文献检索文档翻译深度研究
Suppr Zotero 插件Zotero 插件
邀请有礼套餐&价格历史记录

新学期,新优惠

限时优惠:9月1日-9月22日

30天高级会员仅需29元

1天体验卡首发特惠仅需5.99元

了解详情
不再提醒
插件&应用
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
高级版
套餐订阅购买积分包
AI 工具
文献检索文档翻译深度研究
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2025

RAD21 是参与指导基因组组织的黏合复合物的核心亚基。

RAD21 is the core subunit of the cohesin complex involved in directing genome organization.

机构信息

State Key Laboratory of Membrane Biology, School of Life Sciences, and Biomedical Pioneering Innovation Center (BIOPIC), Peking University, Beijing, 100871, China.

Peking-Tsinghua Center for Life Sciences, The National Laboratory of Protein and Plant Gene Research, College of Life Sciences, Peking University, Beijing, China.

出版信息

Genome Biol. 2023 Jun 28;24(1):155. doi: 10.1186/s13059-023-02982-1.


DOI:10.1186/s13059-023-02982-1
PMID:37381036
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10303866/
Abstract

BACKGROUND: The ring-shaped cohesin complex is an important factor for the formation of chromatin loops and topologically associating domains (TADs) by loop extrusion. However, the regulation of association between cohesin and chromatin is poorly understood. In this study, we use super-resolution imaging to reveal the unique role of cohesin subunit RAD21 in cohesin loading and chromatin structure regulation. RESULTS: We directly visualize that up-regulation of RAD21 leads to excessive chromatin loop extrusion into a vermicelli-like morphology with RAD21 clustered into foci and excessively loaded cohesin bow-tying a TAD to form a beads-on-a-string-type pattern. In contrast, up-regulation of the other four cohesin subunits results in even distributions. Mechanistically, we identify that the essential role of RAD21 is attributed to the RAD21-loader interaction, which facilitates the cohesin loading process rather than increasing the abundance of cohesin complex upon up-regulation of RAD21. Furthermore, Hi-C and genomic analysis reveal how RAD21 up-regulation affects genome-wide higher-order chromatin structure. Accumulated contacts are shown at TAD corners while inter-TAD interactions increase after vermicelli formation. Importantly, we find that in breast cancer cells, the expression of RAD21 is aberrantly high with poor patient survival and RAD21 forms beads in the nucleus. Up-regulated RAD21 in HeLa cells leads to compartment switching and up-regulation of cancer-related genes. CONCLUSIONS: Our results provide key insights into the molecular mechanism by which RAD21 facilitates the cohesin loading process and provide an explanation to how cohesin and loader work cooperatively to promote chromatin extrusion, which has important implications in construction of three-dimensional genome organization.

摘要

背景:环形黏合蛋白复合体是通过环挤出形成染色质环和拓扑关联域(TAD)的重要因素。然而,黏合蛋白与染色质之间的关联调节机制仍不清楚。在本研究中,我们使用超分辨率成像技术揭示了黏合蛋白亚基 RAD21 在黏合蛋白加载和染色质结构调节中的独特作用。

结果:我们直接观察到,RAD21 的上调导致过多的染色质环挤出,形成类似意大利面条状的形态,RAD21 聚集在焦点中,过多的黏合蛋白呈 bow-tying 状,将一个 TAD 绑成串珠状图案。相比之下,其他四个黏合蛋白亚基的上调导致均匀分布。从机制上讲,我们确定 RAD21 的基本作用归因于 RAD21 加载器相互作用,该相互作用促进了黏合蛋白加载过程,而不是在 RAD21 上调时增加黏合蛋白复合物的丰度。此外,Hi-C 和基因组分析揭示了 RAD21 上调如何影响全基因组的高级染色质结构。在 TAD 角处显示出累积的接触,而在形成意大利面条状结构后,TAD 之间的相互作用增加。重要的是,我们发现乳腺癌细胞中 RAD21 的表达异常升高,患者生存率较差,RAD21 在核内形成珠状。HeLa 细胞中上调的 RAD21 导致隔室转换和与癌症相关基因的上调。

结论:我们的研究结果提供了 RAD21 促进黏合蛋白加载过程的分子机制的关键见解,并解释了黏合蛋白和加载器如何协同工作以促进染色质挤出,这对构建三维基因组组织具有重要意义。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d32/10303866/7a5e6a9cd309/13059_2023_2982_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d32/10303866/b9b90f74b88a/13059_2023_2982_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d32/10303866/b790ee303b97/13059_2023_2982_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d32/10303866/18f5d8e6796a/13059_2023_2982_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d32/10303866/92414ebb4971/13059_2023_2982_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d32/10303866/484317fdcb58/13059_2023_2982_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d32/10303866/7a5e6a9cd309/13059_2023_2982_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d32/10303866/b9b90f74b88a/13059_2023_2982_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d32/10303866/b790ee303b97/13059_2023_2982_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d32/10303866/18f5d8e6796a/13059_2023_2982_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d32/10303866/92414ebb4971/13059_2023_2982_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d32/10303866/484317fdcb58/13059_2023_2982_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d32/10303866/7a5e6a9cd309/13059_2023_2982_Fig6_HTML.jpg

相似文献

[1]
RAD21 is the core subunit of the cohesin complex involved in directing genome organization.

