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Mcm10 coordinates the timely assembly and activation of the replication fork helicase

Mcm10 is an essential replication factor that is required for DNA replication in eukaryotes. Two key steps in the initiation of DNA replication are the assembly and activation of Cdc45–Mcm2–7-GINS (CMG) replicative helicase. However, it is not known what coordinates helicase assembly with helicase a...

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Autores principales: Perez-Arnaiz, Patricia, Bruck, Irina, Kaplan, Daniel L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4705653/
https://www.ncbi.nlm.nih.gov/pubmed/26582917
http://dx.doi.org/10.1093/nar/gkv1260
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author Perez-Arnaiz, Patricia
Bruck, Irina
Kaplan, Daniel L.
author_facet Perez-Arnaiz, Patricia
Bruck, Irina
Kaplan, Daniel L.
author_sort Perez-Arnaiz, Patricia
collection PubMed
description Mcm10 is an essential replication factor that is required for DNA replication in eukaryotes. Two key steps in the initiation of DNA replication are the assembly and activation of Cdc45–Mcm2–7-GINS (CMG) replicative helicase. However, it is not known what coordinates helicase assembly with helicase activation. We show in this manuscript, using purified proteins from budding yeast, that Mcm10 directly interacts with the Mcm2–7 complex and Cdc45. In fact, Mcm10 recruits Cdc45 to Mcm2–7 complex in vitro. To study the role of Mcm10 in more detail in vivo we used an auxin inducible degron in which Mcm10 is degraded upon addition of auxin. We show in this manuscript that Mcm10 is required for the timely recruitment of Cdc45 and GINS recruitment to the Mcm2–7 complex in vivo during early S phase. We also found that Mcm10 stimulates Mcm2 phosphorylation by DDK in vivo and in vitro. These findings indicate that Mcm10 plays a critical role in coupling replicative helicase assembly with helicase activation. Mcm10 is first involved in the recruitment of Cdc45 to the Mcm2–7 complex. After Cdc45–Mcm2–7 complex assembly, Mcm10 promotes origin melting by stimulating DDK phosphorylation of Mcm2, which thereby leads to GINS attachment to Mcm2–7.
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spelling pubmed-47056532016-01-11 Mcm10 coordinates the timely assembly and activation of the replication fork helicase Perez-Arnaiz, Patricia Bruck, Irina Kaplan, Daniel L. Nucleic Acids Res Nucleic Acid Enzymes Mcm10 is an essential replication factor that is required for DNA replication in eukaryotes. Two key steps in the initiation of DNA replication are the assembly and activation of Cdc45–Mcm2–7-GINS (CMG) replicative helicase. However, it is not known what coordinates helicase assembly with helicase activation. We show in this manuscript, using purified proteins from budding yeast, that Mcm10 directly interacts with the Mcm2–7 complex and Cdc45. In fact, Mcm10 recruits Cdc45 to Mcm2–7 complex in vitro. To study the role of Mcm10 in more detail in vivo we used an auxin inducible degron in which Mcm10 is degraded upon addition of auxin. We show in this manuscript that Mcm10 is required for the timely recruitment of Cdc45 and GINS recruitment to the Mcm2–7 complex in vivo during early S phase. We also found that Mcm10 stimulates Mcm2 phosphorylation by DDK in vivo and in vitro. These findings indicate that Mcm10 plays a critical role in coupling replicative helicase assembly with helicase activation. Mcm10 is first involved in the recruitment of Cdc45 to the Mcm2–7 complex. After Cdc45–Mcm2–7 complex assembly, Mcm10 promotes origin melting by stimulating DDK phosphorylation of Mcm2, which thereby leads to GINS attachment to Mcm2–7. Oxford University Press 2016-01-08 2015-11-17 /pmc/articles/PMC4705653/ /pubmed/26582917 http://dx.doi.org/10.1093/nar/gkv1260 Text en © The Author(s) 2015. Published by Oxford University Press on behalf of Nucleic Acids Research. 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 reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Nucleic Acid Enzymes
Perez-Arnaiz, Patricia
Bruck, Irina
Kaplan, Daniel L.
Mcm10 coordinates the timely assembly and activation of the replication fork helicase
title Mcm10 coordinates the timely assembly and activation of the replication fork helicase
title_full Mcm10 coordinates the timely assembly and activation of the replication fork helicase
title_fullStr Mcm10 coordinates the timely assembly and activation of the replication fork helicase
title_full_unstemmed Mcm10 coordinates the timely assembly and activation of the replication fork helicase
title_short Mcm10 coordinates the timely assembly and activation of the replication fork helicase
title_sort mcm10 coordinates the timely assembly and activation of the replication fork helicase
topic Nucleic Acid Enzymes
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4705653/
https://www.ncbi.nlm.nih.gov/pubmed/26582917
http://dx.doi.org/10.1093/nar/gkv1260
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