| Literature DB >> 29452641 |
Yogitha Thattikota1, Sylvain Tollis2, Roger Palou3, Justine Vinet3, Mike Tyers3, Damien D'Amours4.
Abstract
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.Entities:
Keywords: Cdc48; SMC; Ufd1-Npl4; VCP; chromatin; chromosome condensation; condensin; genome stability; mitosis
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Year: 2018 PMID: 29452641 DOI: 10.1016/j.molcel.2018.01.030
Source DB: PubMed Journal: Mol Cell ISSN: 1097-2765 Impact factor: 17.970