Genome Biol. 2023-6-28

[2]
Topologically associating domains and chromatin loops depend on cohesin and are regulated by CTCF, WAPL, and PDS5 proteins.

EMBO J. 2017-12-15

[3]
PHF2 regulates genome topology and DNA replication in neural stem cells via cohesin.

Nucleic Acids Res. 2024-7-8

[4]
Sensitivity of cohesin-chromatin association to high-salt treatment corroborates non-topological mode of loop extrusion.

Epigenetics Chromatin. 2021-7-28

[5]
High-speed AFM imaging reveals DNA capture and loop extrusion dynamics by cohesin-NIPBL.

J Biol Chem. 2023-11

[6]
Specific Contributions of Cohesin-SA1 and Cohesin-SA2 to TADs and Polycomb Domains in Embryonic Stem Cells.

Cell Rep. 2019-6-18

[7]
Cohesin-independent STAG proteins interact with RNA and R-loops and promote complex loading.

Elife. 2023-4-3

[8]
Determining cellular CTCF and cohesin abundances to constrain 3D genome models.

Elife. 2019-6-17

[9]
The dynamic role of cohesin in maintaining human genome architecture.

Bioessays. 2023-10

[10]
DNA loop extrusion by human cohesin.

Science. 2019-11-21

引用本文的文献

[1]
Multimodal diagnostic models and subtype analysis for neoadjuvant therapy in breast cancer.

Front Immunol. 2025-3-18

[2]
Increasingly efficient chromatin binding of cohesin and CTCF supports chromatin architecture formation during zebrafish embryogenesis.

Nat Commun. 2025-2-21

[3]
Mature chromatin packing domains persist after RAD21 depletion in 3D.

Sci Adv. 2025-1-24

[4]
Identification of responsible sequences which mutations cause maternal H19-ICR hypermethylation with Beckwith-Wiedemann syndrome-like overgrowth.

Commun Biol. 2024-12-2

[5]
Genetic signatures of variants associated with worse COVID-19 outcomes - a multicentric observational study.

Front Immunol. 2024

[6]
The physical chemistry of interphase loop extrusion.

bioRxiv. 2024-8-24

[7]
Cohesin composition and dosage independently affect early development in zebrafish.

Development. 2024-8-1

[8]
Genomic alteration discordance in the paired primary-recurrent ovarian cancers: based on the comprehensive genomic profiling (CGP) analysis.

J Ovarian Res. 2024-6-27

[9]
From compartments to loops: understanding the unique chromatin organization in neuronal cells.

Epigenetics Chromatin. 2024-5-23

[10]
A comprehensive benchmarking with interpretation and operational guidance for the hierarchy of topologically associating domains.

Nat Commun. 2024-5-23

本文引用的文献

[1]
Loop stacking organizes genome folding from TADs to chromosomes.

Mol Cell. 2023-5-4

[2]
SMC complexes: Lifting the lid on loop extrusion.

Curr Opin Cell Biol. 2022-2

[3]
Transcription-coupled structural dynamics of topologically associating domains regulate replication origin efficiency.

Genome Biol. 2021-7-12

[4]
Hi-C analyses with GENOVA: a case study with cohesin variants.

NAR Genom Bioinform. 2021-5-22

[5]
Bridging-induced phase separation induced by cohesin SMC protein complexes.

Sci Adv. 2021-2

[6]
WAPL maintains a cohesin loading cycle to preserve cell-type-specific distal gene regulation.

Nat Genet. 2021-1

[7]
Opposing Effects of Cohesin and Transcription on CTCF Organization Revealed by Super-resolution Imaging.

Mol Cell. 2020-10-21

[8]
NLRP3 Inflammasome From Bench to Bedside: New Perspectives for Triple Negative Breast Cancer.

Front Oncol. 2020-9-4

[9]
DONSON and FANCM associate with different replisomes distinguished by replication timing and chromatin domain.

Nat Commun. 2020-8-7

[10]
Cell migration inducing hyaluronidase 1 (CEMIP) activates STAT3 pathway to facilitate cell proliferation and migration in breast cancer.

J Recept Signal Transduct Res. 2021-4

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

推荐工具

医学文档翻译智能文献检索