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Physical Proximity of Sister Chromatids Promotes Top2-Dependent Intertwining.
- Source :
-
Molecular cell [Mol Cell] 2016 Oct 06; Vol. 64 (1), pp. 134-147. - Publication Year :
- 2016
-
Abstract
- Sister chromatid intertwines (SCIs), or catenanes, are topological links between replicated chromatids that interfere with chromosome segregation. The formation of SCIs is thought to be a consequence of fork swiveling during DNA replication, and their removal is thought to occur because of the intrinsic feature of type II topoisomerases (Top2) to simplify DNA topology. Here, we report that SCIs are also formed independently of DNA replication during G <subscript>2</subscript> /M by Top2-dependent concatenation of cohesed chromatids due to their physical proximity. We demonstrate that, in contrast to G <subscript>2</subscript> /M, Top2 removes SCIs from cohesed chromatids at the anaphase onset. Importantly, SCI removal in anaphase requires condensin and coincides with the hyperactivation of condensin DNA supercoiling activity. This is consistent with the longstanding proposal that condensin provides a bias in Top2 function toward decatenation. A comprehensive model for the formation and resolution of toxic SCI entanglements on eukaryotic genomes is proposed.<br /> (Crown Copyright © 2016. Published by Elsevier Inc. All rights reserved.)
- Subjects :
- Adenosine Triphosphatases metabolism
Anaphase
Chromatids metabolism
Chromatids ultrastructure
Chromosome Segregation
Chromosomes, Fungal ultrastructure
DNA Topoisomerases, Type II metabolism
DNA, Fungal metabolism
DNA-Binding Proteins metabolism
G2 Phase Cell Cycle Checkpoints
Gene Expression
Multiprotein Complexes metabolism
Saccharomyces cerevisiae metabolism
Saccharomyces cerevisiae ultrastructure
Adenosine Triphosphatases genetics
Chromosomes, Fungal metabolism
DNA Replication
DNA Topoisomerases, Type II genetics
DNA, Fungal genetics
DNA-Binding Proteins genetics
Multiprotein Complexes genetics
Saccharomyces cerevisiae genetics
Subjects
Details
- Language :
- English
- ISSN :
- 1097-4164
- Volume :
- 64
- Issue :
- 1
- Database :
- MEDLINE
- Journal :
- Molecular cell
- Publication Type :
- Academic Journal
- Accession number :
- 27716481
- Full Text :
- https://doi.org/10.1016/j.molcel.2016.09.007