論文

査読有り
2006年7月

Transcriptional repression and DNA hypermethylation of a small set of ES cell marker genes in male germline stem cells

BMC DEVELOPMENTAL BIOLOGY
  • Masanori Imamura
  • ,
  • Kyoko Miura
  • ,
  • Kumiko Iwabuchi
  • ,
  • Tomoko Ichisaka
  • ,
  • Masato Nakagawa
  • ,
  • Jiyoung Lee
  • ,
  • Mito Kanatsu-Shinohara
  • ,
  • Takashi Shinohara
  • ,
  • Shinya Yamanaka

6
開始ページ
34
終了ページ
記述言語
英語
掲載種別
研究論文(学術雑誌)
DOI
10.1186/1471-213X-6-34
出版者・発行元
BIOMED CENTRAL LTD

Background: We previously identified a set of genes called ECATs (ES cell-associated transcripts) that are expressed at high levels in mouse ES cells. Here, we examine the expression and DNA methylation of ECATs in somatic cells and germ cells.
Results: In all ECATs examined, the promoter region had low methylation levels in ES cells, but higher levels in somatic cells. In contrast, in spite of their lack of pluripotency, male germline stem (GS) cells expressed most ECATs and exhibited hypomethylation of ECAT promoter regions. We observed a similar hypomethylation of ECAT loci in adult testis and isolated sperm. Some ECATs were even less methylated in male germ cells than in ES cells. However, a few ECATs were not expressed in GS cells, and most of them targets of Oct3/4 and Sox2. The Octamer/Sox regulatory elements were hypermethylated in these genes. In addition, we found that GS cells express little Sox2 protein and low Oct3/4 protein despite abundant expression of their transcripts.
Conclusion: Our results suggest that DNA hypermethylation and transcriptional repression of a small set of ECATs, together with post-transcriptional repression of Oct3/4 and Sox2, contribute to the loss of pluripotency in male germ cells.

リンク情報
DOI
https://doi.org/10.1186/1471-213X-6-34
PubMed
https://www.ncbi.nlm.nih.gov/pubmed/16859545
Web of Science
https://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=JSTA_CEL&SrcApp=J_Gate_JST&DestLinkType=FullRecord&KeyUT=WOS:000240687300001&DestApp=WOS_CPL
ID情報
  • DOI : 10.1186/1471-213X-6-34
  • ISSN : 1471-213X
  • PubMed ID : 16859545
  • Web of Science ID : WOS:000240687300001

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