多梳抑制复合物1和2在小脑神经发育过程中独立和动态地调节常染色质。

IF 3.7 2区 生物学 Q1 GENETICS & HEREDITY
PLoS Genetics Pub Date : 2025-09-29 eCollection Date: 2025-09-01 DOI:10.1371/journal.pgen.1011843
Aditya Parmar, Anjali Srinivasan, Lena Krockenberger, Abijith Augustine, Owin Gong, Addison C Bullard, Riya Kalra, Leya Ledvin, Dylan Pilz, Jonathan Tawil, Challana E Tea, Kelly C Wang, Olivia Urso, Larissa M Kaube, Ying Sun, Roman Sasik, Kyle J Gaulton, Kathleen M Fisch, Cole J Ferguson
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引用次数: 0

摘要

多梳抑制复合物(Polycomb repression Complexes, prc)以化学修饰组蛋白致密染色质结构和抑制转录而闻名。一般来说,PRC1单泛素化组蛋白2A的赖氨酸119位点(H2AK119ub), PRC2甲基化组蛋白H3赖氨酸27位点(H3K27me3、H3K27me2和H3K27me1),但这些活性的范围和功能由于涉及不同细胞背景和两种复合物组成的多种因素而变得复杂。由于PRC失调与神经发育障碍有关,但对其在神经元中的正常活动知之甚少,我们使用CUT&RUN绘制了出生后两个时间点(第12天和第3个月)小鼠小脑中PRC依赖性组蛋白修饰。我们发现,随着小脑的成熟,H2AK119ub出现在异染色质和常染色质中,在活性增强子和启动子中变得丰富,而在异染色质中被耗尽。出乎意料的是,PRC1产物H2AK119ub在没有PRC2产物H3K27me3伴随的情况下频繁出现;这些位点的染色质状态比H2AK119ub与H3K27me3共定位的位点更具动态性。在神经发育过程中,H2AK119ub在具有活性顺式调节元件染色质特征的位点沉积也倾向于获得与常染色质相关的修饰H3K4me3和H3K27ac。重要的是,H2AK119ub在二价启动子和仅h3k4me3启动子中的沉积减少了下游基因的转录。与肝脏和肾脏相比,H2AK119ub沉积的模式是小脑特有的。然后我们发现PRC2产物H3K27me1形成了常染色质区,与H3K27me3主导的异染色质区交替。在早期和晚期时间点之间,H3K27me1在表达基因体的一个子集中富集,而在大多数其他基因中缺失,而与相应mrna的丰度保持不相关。我们的数据表明,在小脑发育过程中,H2AK119ub和H3K27me1的沉积可能分别微调顺式调控元件和转录的活性,而PRC1和PRC2的活性在成熟的大脑中变得不耦合。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Polycomb repressive complexes 1 and 2 independently and dynamically regulate euchromatin during cerebellar neurodevelopment.

Polycomb Repressive Complexes (PRCs) are known for chemically modifying histones to compact chromatin structure and repress transcription. Broadly speaking, PRC1 monoubiquitinates histone 2A at lysine 119 (H2AK119ub), and PRC2 methylates histone H3 lysine 27 (H3K27me3, H3K27me2 and H3K27me1), but the scope and functions of these activities are complicated by a multiplicity of factors involving distinct cellular contexts and compositions of both complexes. Because epigenetic dysregulation is associated with neurodevelopmental disorders, but little is known about normal PRC activities in neurons, we used CUT&RUN to map PRC-dependent histone modifications in the mouse cerebellum at two postnatal timepoints (day 12 and 3 months). We find that H2AK119ub appears within both heterochromatin and euchromatin as the cerebellum matures, becoming enriched within active enhancers and promoters while being depleted from heterochromatin. Unexpectedly, the PRC1 product H2AK119ub appeared frequently without the accompaniment of the PRC2 product H3K27me3; leading to a much more dynamic chromatin state than when these two marks colocalized. Deposition of H2AK119ub at loci with the chromatin signature of active cis-regulatory elements tended to also gain the euchromatin-associated modifications H3K4me3 and H3K27ac during neurodevelopment. Importantly, deposition of H2AK119ub within both bivalent and H3K4me3-only promoters reduced transcription of downstream genes. The pattern of H2AK119ub deposition was specific to the cerebellum compared to liver and kidney. We then show that the PRC2 product H3K27me1 formed euchromatic zones that alternated with heterochromatic zones dominated by H3K27me3. Between the early and late timepoints H3K27me1 became enriched within a subset of expressed gene bodies and depleted from most other genes while remaining uncorrelated with the abundance of the corresponding mRNAs. Our data lead us to propose that deposition of H2AK119ub and H3K27me1 during cerebellar development likely fine-tunes the activity of cis-regulatory elements and transcription, respectively, and that PRC1 and PRC2 activities become uncoupled in the mature brain.

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PLoS Genetics
PLoS Genetics GENETICS & HEREDITY-
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期刊介绍: PLOS Genetics is run by an international Editorial Board, headed by the Editors-in-Chief, Greg Barsh (HudsonAlpha Institute of Biotechnology, and Stanford University School of Medicine) and Greg Copenhaver (The University of North Carolina at Chapel Hill). Articles published in PLOS Genetics are archived in PubMed Central and cited in PubMed.
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