Institute for Research in Immunology and Cancer, Université de Montréal, C.P. 6128, succursale Centre-ville, Montréal, QC H3C 3J7, Canada; Ottawa Institute of Systems Biology, Department of Cellular and Molecular Medicine, University of Ottawa, Roger Guindon Hall, 451 Smyth Road, Ottawa, ON K1H 8M5, Canada.
Institute for Research in Immunology and Cancer, Université de Montréal, C.P. 6128, succursale Centre-ville, Montréal, QC H3C 3J7, Canada; Wellcome Trust Centre for Cell Biology, University of Edinburgh, Edinburgh EH93BF, UK.
Mol Cell. 2018 Feb 15;69(4):664-676.e5. doi: 10.1016/j.molcel.2018.01.030.
The morphological transformation of amorphous chromatin into distinct chromosomes is a hallmark of mitosis. To achieve this, chromatin must be compacted and remodeled by a ring-shaped enzyme complex known as condensin. However, the mechanistic basis underpinning condensin's role in chromosome remodeling has remained elusive. Here we show that condensin has a strong tendency to trap itself in its own reaction product during chromatin compaction and yet is capable of interacting with chromatin in a highly dynamic manner in vivo. To resolve this apparent paradox, we identified specific chromatin remodelers and AAA-class ATPases that act in a coordinated manner to release condensin from chromatin entrapment. The Cdc48 segregase is the central linchpin of this regulatory mechanism and promotes ubiquitin-dependent cycling of condensin on mitotic chromatin as well as effective chromosome condensation. Collectively, our results show that condensin inhibition by its own reaction product is relieved by forceful enzyme extraction from chromatin.
无定形染色质转化为明显的染色体是有丝分裂的一个标志。为了实现这一点,染色质必须通过一种称为凝聚素的环形酶复合物进行压缩和重塑。然而,凝聚素在染色体重塑中的作用的机械基础仍然难以捉摸。在这里,我们表明,在染色质压缩过程中,凝聚素有很强的倾向将自身困在其自身的反应产物中,但在体内仍能够以高度动态的方式与染色质相互作用。为了解决这个明显的悖论,我们鉴定了特定的染色质重塑因子和 AAA 类 ATP 酶,它们以协调的方式共同作用,将凝聚素从染色质捕获中释放出来。CDC48 解旋酶是该调控机制的核心连接点,它促进凝聚素在有丝分裂染色质上的泛素依赖性循环以及有效的染色体浓缩。总的来说,我们的结果表明,通过从染色质上强制酶提取来缓解凝聚素自身反应产物的抑制作用。