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A conserved Mcm4 motif is required for Mcm2-7 double-hexamer formation and origin DNA unwinding

Licensing of eukaryotic origins of replication requires DNA loading of two copies of the Mcm2-7 replicative helicase to form a head-to-head double-hexamer, ensuring activated helicases depart the origin bidirectionally. To understand the formation and importance of this double-hexamer, we identified...

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Autores principales: Champasa, Kanokwan, Blank, Caitlin, Friedman, Larry J, Gelles, Jeff, Bell, Stephen P
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6701924/
https://www.ncbi.nlm.nih.gov/pubmed/31385807
http://dx.doi.org/10.7554/eLife.45538
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author Champasa, Kanokwan
Blank, Caitlin
Friedman, Larry J
Gelles, Jeff
Bell, Stephen P
author_facet Champasa, Kanokwan
Blank, Caitlin
Friedman, Larry J
Gelles, Jeff
Bell, Stephen P
author_sort Champasa, Kanokwan
collection PubMed
description Licensing of eukaryotic origins of replication requires DNA loading of two copies of the Mcm2-7 replicative helicase to form a head-to-head double-hexamer, ensuring activated helicases depart the origin bidirectionally. To understand the formation and importance of this double-hexamer, we identified mutations in a conserved and essential Mcm4 motif that permit loading of two Mcm2-7 complexes but are defective for double-hexamer formation. Single-molecule studies show mutant Mcm2-7 forms initial hexamer-hexamer interactions; however, the resulting complex is unstable. Kinetic analyses of wild-type and mutant Mcm2-7 reveal a limited time window for double-hexamer formation following second Mcm2-7 association, suggesting that this process is facilitated. Double-hexamer formation is required for extensive origin DNA unwinding but not initial DNA melting or recruitment of helicase-activation proteins (Cdc45, GINS, Mcm10). Our findings elucidate dynamic mechanisms of origin licensing, and identify the transition between initial DNA melting and extensive unwinding as the first initiation event requiring double-hexamer formation.
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spelling pubmed-67019242019-08-21 A conserved Mcm4 motif is required for Mcm2-7 double-hexamer formation and origin DNA unwinding Champasa, Kanokwan Blank, Caitlin Friedman, Larry J Gelles, Jeff Bell, Stephen P eLife Biochemistry and Chemical Biology Licensing of eukaryotic origins of replication requires DNA loading of two copies of the Mcm2-7 replicative helicase to form a head-to-head double-hexamer, ensuring activated helicases depart the origin bidirectionally. To understand the formation and importance of this double-hexamer, we identified mutations in a conserved and essential Mcm4 motif that permit loading of two Mcm2-7 complexes but are defective for double-hexamer formation. Single-molecule studies show mutant Mcm2-7 forms initial hexamer-hexamer interactions; however, the resulting complex is unstable. Kinetic analyses of wild-type and mutant Mcm2-7 reveal a limited time window for double-hexamer formation following second Mcm2-7 association, suggesting that this process is facilitated. Double-hexamer formation is required for extensive origin DNA unwinding but not initial DNA melting or recruitment of helicase-activation proteins (Cdc45, GINS, Mcm10). Our findings elucidate dynamic mechanisms of origin licensing, and identify the transition between initial DNA melting and extensive unwinding as the first initiation event requiring double-hexamer formation. eLife Sciences Publications, Ltd 2019-08-06 /pmc/articles/PMC6701924/ /pubmed/31385807 http://dx.doi.org/10.7554/eLife.45538 Text en © 2019, Champasa et al http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Biochemistry and Chemical Biology
Champasa, Kanokwan
Blank, Caitlin
Friedman, Larry J
Gelles, Jeff
Bell, Stephen P
A conserved Mcm4 motif is required for Mcm2-7 double-hexamer formation and origin DNA unwinding
title A conserved Mcm4 motif is required for Mcm2-7 double-hexamer formation and origin DNA unwinding
title_full A conserved Mcm4 motif is required for Mcm2-7 double-hexamer formation and origin DNA unwinding
title_fullStr A conserved Mcm4 motif is required for Mcm2-7 double-hexamer formation and origin DNA unwinding
title_full_unstemmed A conserved Mcm4 motif is required for Mcm2-7 double-hexamer formation and origin DNA unwinding
title_short A conserved Mcm4 motif is required for Mcm2-7 double-hexamer formation and origin DNA unwinding
title_sort conserved mcm4 motif is required for mcm2-7 double-hexamer formation and origin dna unwinding
topic Biochemistry and Chemical Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6701924/
https://www.ncbi.nlm.nih.gov/pubmed/31385807
http://dx.doi.org/10.7554/eLife.45538
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