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Cdc45-MCM-GINS, a new power player for DNA replication

The identity of the DNA helicase(s) involved in eukaryotic DNA replication is still a matter of debate, but the mini-chromosome maintenance (MCM) proteins are the chief candidate. Six conserved MCM proteins, Mcm2–7, are essential for the initiation and elongation stages of DNA replication, contain A...

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Detalles Bibliográficos
Autores principales: Aparicio, Tomás, Ibarra, Arkaitz, Méndez, Juan
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2006
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1564009/
https://www.ncbi.nlm.nih.gov/pubmed/16930479
http://dx.doi.org/10.1186/1747-1028-1-18
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author Aparicio, Tomás
Ibarra, Arkaitz
Méndez, Juan
author_facet Aparicio, Tomás
Ibarra, Arkaitz
Méndez, Juan
author_sort Aparicio, Tomás
collection PubMed
description The identity of the DNA helicase(s) involved in eukaryotic DNA replication is still a matter of debate, but the mini-chromosome maintenance (MCM) proteins are the chief candidate. Six conserved MCM proteins, Mcm2–7, are essential for the initiation and elongation stages of DNA replication, contain ATP binding pockets and can form a hexameric structure resembling that of known prokaryotic and viral helicases. However, biochemical proof of their presumed function has remained elusive. Several recent reports confirm that the MCM complex is part of the cellular machine responsible for the unwinding of DNA during S phase. In one of these reports, the helicase activity of Mcm2–7 is finally revealed, when they are purified in association with two partners: initiation factor Cdc45 and a four-subunit complex called GINS. The Cdc45-MCM-GINS complex could constitute the core of a larger macromolecular structure that has been termed the "replisome progression complex".
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spelling pubmed-15640092006-09-12 Cdc45-MCM-GINS, a new power player for DNA replication Aparicio, Tomás Ibarra, Arkaitz Méndez, Juan Cell Div Commentaries The identity of the DNA helicase(s) involved in eukaryotic DNA replication is still a matter of debate, but the mini-chromosome maintenance (MCM) proteins are the chief candidate. Six conserved MCM proteins, Mcm2–7, are essential for the initiation and elongation stages of DNA replication, contain ATP binding pockets and can form a hexameric structure resembling that of known prokaryotic and viral helicases. However, biochemical proof of their presumed function has remained elusive. Several recent reports confirm that the MCM complex is part of the cellular machine responsible for the unwinding of DNA during S phase. In one of these reports, the helicase activity of Mcm2–7 is finally revealed, when they are purified in association with two partners: initiation factor Cdc45 and a four-subunit complex called GINS. The Cdc45-MCM-GINS complex could constitute the core of a larger macromolecular structure that has been termed the "replisome progression complex". BioMed Central 2006-08-24 /pmc/articles/PMC1564009/ /pubmed/16930479 http://dx.doi.org/10.1186/1747-1028-1-18 Text en Copyright © 2006 Aparicio et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Commentaries
Aparicio, Tomás
Ibarra, Arkaitz
Méndez, Juan
Cdc45-MCM-GINS, a new power player for DNA replication
title Cdc45-MCM-GINS, a new power player for DNA replication
title_full Cdc45-MCM-GINS, a new power player for DNA replication
title_fullStr Cdc45-MCM-GINS, a new power player for DNA replication
title_full_unstemmed Cdc45-MCM-GINS, a new power player for DNA replication
title_short Cdc45-MCM-GINS, a new power player for DNA replication
title_sort cdc45-mcm-gins, a new power player for dna replication
topic Commentaries
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1564009/
https://www.ncbi.nlm.nih.gov/pubmed/16930479
http://dx.doi.org/10.1186/1747-1028-1-18
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