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一种依赖RNA且相分离的活性亚核区室保护抑制性染色质结构域。

An RNA-dependent and phase-separated active subnuclear compartment safeguards repressive chromatin domains.

作者信息

Lerra Luigi, Panatta Martina, Bär Dominik, Zanini Isabella, Tan Jennifer Yihong, Pisano Agnese, Mungo Chiara, Baroux Célia, Panse Vikram Govind, Marques Ana C, Santoro Raffaella

机构信息

Department of Molecular Mechanisms of Disease (DMMD), University of Zurich, Zurich 8057, Switzerland; RNA Biology Program, Life Science Zurich Graduate School, University of Zurich, Zurich 8057, Switzerland.

Department of Molecular Mechanisms of Disease (DMMD), University of Zurich, Zurich 8057, Switzerland.

出版信息

Mol Cell. 2024 May 2;84(9):1667-1683.e10. doi: 10.1016/j.molcel.2024.03.015. Epub 2024 Apr 9.

DOI:10.1016/j.molcel.2024.03.015
PMID:38599210
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11065421/
Abstract

The nucleus is composed of functionally distinct membraneless compartments that undergo phase separation (PS). However, whether different subnuclear compartments are connected remains elusive. We identified a type of nuclear body with PS features composed of BAZ2A that associates with active chromatin. BAZ2A bodies depend on RNA transcription and BAZ2A non-disordered RNA-binding TAM domain. Although BAZ2A and H3K27me3 occupancies anticorrelate in the linear genome, in the nuclear space, BAZ2A bodies contact H3K27me3 bodies. BAZ2A-body disruption promotes BAZ2A invasion into H3K27me3 domains, causing H3K27me3-body loss and gene upregulation. Weak BAZ2A-RNA interactions, such as with nascent transcripts, promote BAZ2A bodies, whereas the strong binder long non-coding RNA (lncRNA) Malat1 impairs them while mediating BAZ2A association to chromatin at nuclear speckles. In addition to unraveling a direct connection between nuclear active and repressive compartments through PS mechanisms, the results also showed that the strength of RNA-protein interactions regulates this process, contributing to nuclear organization and the regulation of chromatin and gene expression.

摘要

细胞核由经历相分离(PS)的功能不同的无膜区室组成。然而,不同的亚核区室是否相互连接仍不清楚。我们鉴定出一种具有PS特征的核体,其由与活性染色质相关的BAZ2A组成。BAZ2A核体依赖于RNA转录和BAZ2A的非无序RNA结合TAM结构域。尽管在线性基因组中BAZ2A和H3K27me3的占据情况呈反相关,但在核空间中,BAZ2A核体与H3K27me3核体相互接触。破坏BAZ2A核体会促进BAZ2A侵入H3K27me3结构域,导致H3K27me3核体丢失和基因上调。较弱的BAZ2A-RNA相互作用,如与新生转录本的相互作用,会促进BAZ2A核体的形成,而强结合剂长链非编码RNA(lncRNA)Malat1会损害它们,同时介导BAZ2A在核斑点处与染色质的结合。除了通过PS机制揭示核活性区室和抑制区室之间的直接联系外,研究结果还表明RNA-蛋白质相互作用的强度调节这一过程,有助于核组织以及染色质和基因表达的调控。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2359/11065421/81ed24b71f7a/gr7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2359/11065421/dd2fa1acd0d0/fx1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2359/11065421/92fbc5538650/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2359/11065421/7125159cf7d0/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2359/11065421/9cde0db2fbfd/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2359/11065421/6d6089a7059b/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2359/11065421/d9ae849087f3/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2359/11065421/912ab4b90e5c/gr6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2359/11065421/81ed24b71f7a/gr7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2359/11065421/dd2fa1acd0d0/fx1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2359/11065421/92fbc5538650/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2359/11065421/7125159cf7d0/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2359/11065421/9cde0db2fbfd/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2359/11065421/6d6089a7059b/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2359/11065421/d9ae849087f3/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2359/11065421/912ab4b90e5c/gr6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2359/11065421/81ed24b71f7a/gr7.jpg

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SRRM2 organizes splicing condensates to regulate alternative splicing.SRRM2 组织剪接体凝聚物以调节可变剪接。
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