Detailed Information

Cited 4 time in webofscience Cited 5 time in scopus
Metadata Downloads

Nac1 facilitates pluripotency gene activation for establishing somatic cell reprogramming

Full metadata record
DC Field Value Language
dc.contributor.authorChoi, Hwan-
dc.contributor.authorPark, Hyeok Ju-
dc.contributor.authorKim, Hongwon-
dc.contributor.authorKim, Junyeop-
dc.contributor.authorLee, Yong Kyu-
dc.contributor.authorKim, Jongpil-
dc.date.accessioned2023-04-28T02:40:38Z-
dc.date.available2023-04-28T02:40:38Z-
dc.date.issued2019-10-15-
dc.identifier.issn0006-291X-
dc.identifier.issn1090-2104-
dc.identifier.urihttps://scholarworks.dongguk.edu/handle/sw.dongguk/7518-
dc.description.abstractTranscription factors play a central role in pluripotency transcription circuitry for establishing pluripotent reprogramming. Master transcription factors Oct4, Nanog, and Sox2 are known to form the core of the pluripotency transcription network. Other transcription factors also play critical roles for further refining the core circuitry for pluripotency in induced pluripotent stem (iPS) cells. Here, we reported that Nacl interacted with the master pluripotent factors Oct4 and Nanog co-occupies gene promoters bound by these transcriptional factors for establishing pluripotency. Moreover, this interaction coordinates gene expression with H3K4me3 in the somatic cell reprogramming. Knockdown of Nac1 suppressed somatic cell reprogramming, whereas overexpression of Nac1 resulted in enhanced efficiency of induced pluripotent cell generation. Altogether, these results reveal the genome wide role for Nac1 in the contribution to the pluripotency circuitry and the regulation of the establishing pluripotent state. (C) 2019 Elsevier Inc. All rights reserved.-
dc.format.extent6-
dc.language영어-
dc.language.isoENG-
dc.publisherACADEMIC PRESS INC ELSEVIER SCIENCE-
dc.titleNac1 facilitates pluripotency gene activation for establishing somatic cell reprogramming-
dc.typeArticle-
dc.publisher.location미국-
dc.identifier.doi10.1016/j.bbrc.2019.08.043-
dc.identifier.scopusid2-s2.0-85070378555-
dc.identifier.wosid000506401900010-
dc.identifier.bibliographicCitationBIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, v.518, no.2, pp 253 - 258-
dc.citation.titleBIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS-
dc.citation.volume518-
dc.citation.number2-
dc.citation.startPage253-
dc.citation.endPage258-
dc.type.docTypeArticle-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClasssci-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaBiochemistry & Molecular Biology-
dc.relation.journalResearchAreaBiophysics-
dc.relation.journalWebOfScienceCategoryBiochemistry & Molecular Biology-
dc.relation.journalWebOfScienceCategoryBiophysics-
dc.subject.keywordPlusPROTEIN-
dc.subject.keywordPlusCIRCUITRY-
dc.subject.keywordPlusNETWORK-
dc.subject.keywordPlusNANOG-
dc.subject.keywordPlusSTATE-
dc.subject.keywordPlusTET1-
dc.subject.keywordAuthorNucleus accumbens-1-
dc.subject.keywordAuthorPluripotency-
dc.subject.keywordAuthorInduced pluripotent stem cell-
dc.subject.keywordAuthorEmbryonic stem cell-
Files in This Item
There are no files associated with this item.
Appears in
Collections
College of Advanced Convergence Engineering > Department of Computer Science and Artificial Intelligence > 1. Journal Articles
College of Natural Science > Department of Chemistry > 1. Journal Articles

qrcode

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

Related Researcher

Researcher Kim, Jong Pil photo

Kim, Jong Pil
College of Natural Science (Department of Chemistry)
Read more

Altmetrics

Total Views & Downloads

BROWSE