Cited time in webofscience Cited time in scopus

Full metadata record

DC Field Value Language
dc.contributor.author Boo, Kyungjin -
dc.contributor.author Bhin, Jinhyuk -
dc.contributor.author Jeon, Yoon -
dc.contributor.author Kim, Joomyung -
dc.contributor.author Shin, Hi-Jai R. -
dc.contributor.author Park, Jong-Eun -
dc.contributor.author Kim, Kyeongkyu -
dc.contributor.author Kim, Chang Rok -
dc.contributor.author Jang, Hyonchol -
dc.contributor.author Kim, In-Hoo -
dc.contributor.author Kim, V. Narry -
dc.contributor.author Hwang, Daehee -
dc.contributor.author Lee, Ho -
dc.contributor.author Baek, Sung Hee -
dc.date.available 2017-07-11T05:59:04Z -
dc.date.created 2017-04-10 -
dc.date.issued 2015-04 -
dc.identifier.issn 2041-1723 -
dc.identifier.uri http://hdl.handle.net/20.500.11750/2913 -
dc.description.abstract The actions of transcription factors, chromatin modifiers and noncoding RNAs are crucial for the programming of cell states. Although the importance of various epigenetic machineries for controlling pluripotency of embryonic stem (ES) cells has been previously studied, how chromatin modifiers cooperate with specific transcription factors still remains largely elusive. Here, we find that Pontin chromatin remodelling factor plays an essential role as a coactivator for Oct4 for maintenance of pluripotency in mouse ES cells. Genome-wide analyses reveal that Pontin and Oct4 share a substantial set of target genes involved in ES cell maintenance. Intriguingly, we find that the Oct4-dependent coactivator function of Pontin extends to the transcription of large intergenic noncoding RNAs (lincRNAs) and in particular linc1253, a lineage programme repressing lincRNA, is a Pontin-dependent Oct4 target lincRNA. Together, our findings demonstrate that the Oct4-Pontin module plays critical roles in the regulation of genes involved in ES cell fate determination. -
dc.language English -
dc.publisher Nature Publishing Group -
dc.title Pontin functions as an essential coactivator for Oct4-dependent lincRNA expression in mouse embryonic stem cells -
dc.type Article -
dc.identifier.doi 10.1038/ncomms7810 -
dc.identifier.scopusid 2-s2.0-84927637015 -
dc.identifier.bibliographicCitation Nature Communications, v.6 -
dc.description.isOpenAccess TRUE -
dc.subject.keywordPlus NONCODING RNAS -
dc.subject.keywordPlus REGULATES PLURIPOTENCY -
dc.subject.keywordPlus CHROMATIN -
dc.subject.keywordPlus GENE -
dc.subject.keywordPlus DIFFERENTIATION -
dc.subject.keywordPlus TRANSCRIPTION -
dc.subject.keywordPlus INTEGRATION -
dc.subject.keywordPlus CIRCUITRY -
dc.subject.keywordPlus REVEALS -
dc.subject.keywordPlus NETWORK -
dc.citation.title Nature Communications -
dc.citation.volume 6 -
Files in This Item:
10.1038_ncomms7810.pdf

10.1038_ncomms7810.pdf

기타 데이터 / 2.59 MB / Adobe PDF download
Appears in Collections:
Department of New Biology Systems Biology and Medicine Lab 1. Journal Articles

qrcode

  • twitter
  • facebook
  • mendeley

Items in Repository are protected by copyright, with all rights reserved, unless otherwise indicated.

BROWSE