小头症相关转录调节因子AUTS2与Polycomb复合体PRC2在小鼠中协同产生上层神经元。

Kazumi Shimaoka,Kei Hori,Satoshi Miyashita,Yukiko U Inoue,Nao K N Tabe,Asami Sakamoto,Ikuko Hasegawa,Kayo Nishitani,Kunihiko Yamashiro,Saki F Egusa,Shoji Tatsumoto,Yasuhiro Go,Manabu Abe,Kenji Sakimura,Takayoshi Inoue,Takuya Imamura,Mikio Hoshino
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引用次数: 0

摘要

AUTS2综合征以智力残疾和小头畸形为特征,通常与自闭症谱系障碍有关,但其潜在机制,特别是与小头畸形有关的机制仍不完全清楚。在这里,我们分析了转录调节因子AUTS2突变的小鼠,它再现了小头畸形。他们的大脑表现出中间祖细胞(IPCs)分裂减少,导致神经元减少和上层皮层厚度下降。突变动物中AUTS2转录靶点Robo1的表达增加可抑制IPC分裂,转录组学和染色质分析表明,AUTS2主要抑制IPC中Robo1等基因的转录。AUTS2靶基因转录起始位点周围的区域富含抑制性组蛋白修饰H3K27me3,在AUTS2突变体中减少。此外,我们发现AUTS2与Polycomb复合物PRC2相互作用,并与之合作促进IPC分裂。这些发现揭示了在AUTS2综合征中观察到的小头畸形表型。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The microcephaly-associated transcriptional regulator AUTS2 cooperates with Polycomb complex PRC2 to produce upper-layer neurons in mice.
AUTS2 syndrome is characterized by intellectual disability and microcephaly, and is often associated with autism spectrum disorder, but the underlying mechanisms, particularly concerning microcephaly, remain incompletely understood. Here, we analyze mice mutated for the transcriptional regulator AUTS2, which recapitulate microcephaly. Their brains exhibit reduced division of intermediate progenitor cells (IPCs), leading to fewer neurons and decreased thickness in the upper-layer cortex. Increased expression of the AUTS2 transcriptional target Robo1 in the mutant animals suppresses IPC division, and transcriptomic and chromatin profiling shows that AUTS2 primarily represses transcription of genes like Robo1 in IPCs. Regions around the transcriptional start sites of AUTS2 target genes are enriched for the repressive histone modification H3K27me3, which is reduced in Auts2 mutants. Furthermore, we find that AUTS2 interacts with Polycomb complex PRC2, with which it cooperates to promote IPC division. These findings shed light on the microcephaly phenotype observed in the AUTS2 syndrome.
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