Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Tsabar, Michael, Haase, Julian, Harrison, Benjamin, Snider, Chloe E., Eldridge, Brittany, Kaminsky, Lila, Hine, Rebecca M., Haber, James E., Bloom, Kerry
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2016
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
_version_ 1782429801970139136
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
work_keys_str_mv AT tsabarmichael acohesinbasedpartitioningmechanismrevealedupontranscriptionalinactivationofcentromere
AT haasejulian acohesinbasedpartitioningmechanismrevealedupontranscriptionalinactivationofcentromere
AT harrisonbenjamin acohesinbasedpartitioningmechanismrevealedupontranscriptionalinactivationofcentromere
AT sniderchloee acohesinbasedpartitioningmechanismrevealedupontranscriptionalinactivationofcentromere
AT eldridgebrittany acohesinbasedpartitioningmechanismrevealedupontranscriptionalinactivationofcentromere
AT kaminskylila acohesinbasedpartitioningmechanismrevealedupontranscriptionalinactivationofcentromere
AT hinerebeccam acohesinbasedpartitioningmechanismrevealedupontranscriptionalinactivationofcentromere
AT haberjamese acohesinbasedpartitioningmechanismrevealedupontranscriptionalinactivationofcentromere
AT bloomkerry acohesinbasedpartitioningmechanismrevealedupontranscriptionalinactivationofcentromere
AT tsabarmichael cohesinbasedpartitioningmechanismrevealedupontranscriptionalinactivationofcentromere
AT haasejulian cohesinbasedpartitioningmechanismrevealedupontranscriptionalinactivationofcentromere
AT harrisonbenjamin cohesinbasedpartitioningmechanismrevealedupontranscriptionalinactivationofcentromere
AT sniderchloee cohesinbasedpartitioningmechanismrevealedupontranscriptionalinactivationofcentromere
AT eldridgebrittany cohesinbasedpartitioningmechanismrevealedupontranscriptionalinactivationofcentromere
AT kaminskylila cohesinbasedpartitioningmechanismrevealedupontranscriptionalinactivationofcentromere
AT hinerebeccam cohesinbasedpartitioningmechanismrevealedupontranscriptionalinactivationofcentromere
AT haberjamese cohesinbasedpartitioningmechanismrevealedupontranscriptionalinactivationofcentromere
AT bloomkerry cohesinbasedpartitioningmechanismrevealedupontranscriptionalinactivationofcentromere