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与小头畸形相关的转录调节因子AUTS2与多梳蛋白复合体PRC2协同作用,在小鼠体内产生上层神经元。

The microcephaly-associated transcriptional regulator AUTS2 cooperates with Polycomb complex PRC2 to produce upper-layer neurons in mice.

作者信息

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

机构信息

Department of Biochemistry and Cellular Biology, National Institute of Neuroscience, National Center of Neurology and Psychiatry (NCNP), Tokyo, 187-8502, Japan.

Department of NCNP Brain Physiology and Pathology, Institute of Science Tokyo, Tokyo, 113-8510, Japan.

出版信息

EMBO J. 2025 Mar;44(5):1354-1378. doi: 10.1038/s44318-024-00343-7. Epub 2025 Jan 15.

Abstract

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.

摘要

AUTS2综合征的特征是智力残疾和小头畸形,且常与自闭症谱系障碍相关,但潜在机制,尤其是与小头畸形相关的机制,仍未完全明确。在此,我们分析了转录调节因子AUTS2发生突变的小鼠,这些小鼠重现了小头畸形。它们的大脑显示中间祖细胞(IPC)的分裂减少,导致神经元数量减少以及上层皮质厚度降低。突变动物中AUTS2转录靶点Robo1的表达增加会抑制IPC分裂,转录组和染色质分析表明,AUTS2主要在IPC中抑制像Robo1这样的基因的转录。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,而在Auts2突变体中该修饰减少。此外,我们发现AUTS2与多梳蛋白复合体PRC2相互作用,并与其合作促进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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f6f8/11876313/82a52c11291f/44318_2024_343_Fig1_HTML.jpg

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