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Dynamic centriolar localization of Polo and Centrobin in early mitosis primes centrosome asymmetry
Centrosomes, the main microtubule organizing centers (MTOCs) of metazoan cells, contain an older “mother” and a younger “daughter” centriole. Stem cells either inherit the mother or daughter-centriole-containing centrosome, providing a possible mechanism for biased delivery of cell fate determinants...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7433902/ https://www.ncbi.nlm.nih.gov/pubmed/32760088 http://dx.doi.org/10.1371/journal.pbio.3000762 |
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author | Gallaud, Emmanuel Ramdas Nair, Anjana Horsley, Nicole Monnard, Arnaud Singh, Priyanka Pham, Tri Thanh Salvador Garcia, David Ferrand, Alexia Cabernard, Clemens |
author_facet | Gallaud, Emmanuel Ramdas Nair, Anjana Horsley, Nicole Monnard, Arnaud Singh, Priyanka Pham, Tri Thanh Salvador Garcia, David Ferrand, Alexia Cabernard, Clemens |
author_sort | Gallaud, Emmanuel |
collection | PubMed |
description | Centrosomes, the main microtubule organizing centers (MTOCs) of metazoan cells, contain an older “mother” and a younger “daughter” centriole. Stem cells either inherit the mother or daughter-centriole-containing centrosome, providing a possible mechanism for biased delivery of cell fate determinants. However, the mechanisms regulating centrosome asymmetry and biased centrosome segregation are unclear. Using 3D-structured illumination microscopy (3D-SIM) and live-cell imaging, we show in fly neural stem cells (neuroblasts) that the mitotic kinase Polo and its centriolar protein substrate Centrobin (Cnb) accumulate on the daughter centriole during mitosis, thereby generating molecularly distinct mother and daughter centrioles before interphase. Cnb’s asymmetric localization, potentially involving a direct relocalization mechanism, is regulated by Polo-mediated phosphorylation, whereas Polo’s daughter centriole enrichment requires both Wdr62 and Cnb. Based on optogenetic protein mislocalization experiments, we propose that the establishment of centriole asymmetry in mitosis primes biased interphase MTOC activity, necessary for correct spindle orientation. |
format | Online Article Text |
id | pubmed-7433902 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-74339022020-08-25 Dynamic centriolar localization of Polo and Centrobin in early mitosis primes centrosome asymmetry Gallaud, Emmanuel Ramdas Nair, Anjana Horsley, Nicole Monnard, Arnaud Singh, Priyanka Pham, Tri Thanh Salvador Garcia, David Ferrand, Alexia Cabernard, Clemens PLoS Biol Research Article Centrosomes, the main microtubule organizing centers (MTOCs) of metazoan cells, contain an older “mother” and a younger “daughter” centriole. Stem cells either inherit the mother or daughter-centriole-containing centrosome, providing a possible mechanism for biased delivery of cell fate determinants. However, the mechanisms regulating centrosome asymmetry and biased centrosome segregation are unclear. Using 3D-structured illumination microscopy (3D-SIM) and live-cell imaging, we show in fly neural stem cells (neuroblasts) that the mitotic kinase Polo and its centriolar protein substrate Centrobin (Cnb) accumulate on the daughter centriole during mitosis, thereby generating molecularly distinct mother and daughter centrioles before interphase. Cnb’s asymmetric localization, potentially involving a direct relocalization mechanism, is regulated by Polo-mediated phosphorylation, whereas Polo’s daughter centriole enrichment requires both Wdr62 and Cnb. Based on optogenetic protein mislocalization experiments, we propose that the establishment of centriole asymmetry in mitosis primes biased interphase MTOC activity, necessary for correct spindle orientation. Public Library of Science 2020-08-06 /pmc/articles/PMC7433902/ /pubmed/32760088 http://dx.doi.org/10.1371/journal.pbio.3000762 Text en © 2020 Gallaud 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 (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Gallaud, Emmanuel Ramdas Nair, Anjana Horsley, Nicole Monnard, Arnaud Singh, Priyanka Pham, Tri Thanh Salvador Garcia, David Ferrand, Alexia Cabernard, Clemens Dynamic centriolar localization of Polo and Centrobin in early mitosis primes centrosome asymmetry |
title | Dynamic centriolar localization of Polo and Centrobin in early mitosis primes centrosome asymmetry |
title_full | Dynamic centriolar localization of Polo and Centrobin in early mitosis primes centrosome asymmetry |
title_fullStr | Dynamic centriolar localization of Polo and Centrobin in early mitosis primes centrosome asymmetry |
title_full_unstemmed | Dynamic centriolar localization of Polo and Centrobin in early mitosis primes centrosome asymmetry |
title_short | Dynamic centriolar localization of Polo and Centrobin in early mitosis primes centrosome asymmetry |
title_sort | dynamic centriolar localization of polo and centrobin in early mitosis primes centrosome asymmetry |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7433902/ https://www.ncbi.nlm.nih.gov/pubmed/32760088 http://dx.doi.org/10.1371/journal.pbio.3000762 |
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