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Mice lacking methyl-CpG binding protein 1 have deficits in adult neurogenesis and hippocampal function

  • Xinyu Zhao
  • , Tetsuya Ueba
  • , Brian R. Christie
  • , Basam Barkho
  • , Michael J. McConnell
  • , Kinichi Nakashima
  • , Edward S. Lein
  • , Brennan D. Eadie
  • , Andrew R. Willhoite
  • , Alysson R. Muotri
  • , Robert G. Summers
  • , Jerold Chun
  • , Kuo Fen Lee
  • , Fred H. Gage

研究成果: ジャーナルへの寄稿 › 学術誌 › 査読

抄録

DNA methylation-mediated epigenetic regulation plays critical roles in regulating mammalian gene expression, but its role in normal brain function is not clear. Methyl-CpG binding protein 1 (MBD1), a member of the methylated DNA-binding protein family, has been shown to bind methylated gene promoters and facilitate transcriptional repression in vitro. Here we report the generation and analysis of MBD1-/- mice. MBD1-/- mice had no detectable developmental defects and appeared healthy throughout life. However, we found that MBD1-/- neural stem cells exhibited reduced neuronal differentiation and increased genomic instability. Furthermore, adult MBD1-/- mice had decreased neurogenesis, impaired spatial learning, and a significant reduction in long-term potentiation in the dentate gyrus of the hippocampus. Our findings indicate that DNA methylation is important in maintaining cellular genomic stability and is crucial for normal neural stem cell and brain functions.

本文言語英語
ページ(範囲)6777-6782
ページ数6
ジャーナルProceedings of the National Academy of Sciences of the United States of America
巻100
号11
DOI
出版ステータス出版済み - 5月 27 2003
外部発表はい

!!!All Science Journal Classification (ASJC) codes

  • 一般

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