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dc.contributor.authorKitagawa, Yohkoen
dc.contributor.authorIkenaka, Akihiroen
dc.contributor.authorSugimura, Ryohichien
dc.contributor.authorNiwa, Akiraen
dc.contributor.authorSaito, Megumu K.en
dc.contributor.alternative北川, 瑶子ja
dc.contributor.alternative池中, 亮裕ja
dc.contributor.alternative杉村, 竜一ja
dc.contributor.alternative丹羽, 明ja
dc.contributor.alternative齋藤, 潤ja
dc.date.accessioned2023-10-02T07:26:30Z-
dc.date.available2023-10-02T07:26:30Z-
dc.date.issued2023-10-20-
dc.identifier.urihttp://hdl.handle.net/2433/285251-
dc.description血球細胞分化に必要な新たな因子を同定. 京都大学プレスリリース. 2023-09-29.ja
dc.descriptionDelineating the dynamic transcriptional and epigenetic landscape regulating hematopoiesis. 京都大学プレスリリース. 2023-10-17.en
dc.description.abstractCell differentiation is achieved by acquiring a cell type-specific transcriptional program and epigenetic landscape. While the cell type-specific patterning of enhancers has been shown to precede cell fate decisions, it remains unclear how regulators of these enhancers are induced to initiate cell specification and how they appropriately restrict cells that differentiate. Here, using embryonic stem cell–derived hematopoietic cell differentiation cultures, we show the activation of some hematopoietic enhancers during arterialization of hemogenic endothelium, a prerequisite for hematopoiesis. We further reveal that ZEB2, a factor involved in the transcriptional regulation of arterial endothelial cells, and a hematopoietic regulator MEIS1 are independently required for activating these enhancers. Concomitantly, ZEB2 or MEIS1 deficiency impaired hematopoietic cell development. These results suggest that multiple regulators expressed from an earlier developmental stage non-redundantly contribute to the establishment of hematopoietic enhancer landscape, thereby restricting cell differentiation despite the unrestricted expression of these regulators to hematopoietic cells.en
dc.language.isoeng-
dc.publisherElsevier BVen
dc.rights© 2023 The Authors.en
dc.rightsThis is an open access article under the CC BY-NC-ND license.en
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/-
dc.subjectNatural sciencesen
dc.subjectBiological sciencesen
dc.subjectDevelopmental biologyen
dc.titleZEB2 and MEIS1 independently contribute to hematopoiesis via early hematopoietic enhancer activationen
dc.typejournal article-
dc.type.niitypeJournal Article-
dc.identifier.jtitleiScienceen
dc.identifier.volume26-
dc.identifier.issue10-
dc.relation.doi10.1016/j.isci.2023.107893-
dc.textversionpublisher-
dc.identifier.artnum107893-
dc.addressDepartment of Clinical Application, Center for iPS Cell Research and Application, Kyoto Universityen
dc.addressDepartment of Clinical Application, Center for iPS Cell Research and Application, Kyoto Universityen
dc.addressDepartment of Clinical Application, Center for iPS Cell Research and Application, Kyoto University; Present address: Li Ka Shing Faculty of Medicine, University of Hong Kongen
dc.addressDepartment of Clinical Application, Center for iPS Cell Research and Application, Kyoto Universityen
dc.addressDepartment of Clinical Application, Center for iPS Cell Research and Application, Kyoto Universityen
dc.identifier.pmid37771659-
dc.relation.urlhttps://www.cira.kyoto-u.ac.jp/j/pressrelease/news/230929-100000.html-
dc.relation.urlhttps://www.cira.kyoto-u.ac.jp/e/pressrelease/news/231017-110000.html-
dcterms.accessRightsopen access-
datacite.awardNumber18J02122-
datacite.awardNumber18K14713-
datacite.awardNumber20K15800-
datacite.awardNumber.urihttps://kaken.nii.ac.jp/grant/KAKENHI-PROJECT-18J02122/-
datacite.awardNumber.urihttps://kaken.nii.ac.jp/grant/KAKENHI-PROJECT-18K14713/-
datacite.awardNumber.urihttps://kaken.nii.ac.jp/grant/KAKENHI-PROJECT-20K15800/-
dc.identifier.eissn2589-0042-
jpcoar.funderName日本学術振興会ja
jpcoar.funderName日本学術振興会ja
jpcoar.funderName日本学術振興会ja
jpcoar.awardTitle造血幹細胞分化におけるエピゲノム制御解明ja
jpcoar.awardTitleヒト造血幹細胞の多分化能を操るエンハンサー制御機構解明ja
jpcoar.awardTitle動脈内皮プログラムが誘導する血球分化の転写エピゲノム制御解明ja
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