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Chromosome Duplication in Saccharomyces cerevisiae

The accurate and complete replication of genomic DNA is essential for all life. In eukaryotic cells, the assembly of the multi-enzyme replisomes that perform replication is divided into stages that occur at distinct phases of the cell cycle. Replicative DNA helicases are loaded around origins of DNA...

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Detalles Bibliográficos
Autores principales: Bell, Stephen P., Labib, Karim
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Genetics Society of America 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4937469/
https://www.ncbi.nlm.nih.gov/pubmed/27384026
http://dx.doi.org/10.1534/genetics.115.186452
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author Bell, Stephen P.
Labib, Karim
author_facet Bell, Stephen P.
Labib, Karim
author_sort Bell, Stephen P.
collection PubMed
description The accurate and complete replication of genomic DNA is essential for all life. In eukaryotic cells, the assembly of the multi-enzyme replisomes that perform replication is divided into stages that occur at distinct phases of the cell cycle. Replicative DNA helicases are loaded around origins of DNA replication exclusively during G(1) phase. The loaded helicases are then activated during S phase and associate with the replicative DNA polymerases and other accessory proteins. The function of the resulting replisomes is monitored by checkpoint proteins that protect arrested replisomes and inhibit new initiation when replication is inhibited. The replisome also coordinates nucleosome disassembly, assembly, and the establishment of sister chromatid cohesion. Finally, when two replisomes converge they are disassembled. Studies in Saccharomyces cerevisiae have led the way in our understanding of these processes. Here, we review our increasingly molecular understanding of these events and their regulation.
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spelling pubmed-49374692017-04-06 Chromosome Duplication in Saccharomyces cerevisiae Bell, Stephen P. Labib, Karim Genetics YeastBook The accurate and complete replication of genomic DNA is essential for all life. In eukaryotic cells, the assembly of the multi-enzyme replisomes that perform replication is divided into stages that occur at distinct phases of the cell cycle. Replicative DNA helicases are loaded around origins of DNA replication exclusively during G(1) phase. The loaded helicases are then activated during S phase and associate with the replicative DNA polymerases and other accessory proteins. The function of the resulting replisomes is monitored by checkpoint proteins that protect arrested replisomes and inhibit new initiation when replication is inhibited. The replisome also coordinates nucleosome disassembly, assembly, and the establishment of sister chromatid cohesion. Finally, when two replisomes converge they are disassembled. Studies in Saccharomyces cerevisiae have led the way in our understanding of these processes. Here, we review our increasingly molecular understanding of these events and their regulation. Genetics Society of America 2016-07 2016-06-27 /pmc/articles/PMC4937469/ /pubmed/27384026 http://dx.doi.org/10.1534/genetics.115.186452 Text en Copyright © 2016 Bell and Labib Available freely online through the author-supported open access option. This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle YeastBook
Bell, Stephen P.
Labib, Karim
Chromosome Duplication in Saccharomyces cerevisiae
title Chromosome Duplication in Saccharomyces cerevisiae
title_full Chromosome Duplication in Saccharomyces cerevisiae
title_fullStr Chromosome Duplication in Saccharomyces cerevisiae
title_full_unstemmed Chromosome Duplication in Saccharomyces cerevisiae
title_short Chromosome Duplication in Saccharomyces cerevisiae
title_sort chromosome duplication in saccharomyces cerevisiae
topic YeastBook
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4937469/
https://www.ncbi.nlm.nih.gov/pubmed/27384026
http://dx.doi.org/10.1534/genetics.115.186452
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