One Argonaute family member, Eif2c2 (Ago2), is essential for development and appears not to be involved in DNA methylation

被引:109
作者
Morita, Sumiyo
Horii, Takuro
Kimura, Mika
Goto, Yuji
Ochiya, Takahiro
Hatada, Izuho
机构
[1] Gunma Univ, Inst Mol & Cellular Regulat, Biosignal Genome Resource Ctr, Lab Genome Sci, Maebashi, Gunma 3718512, Japan
[2] Japan Sci & Technol Corp, PREST, Kawaguchi, Saitama 3320012, Japan
[3] Kyoto Univ, Fac Med, Horizontal Med Res Org, Sakyo Ku, Kyoto 6068501, Japan
[4] Natl Canc Ctr, Res Inst, Sect Studies Metastasis, Chuo Ku, Tokyo 1040045, Japan
基金
日本科学技术振兴机构;
关键词
RNAi; Eif2c2; dicer; microRNA; mouse; development;
D O I
10.1016/j.ygeno.2007.01.004
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
To elucidate the epigenetic role of RNAi in mammals, we disrupted the gene for Eif2c2 (Ago2), which works as the sole slicer of RNAi in the Argonaute family. In mice, disruption of Eif2c2 leads to embryonic lethality early in development after the implantation stage. This phenotype is completely different from that in a previous report, but somewhat similar to the disruption of Dicer1, another important component of RNAi. We also show that Eif2c2 is not required for the maintenance of DNA methylation in imprinted genes, centromeric repeats, and Xist. This suggests that developmental defects in the Eif2c2-deficient mouse are caused not at the transcriptional level, but rather at the posttranscriptional level through the miRNA-protein complex. (c) 2007 Elsevier Inc. All rights reserved.
引用
收藏
页码:687 / 696
页数:10
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