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A Cohesin-Based Partitioning Mechanism Revealed upon Transcriptional Inactivation of Centromere
Transcriptional inactivation of the budding yeast centromere has been a widely used tool in studies of chromosome segregation and aneuploidy. In haploid cells when an essential chromosome contains a single conditionally inactivated centromere (GAL-CEN), cell growth rate is slowed and segregation fid...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4851351/ https://www.ncbi.nlm.nih.gov/pubmed/27128635 http://dx.doi.org/10.1371/journal.pgen.1006021 |
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author | Tsabar, Michael Haase, Julian Harrison, Benjamin Snider, Chloe E. Eldridge, Brittany Kaminsky, Lila Hine, Rebecca M. Haber, James E. Bloom, Kerry |
author_facet | Tsabar, Michael Haase, Julian Harrison, Benjamin Snider, Chloe E. Eldridge, Brittany Kaminsky, Lila Hine, Rebecca M. Haber, James E. Bloom, Kerry |
author_sort | Tsabar, Michael |
collection | PubMed |
description | Transcriptional inactivation of the budding yeast centromere has been a widely used tool in studies of chromosome segregation and aneuploidy. In haploid cells when an essential chromosome contains a single conditionally inactivated centromere (GAL-CEN), cell growth rate is slowed and segregation fidelity is reduced; but colony formation is nearly 100%. Pedigree analysis revealed that only 30% of the time both mother and daughter cell inherit the GAL-CEN chromosome. The reduced segregation capacity of the GAL-CEN chromosome is further compromised upon reduction of pericentric cohesin (mcm21∆), as reflected in a further diminishment of the Mif2 kinetochore protein at GAL-CEN. By redistributing cohesin from the nucleolus to the pericentromere (by deleting SIR2), there is increased presence of the kinetochore protein Mif2 at GAL-CEN and restoration of cell viability. These studies identify the ability of cohesin to promote chromosome segregation via kinetochore assembly, in a situation where the centromere has been severely compromised. |
format | Online Article Text |
id | pubmed-4851351 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-48513512016-05-07 A Cohesin-Based Partitioning Mechanism Revealed upon Transcriptional Inactivation of Centromere Tsabar, Michael Haase, Julian Harrison, Benjamin Snider, Chloe E. Eldridge, Brittany Kaminsky, Lila Hine, Rebecca M. Haber, James E. Bloom, Kerry PLoS Genet Research Article Transcriptional inactivation of the budding yeast centromere has been a widely used tool in studies of chromosome segregation and aneuploidy. In haploid cells when an essential chromosome contains a single conditionally inactivated centromere (GAL-CEN), cell growth rate is slowed and segregation fidelity is reduced; but colony formation is nearly 100%. Pedigree analysis revealed that only 30% of the time both mother and daughter cell inherit the GAL-CEN chromosome. The reduced segregation capacity of the GAL-CEN chromosome is further compromised upon reduction of pericentric cohesin (mcm21∆), as reflected in a further diminishment of the Mif2 kinetochore protein at GAL-CEN. By redistributing cohesin from the nucleolus to the pericentromere (by deleting SIR2), there is increased presence of the kinetochore protein Mif2 at GAL-CEN and restoration of cell viability. These studies identify the ability of cohesin to promote chromosome segregation via kinetochore assembly, in a situation where the centromere has been severely compromised. Public Library of Science 2016-04-29 /pmc/articles/PMC4851351/ /pubmed/27128635 http://dx.doi.org/10.1371/journal.pgen.1006021 Text en © 2016 Tsabar et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Tsabar, Michael Haase, Julian Harrison, Benjamin Snider, Chloe E. Eldridge, Brittany Kaminsky, Lila Hine, Rebecca M. Haber, James E. Bloom, Kerry A Cohesin-Based Partitioning Mechanism Revealed upon Transcriptional Inactivation of Centromere |
title | A Cohesin-Based Partitioning Mechanism Revealed upon Transcriptional Inactivation of Centromere |
title_full | A Cohesin-Based Partitioning Mechanism Revealed upon Transcriptional Inactivation of Centromere |
title_fullStr | A Cohesin-Based Partitioning Mechanism Revealed upon Transcriptional Inactivation of Centromere |
title_full_unstemmed | A Cohesin-Based Partitioning Mechanism Revealed upon Transcriptional Inactivation of Centromere |
title_short | A Cohesin-Based Partitioning Mechanism Revealed upon Transcriptional Inactivation of Centromere |
title_sort | cohesin-based partitioning mechanism revealed upon transcriptional inactivation of centromere |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4851351/ https://www.ncbi.nlm.nih.gov/pubmed/27128635 http://dx.doi.org/10.1371/journal.pgen.1006021 |
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