Cited 5 time in
Nac1 facilitates pluripotency gene activation for establishing somatic cell reprogramming
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Choi, Hwan | - |
| dc.contributor.author | Park, Hyeok Ju | - |
| dc.contributor.author | Kim, Hongwon | - |
| dc.contributor.author | Kim, Junyeop | - |
| dc.contributor.author | Lee, Yong Kyu | - |
| dc.contributor.author | Kim, Jongpil | - |
| dc.date.accessioned | 2023-04-28T02:40:38Z | - |
| dc.date.available | 2023-04-28T02:40:38Z | - |
| dc.date.issued | 2019-10-15 | - |
| dc.identifier.issn | 0006-291X | - |
| dc.identifier.issn | 1090-2104 | - |
| dc.identifier.uri | https://scholarworks.dongguk.edu/handle/sw.dongguk/7518 | - |
| dc.description.abstract | Transcription 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.extent | 6 | - |
| dc.language | 영어 | - |
| dc.language.iso | ENG | - |
| dc.publisher | ACADEMIC PRESS INC ELSEVIER SCIENCE | - |
| dc.title | Nac1 facilitates pluripotency gene activation for establishing somatic cell reprogramming | - |
| dc.type | Article | - |
| dc.publisher.location | 미국 | - |
| dc.identifier.doi | 10.1016/j.bbrc.2019.08.043 | - |
| dc.identifier.scopusid | 2-s2.0-85070378555 | - |
| dc.identifier.wosid | 000506401900010 | - |
| dc.identifier.bibliographicCitation | BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, v.518, no.2, pp 253 - 258 | - |
| dc.citation.title | BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS | - |
| dc.citation.volume | 518 | - |
| dc.citation.number | 2 | - |
| dc.citation.startPage | 253 | - |
| dc.citation.endPage | 258 | - |
| dc.type.docType | Article | - |
| dc.description.isOpenAccess | N | - |
| dc.description.journalRegisteredClass | sci | - |
| dc.description.journalRegisteredClass | scie | - |
| dc.description.journalRegisteredClass | scopus | - |
| dc.relation.journalResearchArea | Biochemistry & Molecular Biology | - |
| dc.relation.journalResearchArea | Biophysics | - |
| dc.relation.journalWebOfScienceCategory | Biochemistry & Molecular Biology | - |
| dc.relation.journalWebOfScienceCategory | Biophysics | - |
| dc.subject.keywordPlus | PROTEIN | - |
| dc.subject.keywordPlus | CIRCUITRY | - |
| dc.subject.keywordPlus | NETWORK | - |
| dc.subject.keywordPlus | NANOG | - |
| dc.subject.keywordPlus | STATE | - |
| dc.subject.keywordPlus | TET1 | - |
| dc.subject.keywordAuthor | Nucleus accumbens-1 | - |
| dc.subject.keywordAuthor | Pluripotency | - |
| dc.subject.keywordAuthor | Induced pluripotent stem cell | - |
| dc.subject.keywordAuthor | Embryonic stem cell | - |
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