Cargando…

The budding yeast RSC complex maintains ploidy by promoting spindle pole body insertion

Ploidy is tightly regulated in eukaryotic cells and is critical for cell function and survival. Cells coordinate multiple pathways to ensure replicated DNA is segregated accurately to prevent abnormal changes in chromosome number. In this study, we characterize an unanticipated role for the Saccharo...

Descripción completa

Detalles Bibliográficos
Autores principales: Sing, Tina L., Hung, Minnie P., Ohnuki, Shinsuke, Suzuki, Godai, San Luis, Bryan-Joseph, McClain, Melainia, Unruh, Jay R., Yu, Zulin, Ou, Jiongwen, Marshall-Sheppard, Jesse, Huh, Won-Ki, Costanzo, Michael, Boone, Charles, Ohya, Yoshikazu, Jaspersen, Sue L., Brown, Grant W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Rockefeller University Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6028538/
https://www.ncbi.nlm.nih.gov/pubmed/29875260
http://dx.doi.org/10.1083/jcb.201709009
_version_ 1783336784741007360
author Sing, Tina L.
Hung, Minnie P.
Ohnuki, Shinsuke
Suzuki, Godai
San Luis, Bryan-Joseph
McClain, Melainia
Unruh, Jay R.
Yu, Zulin
Ou, Jiongwen
Marshall-Sheppard, Jesse
Huh, Won-Ki
Costanzo, Michael
Boone, Charles
Ohya, Yoshikazu
Jaspersen, Sue L.
Brown, Grant W.
author_facet Sing, Tina L.
Hung, Minnie P.
Ohnuki, Shinsuke
Suzuki, Godai
San Luis, Bryan-Joseph
McClain, Melainia
Unruh, Jay R.
Yu, Zulin
Ou, Jiongwen
Marshall-Sheppard, Jesse
Huh, Won-Ki
Costanzo, Michael
Boone, Charles
Ohya, Yoshikazu
Jaspersen, Sue L.
Brown, Grant W.
author_sort Sing, Tina L.
collection PubMed
description Ploidy is tightly regulated in eukaryotic cells and is critical for cell function and survival. Cells coordinate multiple pathways to ensure replicated DNA is segregated accurately to prevent abnormal changes in chromosome number. In this study, we characterize an unanticipated role for the Saccharomyces cerevisiae “remodels the structure of chromatin” (RSC) complex in ploidy maintenance. We show that deletion of any of six nonessential RSC genes causes a rapid transition from haploid to diploid DNA content because of nondisjunction events. Diploidization is accompanied by diagnostic changes in cell morphology and is stably maintained without further ploidy increases. We find that RSC promotes chromosome segregation by facilitating spindle pole body (SPB) duplication. More specifically, RSC plays a role in distributing two SPB insertion factors, Nbp1 and Ndc1, to the new SPB. Thus, we provide insight into a role for a SWI/SNF family complex in SPB duplication and ploidy maintenance.
format Online
Article
Text
id pubmed-6028538
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher Rockefeller University Press
record_format MEDLINE/PubMed
spelling pubmed-60285382019-01-02 The budding yeast RSC complex maintains ploidy by promoting spindle pole body insertion Sing, Tina L. Hung, Minnie P. Ohnuki, Shinsuke Suzuki, Godai San Luis, Bryan-Joseph McClain, Melainia Unruh, Jay R. Yu, Zulin Ou, Jiongwen Marshall-Sheppard, Jesse Huh, Won-Ki Costanzo, Michael Boone, Charles Ohya, Yoshikazu Jaspersen, Sue L. Brown, Grant W. J Cell Biol Research Articles Ploidy is tightly regulated in eukaryotic cells and is critical for cell function and survival. Cells coordinate multiple pathways to ensure replicated DNA is segregated accurately to prevent abnormal changes in chromosome number. In this study, we characterize an unanticipated role for the Saccharomyces cerevisiae “remodels the structure of chromatin” (RSC) complex in ploidy maintenance. We show that deletion of any of six nonessential RSC genes causes a rapid transition from haploid to diploid DNA content because of nondisjunction events. Diploidization is accompanied by diagnostic changes in cell morphology and is stably maintained without further ploidy increases. We find that RSC promotes chromosome segregation by facilitating spindle pole body (SPB) duplication. More specifically, RSC plays a role in distributing two SPB insertion factors, Nbp1 and Ndc1, to the new SPB. Thus, we provide insight into a role for a SWI/SNF family complex in SPB duplication and ploidy maintenance. Rockefeller University Press 2018-07-02 /pmc/articles/PMC6028538/ /pubmed/29875260 http://dx.doi.org/10.1083/jcb.201709009 Text en © 2018 Sing 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
