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

被引:100
作者
Imamura, Masanori
Miura, Kyoko
Iwabuchi, Kumiko
Ichisaka, Tomoko
Nakagawa, Masato
Lee, Jiyoung
Kanatsu-Shinohara, Mito
Shinohara, Takashi
Yamanaka, Shinya [1 ]
机构
[1] Kyoto Univ, Inst Frontier Med Sci, Dept Stem Cell Biol, Kyoto 6068507, Japan
[2] Kyoto Univ, Grad Sch Med, Dept Mol Genet, Kyoto 6068507, Japan
[3] Kyoto Univ, Grad Sch Med, Horizontal Med Res Org, Kyoto 6068501, Japan
来源
BMC DEVELOPMENTAL BIOLOGY | 2006年 / 6卷
关键词
D O I
10.1186/1471-213X-6-34
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
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.
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页数:16
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