Cargando…
Mitotic chromosome alignment ensures mitotic fidelity by promoting interchromosomal compaction during anaphase
Chromosome alignment at the equator of the mitotic spindle is a highly conserved step during cell division; however, its importance to genomic stability and cellular fitness is not understood. Normal mammalian somatic cells lacking KIF18A function complete cell division without aligning chromosomes....
Autores principales: | , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Rockefeller University Press
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6446859/ https://www.ncbi.nlm.nih.gov/pubmed/30733233 http://dx.doi.org/10.1083/jcb.201807228 |
_version_ | 1783408430196719616 |
---|---|
author | Fonseca, Cindy L. Malaby, Heidi L.H. Sepaniac, Leslie A. Martin, Whitney Byers, Candice Czechanski, Anne Messinger, Dana Tang, Mary Ohi, Ryoma Reinholdt, Laura G. Stumpff, Jason |
author_facet | Fonseca, Cindy L. Malaby, Heidi L.H. Sepaniac, Leslie A. Martin, Whitney Byers, Candice Czechanski, Anne Messinger, Dana Tang, Mary Ohi, Ryoma Reinholdt, Laura G. Stumpff, Jason |
author_sort | Fonseca, Cindy L. |
collection | PubMed |
description | Chromosome alignment at the equator of the mitotic spindle is a highly conserved step during cell division; however, its importance to genomic stability and cellular fitness is not understood. Normal mammalian somatic cells lacking KIF18A function complete cell division without aligning chromosomes. These alignment-deficient cells display normal chromosome copy numbers in vitro and in vivo, suggesting that chromosome alignment is largely dispensable for maintenance of euploidy. However, we find that loss of chromosome alignment leads to interchromosomal compaction defects during anaphase, abnormal organization of chromosomes into a single nucleus at mitotic exit, and the formation of micronuclei in vitro and in vivo. These defects slow cell proliferation and are associated with impaired postnatal growth and survival in mice. Our studies support a model in which the alignment of mitotic chromosomes promotes proper organization of chromosomes into a single nucleus and continued proliferation by ensuring that chromosomes segregate as a compact mass during anaphase. |
format | Online Article Text |
id | pubmed-6446859 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-64468592019-10-01 Mitotic chromosome alignment ensures mitotic fidelity by promoting interchromosomal compaction during anaphase Fonseca, Cindy L. Malaby, Heidi L.H. Sepaniac, Leslie A. Martin, Whitney Byers, Candice Czechanski, Anne Messinger, Dana Tang, Mary Ohi, Ryoma Reinholdt, Laura G. Stumpff, Jason J Cell Biol Research Articles Chromosome alignment at the equator of the mitotic spindle is a highly conserved step during cell division; however, its importance to genomic stability and cellular fitness is not understood. Normal mammalian somatic cells lacking KIF18A function complete cell division without aligning chromosomes. These alignment-deficient cells display normal chromosome copy numbers in vitro and in vivo, suggesting that chromosome alignment is largely dispensable for maintenance of euploidy. However, we find that loss of chromosome alignment leads to interchromosomal compaction defects during anaphase, abnormal organization of chromosomes into a single nucleus at mitotic exit, and the formation of micronuclei in vitro and in vivo. These defects slow cell proliferation and are associated with impaired postnatal growth and survival in mice. Our studies support a model in which the alignment of mitotic chromosomes promotes proper organization of chromosomes into a single nucleus and continued proliferation by ensuring that chromosomes segregate as a compact mass during anaphase. Rockefeller University Press 2019-04-01 2019-02-07 /pmc/articles/PMC6446859/ /pubmed/30733233 http://dx.doi.org/10.1083/jcb.201807228 Text en © 2019 Fonseca et al. http://www.rupress.org/terms/https://creativecommons.org/licenses/by-nc-sa/4.0/This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms/). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 International license, as described at https://creativecommons.org/licenses/by-nc-sa/4.0/). |
spellingShingle | Research Articles Fonseca, Cindy L. Malaby, Heidi L.H. Sepaniac, Leslie A. Martin, Whitney Byers, Candice Czechanski, Anne Messinger, Dana Tang, Mary Ohi, Ryoma Reinholdt, Laura G. Stumpff, Jason Mitotic chromosome alignment ensures mitotic fidelity by promoting interchromosomal compaction during anaphase |
title | Mitotic chromosome alignment ensures mitotic fidelity by promoting interchromosomal compaction during anaphase |
title_full | Mitotic chromosome alignment ensures mitotic fidelity by promoting interchromosomal compaction during anaphase |
title_fullStr | Mitotic chromosome alignment ensures mitotic fidelity by promoting interchromosomal compaction during anaphase |
title_full_unstemmed | Mitotic chromosome alignment ensures mitotic fidelity by promoting interchromosomal compaction during anaphase |
title_short | Mitotic chromosome alignment ensures mitotic fidelity by promoting interchromosomal compaction during anaphase |
title_sort | mitotic chromosome alignment ensures mitotic fidelity by promoting interchromosomal compaction during anaphase |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6446859/ https://www.ncbi.nlm.nih.gov/pubmed/30733233 http://dx.doi.org/10.1083/jcb.201807228 |
work_keys_str_mv | AT fonsecacindyl mitoticchromosomealignmentensuresmitoticfidelitybypromotinginterchromosomalcompactionduringanaphase AT malabyheidilh mitoticchromosomealignmentensuresmitoticfidelitybypromotinginterchromosomalcompactionduringanaphase AT sepaniaclesliea mitoticchromosomealignmentensuresmitoticfidelitybypromotinginterchromosomalcompactionduringanaphase AT martinwhitney mitoticchromosomealignmentensuresmitoticfidelitybypromotinginterchromosomalcompactionduringanaphase AT byerscandice mitoticchromosomealignmentensuresmitoticfidelitybypromotinginterchromosomalcompactionduringanaphase AT czechanskianne mitoticchromosomealignmentensuresmitoticfidelitybypromotinginterchromosomalcompactionduringanaphase AT messingerdana mitoticchromosomealignmentensuresmitoticfidelitybypromotinginterchromosomalcompactionduringanaphase AT tangmary mitoticchromosomealignmentensuresmitoticfidelitybypromotinginterchromosomalcompactionduringanaphase AT ohiryoma mitoticchromosomealignmentensuresmitoticfidelitybypromotinginterchromosomalcompactionduringanaphase AT reinholdtlaurag mitoticchromosomealignmentensuresmitoticfidelitybypromotinginterchromosomalcompactionduringanaphase AT stumpffjason mitoticchromosomealignmentensuresmitoticfidelitybypromotinginterchromosomalcompactionduringanaphase |