Distinct enhancer activity of Oct4 in naive and primed mouse pluripotency

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dc.contributor.authorH W Choi-
dc.contributor.authorJ Y Joo-
dc.contributor.authorY J Hong-
dc.contributor.authorJ S Kim-
dc.contributor.authorH Song-
dc.contributor.authorJeong Woong Lee-
dc.contributor.authorG Wu-
dc.contributor.authorH R Scholer-
dc.contributor.authorJ T Do-
dc.date.accessioned2017-04-19T10:30:52Z-
dc.date.available2017-04-19T10:30:52Z-
dc.date.issued2016-
dc.identifier.issn2213-6711-
dc.identifier.uri10.1016/j.stemcr.2016.09.012ko
dc.identifier.urihttps://oak.kribb.re.kr/handle/201005/13585-
dc.description.abstractNaive and primed pluripotent stem cells (PSCs) and germ cells express the Oct4 gene. The Oct4 gene contains two cis-regulatory elements, the distal enhancer (DE) and proximal enhancer (PE), which differentially control Oct4 expression in a cell-type-specific and stage-specific manner. Here, we generated double transgenic mice carrying both Oct4-ΔPE-GFP and Oct4-ΔDE-tdTomato (RFP), enabling us to simultaneously monitor the activity of DE and PE. Oct4 expression is stage-specifically regulated by DE and PE during embryonic and germ cell development. Using this dual reporter system, we successfully cultured pure populations of naive (GFP+RFP-) and primed (GFP-RFP+) PSCs. We found that GFP+RFP- cells were metastable (not naive) in serum-containing medium; stable naive pluripotent cells were observed in medium containing two inhibitors (Meki and GSKi) but lacked serum. Finally, we suggest that the activity of Oct4 DE and PE is regulated by the repressive histone marks and DNA methylation in a cell-type-specific manner-
dc.publisherElsevier-Cell Press-
dc.titleDistinct enhancer activity of Oct4 in naive and primed mouse pluripotency-
dc.title.alternativeDistinct enhancer activity of Oct4 in naive and primed mouse pluripotency-
dc.typeArticle-
dc.citation.titleStem Cell Reports-
dc.citation.number5-
dc.citation.endPage926-
dc.citation.startPage911-
dc.citation.volume7-
dc.contributor.affiliatedAuthorJeong Woong Lee-
dc.contributor.alternativeName최현우-
dc.contributor.alternativeName주진영-
dc.contributor.alternativeName홍연주-
dc.contributor.alternativeName김종수-
dc.contributor.alternativeName송혁-
dc.contributor.alternativeName이정웅-
dc.contributor.alternativeNameWu-
dc.contributor.alternativeNameScholer-
dc.contributor.alternativeName도정태-
dc.identifier.bibliographicCitationStem Cell Reports, vol. 7, no. 5, pp. 911-926-
dc.identifier.doi10.1016/j.stemcr.2016.09.012-
dc.subject.keywordenhancer-
dc.subject.keywordnaive pluripotency-
dc.subject.keywordOct4-
dc.subject.keywordprimed pluripotency-
dc.subject.localEnhancer-
dc.subject.localenhancer-
dc.subject.localnaive pluripotency-
dc.subject.localOct-4-
dc.subject.localOct4-
dc.subject.localprimed pluripotency-
dc.description.journalClassY-
Appears in Collections:
Division of A.I. & Biomedical Research > Biotherapeutics Translational Research Center > 1. Journal Articles
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