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dc.contributor.authorIwasaki, Mioen
dc.contributor.authorKawahara, Yukaen
dc.contributor.authorOkubo, Chikakoen
dc.contributor.authorYamakawa, Tatsuyaen
dc.contributor.authorNakamura, Michikoen
dc.contributor.authorTabata, Tsuyoshien
dc.contributor.authorNishi, Yoheien
dc.contributor.authorNarita, Megumien
dc.contributor.authorOhta, Akiraen
dc.contributor.authorSaito, Hirohideen
dc.contributor.authorYamamoto, Takuyaen
dc.contributor.authorNakagawa, Masatoen
dc.contributor.authorYamanaka, Shinyaen
dc.contributor.authorTakahashi, Kazutoshien
dc.contributor.alternative岩崎, 未央ja
dc.contributor.alternative川原, 優香ja
dc.contributor.alternative大久保, 周子ja
dc.contributor.alternative山川, 達也ja
dc.contributor.alternative中村, 美千子ja
dc.contributor.alternative田畑, 剛ja
dc.contributor.alternative西, 洋平ja
dc.contributor.alternative成田, 恵ja
dc.contributor.alternative太田, 章ja
dc.contributor.alternative齊藤, 博英ja
dc.contributor.alternative山本, 拓也ja
dc.contributor.alternative中川, 誠人ja
dc.contributor.alternative山中, 伸弥ja
dc.contributor.alternative高橋, 和利ja
dc.date.accessioned2022-05-17T04:48:04Z-
dc.date.available2022-05-17T04:48:04Z-
dc.date.issued2022-05-
dc.identifier.urihttp://hdl.handle.net/2433/270024-
dc.descriptionヒトのiPS細胞やES細胞の生存に必要な遺伝子の発見 --これまで見過ごされていた、タンパク質レベルで量が制御されている遺伝子群の制御機構解明に向けて--. 京都大学プレスリリース. 2022-05-13.ja
dc.descriptionDiscovery of genes required for survival of human iPS and ES cells. 京都大学プレスリリース. 2022-05-16.en
dc.description.abstractThe effects of transcription factors on the maintenance and differentiation of human-induced or embryonic pluripotent stem cells (iPSCs/ESCs) have been well studied. However, the importance of posttranscriptional regulatory mechanisms, which cause the quantitative dissociation of mRNA and protein expression, has not been explored in detail. Here, by combining transcriptome and proteome profiling, we identified 228 posttranscriptionally regulated genes with strict upregulation of the protein level in iPSCs/ESCs. Among them, we found 84 genes were vital for the survival of iPSCs and HDFs, including 20 genes that were specifically necessary for iPSC survival. These 20 proteins were upregulated only in iPSCs/ESCs and not in differentiated cells derived from the three germ layers. Although there are still unknown mechanisms that downregulate protein levels in HDFs, these results reveal that posttranscriptionally regulated genes have a crucial role in iPSC survival.en
dc.language.isoeng-
dc.publisherElsevier BVen
dc.rights© 2022 The Authors.en
dc.rightsThis is an open access article under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International license.en
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/-
dc.subjectBiological sciencesen
dc.subjectStem cells researchen
dc.subjectOmicsen
dc.titleMulti-omics approach reveals post-transcriptionally regulated genes are essential for human pluripotent stem cellsen
dc.typejournal article-
dc.type.niitypeJournal Article-
dc.identifier.jtitleiScienceen
dc.identifier.volume25-
dc.identifier.issue5-
dc.relation.doi10.1016/j.isci.2022.104289-
dc.textversionpublisher-
dc.identifier.artnum104289-
dc.addressDepartment of Life Science Frontiers, Center for iPS Cell Research and Application, Kyoto Universityen
dc.addressDepartment of Life Science Frontiers, Center for iPS Cell Research and Application, Kyoto Universityen
dc.addressDepartment of Life Science Frontiers, Center for iPS Cell Research and Application, Kyoto Universityen
dc.addressDepartment of Life Science Frontiers, Center for iPS Cell Research and Application, Kyoto Universityen
dc.addressDepartment of Life Science Frontiers, Center for iPS Cell Research and Application, Kyoto Universityen
dc.addressDepartment of Life Science Frontiers, Center for iPS Cell Research and Application, Kyoto Universityen
dc.addressDepartment of Life Science Frontiers, Center for iPS Cell Research and Application, Kyoto University; iPSC-Based Drug Discovery and Development Team, RIKEN Bio Resource Research Center (BRC)en
dc.addressDepartment of Life Science Frontiers, Center for iPS Cell Research and Application, Kyoto Universityen
dc.addressDepartment of Life Science Frontiers, Center for iPS Cell Research and Application, Kyoto Universityen
dc.addressDepartment of Life Science Frontiers, Center for iPS Cell Research and Application, Kyoto Universityen
dc.addressDepartment of Life Science Frontiers, Center for iPS Cell Research and Application, Kyoto University; Institute for the Advanced Study of Human Biology (WPI-ASHBi), Kyoto University; Medical-risk Avoidance based on iPS Cells Team, RIKEN Center for Advanced Intelligence Project (AIP)en
dc.addressDepartment of Life Science Frontiers, Center for iPS Cell Research and Application, Kyoto Universityen
dc.addressDepartment of Life Science Frontiers, Center for iPS Cell Research and Application, Kyoto University; Gladstone Institute of Cardiovascular Disease; Department of Anatomy, University of California, San Franciscoen
dc.addressDepartment of Life Science Frontiers, Center for iPS Cell Research and Application, Kyoto Universityen
dc.identifier.pmid35573189-
dc.relation.urlhttps://www.cira.kyoto-u.ac.jp/j/pressrelease/news/220513-140000.html-
dcterms.accessRightsopen access-
datacite.awardNumber19K16104-
datacite.awardNumber.urihttps://kaken.nii.ac.jp/grant/KAKENHI-PROJECT-19K16104/-
dc.identifier.eissn2589-0042-
jpcoar.funderName日本学術振興会ja
jpcoar.awardTitleタンパク質の量制御機構と分化特異性の解析ja
出現コレクション:学術雑誌掲載論文等

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