaments of Scx-deficient mice generated by transcription activator-like effector nucleases-mediated gene disruption. Tnmd mRNA levels were dramatically decreased during serial passages of rat tenocytes. Scx silencing by small interfering RNA significantly suppressed endogenous Tnmd mRNA levels in tenocytes. Mouse Tnmd contains five E-box sites in the ~1-kb 5′-flanking region. A 174-base pair genomic fragment containing a TATA box drives transcription in tenocytes. Enhancer activity was increased in the upstream region (−1030 to −295) of Tnmd in tenocytes, but not in NIH3T3 and C3H10T1/2 cells. Preferential binding of both Scx and Twist1 as a heterodimer with E12 or E47 to CAGATG or CATCTG and transactivation of the 5′-flanking region were confirmed by electrophoresis mobility shift and dual luciferase assays, respectively. Scx directly transactivates Tnmd via these E-boxes to positively regulate tenocyte differentiation and maturation.en
dc.format.mimetypeapplication/pdf-
dc.language.isoeng-
dc.publisherSpringer Natureen
dc.rights© The Author(s) 2018. This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.en
dc.titleScleraxis is a transcriptional activator that regulates the expression of Tenomodulin, a marker of mature tenocytes and ligamentocytesen
dc.typejournal article-
dc.type.niitypeJournal Article-
dc.identifier.jtitleScientific Reportsen
dc.identifier.volume8-
dc.relation.doi10.1038/s41598-018-21194-3-
dc.textversionpublisher-
dc.identifier.artnum3155-
dc.addressDepartment of Molecular Biology and Biochemistry, Division of Dental Sciences, Graduate School of Biomedical and Health Sciences, Hiroshima Universityen
dc.addressLaboratory of Cellular Differentiation, Institute for Frontier Life and Medical Sciences, Kyoto Universityen
dc.addressLaboratory of Cellular Differentiation, Institute for Frontier Life and Medical Sciences, Kyoto University・Functional Morphology Laboratory, Department of Clinical Pharmacy, Faculty of Pharmacy, Yokohama University of Pharmacyen
dc.addressDepartment of Molecular Biology and Biochemistry, Division of Dental Sciences, Graduate School of Biomedical and Health Sciences, Hiroshima Universityen
dc.addressDepartment of Molecular Biology and Biochemistry, Division of Dental Sciences, Graduate School of Biomedical and Health Sciences, Hiroshima Universityen
dc.addressLaboratory of Cellular Differentiation, Institute for Frontier Life and Medical Sciences, Kyoto Universityen
dc.addressLaboratory of Integrative Biological Science, Institute for Frontier Life and Medical Sciences, Kyoto Universityen
dc.addressDepartment of Mathematical and Life Sciences, Graduate School of Science, Hiroshima Universityen
dc.addressDepartment of Mathematical and Life Sciences, Graduate School of Science, Hiroshima Universityen
dc.addressLaboratory of Integrative Biological Science, Institute for Frontier Life and Medical Sciences, Kyoto Universityen
dc.addressLaboratory of Cellular Differentiation, Institute for Frontier Life and Medical Sciences, Kyoto Universityen
dc.identifier.pmid29453333-
dcterms.accessRightsopen access-
datacite.awardNumberJP26293395-
datacite.awardNumberJP22390289-
jpcoar.funderName日本学術振興会ja
jpcoar.funderName日本学術振興会ja
jpcoar.funderName.alternativeJapan Society for the Promotion of Science (JSPS)en
jpcoar.funderName.alternativeJapan Society for the Promotion of Science (JSPS)en
出現コレクション:学術雑誌掲載論文等

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