Sing, Tina L.
Hung, Minnie P.
Ohnuki, Shinsuke
Suzuki, Godai
San Luis, Bryan-Joseph
McClain, Melainia
Unruh, Jay R.
Yu, Zulin
Ou, Jiongwen
Marshall-Sheppard, Jesse
Huh, Won-Ki
Costanzo, Michael
Boone, Charles
Ohya, Yoshikazu
Jaspersen, Sue L.
Brown, Grant W.
The budding yeast RSC complex maintains ploidy by promoting spindle pole body insertion
title The budding yeast RSC complex maintains ploidy by promoting spindle pole body insertion
title_full The budding yeast RSC complex maintains ploidy by promoting spindle pole body insertion
title_fullStr The budding yeast RSC complex maintains ploidy by promoting spindle pole body insertion
title_full_unstemmed The budding yeast RSC complex maintains ploidy by promoting spindle pole body insertion
title_short The budding yeast RSC complex maintains ploidy by promoting spindle pole body insertion
title_sort budding yeast rsc complex maintains ploidy by promoting spindle pole body insertion
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6028538/
https://www.ncbi.nlm.nih.gov/pubmed/29875260
http://dx.doi.org/10.1083/jcb.201709009
work_keys_str_mv AT singtinal thebuddingyeastrsccomplexmaintainsploidybypromotingspindlepolebodyinsertion
AT hungminniep thebuddingyeastrsccomplexmaintainsploidybypromotingspindlepolebodyinsertion
AT ohnukishinsuke thebuddingyeastrsccomplexmaintainsploidybypromotingspindlepolebodyinsertion
AT suzukigodai thebuddingyeastrsccomplexmaintainsploidybypromotingspindlepolebodyinsertion
AT sanluisbryanjoseph thebuddingyeastrsccomplexmaintainsploidybypromotingspindlepolebodyinsertion
AT mcclainmelainia thebuddingyeastrsccomplexmaintainsploidybypromotingspindlepolebodyinsertion
AT unruhjayr thebuddingyeastrsccomplexmaintainsploidybypromotingspindlepolebodyinsertion
AT yuzulin thebuddingyeastrsccomplexmaintainsploidybypromotingspindlepolebodyinsertion
AT oujiongwen thebuddingyeastrsccomplexmaintainsploidybypromotingspindlepolebodyinsertion
AT marshallsheppardjesse thebuddingyeastrsccomplexmaintainsploidybypromotingspindlepolebodyinsertion
AT huhwonki thebuddingyeastrsccomplexmaintainsploidybypromotingspindlepolebodyinsertion
AT costanzomichael thebuddingyeastrsccomplexmaintainsploidybypromotingspindlepolebodyinsertion
AT boonecharles thebuddingyeastrsccomplexmaintainsploidybypromotingspindlepolebodyinsertion
AT ohyayoshikazu thebuddingyeastrsccomplexmaintainsploidybypromotingspindlepolebodyinsertion
AT jaspersensuel thebuddingyeastrsccomplexmaintainsploidybypromotingspindlepolebodyinsertion
AT browngrantw thebuddingyeastrsccomplexmaintainsploidybypromotingspindlepolebodyinsertion
AT singtinal buddingyeastrsccomplexmaintainsploidybypromotingspindlepolebodyinsertion
AT hungminniep buddingyeastrsccomplexmaintainsploidybypromotingspindlepolebodyinsertion
AT ohnukishinsuke buddingyeastrsccomplexmaintainsploidybypromotingspindlepolebodyinsertion
AT suzukigodai buddingyeastrsccomplexmaintainsploidybypromotingspindlepolebodyinsertion
AT sanluisbryanjoseph buddingyeastrsccomplexmaintainsploidybypromotingspindlepolebodyinsertion
AT mcclainmelainia buddingyeastrsccomplexmaintainsploidybypromotingspindlepolebodyinsertion
AT unruhjayr buddingyeastrsccomplexmaintainsploidybypromotingspindlepolebodyinsertion
AT yuzulin buddingyeastrsccomplexmaintainsploidybypromotingspindlepolebodyinsertion
AT oujiongwen buddingyeastrsccomplexmaintainsploidybypromotingspindlepolebodyinsertion
AT marshallsheppardjesse buddingyeastrsccomplexmaintainsploidybypromotingspindlepolebodyinsertion
AT huhwonki buddingyeastrsccomplexmaintainsploidybypromotingspindlepolebodyinsertion
AT costanzomichael buddingyeastrsccomplexmaintainsploidybypromotingspindlepolebodyinsertion
AT boonecharles buddingyeastrsccomplexmaintainsploidybypromotingspindlepolebodyinsertion
AT ohyayoshikazu buddingyeastrsccomplexmaintainsploidybypromotingspindlepolebodyinsertion
AT jaspersensuel buddingyeastrsccomplexmaintainsploidybypromotingspindlepolebodyinsertion
AT browngrantw buddingyeastrsccomplexmaintainsploidybypromotingspindlepolebodyinsertion