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The Scc2/Scc4 cohesin loader determines the distribution of cohesin on budding yeast chromosomes.Scc2/Scc4黏连蛋白装载复合体决定了黏连蛋白在芽殖酵母染色体上的分布。
Genes Dev. 2009 Oct 1;23(19):2345-57. doi: 10.1101/gad.1819409.
2
Mediator recruits the cohesin loader Scc2 to RNA Pol II-transcribed genes and promotes sister chromatid cohesion.中介体招募黏合素加载器 Scc2 到 RNA Pol II 转录的基因,并促进姐妹染色单体黏合。
Curr Biol. 2022 Jul 11;32(13):2884-2896.e6. doi: 10.1016/j.cub.2022.05.019. Epub 2022 Jun 1.
3
Cell cycle-specific cleavage of Scc2 regulates its cohesin deposition activity.细胞周期特异性切割 Scc2 调节其黏连蛋白沉积活性。
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4
Structure of the cohesin loader Scc2.着丝粒复合物加载器 Scc2 的结构。
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Identification of Functional Domains in the Cohesin Loader Subunit Scc4 by a Random Insertion/Dominant Negative Screen.通过随机插入/显性负筛选鉴定黏连蛋白装载亚基Scc4中的功能结构域
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Phosphorylation of the Scc2 cohesin deposition complex subunit regulates chromosome condensation through cohesin integrity.Scc2黏连蛋白沉积复合体亚基的磷酸化通过黏连蛋白的完整性来调节染色体凝聚。
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PLoS One. 2013 Sep 26;8(9):e75435. doi: 10.1371/journal.pone.0075435. eCollection 2013.
8
Structural evidence for Scc4-dependent localization of cohesin loading.黏连蛋白装载依赖Scc4定位的结构证据。
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Human Scc4 is required for cohesin binding to chromatin, sister-chromatid cohesion, and mitotic progression.人源Scc4是黏连蛋白与染色质结合、姐妹染色单体黏连及有丝分裂进程所必需的。
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Orc4 spatiotemporally stabilizes centromeric chromatin.Orc4 使着丝粒染色质在时空上稳定。
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The cohesin loader SCC2 contains a PHD finger that is required for meiosis in land plants.着丝粒复合物加载器 SCC2 包含一个 PHD 指,该指对于陆地植物的减数分裂是必需的。
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Depletion of Limiting rDNA Structural Complexes Triggers Chromosomal Instability and Replicative Aging of .耗尽限制 rDNA 结构复合物会引发染色体不稳定性和复制性衰老。
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A streamlined cohesin apparatus is sufficient for mitosis and meiosis in the protist Tetrahymena.一种简化的黏连蛋白装置足以支持原生生物四膜虫的有丝分裂和减数分裂。
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9
Localization of Cdc7 Protein Kinase During DNA Replication in .Cdc7蛋白激酶在……DNA复制过程中的定位
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10
Identification of Functional Domains in the Cohesin Loader Subunit Scc4 by a Random Insertion/Dominant Negative Screen.通过随机插入/显性负筛选鉴定黏连蛋白装载亚基Scc4中的功能结构域
G3 (Bethesda). 2016 Aug 9;6(8):2655-63. doi: 10.1534/g3.116.031674.

本文引用的文献

1
Building sister chromatid cohesion: smc3 acetylation counteracts an antiestablishment activity.建立姐妹染色单体黏连:SMC3乙酰化抵消一种抗建立活性。
Mol Cell. 2009 Mar 27;33(6):763-74. doi: 10.1016/j.molcel.2009.02.028.
2
Intersection of ChIP and FLIP, genomic methods to study the dynamics of the cohesin proteins.染色质免疫沉淀(ChIP)与荧光损失在光漂白(FLIP)的交叉应用,用于研究黏连蛋白动力学的基因组学方法。
Chromosome Res. 2009;17(2):155-63. doi: 10.1007/s10577-008-9007-9.
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A handcuff model for the cohesin complex.黏连蛋白复合物的手铐模型。
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The cohesin complex and its roles in chromosome biology.黏连蛋白复合体及其在染色体生物学中的作用。
Genes Dev. 2008 Nov 15;22(22):3089-114. doi: 10.1101/gad.1724308.
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A molecular determinant for the establishment of sister chromatid cohesion.一种用于建立姐妹染色单体黏连的分子决定因素。
Science. 2008 Jul 25;321(5888):566-9. doi: 10.1126/science.1157880.
6
Eco1-dependent cohesin acetylation during establishment of sister chromatid cohesion.在姐妹染色单体黏连建立过程中依赖Eco1的黏连蛋白乙酰化作用
Science. 2008 Jul 25;321(5888):563-6. doi: 10.1126/science.1157774.
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Sister chromatid cohesion: a simple concept with a complex reality.姐妹染色单体黏连:一个概念简单但实际情况复杂的现象
Annu Rev Cell Dev Biol. 2008;24:105-29. doi: 10.1146/annurev.cellbio.24.110707.175350.
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CTCF physically links cohesin to chromatin.CTCF将黏连蛋白物理连接至染色质。
Proc Natl Acad Sci U S A. 2008 Jun 17;105(24):8309-14. doi: 10.1073/pnas.0801273105. Epub 2008 Jun 11.
9
Cell-type-specific TEV protease cleavage reveals cohesin functions in Drosophila neurons.细胞类型特异性的TEV蛋白酶切割揭示了黏连蛋白在果蝇神经元中的功能。
Dev Cell. 2008 Feb;14(2):239-51. doi: 10.1016/j.devcel.2007.12.009.
10
piggyBac-based mosaic screen identifies a postmitotic function for cohesin in regulating developmental axon pruning.基于piggyBac的镶嵌筛选确定了黏连蛋白在调节发育性轴突修剪中的有丝分裂后功能。
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Scc2/Scc4黏连蛋白装载复合体决定了黏连蛋白在芽殖酵母染色体上的分布。

