Cargando…
Spatiotemporal expression of regulatory kinases directs the transition from mitosis to cellular morphogenesis in Drosophila
Embryogenesis depends on a tightly regulated balance between mitosis, differentiation, and morphogenesis. Understanding how the embryo uses a relatively small number of proteins to transition between growth and morphogenesis is a central question of developmental biology, but the mechanisms controll...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8828718/ https://www.ncbi.nlm.nih.gov/pubmed/35140224 http://dx.doi.org/10.1038/s41467-022-28322-8 |
_version_ | 1784647903408553984 |
---|---|
author | Yang, Shuo McAdow, Jennifer Du, Yingqiu Trigg, Jennifer Taghert, Paul H. Johnson, Aaron N. |
author_facet | Yang, Shuo McAdow, Jennifer Du, Yingqiu Trigg, Jennifer Taghert, Paul H. Johnson, Aaron N. |
author_sort | Yang, Shuo |
collection | PubMed |
description | Embryogenesis depends on a tightly regulated balance between mitosis, differentiation, and morphogenesis. Understanding how the embryo uses a relatively small number of proteins to transition between growth and morphogenesis is a central question of developmental biology, but the mechanisms controlling mitosis and differentiation are considered to be fundamentally distinct. Here we show the mitotic kinase Polo, which regulates all steps of mitosis in Drosophila, also directs cellular morphogenesis after cell cycle exit. In mitotic cells, the Aurora kinases activate Polo to control a cytoskeletal regulatory module that directs cytokinesis. We show that in the post-mitotic mesoderm, the control of Polo activity transitions from the Aurora kinases to the uncharacterized kinase Back Seat Driver (Bsd), where Bsd and Polo cooperate to regulate muscle morphogenesis. Polo and its effectors therefore direct mitosis and cellular morphogenesis, but the transition from growth to morphogenesis is determined by the spatiotemporal expression of upstream activating kinases. |
format | Online Article Text |
id | pubmed-8828718 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-88287182022-03-04 Spatiotemporal expression of regulatory kinases directs the transition from mitosis to cellular morphogenesis in Drosophila Yang, Shuo McAdow, Jennifer Du, Yingqiu Trigg, Jennifer Taghert, Paul H. Johnson, Aaron N. Nat Commun Article Embryogenesis depends on a tightly regulated balance between mitosis, differentiation, and morphogenesis. Understanding how the embryo uses a relatively small number of proteins to transition between growth and morphogenesis is a central question of developmental biology, but the mechanisms controlling mitosis and differentiation are considered to be fundamentally distinct. Here we show the mitotic kinase Polo, which regulates all steps of mitosis in Drosophila, also directs cellular morphogenesis after cell cycle exit. In mitotic cells, the Aurora kinases activate Polo to control a cytoskeletal regulatory module that directs cytokinesis. We show that in the post-mitotic mesoderm, the control of Polo activity transitions from the Aurora kinases to the uncharacterized kinase Back Seat Driver (Bsd), where Bsd and Polo cooperate to regulate muscle morphogenesis. Polo and its effectors therefore direct mitosis and cellular morphogenesis, but the transition from growth to morphogenesis is determined by the spatiotemporal expression of upstream activating kinases. Nature Publishing Group UK 2022-02-09 /pmc/articles/PMC8828718/ /pubmed/35140224 http://dx.doi.org/10.1038/s41467-022-28322-8 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Yang, Shuo McAdow, Jennifer Du, Yingqiu Trigg, Jennifer Taghert, Paul H. Johnson, Aaron N. Spatiotemporal expression of regulatory kinases directs the transition from mitosis to cellular morphogenesis in Drosophila |
title | Spatiotemporal expression of regulatory kinases directs the transition from mitosis to cellular morphogenesis in Drosophila |
title_full | Spatiotemporal expression of regulatory kinases directs the transition from mitosis to cellular morphogenesis in Drosophila |
title_fullStr | Spatiotemporal expression of regulatory kinases directs the transition from mitosis to cellular morphogenesis in Drosophila |
title_full_unstemmed | Spatiotemporal expression of regulatory kinases directs the transition from mitosis to cellular morphogenesis in Drosophila |
title_short | Spatiotemporal expression of regulatory kinases directs the transition from mitosis to cellular morphogenesis in Drosophila |
title_sort | spatiotemporal expression of regulatory kinases directs the transition from mitosis to cellular morphogenesis in drosophila |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8828718/ https://www.ncbi.nlm.nih.gov/pubmed/35140224 http://dx.doi.org/10.1038/s41467-022-28322-8 |
work_keys_str_mv | AT yangshuo spatiotemporalexpressionofregulatorykinasesdirectsthetransitionfrommitosistocellularmorphogenesisindrosophila AT mcadowjennifer spatiotemporalexpressionofregulatorykinasesdirectsthetransitionfrommitosistocellularmorphogenesisindrosophila AT duyingqiu spatiotemporalexpressionofregulatorykinasesdirectsthetransitionfrommitosistocellularmorphogenesisindrosophila AT triggjennifer spatiotemporalexpressionofregulatorykinasesdirectsthetransitionfrommitosistocellularmorphogenesisindrosophila AT taghertpaulh spatiotemporalexpressionofregulatorykinasesdirectsthetransitionfrommitosistocellularmorphogenesisindrosophila AT johnsonaaronn spatiotemporalexpressionofregulatorykinasesdirectsthetransitionfrommitosistocellularmorphogenesisindrosophila |