Depletion or cleavage of cohesin during anaphase differentially affects chromatin structure and segregation

Chromosome segregation requires both the separation of sister chromatids and the sustained condensation of chromatids during anaphase. In yeast cells, cohesin is not only required for sister chromatid cohesion but also plays a major role determining the structure of individual chromatids in metaphas...

Full description

Bibliographic Details
Main Authors: Jonay Garcia-Luis, Hélène Bordelet, Agnès Thierry, Romain Koszul, Luis Aragon
Format: Article
Language:English
Published: eLife Sciences Publications Ltd 2022-10-01
Series:eLife
Subjects:
Online Access:https://elifesciences.org/articles/80147
_version_ 1798029312414187520
author Jonay Garcia-Luis
Hélène Bordelet
Agnès Thierry
Romain Koszul
Luis Aragon
author_facet Jonay Garcia-Luis
Hélène Bordelet
Agnès Thierry
Romain Koszul
Luis Aragon
author_sort Jonay Garcia-Luis
collection DOAJ
description Chromosome segregation requires both the separation of sister chromatids and the sustained condensation of chromatids during anaphase. In yeast cells, cohesin is not only required for sister chromatid cohesion but also plays a major role determining the structure of individual chromatids in metaphase. Separase cleavage is thought to remove all cohesin complexes from chromosomes to initiate anaphase. It is thus not clear how the length and organisation of segregating chromatids is maintained during anaphase in the absence of cohesin. Here, we show that degradation of cohesin at the anaphase onset causes aberrant chromatid segregation. Hi-C analysis on segregating chromatids demonstrates that cohesin depletion causes loss of intrachromatid organisation. Surprisingly, tobacco etch virus (TEV)-mediated cleavage of cohesin does not dramatically disrupt chromatid organisation in anaphase, explaining why bulk segregation is achieved. In addition, we identified a small pool of cohesin complexes bound to telophase chromosomes in wild-type cells and show that they play a role in the organisation of centromeric regions. Our data demonstrates that in yeast cells cohesin function is not over in metaphase, but extends to the anaphase period when chromatids are segregating.
first_indexed 2024-04-11T19:22:17Z
format Article
id doaj.art-79ff806a1b13495fb450c4c4437f9c52
institution Directory Open Access Journal
issn 2050-084X
language English
last_indexed 2024-04-11T19:22:17Z
publishDate 2022-10-01
publisher eLife Sciences Publications Ltd
record_format Article
series eLife
spelling doaj.art-79ff806a1b13495fb450c4c4437f9c522022-12-22T04:07:16ZengeLife Sciences Publications LtdeLife2050-084X2022-10-011110.7554/eLife.80147Depletion or cleavage of cohesin during anaphase differentially affects chromatin structure and segregationJonay Garcia-Luis0Hélène Bordelet1https://orcid.org/0000-0002-8190-2326Agnès Thierry2Romain Koszul3https://orcid.org/0000-0002-3086-1173Luis Aragon4https://orcid.org/0000-0003-0634-6742DNA motors Group, MRC London Institute of Medical Sciences, London, United KingdomInstitut Pasteur, CNRS UMR 3525, Université Paris Cité, Unité Régulation Spatiale des Génomes, Paris, FranceInstitut Pasteur, CNRS UMR 3525, Université Paris Cité, Unité Régulation Spatiale des Génomes, Paris, FranceInstitut Pasteur, CNRS UMR 3525, Université Paris Cité, Unité Régulation Spatiale des Génomes, Paris, FranceDNA motors Group, MRC London Institute of Medical Sciences, London, United KingdomChromosome segregation requires both the separation of sister chromatids and the sustained condensation of chromatids during anaphase. In yeast cells, cohesin is not only required for sister chromatid cohesion but also plays a major role determining the structure of individual chromatids in metaphase. Separase cleavage is thought to remove all cohesin complexes from chromosomes to initiate anaphase. It is thus not clear how the length and organisation of segregating chromatids is maintained during anaphase in the absence of cohesin. Here, we show that degradation of cohesin at the anaphase onset causes aberrant chromatid segregation. Hi-C analysis on segregating chromatids demonstrates that cohesin depletion causes loss of intrachromatid organisation. Surprisingly, tobacco etch virus (TEV)-mediated cleavage of cohesin does not dramatically disrupt chromatid organisation in anaphase, explaining why bulk segregation is achieved. In addition, we identified a small pool of cohesin complexes bound to telophase chromosomes in wild-type cells and show that they play a role in the organisation of centromeric regions. Our data demonstrates that in yeast cells cohesin function is not over in metaphase, but extends to the anaphase period when chromatids are segregating.https://elifesciences.org/articles/80147cohesinchromosome segregationchromosome condensation
spellingShingle Jonay Garcia-Luis
Hélène Bordelet
Agnès Thierry
Romain Koszul
Luis Aragon
Depletion or cleavage of cohesin during anaphase differentially affects chromatin structure and segregation
eLife
cohesin
chromosome segregation
chromosome condensation
title Depletion or cleavage of cohesin during anaphase differentially affects chromatin structure and segregation
title_full Depletion or cleavage of cohesin during anaphase differentially affects chromatin structure and segregation
title_fullStr Depletion or cleavage of cohesin during anaphase differentially affects chromatin structure and segregation
title_full_unstemmed Depletion or cleavage of cohesin during anaphase differentially affects chromatin structure and segregation
title_short Depletion or cleavage of cohesin during anaphase differentially affects chromatin structure and segregation
title_sort depletion or cleavage of cohesin during anaphase differentially affects chromatin structure and segregation
topic cohesin
chromosome segregation
chromosome condensation
url https://elifesciences.org/articles/80147
work_keys_str_mv AT jonaygarcialuis depletionorcleavageofcohesinduringanaphasedifferentiallyaffectschromatinstructureandsegregation
AT helenebordelet depletionorcleavageofcohesinduringanaphasedifferentiallyaffectschromatinstructureandsegregation
AT agnesthierry depletionorcleavageofcohesinduringanaphasedifferentiallyaffectschromatinstructureandsegregation
AT romainkoszul depletionorcleavageofcohesinduringanaphasedifferentiallyaffectschromatinstructureandsegregation
AT luisaragon depletionorcleavageofcohesinduringanaphasedifferentiallyaffectschromatinstructureandsegregation