The Scc2/Scc4 cohesin loader determines the distribution of cohesin on budding yeast chromosomes.

作者信息

Kogut Igor, Wang Jianbin, Guacci Vincent, Mistry Rohinton K, Megee Paul C

机构信息

Department of Biochemistry and Molecular Genetics, University of Colorado Denver School of Medicine, Aurora, Colorado 80045, USA.

出版信息

Genes Dev. 2009 Oct 1;23(19):2345-57. doi: 10.1101/gad.1819409.

DOI:10.1101/gad.1819409
PMID:19797771
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2758738/
Abstract

Cohesins mediate sister chromatid cohesion and DNA repair and also function in gene regulation. Chromosomal cohesins are distributed nonrandomly, and their deposition requires the heterodimeric Scc2/Scc4 loader. Whether Scc2/Scc4 establishes nonrandom cohesin distributions on chromosomes is poorly characterized, however. To better understand the spatial regulation of cohesin association, we mapped budding yeast Scc2 and Scc4 chromosomal distributions. We find that Scc2/Scc4 resides at previously mapped cohesin-associated regions (CARs) in pericentromeric and arm regions, and that Scc2/Scc4-cohesin colocalization persists after the initial deposition of cohesins in G1/S phase. Pericentromeric Scc2/Scc4 enrichment is kinetochore-dependent, and both Scc2/Scc4 and cohesin associations are coordinately reduced in these regions following chromosome biorientation. Thus, these characteristics of Scc2/Scc4 binding closely recapitulate those of cohesin. Although present in G1, Scc2/Scc4 initially has a poor affinity for CARs, but its affinity increases as cells traverse the cell cycle. Scc2/Scc4 association with CARs is independent of cohesin, however. Taken together, these observations are inconsistent with a previous suggestion that cohesins are relocated by translocating RNA polymerases from separate loading sites to intergenic regions between convergently transcribed genes. Rather, our findings suggest that budding yeast cohesins are targeted to CARs largely by Scc2/Scc4 loader association at these locations.

摘要

黏连蛋白介导姐妹染色单体黏连和DNA修复,并且在基因调控中也发挥作用。染色体黏连蛋白呈非随机分布,其沉积需要异二聚体Scc2/Scc4装载蛋白。然而,Scc2/Scc4是否在染色体上建立非随机的黏连蛋白分布还不清楚。为了更好地理解黏连蛋白结合的空间调控,我们绘制了芽殖酵母Scc2和Scc4的染色体分布图谱。我们发现Scc2/Scc4位于着丝粒周围和臂区域中先前定位的黏连蛋白相关区域(CARs),并且在G1/S期黏连蛋白初始沉积后,Scc2/Scc4-黏连蛋白共定位持续存在。着丝粒周围Scc2/Scc4的富集依赖于动粒,并且在染色体双定向后,这些区域中Scc2/Scc4和黏连蛋白的结合都协同减少。因此,Scc2/Scc4结合的这些特征与黏连蛋白的特征密切相似。尽管Scc2/Scc4在G1期存在,但其最初对CARs的亲和力较差,但随着细胞穿越细胞周期,其亲和力会增加。然而,Scc2/Scc4与CARs的结合独立于黏连蛋白。综上所述,这些观察结果与之前的一种观点不一致,该观点认为黏连蛋白通过将RNA聚合酶从单独的装载位点转移到同向转录基因之间的基因间区域而重新定位。相反,我们的研究结果表明,芽殖酵母黏连蛋白主要通过Scc2/Scc4装载蛋白在这些位置的结合而靶向CARs。