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Condensin association with histone H2A shapes mitotic chromosomes

Chromosome structure is dynamically regulated during cell division, and this regulation is dependent, in part, on condensin. The localization of condensin at chromosome arms is crucial for chromosome partitioning during anaphase. Condensin is also enriched at kinetochores but its precise role and lo...

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Published in:Nature (London) 2011-06, Vol.474 (7352), p.477-483
Main Authors: Tada, Kenji, Susumu, Hiroaki, Sakuno, Takeshi, Watanabe, Yoshinori
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Susumu, Hiroaki
Sakuno, Takeshi
Watanabe, Yoshinori
description Chromosome structure is dynamically regulated during cell division, and this regulation is dependent, in part, on condensin. The localization of condensin at chromosome arms is crucial for chromosome partitioning during anaphase. Condensin is also enriched at kinetochores but its precise role and loading machinery remain unclear. Here we show that fission yeast ( Schizosaccharomyces pombe ) kinetochore proteins Pcs1 and Mde4—homologues of budding yeast ( Saccharomyces cerevisiae ) monopolin subunits and known to prevent merotelic kinetochore orientation—act as a condensin ‘recruiter’ at kinetochores, and that condensin itself may act to clamp microtubule binding sites during metaphase. In addition to the regional recruitment factors, overall condensin association with chromatin is governed by the chromosomal passenger kinase Aurora B. Aurora-B-dependent phosphorylation of condensin promotes its association with histone H2A and H2A.Z, which we identify as conserved chromatin ‘receptors’ of condensin. Condensin phosphorylation and its deposition onto chromosome arms reach a peak during anaphase, when Aurora B kinase relocates from centromeres to the spindle midzone, where the separating chromosome arms are positioned. Our results elucidate the molecular basis for the spatiotemporal regulation of mitotic chromosome architecture, which is crucial for chromosome partitioning. Recruiting condensin During mitosis, chromosomes are made compact and rigid by the action of condensin. This protein is thought to have different roles in the chromosome arms and at the kinetochore, but how it is localized to these regions is unclear. Tada et al . show that the kinetochore protein monopolin is a recruiter for centromeric condensin. In addition, phosphorylation by Aurora B kinase promotes condensin binding to certain histones. Aurora B localization varies through the cell cycle, which may account for cell-cycle-linked recruitment of condensin at the kinetochore.
doi_str_mv 10.1038/nature10179
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Condensin phosphorylation and its deposition onto chromosome arms reach a peak during anaphase, when Aurora B kinase relocates from centromeres to the spindle midzone, where the separating chromosome arms are positioned. Our results elucidate the molecular basis for the spatiotemporal regulation of mitotic chromosome architecture, which is crucial for chromosome partitioning. Recruiting condensin During mitosis, chromosomes are made compact and rigid by the action of condensin. This protein is thought to have different roles in the chromosome arms and at the kinetochore, but how it is localized to these regions is unclear. Tada et al . show that the kinetochore protein monopolin is a recruiter for centromeric condensin. In addition, phosphorylation by Aurora B kinase promotes condensin binding to certain histones. Aurora B localization varies through the cell cycle, which may account for cell-cycle-linked recruitment of condensin at the kinetochore.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>21633354</pmid><doi>10.1038/nature10179</doi><tpages>7</tpages></addata></record>
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identifier ISSN: 0028-0836
ispartof Nature (London), 2011-06, Vol.474 (7352), p.477-483
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1476-4687
language eng
recordid cdi_proquest_miscellaneous_968159084
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subjects 631/80/641/1655
631/80/641/2358
Adenosine Triphosphatases - metabolism
Aurora Kinase B
Aurora Kinases
Binding Sites
Biological and medical sciences
cdc25 Phosphatases - genetics
cdc25 Phosphatases - metabolism
Cell Cycle Proteins - metabolism
Cell cycle, cell proliferation
Cell physiology
Chromatin
Chromatin - metabolism
Chromosomal Proteins, Non-Histone - metabolism
Chromosomes
Chromosomes, Fungal - metabolism
DNA-Binding Proteins - metabolism
Fundamental and applied biological sciences. Psychology
Genetic aspects
Genetics
HeLa Cells
Histones
Histones - metabolism
Humanities and Social Sciences
Humans
Kinetochores - metabolism
Microtubules - metabolism
Mitosis
Molecular and cellular biology
multidisciplinary
Multiprotein Complexes - metabolism
Mutation
Nuclear Proteins - metabolism
Phosphorylation
Physiological aspects
Protein Binding
Protein Transport
Protein-Serine-Threonine Kinases - metabolism
Saccharomyces cerevisiae
Schizosaccharomyces - cytology
Schizosaccharomyces - metabolism
Schizosaccharomyces pombe
Schizosaccharomyces pombe Proteins - metabolism
Science
Studies
Yeast
Yeasts
title Condensin association with histone H2A shapes mitotic chromosomes
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-05T12%3A32%3A11IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-gale_proqu&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Condensin%20association%20with%20histone%20H2A%20shapes%20mitotic%20chromosomes&rft.jtitle=Nature%20(London)&rft.au=Tada,%20Kenji&rft.date=2011-06-01&rft.volume=474&rft.issue=7352&rft.spage=477&rft.epage=483&rft.pages=477-483&rft.issn=0028-0836&rft.eissn=1476-4687&rft.coden=NATUAS&rft_id=info:doi/10.1038/nature10179&rft_dat=%3Cgale_proqu%3EA632498092%3C/gale_proqu%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c616t-9d07368ee873afbc0b54656e0ac613ac3258c286a964336a5786f76535a7a8f83%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=874644291&rft_id=info:pmid/21633354&rft_galeid=A632498092&rfr_iscdi=true