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{"title":"Reconstitution of Mitotic Chromatids In Vitro","authors":"Keishi Shintomi, Tatsuya Hirano","doi":"10.1002/cpcb.48","DOIUrl":null,"url":null,"abstract":"<p>The mitotic chromosome, which is composed of a pair of sister chromatids, is a large macromolecular assembly that ensures faithful transmission of genetic information into daughter cells. Despite its fundamental importance, how a nucleosome fiber is folded and assembled into a large-scale chromatid structure remains poorly understood. To address this question, we have established a biochemically tractable system in which mitotic chromatids can be reconstituted in vitro by mixing a simple substrate (sperm nucleus) and a limited number of purified factors. The minimum set of required factors includes core histones, three histone chaperones, topoisomerase II, and condensin I. In this article, we describe a set of protocols for the preparation of key reagents and the setup of reconstitution reactions. We believe that this classical approach of biochemical reconstitution will be of great help to dissect the mechanisms of action of individual factors during mitotic chromatid assembly and to assess the contribution of nucleosome dynamics to this process from a fresh angle. © 2018 by John Wiley & Sons, Inc.</p>","PeriodicalId":40051,"journal":{"name":"Current Protocols in Cell Biology","volume":"79 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2018-05-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1002/cpcb.48","citationCount":"3","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Current Protocols in Cell Biology","FirstCategoryId":"1085","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/cpcb.48","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"Biochemistry, Genetics and Molecular Biology","Score":null,"Total":0}
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Abstract
The mitotic chromosome, which is composed of a pair of sister chromatids, is a large macromolecular assembly that ensures faithful transmission of genetic information into daughter cells. Despite its fundamental importance, how a nucleosome fiber is folded and assembled into a large-scale chromatid structure remains poorly understood. To address this question, we have established a biochemically tractable system in which mitotic chromatids can be reconstituted in vitro by mixing a simple substrate (sperm nucleus) and a limited number of purified factors. The minimum set of required factors includes core histones, three histone chaperones, topoisomerase II, and condensin I. In this article, we describe a set of protocols for the preparation of key reagents and the setup of reconstitution reactions. We believe that this classical approach of biochemical reconstitution will be of great help to dissect the mechanisms of action of individual factors during mitotic chromatid assembly and to assess the contribution of nucleosome dynamics to this process from a fresh angle. © 2018 by John Wiley & Sons, Inc.
有丝分裂染色单体的体外重组
有丝分裂染色体由一对姐妹染色单体组成,是一个大型的大分子组合,确保遗传信息忠实地传递到子细胞。尽管核小体纤维具有基本的重要性,但人们对其折叠和组装成大规模染色单体结构的方式仍然知之甚少。为了解决这个问题,我们建立了一个生物化学易于处理的系统,在这个系统中,有丝分裂染色单体可以通过混合一个简单的底物(精子核)和有限数量的纯化因子在体外重建。所需的最小因子集包括核心组蛋白、三种组蛋白伴侣、拓扑异构酶II和凝聚蛋白i。在本文中,我们描述了一套关键试剂的制备和重组反应的设置方案。我们相信,这种经典的生化重建方法将有助于剖析有丝分裂染色单体组装过程中单个因子的作用机制,并从一个新的角度评估核小体动力学对这一过程的贡献。©2018 by John Wiley &儿子,Inc。
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