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Meiotic control of the APC/C: similarities & differences from mitosis

The anaphase promoting complex is a highly conserved E3 ligase complex that mediates the destruction of key regulatory proteins during both mitotic and meiotic divisions. In order to maintain ploidy, this destruction must occur after the regulatory proteins have executed their function. Thus, the re...

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Autores principales: Cooper, Katrina F, Strich, Randy
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3162515/
https://www.ncbi.nlm.nih.gov/pubmed/21806783
http://dx.doi.org/10.1186/1747-1028-6-16
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author Cooper, Katrina F
Strich, Randy
author_facet Cooper, Katrina F
Strich, Randy
author_sort Cooper, Katrina F
collection PubMed
description The anaphase promoting complex is a highly conserved E3 ligase complex that mediates the destruction of key regulatory proteins during both mitotic and meiotic divisions. In order to maintain ploidy, this destruction must occur after the regulatory proteins have executed their function. Thus, the regulation of APC/C activity itself is critical for maintaining ploidy during all types of cell divisions. During mitotic cell division, two conserved activator proteins called Cdc20 and Cdh1 are required for both APC/C activation and substrate selection. However, significantly less is known about how these proteins regulate APC/C activity during the specialized meiotic nuclear divisions. In addition, both budding yeast and flies utilize a third meiosis-specific activator. In Saccharomyces cerevisiae, this meiosis-specific activator is called Ama1. This review summarizes our knowledge of how Cdc20 and Ama1 coordinate APC/C activity to regulate the meiotic nuclear divisions in yeast.
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spelling pubmed-31625152011-08-27 Meiotic control of the APC/C: similarities & differences from mitosis Cooper, Katrina F Strich, Randy Cell Div Review The anaphase promoting complex is a highly conserved E3 ligase complex that mediates the destruction of key regulatory proteins during both mitotic and meiotic divisions. In order to maintain ploidy, this destruction must occur after the regulatory proteins have executed their function. Thus, the regulation of APC/C activity itself is critical for maintaining ploidy during all types of cell divisions. During mitotic cell division, two conserved activator proteins called Cdc20 and Cdh1 are required for both APC/C activation and substrate selection. However, significantly less is known about how these proteins regulate APC/C activity during the specialized meiotic nuclear divisions. In addition, both budding yeast and flies utilize a third meiosis-specific activator. In Saccharomyces cerevisiae, this meiosis-specific activator is called Ama1. This review summarizes our knowledge of how Cdc20 and Ama1 coordinate APC/C activity to regulate the meiotic nuclear divisions in yeast. BioMed Central 2011-08-01 /pmc/articles/PMC3162515/ /pubmed/21806783 http://dx.doi.org/10.1186/1747-1028-6-16 Text en Copyright ©2011 Cooper and Strich; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review
Cooper, Katrina F
Strich, Randy
Meiotic control of the APC/C: similarities & differences from mitosis
title Meiotic control of the APC/C: similarities & differences from mitosis
title_full Meiotic control of the APC/C: similarities & differences from mitosis
title_fullStr Meiotic control of the APC/C: similarities & differences from mitosis
title_full_unstemmed Meiotic control of the APC/C: similarities & differences from mitosis
title_short Meiotic control of the APC/C: similarities & differences from mitosis
title_sort meiotic control of the apc/c: similarities & differences from mitosis
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3162515/
https://www.ncbi.nlm.nih.gov/pubmed/21806783
http://dx.doi.org/10.1186/1747-1028-6-16
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