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2
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本文引用的文献

1
Replisome-Cohesin Interfacing: A Molecular Perspective.复制体-黏合蛋白界面:分子视角。
Bioessays. 2018 Oct;40(10):e1800109. doi: 10.1002/bies.201800109. Epub 2018 Aug 14.
2
Dynamic condensates activate transcription.动态凝聚物激活转录。
Science. 2018 Jul 27;361(6400):329-330. doi: 10.1126/science.aau4795.
3
A Muscle-Specific Enhancer RNA Mediates Cohesin Recruitment and Regulates Transcription In trans.肌特异性增强子 RNA 介导黏着蛋白募集并调节反式转录。
Mol Cell. 2018 Jul 5;71(1):129-141.e8. doi: 10.1016/j.molcel.2018.06.008.
4
Cell-Cycle Regulation of Dynamic Chromosome Association of the Condensin Complex.着丝粒复合体动态染色体结合的细胞周期调控。
Cell Rep. 2018 May 22;23(8):2308-2317. doi: 10.1016/j.celrep.2018.04.082.
5
Suppressor mutation analysis combined with 3D modeling explains cohesin's capacity to hold and release DNA.抑制突变分析与 3D 建模相结合,解释了黏连蛋白保持和释放 DNA 的能力。
Proc Natl Acad Sci U S A. 2018 May 22;115(21):E4833-E4842. doi: 10.1073/pnas.1803564115. Epub 2018 May 7.
6
Emerging Evidence of Chromosome Folding by Loop Extrusion.通过环状挤压实现染色体折叠的新证据
Cold Spring Harb Symp Quant Biol. 2017;82:45-55. doi: 10.1101/sqb.2017.82.034710. Epub 2018 May 4.
7
The Energetics and Physiological Impact of Cohesin Extrusion.着丝粒蛋白复合体挤出的能量学和生理学影响
Cell. 2018 May 17;173(5):1165-1178.e20. doi: 10.1016/j.cell.2018.03.072. Epub 2018 Apr 26.
8
A quantitative map of human Condensins provides new insights into mitotic chromosome architecture.人类凝缩蛋白的定量图谱为有丝分裂染色体结构提供了新的见解。
J Cell Biol. 2018 Jul 2;217(7):2309-2328. doi: 10.1083/jcb.201801048. Epub 2018 Apr 9.
9
SMC Complexes: Universal DNA Looping Machines with Distinct Regulators.SMC 复合物:具有独特调控因子的通用 DNA 环化机器。
Trends Genet. 2018 Jun;34(6):477-487. doi: 10.1016/j.tig.2018.03.003. Epub 2018 Mar 29.
10
Dissecting super-enhancer hierarchy based on chromatin interactions.基于染色质相互作用剖析超级增强子层级结构。
Nat Commun. 2018 Mar 5;9(1):943. doi: 10.1038/s41467-018-03279-9.

凝聚素和黏合素——两者并不相同!

Condensins and cohesins - one of these things is not like the other!

机构信息

Department of Biological Sciences, 111 Research Drive, Lehigh University, Bethlehem, PA 18015, USA

出版信息

J Cell Sci. 2019 Feb 7;132(3):jcs220491. doi: 10.1242/jcs.220491.

DOI:10.1242/jcs.220491
PMID:30733374
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6382015/
Abstract

Condensins and cohesins are highly conserved complexes that tether together DNA loci within a single DNA molecule to produce DNA loops. Condensin and cohesin structures, however, are different, and the DNA loops produced by each underlie distinct cell processes. Condensin rods compact chromosomes during mitosis, with condensin I and II complexes producing spatially defined and nested looping in metazoan cells. Structurally adaptive cohesin rings produce loops, which organize the genome during interphase. Cohesin-mediated loops, termed topologically associating domains or TADs, antagonize the formation of epigenetically defined but untethered DNA volumes, termed compartments. While condensin complexes formed through -interactions must maintain chromatin compaction throughout mitosis, cohesins remain highly dynamic during interphase to allow for transcription-mediated responses to external cues and the execution of developmental programs. Here, I review differences in condensin and cohesin structures, and highlight recent advances regarding the intramolecular or -based tetherings through which condensins compact DNA during mitosis and cohesins organize the genome during interphase.

摘要

凝聚素和黏合素是高度保守的复合物,可将单个 DNA 分子内的 DNA 位点连接在一起,形成 DNA 环。然而,凝聚素和黏合素的结构不同,它们各自产生的 DNA 环在不同的细胞过程中发挥作用。在有丝分裂过程中,凝聚素杆状结构使染色体浓缩,其中凝聚素 I 和 II 复合物在后生动物细胞中产生空间限定的嵌套环。结构适应性黏合素环产生的环在有丝分裂间期组织基因组。黏合素介导的环,称为拓扑关联域或 TAD,拮抗由表观遗传定义但未连接的 DNA 体积形成,称为隔室。虽然通过 -相互作用形成的凝聚素复合物在有丝分裂过程中必须维持染色质的浓缩,但黏合素在有丝分裂间期仍保持高度动态,以允许转录介导的对外界信号的反应,并执行发育程序。在这里,我回顾了凝聚素和黏合素结构的差异,并强调了最近在凝聚素通过 -相互作用在有丝分裂期间压缩 DNA 以及黏合素在有丝分裂间期组织基因组方面的进展。