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Recruitment of Fkh1 to replication origins requires precisely positioned Fkh1/2 binding sites and concurrent assembly of the pre-replicative complex

In budding yeast, activation of many DNA replication origins is regulated by their chromatin environment, whereas others fire in early S phase regardless of their chromosomal location. Several location-independent origins contain at least two divergently oriented binding sites for Forkhead (Fkh) tra...

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Autores principales: Reinapae, Allan, Jalakas, Kristiina, Avvakumov, Nikita, Lõoke, Marko, Kristjuhan, Kersti, Kristjuhan, Arnold
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5308776/
https://www.ncbi.nlm.nih.gov/pubmed/28141805
http://dx.doi.org/10.1371/journal.pgen.1006588
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author Reinapae, Allan
Jalakas, Kristiina
Avvakumov, Nikita
Lõoke, Marko
Kristjuhan, Kersti
Kristjuhan, Arnold
author_facet Reinapae, Allan
Jalakas, Kristiina
Avvakumov, Nikita
Lõoke, Marko
Kristjuhan, Kersti
Kristjuhan, Arnold
author_sort Reinapae, Allan
collection PubMed
description In budding yeast, activation of many DNA replication origins is regulated by their chromatin environment, whereas others fire in early S phase regardless of their chromosomal location. Several location-independent origins contain at least two divergently oriented binding sites for Forkhead (Fkh) transcription factors in close proximity to their ARS consensus sequence. To explore whether recruitment of Forkhead proteins to replication origins is dependent on the spatial arrangement of Fkh1/2 binding sites, we changed the spacing and orientation of the sites in early replication origins ARS305 and ARS607. We followed recruitment of the Fkh1 protein to origins by chromatin immunoprecipitation and tested the ability of these origins to fire in early S phase. Our results demonstrate that precise spatial and directional arrangement of Fkh1/2 sites is crucial for efficient binding of the Fkh1 protein and for early firing of the origins. We also show that recruitment of Fkh1 to the origins depends on formation of the pre-replicative complex (pre-RC) and loading of the Mcm2-7 helicase, indicating that the origins are regulated by cooperative action of Fkh1 and the pre-RC. These results reveal that DNA binding of Forkhead factors does not depend merely on the presence of its binding sites but on their precise arrangement and is strongly influenced by other protein complexes in the vicinity.
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spelling pubmed-53087762017-03-03 Recruitment of Fkh1 to replication origins requires precisely positioned Fkh1/2 binding sites and concurrent assembly of the pre-replicative complex Reinapae, Allan Jalakas, Kristiina Avvakumov, Nikita Lõoke, Marko Kristjuhan, Kersti Kristjuhan, Arnold PLoS Genet Research Article In budding yeast, activation of many DNA replication origins is regulated by their chromatin environment, whereas others fire in early S phase regardless of their chromosomal location. Several location-independent origins contain at least two divergently oriented binding sites for Forkhead (Fkh) transcription factors in close proximity to their ARS consensus sequence. To explore whether recruitment of Forkhead proteins to replication origins is dependent on the spatial arrangement of Fkh1/2 binding sites, we changed the spacing and orientation of the sites in early replication origins ARS305 and ARS607. We followed recruitment of the Fkh1 protein to origins by chromatin immunoprecipitation and tested the ability of these origins to fire in early S phase. Our results demonstrate that precise spatial and directional arrangement of Fkh1/2 sites is crucial for efficient binding of the Fkh1 protein and for early firing of the origins. We also show that recruitment of Fkh1 to the origins depends on formation of the pre-replicative complex (pre-RC) and loading of the Mcm2-7 helicase, indicating that the origins are regulated by cooperative action of Fkh1 and the pre-RC. These results reveal that DNA binding of Forkhead factors does not depend merely on the presence of its binding sites but on their precise arrangement and is strongly influenced by other protein complexes in the vicinity. Public Library of Science 2017-01-31 /pmc/articles/PMC5308776/ /pubmed/28141805 http://dx.doi.org/10.1371/journal.pgen.1006588 Text en © 2017 Reinapae et al 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 use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Reinapae, Allan
Jalakas, Kristiina
Avvakumov, Nikita
Lõoke, Marko
Kristjuhan, Kersti
Kristjuhan, Arnold
Recruitment of Fkh1 to replication origins requires precisely positioned Fkh1/2 binding sites and concurrent assembly of the pre-replicative complex
title Recruitment of Fkh1 to replication origins requires precisely positioned Fkh1/2 binding sites and concurrent assembly of the pre-replicative complex
title_full Recruitment of Fkh1 to replication origins requires precisely positioned Fkh1/2 binding sites and concurrent assembly of the pre-replicative complex
title_fullStr Recruitment of Fkh1 to replication origins requires precisely positioned Fkh1/2 binding sites and concurrent assembly of the pre-replicative complex
title_full_unstemmed Recruitment of Fkh1 to replication origins requires precisely positioned Fkh1/2 binding sites and concurrent assembly of the pre-replicative complex
title_short Recruitment of Fkh1 to replication origins requires precisely positioned Fkh1/2 binding sites and concurrent assembly of the pre-replicative complex
title_sort recruitment of fkh1 to replication origins requires precisely positioned fkh1/2 binding sites and concurrent assembly of the pre-replicative complex
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5308776/
https://www.ncbi.nlm.nih.gov/pubmed/28141805
http://dx.doi.org/10.1371/journal.pgen.1006588
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