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Recruitment of Polo Kinase to the Spindle Midzone during Cytokinesis Requires the Feo/Klp3A Complex
BACKGROUND: Polo-like kinases control multiple events during cell division, including mitotic entry, centrosome organization, spindle formation, chromosome segregation and cytokinesis. Their roles during cytokinesis, however, are not well understood because the requirement of these kinases during ea...
Autores principales: | , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Public Library of Science
2007
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1894651/ https://www.ncbi.nlm.nih.gov/pubmed/17593971 http://dx.doi.org/10.1371/journal.pone.0000572 |
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author | D'Avino, Pier Paolo Archambault, Vincent Przewloka, Marcin R. Zhang, Wei Lilley, Kathryn S. Laue, Ernest Glover, David M. |
author_facet | D'Avino, Pier Paolo Archambault, Vincent Przewloka, Marcin R. Zhang, Wei Lilley, Kathryn S. Laue, Ernest Glover, David M. |
author_sort | D'Avino, Pier Paolo |
collection | PubMed |
description | BACKGROUND: Polo-like kinases control multiple events during cell division, including mitotic entry, centrosome organization, spindle formation, chromosome segregation and cytokinesis. Their roles during cytokinesis, however, are not well understood because the requirement of these kinases during early stages of mitosis complicates the study of their functions after anaphase onset. METHODOLOGY/PRINCIPAL FINDINGS: We used time-lapse microscopy to analyze the dynamics of Polo::GFP in Drosophila tissue culture cells during mitosis. After anaphase onset, Polo::GFP concentrated at the spindle midzone, but also diffused along the entire length of the central spindle. Using RNA interference we demonstrate that the microtubule-associated proteins Feo and Klp3A are required for Polo recruitment to the spindle midzone, but not the kinesin Pavarotti as previously thought. Moreover, we show that Feo and Klp3A form a complex and that Polo co-localizes with both proteins during cytokinesis. CONCLUSION/SIGNIFICANCE: Our results reveal that the Feo/Klp3A complex is necessary for Polo recruitment to the spindle midzone. A similar finding has also been recently reported in mammalian cells [1], suggesting that this basic mechanism has been conserved during evolution, albeit with some differences. Finally, since cleavage furrow formation and ingression are unaffected following feo RNAi, our data imply that Polo recruitment to the central spindle is not required for furrowing, but some other aspect of cytokinesis. |
format | Text |
id | pubmed-1894651 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2007 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-18946512007-06-27 Recruitment of Polo Kinase to the Spindle Midzone during Cytokinesis Requires the Feo/Klp3A Complex D'Avino, Pier Paolo Archambault, Vincent Przewloka, Marcin R. Zhang, Wei Lilley, Kathryn S. Laue, Ernest Glover, David M. PLoS One Research Article BACKGROUND: Polo-like kinases control multiple events during cell division, including mitotic entry, centrosome organization, spindle formation, chromosome segregation and cytokinesis. Their roles during cytokinesis, however, are not well understood because the requirement of these kinases during early stages of mitosis complicates the study of their functions after anaphase onset. METHODOLOGY/PRINCIPAL FINDINGS: We used time-lapse microscopy to analyze the dynamics of Polo::GFP in Drosophila tissue culture cells during mitosis. After anaphase onset, Polo::GFP concentrated at the spindle midzone, but also diffused along the entire length of the central spindle. Using RNA interference we demonstrate that the microtubule-associated proteins Feo and Klp3A are required for Polo recruitment to the spindle midzone, but not the kinesin Pavarotti as previously thought. Moreover, we show that Feo and Klp3A form a complex and that Polo co-localizes with both proteins during cytokinesis. CONCLUSION/SIGNIFICANCE: Our results reveal that the Feo/Klp3A complex is necessary for Polo recruitment to the spindle midzone. A similar finding has also been recently reported in mammalian cells [1], suggesting that this basic mechanism has been conserved during evolution, albeit with some differences. Finally, since cleavage furrow formation and ingression are unaffected following feo RNAi, our data imply that Polo recruitment to the central spindle is not required for furrowing, but some other aspect of cytokinesis. Public Library of Science 2007-06-27 /pmc/articles/PMC1894651/ /pubmed/17593971 http://dx.doi.org/10.1371/journal.pone.0000572 Text en D'Avino et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article D'Avino, Pier Paolo Archambault, Vincent Przewloka, Marcin R. Zhang, Wei Lilley, Kathryn S. Laue, Ernest Glover, David M. Recruitment of Polo Kinase to the Spindle Midzone during Cytokinesis Requires the Feo/Klp3A Complex |
title | Recruitment of Polo Kinase to the Spindle Midzone during Cytokinesis Requires the Feo/Klp3A Complex |
title_full | Recruitment of Polo Kinase to the Spindle Midzone during Cytokinesis Requires the Feo/Klp3A Complex |
title_fullStr | Recruitment of Polo Kinase to the Spindle Midzone during Cytokinesis Requires the Feo/Klp3A Complex |
title_full_unstemmed | Recruitment of Polo Kinase to the Spindle Midzone during Cytokinesis Requires the Feo/Klp3A Complex |
title_short | Recruitment of Polo Kinase to the Spindle Midzone during Cytokinesis Requires the Feo/Klp3A Complex |
title_sort | recruitment of polo kinase to the spindle midzone during cytokinesis requires the feo/klp3a complex |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1894651/ https://www.ncbi.nlm.nih.gov/pubmed/17593971 http://dx.doi.org/10.1371/journal.pone.0000572 |
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