Department of Systems Biology, University of Massachusetts Medical School, Worcester, MA, U.S.A.
Howard Hughes Medical Institute, Chevy Chase, MD, U.S.A.
Biochem J. 2022 Oct 28;479(20):2153-2173. doi: 10.1042/BCJ20210140.
Over the last several years enormous progress has been made in identifying the molecular machines, including condensins and topoisomerases that fold mitotic chromosomes. The discovery that condensins generate chromatin loops through loop extrusion has revolutionized, and energized, the field of chromosome folding. To understand how these machines fold chromosomes with the appropriate dimensions, while disentangling sister chromatids, it needs to be determined how they are regulated and deployed. Here, we outline the current understanding of how these machines and factors are regulated through cell cycle dependent expression, chromatin localization, activation and inactivation through post-translational modifications, and through associations with each other, with other factors and with the chromatin template itself. There are still many open questions about how condensins and topoisomerases are regulated but given the pace of progress in the chromosome folding field, it seems likely that many of these will be answered in the years ahead.
在过去的几年中,在鉴定分子机器方面取得了巨大的进展,包括使有丝分裂染色体折叠的凝缩素和拓扑异构酶。凝缩素通过环挤压产生染色质环的发现彻底改变了染色体折叠领域,并为其注入了新的活力。为了了解这些机器如何在解开姐妹染色单体的同时以适当的尺寸折叠染色体,需要确定它们是如何被调节和部署的。在这里,我们概述了目前对这些机器和因素如何通过细胞周期依赖性表达、染色质定位、通过翻译后修饰的激活和失活,以及通过彼此之间、与其他因素和与染色质模板本身的关联进行调节的理解。关于凝缩素和拓扑异构酶是如何被调节的,仍然有许多悬而未决的问题,但考虑到染色体折叠领域的进展速度,在未来几年内,其中许多问题似乎都将得到解答。