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COMPASS 和 SWI/SNF 复合物在发育和疾病中的作用。

COMPASS and SWI/SNF complexes in development and disease.

机构信息

Simpson Querrey Institute for Epigenetics, Northwestern University Feinberg School of Medicine, Chicago, IL, USA.

Department of Biochemistry and Molecular Genetics, Northwestern University Feinberg School of Medicine, Chicago, IL, USA.

出版信息

Nat Rev Genet. 2021 Jan;22(1):38-58. doi: 10.1038/s41576-020-0278-0. Epub 2020 Sep 21.

DOI:10.1038/s41576-020-0278-0
PMID:32958894
Abstract

The Trithorax group (TrxG) of proteins is a large family of epigenetic regulators that form multiprotein complexes to counteract repressive developmental gene expression programmes established by the Polycomb group of proteins and to promote and maintain an active state of gene expression. Recent studies are providing new insights into how two crucial families of the TrxG - the COMPASS family of histone H3 lysine 4 methyltransferases and the SWI/SNF family of chromatin remodelling complexes - regulate gene expression and developmental programmes, and how misregulation of their activities through genetic abnormalities leads to pathologies such as developmental disorders and malignancies.

摘要

Trithorax 组(TrxG)蛋白是一个大型的表观遗传调控因子家族,它们形成多蛋白复合物,以抵消由 Polycomb 组蛋白建立的抑制性发育基因表达程序,并促进和维持基因表达的活跃状态。最近的研究为我们提供了新的见解,了解 TrxG 的两个关键家族——组蛋白 H3 赖氨酸 4 甲基转移酶的 COMPASS 家族和染色质重塑复合物的 SWI/SNF 家族——如何调节基因表达和发育程序,以及它们的活性如何通过遗传异常失调导致发育障碍和恶性肿瘤等病理。

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COMPASS and SWI/SNF complexes in development and disease.COMPASS 和 SWI/SNF 复合物在发育和疾病中的作用。
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本文引用的文献

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Coordinated regulation of cellular identity-associated H3K4me3 breadth by the COMPASS family.COMPASS家族对细胞身份相关的H3K4me3宽度的协同调控。
Sci Adv. 2020 Jun 24;6(26):eaaz4764. doi: 10.1126/sciadv.aaz4764. eCollection 2020 Jun.
2
Uncoupling histone H3K4 trimethylation from developmental gene expression via an equilibrium of COMPASS, Polycomb and DNA methylation.通过 COMPASS、Polycomb 和 DNA 甲基化之间的平衡,将组蛋白 H3K4 三甲基化与发育基因表达解偶联。
Nat Genet. 2020 Jun;52(6):615-625. doi: 10.1038/s41588-020-0618-1. Epub 2020 May 11.
3
Loss of the neural-specific BAF subunit ACTL6B relieves repression of early response genes and causes recessive autism.
Mgv1-Rlm1轴在靶基因启动子处协调SAGA和SWI/SNF复合物。
Nucleic Acids Res. 2025 Jul 8;53(13). doi: 10.1093/nar/gkaf653.
4
PDZ-directed substrate recruitment is the primary determinant of specific 4E-BP1 dephosphorylation by PP1-Neurabin.由PP1-神经肌动蛋白结合蛋白介导的PDZ结构域靶向底物招募是4E-BP1被PP1-神经肌动蛋白特异性去磷酸化的主要决定因素。
Elife. 2025 Jun 23;13:RP103403. doi: 10.7554/eLife.103403.
5
Cell fate specification during respiratory development requires ARID1A-containing canonical BAF complex activity.呼吸发育过程中的细胞命运特化需要含有ARID1A的经典BAF复合物活性。
bioRxiv. 2025 Jun 5:2025.06.02.657302. doi: 10.1101/2025.06.02.657302.
6
Chromatin modifiers in neurodevelopment.神经发育中的染色质修饰因子
Front Mol Neurosci. 2025 May 21;18:1551107. doi: 10.3389/fnmol.2025.1551107. eCollection 2025.
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KMT2D coordinates antiviral CD4 T cell responses through opposing effects on T follicular helper and cytotoxic gene expression.KMT2D通过对滤泡辅助性T细胞和细胞毒性基因表达的相反作用来协调抗病毒CD4 T细胞反应。
Cell Rep. 2025 Jun 24;44(6):115775. doi: 10.1016/j.celrep.2025.115775. Epub 2025 Jun 2.
8
Division of labor among H3K4 methyltransferases defines distinct facets of homeostatic plasticity.H3K4 甲基转移酶之间的分工定义了稳态可塑性的不同方面。
Cell Rep. 2025 May 21;44(6):115746. doi: 10.1016/j.celrep.2025.115746.
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Proc Natl Acad Sci U S A. 2025 May 20;122(20):e2422971122. doi: 10.1073/pnas.2422971122. Epub 2025 May 15.
10
Molecular and clinical aspects of histone-related disorders.组蛋白相关疾病的分子与临床研究进展
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神经特异性 BAF 亚基 ACTL6B 的缺失解除了早期反应基因的抑制,导致隐性自闭症。
Proc Natl Acad Sci U S A. 2020 May 5;117(18):10055-10066. doi: 10.1073/pnas.1908238117. Epub 2020 Apr 20.
4
The Bivalent Genome: Characterization, Structure, and Regulation.二倍体基因组:特征、结构和调控。
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Selective binding of the PHD6 finger of MLL4 to histone H4K16ac links MLL4 and MOF.MLL4 的 PHD6 指对组蛋白 H4K16ac 的选择性结合将 MLL4 和 MOF 联系在一起。
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Dangerous liaisons: interplay between SWI/SNF, NuRD, and Polycomb in chromatin regulation and cancer.危险的勾结:SWI/SNF、NuRD 和 Polycomb 在染色质调控和癌症中的相互作用。
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