論文

国際誌
2019年7月1日

GPAT2 is required for piRNA biogenesis, transposon silencing, and maintenance of spermatogonia in mice†.

Biology of reproduction
  • Yusuke Shiromoto
  • ,
  • Satomi Kuramochi-Miyagawa
  • ,
  • Ippei Nagamori
  • ,
  • Shinichiro Chuma
  • ,
  • Tatsuhiko Arakawa
  • ,
  • Toru Nishimura
  • ,
  • Hidetoshi Hasuwa
  • ,
  • Taro Tachibana
  • ,
  • Masahito Ikawa
  • ,
  • Toru Nakano

101
1
開始ページ
248
終了ページ
256
記述言語
英語
掲載種別
研究論文(学術雑誌)
DOI
10.1093/biolre/ioz056

PIWI-interacting RNAs (piRNAs), a subclass of germ cell-specific noncoding small RNAs, are essential for de novo DNA methylation of retrotransposon genes in embryonic testes. PIWIL2/MILI, one of three mouse PIWI family members, is indispensable for piRNA production, DNA methylation of retrotransposons presumably via piRNA, and normal spermatogenesis. In vitro analysis using germline stem cells (GS cells) revealed that glycerol-3-phosphate acyltransferase 2 (GPAT2), which is a mitochondrial outer membrane protein involved in generation of lysophosphatidic acid (LPA) and highly expressed in testes, plays important roles in spermatogenesis. Namely, GPAT2 binds to PIWIL2 and is closely involved in the biogenesis of piRNAs; this process is independent of its enzymatic activity on LPA. However, GS cells recapitulate only a limited phase of spermatogenesis and the biological functions of GPAT2 remain largely unknown. In this study, we generated GPAT2-deficient mice and conducted comprehensive analyses. The deficient mice showed defective piRNA production and subsequent de-silencing of IAP and Line-1 retrotransposons in fetal testes. In addition, apoptosis of pachytene spermatocytes was observed. These abnormalities were all common to the phenotype of PIWIL2-deficient mice, in which piRNA production was impaired. GPAT2-deficient mice exhibited apoptosis in spermatogonia at the neonatal stage, which was not observed in PIWIL2-deficient mice. These data show that GPAT2 plays a critical role in preventing apoptosis in spermatogonia.

リンク情報
DOI
https://doi.org/10.1093/biolre/ioz056
PubMed
https://www.ncbi.nlm.nih.gov/pubmed/30951587

エクスポート
BibTeX RIS