An AUTS2-Polycomb complex activates gene expression in the CNS

被引:242
作者
Gao, Zhonghua [1 ]
Lee, Pedro [1 ]
Stafford, James M. [1 ]
von Schimmelmann, Melanie [2 ]
Schaefer, Anne [2 ]
Reinberg, Danny [1 ]
机构
[1] NYU, Howard Hughes Med Inst, Langone Sch Med, Dept Biochem & Mol Pharmacol, New York, NY 10016 USA
[2] Mt Sinai Sch Med, Dept Neurosci, Friedman Brain Inst, New York, NY 10029 USA
关键词
HISTONE METHYLTRANSFERASE ACTIVITY; STEM-CELLS; POLYCOMB; PROTEIN; MECHANISMS; CHROMATIN; ENHANCER; H2A; UBIQUITYLATION; VOCALIZATIONS;
D O I
10.1038/nature13921
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
Naturally occurring variations of Polycomb repressive complex 1 (PRC1) comprise a core assembly of Polycomb group proteins and additional factors that include, surprisingly, autism susceptibility candidate 2 (AUTS2). Although AUTS2 is often disrupted in patients with neuronal disorders, the mechanism underlying the pathogenesis is unclear. We investigated the role of AUTS2 as part of a previously identified PRC1 complex (PRC1-AUTS2), and in the context of neurodevelopment. In contrast to the canonical role of PRC1 in gene repression, PRC1-AUTS2 activates transcription. Biochemical studies demonstrate that the CK2 component of PRC1-AUTS2 neutralizes PRC1 repressive activity, whereas AUTS2-mediated recruitment of P300 leads to gene activation. Chromatin immunoprecipitation followed by sequencing (ChIP-seq) demonstrated that AUTS2 regulates neuronal gene expression through promoter association. Conditional targeting of Auts2 in the mouse central nervous system (CNS) leads to various developmental defects. These findings reveal a natural means of subverting PRC1 activity, linking key epigenetic modulators with neuronal functions and diseases.
引用
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页码:349 / +
页数:18
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