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

被引:286
作者
Zhao, XY
Ueba, T
Christie, BR
Barkho, B
McConnell, MJ
Nakashima, K
Lein, ES
Eadie, BD
Willhoite, AR
Muotri, AR
Summers, RG
Chun, J
Lee, KF
Gage, FH
机构
[1] Salk Inst Biol Studies, Genet Lab, San Diego, CA 92186 USA
[2] Salk Inst Biol Studies, Peptide Biol lab, San Diego, CA 92186 USA
[3] Univ Calif San Diego, Dept Pharmacol, La Jolla, CA 92093 USA
[4] Univ British Columbia, Dept Psychol, Vancouver, BC V6T 1Z4, Canada
关键词
D O I
10.1073/pnas.1131928100
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
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.
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页码:6777 / 6782
页数:6
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