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Kinetochores Coordinate Pericentromeric Cohesion and Early DNA Replication by Cdc7-Dbf4 Kinase Recruitment
Centromeres play several important roles in ensuring proper chromosome segregation. Not only do they promote kinetochore assembly for microtubule attachment, but they also support robust sister chromatid cohesion at pericentromeres and facilitate replication of centromeric DNA early in S phase. Howe...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cell Press
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3679449/ https://www.ncbi.nlm.nih.gov/pubmed/23746350 http://dx.doi.org/10.1016/j.molcel.2013.05.011 |
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author | Natsume, Toyoaki Müller, Carolin A. Katou, Yuki Retkute, Renata Gierliński, Marek Araki, Hiroyuki Blow, J. Julian Shirahige, Katsuhiko Nieduszynski, Conrad A. Tanaka, Tomoyuki U. |
author_facet | Natsume, Toyoaki Müller, Carolin A. Katou, Yuki Retkute, Renata Gierliński, Marek Araki, Hiroyuki Blow, J. Julian Shirahige, Katsuhiko Nieduszynski, Conrad A. Tanaka, Tomoyuki U. |
author_sort | Natsume, Toyoaki |
collection | PubMed |
description | Centromeres play several important roles in ensuring proper chromosome segregation. Not only do they promote kinetochore assembly for microtubule attachment, but they also support robust sister chromatid cohesion at pericentromeres and facilitate replication of centromeric DNA early in S phase. However, it is still elusive how centromeres orchestrate all these functions at the same site. Here, we show that the budding yeast Dbf4-dependent kinase (DDK) accumulates at kinetochores in telophase, facilitated by the Ctf19 kinetochore complex. This promptly recruits Sld3–Sld7 replication initiator proteins to pericentromeric replication origins so that they initiate replication early in S phase. Furthermore, DDK at kinetochores independently recruits the Scc2–Scc4 cohesin loader to centromeres in G1 phase. This enhances cohesin loading and facilitates robust pericentromeric cohesion in S phase. Thus, we have found the central mechanism by which kinetochores orchestrate early S phase DNA replication and robust sister chromatid cohesion at microtubule attachment sites. |
format | Online Article Text |
id | pubmed-3679449 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Cell Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-36794492013-06-12 Kinetochores Coordinate Pericentromeric Cohesion and Early DNA Replication by Cdc7-Dbf4 Kinase Recruitment Natsume, Toyoaki Müller, Carolin A. Katou, Yuki Retkute, Renata Gierliński, Marek Araki, Hiroyuki Blow, J. Julian Shirahige, Katsuhiko Nieduszynski, Conrad A. Tanaka, Tomoyuki U. Mol Cell Article Centromeres play several important roles in ensuring proper chromosome segregation. Not only do they promote kinetochore assembly for microtubule attachment, but they also support robust sister chromatid cohesion at pericentromeres and facilitate replication of centromeric DNA early in S phase. However, it is still elusive how centromeres orchestrate all these functions at the same site. Here, we show that the budding yeast Dbf4-dependent kinase (DDK) accumulates at kinetochores in telophase, facilitated by the Ctf19 kinetochore complex. This promptly recruits Sld3–Sld7 replication initiator proteins to pericentromeric replication origins so that they initiate replication early in S phase. Furthermore, DDK at kinetochores independently recruits the Scc2–Scc4 cohesin loader to centromeres in G1 phase. This enhances cohesin loading and facilitates robust pericentromeric cohesion in S phase. Thus, we have found the central mechanism by which kinetochores orchestrate early S phase DNA replication and robust sister chromatid cohesion at microtubule attachment sites. Cell Press 2013-06-06 /pmc/articles/PMC3679449/ /pubmed/23746350 http://dx.doi.org/10.1016/j.molcel.2013.05.011 Text en © 2013 ELL & Excerpta Medica. https://creativecommons.org/licenses/by/3.0/ Open Access under CC BY 3.0 (https://creativecommons.org/licenses/by/3.0/) license |
spellingShingle | Article Natsume, Toyoaki Müller, Carolin A. Katou, Yuki Retkute, Renata Gierliński, Marek Araki, Hiroyuki Blow, J. Julian Shirahige, Katsuhiko Nieduszynski, Conrad A. Tanaka, Tomoyuki U. Kinetochores Coordinate Pericentromeric Cohesion and Early DNA Replication by Cdc7-Dbf4 Kinase Recruitment |
title | Kinetochores Coordinate Pericentromeric Cohesion and Early DNA Replication by Cdc7-Dbf4 Kinase Recruitment |
title_full | Kinetochores Coordinate Pericentromeric Cohesion and Early DNA Replication by Cdc7-Dbf4 Kinase Recruitment |
title_fullStr | Kinetochores Coordinate Pericentromeric Cohesion and Early DNA Replication by Cdc7-Dbf4 Kinase Recruitment |
title_full_unstemmed | Kinetochores Coordinate Pericentromeric Cohesion and Early DNA Replication by Cdc7-Dbf4 Kinase Recruitment |
title_short | Kinetochores Coordinate Pericentromeric Cohesion and Early DNA Replication by Cdc7-Dbf4 Kinase Recruitment |
title_sort | kinetochores coordinate pericentromeric cohesion and early dna replication by cdc7-dbf4 kinase recruitment |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3679449/ https://www.ncbi.nlm.nih.gov/pubmed/23746350 http://dx.doi.org/10.1016/j.molcel.2013.05.011 |
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