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Roles of CDK and DDK in Genome Duplication and Maintenance: Meiotic Singularities
Cells reproduce using two types of divisions: mitosis, which generates two daughter cells each with the same genomic content as the mother cell, and meiosis, which reduces the number of chromosomes of the parent cell by half and gives rise to four gametes. The mechanisms that promote the proper prog...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5368709/ https://www.ncbi.nlm.nih.gov/pubmed/28335524 http://dx.doi.org/10.3390/genes8030105 |
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author | Gómez-Escoda, Blanca Wu, Pei-Yun Jenny |
author_facet | Gómez-Escoda, Blanca Wu, Pei-Yun Jenny |
author_sort | Gómez-Escoda, Blanca |
collection | PubMed |
description | Cells reproduce using two types of divisions: mitosis, which generates two daughter cells each with the same genomic content as the mother cell, and meiosis, which reduces the number of chromosomes of the parent cell by half and gives rise to four gametes. The mechanisms that promote the proper progression of the mitotic and meiotic cycles are highly conserved and controlled. They require the activities of two types of serine-threonine kinases, the cyclin-dependent kinases (CDKs) and the Dbf4-dependent kinase (DDK). CDK and DDK are essential for genome duplication and maintenance in both mitotic and meiotic divisions. In this review, we aim to highlight how these kinases cooperate to orchestrate diverse processes during cellular reproduction, focusing on meiosis-specific adaptions of their regulation and functions in DNA metabolism. |
format | Online Article Text |
id | pubmed-5368709 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-53687092017-04-05 Roles of CDK and DDK in Genome Duplication and Maintenance: Meiotic Singularities Gómez-Escoda, Blanca Wu, Pei-Yun Jenny Genes (Basel) Review Cells reproduce using two types of divisions: mitosis, which generates two daughter cells each with the same genomic content as the mother cell, and meiosis, which reduces the number of chromosomes of the parent cell by half and gives rise to four gametes. The mechanisms that promote the proper progression of the mitotic and meiotic cycles are highly conserved and controlled. They require the activities of two types of serine-threonine kinases, the cyclin-dependent kinases (CDKs) and the Dbf4-dependent kinase (DDK). CDK and DDK are essential for genome duplication and maintenance in both mitotic and meiotic divisions. In this review, we aim to highlight how these kinases cooperate to orchestrate diverse processes during cellular reproduction, focusing on meiosis-specific adaptions of their regulation and functions in DNA metabolism. MDPI 2017-03-20 /pmc/articles/PMC5368709/ /pubmed/28335524 http://dx.doi.org/10.3390/genes8030105 Text en © 2017 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Gómez-Escoda, Blanca Wu, Pei-Yun Jenny Roles of CDK and DDK in Genome Duplication and Maintenance: Meiotic Singularities |
title | Roles of CDK and DDK in Genome Duplication and Maintenance: Meiotic Singularities |
title_full | Roles of CDK and DDK in Genome Duplication and Maintenance: Meiotic Singularities |
title_fullStr | Roles of CDK and DDK in Genome Duplication and Maintenance: Meiotic Singularities |
title_full_unstemmed | Roles of CDK and DDK in Genome Duplication and Maintenance: Meiotic Singularities |
title_short | Roles of CDK and DDK in Genome Duplication and Maintenance: Meiotic Singularities |
title_sort | roles of cdk and ddk in genome duplication and maintenance: meiotic singularities |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5368709/ https://www.ncbi.nlm.nih.gov/pubmed/28335524 http://dx.doi.org/10.3390/genes8030105 |
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