Epigenetic modification of retinoic acid-treated human embryonic stem cells

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dc.contributor.authorCheong, Hyun Subko
dc.contributor.authorLee, Han Chulko
dc.contributor.authorPark, Byung Laeko
dc.contributor.authorKim, Hyeminko
dc.contributor.authorJang, Min Jinko
dc.contributor.authorHan, Yong Mahnko
dc.contributor.authorKim, Seun-Youngko
dc.contributor.authorKim, Yong Sungko
dc.contributor.authorShin, Hyoung Dooko
dc.date.accessioned2013-03-09T20:40:24Z-
dc.date.available2013-03-09T20:40:24Z-
dc.date.created2012-02-06-
dc.date.created2012-02-06-
dc.date.issued2010-12-
dc.identifier.citationBMB REPORTS, v.43, no.12, pp.830 - 835-
dc.identifier.issn1976-6696-
dc.identifier.urihttp://hdl.handle.net/10203/97423-
dc.description.abstractEpigenetic modification of the genome through DNA methylation is the key to maintaining the differentiated state of human embryonic stem cells (hESCs), and it must be reset during differentiation by retinoic acid (RA) treatment. A genome-wide methylation/gene expression assay was performed in order to identify epigenetic modifications of RA-treated hESCs. Between undifferentiated and RA-treated hESCs, 166 differentially methylated CpG sites and 2,013 differentially expressed genes were discovered. Combined analysis of methylation and expression data revealed that 19 genes (STAP2, VAMP8, C10orf26, WFIKKN1, ELF3, C1QTNF6, C10orf10, MRGPRF, ARSE, LSAMP, CENTD3, LDB2, POU5F1, GSPT2, THY1, ZNF574, MSX1, SCMH1, and RARB) were highly correlated with each other. The results provided in this study will facilitate future investigations into the interplay between DNA methylation and gene expression through further functional and biological studies. [BMB reports 2010; 43(12): 830-835]-
dc.languageEnglish-
dc.publisherKOREAN SOCIETY BIOCHEMISTRY MOLECULAR BIOLOGY-
dc.subjectDNA METHYLATION-
dc.subjectGENE-EXPRESSION-
dc.subjectPROMOTER HYPERMETHYLATION-
dc.subjectPROSTATE-CANCER-
dc.subjectCARCINOMA-CELLS-
dc.subjectMARKER GENES-
dc.subjectDIFFERENTIATION-
dc.subjectPROTEIN-
dc.subjectLINES-
dc.subjectGENOME-
dc.titleEpigenetic modification of retinoic acid-treated human embryonic stem cells-
dc.typeArticle-
dc.identifier.wosid000285816300010-
dc.identifier.scopusid2-s2.0-78650700269-
dc.type.rimsART-
dc.citation.volume43-
dc.citation.issue12-
dc.citation.beginningpage830-
dc.citation.endingpage835-
dc.citation.publicationnameBMB REPORTS-
dc.identifier.doi10.5483/BMBRep.2010.43.12.830-
dc.contributor.localauthorHan, Yong Mahn-
dc.contributor.nonIdAuthorCheong, Hyun Sub-
dc.contributor.nonIdAuthorLee, Han Chul-
dc.contributor.nonIdAuthorPark, Byung Lae-
dc.contributor.nonIdAuthorKim, Hyemin-
dc.contributor.nonIdAuthorJang, Min Jin-
dc.contributor.nonIdAuthorKim, Seun-Young-
dc.contributor.nonIdAuthorKim, Yong Sung-
dc.contributor.nonIdAuthorShin, Hyoung Doo-
dc.description.isOpenAccessY-
dc.type.journalArticleArticle-
dc.subject.keywordAuthorDNA methylation-
dc.subject.keywordAuthorEpigenetic modification-
dc.subject.keywordAuthorGene expression-
dc.subject.keywordAuthorHuman embryonic stem cell-
dc.subject.keywordAuthorRetinoic acid-
dc.subject.keywordPlusDNA METHYLATION-
dc.subject.keywordPlusGENE-EXPRESSION-
dc.subject.keywordPlusPROMOTER HYPERMETHYLATION-
dc.subject.keywordPlusPROSTATE-CANCER-
dc.subject.keywordPlusCARCINOMA-CELLS-
dc.subject.keywordPlusMARKER GENES-
dc.subject.keywordPlusDIFFERENTIATION-
dc.subject.keywordPlusPROTEIN-
dc.subject.keywordPlusLINES-
dc.subject.keywordPlusGENOME-
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