Leibniz Institute for Age Research, Fritz Lipmann Institute (FLI), Beutenbergstrasse 11, 07745 Jena, Germany.
Disease Genomics and Individualized Medicine Laboratory, Beijing Institute of Genomics, Chinese Academy of Sciences, 1-7 Beichen West Road, Chaoyang District, Beijing 100101, P.R. China; University of Chinese Academy of Sciences, 19A Yuquan Road, Beijing 100049, P.R. China.
Cell Stem Cell. 2014 May 1;14(5):632-43. doi: 10.1016/j.stem.2014.04.001.
Fate decisions in neural progenitor cells are orchestrated via multiple pathways, and the role of histone acetylation in these decisions has been ascribed to a general function promoting gene activation. Here, we show that the histone acetyltransferase (HAT) cofactor transformation/transcription domain-associated protein (Trrap) specifically regulates activation of cell-cycle genes, thereby integrating discrete cell-intrinsic programs of cell-cycle progression and epigenetic regulation of gene transcription in order to control neurogenesis. Deletion of Trrap impairs recruitment of HATs and transcriptional machinery specifically to E2F cell-cycle target genes, disrupting their transcription with consequent cell-cycle lengthening specifically within cortical apical neural progenitors (APs). Consistently, Trrap conditional mutants exhibit microcephaly because of premature differentiation of APs into intermediate basal progenitors and neurons, and overexpressing cell-cycle regulators in vivo can rescue these premature differentiation defects. These results demonstrate an essential and highly specific role for Trrap-mediated histone regulation in controlling cell-cycle progression and neurogenesis.
神经祖细胞中的命运决定是通过多种途径进行协调的,组蛋白乙酰化在这些决定中的作用归因于促进基因激活的一般功能。在这里,我们表明组蛋白乙酰转移酶 (HAT) 共因子转化/转录结构域相关蛋白 (Trrap) 特异性调节细胞周期基因的激活,从而整合离散的细胞内在细胞周期进程程序和基因转录的表观遗传调控,以控制神经发生。Trrap 的缺失会特异性地破坏 HAT 和转录机制向 E2F 细胞周期靶基因的募集,从而破坏它们的转录,导致细胞周期在皮质顶神经祖细胞 (APs) 中特异性延长。一致地,Trrap 条件性突变体由于 APs 过早分化为中间基底祖细胞和神经元而出现小头畸形,并且体内过表达细胞周期调节剂可以挽救这些过早分化缺陷。这些结果表明 Trrap 介导的组蛋白调控在控制细胞周期进程和神经发生中具有重要且高度特异性的作用。