Diverse gene regulatory mechanisms mediated by Polycomb group proteins during neural development

被引:9
|
作者
Tsuboi, Masafumi [1 ]
Hirabayashi, Yusuke [1 ]
Gotoh, Yukiko [2 ,3 ]
机构
[1] Univ Tokyo, Grad Sch Engn, Tokyo 1130033, Japan
[2] Univ Tokyo, Grad Sch Pharmaceut Sci, Tokyo 1130033, Japan
[3] Univ Tokyo, Int Res Ctr Neurointelligence WPI IRCN, Tokyo 1130033, Japan
关键词
HISTONE H2A UBIQUITINATION; RNA-POLYMERASE-II; REPRESSIVE COMPLEX 1; CHROMATIN-STRUCTURE; PRC2; RECRUITMENT; BIVALENT GENES; SELF-RENEWAL; CPG ISLANDS; SAM DOMAIN; STEM-CELLS;
D O I
10.1016/j.conb.2019.07.003
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
While all the developmental genes are temporarily repressed for future activation in the pluripotent stern cells, non-neural genes become persistently repressed in the course of commitment to the neuronal lineage. Although Polycomb group proteins (PcG) are key factors for both temporary and persistent repression of the developmental genes, how the same group of proteins can differentially repress target genes remains unclarified. The identification of a variety of PcG complexes and activities sheds light on these issues. In this review, based on the recent findings including those with the use of interactome and Chromosome Conformation Capture (3C)-type analyses, we summarize the molecular mechanisms of PcG-mediated gene regulation and discuss how PcG regulates cell fate specification during neural development.
引用
收藏
页码:164 / 173
页数:10
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