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DNA replication licensing factor Cdc6 and Plk4 kinase antagonistically regulate centrosome duplication via Sas-6
Centrosome number is tightly controlled during the cell cycle to ensure proper spindle assembly and cell division. However, the underlying mechanism that controls centrosome number remains largely unclear. We show herein that the DNA replication licensing factor Cdc6 is recruited to the proximal sid...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5414174/ https://www.ncbi.nlm.nih.gov/pubmed/28447620 http://dx.doi.org/10.1038/ncomms15164 |
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author | Xu, Xiaowei Huang, Shijiao Zhang, Boyan Huang, Fan Chi, Wangfei Fu, Jingyan Wang, Gang Li, Si Jiang, Qing Zhang, Chuanmao |
author_facet | Xu, Xiaowei Huang, Shijiao Zhang, Boyan Huang, Fan Chi, Wangfei Fu, Jingyan Wang, Gang Li, Si Jiang, Qing Zhang, Chuanmao |
author_sort | Xu, Xiaowei |
collection | PubMed |
description | Centrosome number is tightly controlled during the cell cycle to ensure proper spindle assembly and cell division. However, the underlying mechanism that controls centrosome number remains largely unclear. We show herein that the DNA replication licensing factor Cdc6 is recruited to the proximal side of the centrioles via cyclin A to negatively regulate centrosome duplication by binding and inhibiting the cartwheel protein Sas-6 from forming a stable complex with another centriole duplication core protein, STIL. We further demonstrate that Cdc6 colocalizes with Plk4 at the centrosome, and interacts with Plk4 during S phase. Plk4 disrupts the interaction between Sas-6 and Cdc6, and suppresses the inhibitory role of Cdc6 on Sas-6 by phosphorylating Cdc6. Overexpressing wild-type Cdc6 or Plk4-unphosphorylatable Cdc6 mutant 2A reduces centrosome over-duplication caused by Plk4 overexpression or hydroxyurea treatment. Taken together, our data demonstrate that Cdc6 and Plk4 antagonistically control proper centrosome duplication during the cell cycle. |
format | Online Article Text |
id | pubmed-5414174 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-54141742017-05-17 DNA replication licensing factor Cdc6 and Plk4 kinase antagonistically regulate centrosome duplication via Sas-6 Xu, Xiaowei Huang, Shijiao Zhang, Boyan Huang, Fan Chi, Wangfei Fu, Jingyan Wang, Gang Li, Si Jiang, Qing Zhang, Chuanmao Nat Commun Article Centrosome number is tightly controlled during the cell cycle to ensure proper spindle assembly and cell division. However, the underlying mechanism that controls centrosome number remains largely unclear. We show herein that the DNA replication licensing factor Cdc6 is recruited to the proximal side of the centrioles via cyclin A to negatively regulate centrosome duplication by binding and inhibiting the cartwheel protein Sas-6 from forming a stable complex with another centriole duplication core protein, STIL. We further demonstrate that Cdc6 colocalizes with Plk4 at the centrosome, and interacts with Plk4 during S phase. Plk4 disrupts the interaction between Sas-6 and Cdc6, and suppresses the inhibitory role of Cdc6 on Sas-6 by phosphorylating Cdc6. Overexpressing wild-type Cdc6 or Plk4-unphosphorylatable Cdc6 mutant 2A reduces centrosome over-duplication caused by Plk4 overexpression or hydroxyurea treatment. Taken together, our data demonstrate that Cdc6 and Plk4 antagonistically control proper centrosome duplication during the cell cycle. Nature Publishing Group 2017-04-27 /pmc/articles/PMC5414174/ /pubmed/28447620 http://dx.doi.org/10.1038/ncomms15164 Text en Copyright © 2017, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Xu, Xiaowei Huang, Shijiao Zhang, Boyan Huang, Fan Chi, Wangfei Fu, Jingyan Wang, Gang Li, Si Jiang, Qing Zhang, Chuanmao DNA replication licensing factor Cdc6 and Plk4 kinase antagonistically regulate centrosome duplication via Sas-6 |
title | DNA replication licensing factor Cdc6 and Plk4 kinase antagonistically regulate centrosome duplication via Sas-6 |
title_full | DNA replication licensing factor Cdc6 and Plk4 kinase antagonistically regulate centrosome duplication via Sas-6 |
title_fullStr | DNA replication licensing factor Cdc6 and Plk4 kinase antagonistically regulate centrosome duplication via Sas-6 |
title_full_unstemmed | DNA replication licensing factor Cdc6 and Plk4 kinase antagonistically regulate centrosome duplication via Sas-6 |
title_short | DNA replication licensing factor Cdc6 and Plk4 kinase antagonistically regulate centrosome duplication via Sas-6 |
title_sort | dna replication licensing factor cdc6 and plk4 kinase antagonistically regulate centrosome duplication via sas-6 |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5414174/ https://www.ncbi.nlm.nih.gov/pubmed/28447620 http://dx.doi.org/10.1038/ncomms15164 |
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