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journal.pone.0020461.pdf1.17 MBAdobe PDF見る/開く
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dc.contributor.authorIwabuchi, Kumiko Aen
dc.contributor.authorYamakawa, Tatsuyaen
dc.contributor.authorSato, Yoshikoen
dc.contributor.authorIchisaka, Tomokoen
dc.contributor.authorTakahashi, Kazutoshien
dc.contributor.authorOkita, Keisukeen
dc.contributor.authorYamanaka, Shinyaen
dc.contributor.alternative岩渕, 久美子ja
dc.contributor.alternative山川, 達也ja
dc.contributor.alternative佐藤, 美子ja
dc.contributor.alternative一阪, 朋子ja
dc.contributor.alternative高橋, 和利ja
dc.contributor.alternative沖田, 圭介ja
dc.contributor.alternative山中, 伸弥ja
dc.date.accessioned2012-10-17T07:37:46Z-
dc.date.available2012-10-17T07:37:46Z-
dc.date.issued2011-05-26-
dc.identifier.issn1932-6203-
dc.identifier.urihttp://hdl.handle.net/2433/160141-
dc.description.abstractThe principal factors that lead to proliferation and pluripotency in embryonic stem cells (ESCs) have been vigorously investigated. However, the global network of factors and their full signaling cascade is still unclear. In this study, we found that ECAT11 (L1td1) is one of the ESC-associated transcripts harboring a truncated fragment of ORF-1, a component of the L1 retrotransposable element. We generated an ECAT11 knock-in mouse by replacing its coding region with green fluorescent protein. In the early stage of development, the fluorescence was observed at the inner cell mass of blastocysts and epiblasts. Despite this specific expression, ECAT11-null mice grow normally and are fertile. In addition, ECAT11 was dispensable for both the proliferation and pluripotency of ESCs.We found rapid and robust activation of ECAT11 in fibroblasts after the forced expression of transcription factors that can give rise pluripotency in somatic cells. However, iPS cells could be established from ECAT11-null fibroblasts. Our data demonstrate the dispensability of ECAT11/L1td1 in pluripotency, despite its specific expression.en
dc.format.mimetypeapplication/pdf-
dc.language.isoeng-
dc.publisherPublic Library of Scienceen
dc.rights© 2011 Iwabuchi et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.en
dc.subject.meshAmino Acid Sequenceen
dc.subject.meshAnimalsen
dc.subject.meshEmbryo, Mammalian/cytologyen
dc.subject.meshEmbryo, Mammalian/metabolismen
dc.subject.meshEmbryonic Stem Cells/cytologyen
dc.subject.meshEmbryonic Stem Cells/metabolismen
dc.subject.meshFibroblasts/metabolismen
dc.subject.meshGene Expression Regulation, Developmentalen
dc.subject.meshGene Knock-In Techniquesen
dc.subject.meshGenes, Reporteren
dc.subject.meshGreen Fluorescent Proteins/metabolismen
dc.subject.meshInduced Pluripotent Stem Cells/cytologyen
dc.subject.meshInduced Pluripotent Stem Cells/metabolismen
dc.subject.meshMiceen
dc.subject.meshMolecular Sequence Dataen
dc.subject.meshPromoter Regions, Genetic/geneticsen
dc.subject.meshProtein Transporten
dc.subject.meshProteins/chemistryen
dc.subject.meshProteins/geneticsen
dc.subject.meshProteins/metabolismen
dc.subject.meshRNA-Binding Proteinsen
dc.subject.meshTranscription Factors/geneticsen
dc.subject.meshTranscription Factors/metabolismen
dc.titleECAT11/L1td1 is enriched in ESCs and rapidly activated during iPSC generation, but it is dispensable for the maintenance and induction of pluripotency.en
dc.typejournal article-
dc.type.niitypeJournal Article-
dc.identifier.jtitlePloS oneen
dc.identifier.volume6-
dc.identifier.issue5-
dc.relation.doi10.1371/journal.pone.0020461-
dc.textversionpublisher-
dc.identifier.artnume20461-
dc.identifier.pmid21637830-
dcterms.accessRightsopen access-
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