自闭症相关染色质调控因子的多效性

Micaela Lasser, Nawei Sun, Yuxiao Xu, Sheng Wang, Sam Drake, Karen Law, Silvano Gonzalez, Belinda Wang, Vanessa Drury, Octavio Castillo, Y. Zaltsman, Jeanselle Dea, Ethel Bader, Kate McCluskey, M. State, A. Willsey, H. Willsey
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引用次数: 2

摘要

高置信度自闭症谱系障碍(hcASD)风险基因的基因本体论分析历来强调染色质调控和突触功能是病理生物学的主要贡献者。我们最近在体内的功能研究也涉及到微管生物学,并确定了细胞增殖中断是ASD的一种趋同表型。由于已知许多染色质调节因子,包括ASD风险基因ADNP和CHD3,可以直接调节微管蛋白和组蛋白,我们研究了与ASD最密切相关的五种染色质调节因子(ADNP、CHD8、CHD2、POGZ和SUV420H1/KMT5B),特别是在微管生物学方面。我们观察到,在体外和体内,这五种细胞都定位于有丝分裂纺锤体的微管。对CHD2的进一步深入研究提供了证据,表明患者来源的突变导致一系列与微管相关的表型,包括有丝分裂纺锤体蛋白定位中断、纺锤体缺陷、细胞周期延迟、DNA损伤和细胞死亡。最后,我们观察到ASD遗传风险在微管相关蛋白中显著富集,表明其具有更广泛的相关性。总之,这些结果提供了进一步的证据,表明微管蛋白生物学和细胞增殖在ASD中的作用值得进一步研究,并突出了仅仅依靠注释基因功能来寻找病理机制的缺陷。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Pleiotropy of autism-associated chromatin regulators
Gene ontology analyses of high confidence autism spectrum disorder (hcASD) risk genes have historically highlighted chromatin regulation and synaptic function as major contributors to pathobiology. Our recent functional work in vivo has additionally implicated microtubule biology and identified disrupted cellular proliferation as a convergent ASD phenotype. As many chromatin regulators, including ASD risk genes ADNP and CHD3, are known to directly regulate both tubulins and histones, we studied the five chromatin regulators most strongly associated with ASD (ADNP, CHD8, CHD2, POGZ, and SUV420H1/KMT5B) specifically with respect to microtubule biology. We observe that all five localize to microtubules of the mitotic spindle in vitro and in vivo. Further in-depth investigation of CHD2 provides evidence that patient-derived mutations lead to a range of microtubule-related phenotypes, including disrupted localization of the protein at the mitotic spindle, spindle defects, cell cycle stalling, DNA damage, and cell death. Lastly, we observe that ASD genetic risk is significantly enriched among microtubule-associated proteins, suggesting broader relevance. Together, these results provide further evidence that the role of tubulin biology and cellular proliferation in ASD warrant further investigation and highlight the pitfalls of relying solely on annotated gene functions in the search for pathological mechanisms.
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