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Making the Auroras glow: regulation of Aurora A and B kinase function by interacting proteins
The conserved Aurora family of protein kinases have emerged as crucial regulators of mitosis and cytokinesis. Despite their high degree of homology, Aurora A and B have very distinctive localisations and functions: Aurora A associates with the spindle poles to regulate entry into mitosis, centrosome...
Autores principales: | , , |
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Formato: | Texto |
Lenguaje: | English |
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Elsevier
2009
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2806521/ https://www.ncbi.nlm.nih.gov/pubmed/19836940 http://dx.doi.org/10.1016/j.ceb.2009.09.008 |
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author | Carmena, Mar Ruchaud, Sandrine Earnshaw, William C |
author_facet | Carmena, Mar Ruchaud, Sandrine Earnshaw, William C |
author_sort | Carmena, Mar |
collection | PubMed |
description | The conserved Aurora family of protein kinases have emerged as crucial regulators of mitosis and cytokinesis. Despite their high degree of homology, Aurora A and B have very distinctive localisations and functions: Aurora A associates with the spindle poles to regulate entry into mitosis, centrosome maturation and spindle assembly; Aurora B is a member of the Chromosomal Passenger Complex (CPC) that transfers from the inner centromere in early mitosis to the spindle midzone, equatorial cortex and midbody in late mitosis and cytokinesis. Aurora B functions include regulation of chromosome–microtubule interactions, cohesion, spindle stability and cytokinesis. This review will focus on how interacting proteins make this functional diversity possible by targeting the kinases to different subcellular locations and regulating their activity. |
format | Text |
id | pubmed-2806521 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-28065212010-01-28 Making the Auroras glow: regulation of Aurora A and B kinase function by interacting proteins Carmena, Mar Ruchaud, Sandrine Earnshaw, William C Curr Opin Cell Biol Article The conserved Aurora family of protein kinases have emerged as crucial regulators of mitosis and cytokinesis. Despite their high degree of homology, Aurora A and B have very distinctive localisations and functions: Aurora A associates with the spindle poles to regulate entry into mitosis, centrosome maturation and spindle assembly; Aurora B is a member of the Chromosomal Passenger Complex (CPC) that transfers from the inner centromere in early mitosis to the spindle midzone, equatorial cortex and midbody in late mitosis and cytokinesis. Aurora B functions include regulation of chromosome–microtubule interactions, cohesion, spindle stability and cytokinesis. This review will focus on how interacting proteins make this functional diversity possible by targeting the kinases to different subcellular locations and regulating their activity. Elsevier 2009-12 /pmc/articles/PMC2806521/ /pubmed/19836940 http://dx.doi.org/10.1016/j.ceb.2009.09.008 Text en © 2009 Elsevier Ltd. https://creativecommons.org/licenses/by/3.0/ Open Access under CC BY 3.0 (https://creativecommons.org/licenses/by/3.0/) license |
spellingShingle | Article Carmena, Mar Ruchaud, Sandrine Earnshaw, William C Making the Auroras glow: regulation of Aurora A and B kinase function by interacting proteins |
title | Making the Auroras glow: regulation of Aurora A and B kinase function by interacting proteins |
title_full | Making the Auroras glow: regulation of Aurora A and B kinase function by interacting proteins |
title_fullStr | Making the Auroras glow: regulation of Aurora A and B kinase function by interacting proteins |
title_full_unstemmed | Making the Auroras glow: regulation of Aurora A and B kinase function by interacting proteins |
title_short | Making the Auroras glow: regulation of Aurora A and B kinase function by interacting proteins |
title_sort | making the auroras glow: regulation of aurora a and b kinase function by interacting proteins |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2806521/ https://www.ncbi.nlm.nih.gov/pubmed/19836940 http://dx.doi.org/10.1016/j.ceb.2009.09.008 |
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