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Par complex cluster formation mediated by phase separation
The evolutionarily conserved Par3/Par6/aPKC complex regulates the polarity establishment of diverse cell types and distinct polarity-driven functions. However, how the Par complex is concentrated beneath the membrane to initiate cell polarization remains unclear. Here we show that the Par complex ex...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7211019/ https://www.ncbi.nlm.nih.gov/pubmed/32385244 http://dx.doi.org/10.1038/s41467-020-16135-6 |
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author | Liu, Ziheng Yang, Ying Gu, Aihong Xu, Jiawen Mao, Ying Lu, Haojie Hu, Weiguo Lei, Qun-Ying Li, Zhouhua Zhang, Mingjie Cai, Yu Wen, Wenyu |
author_facet | Liu, Ziheng Yang, Ying Gu, Aihong Xu, Jiawen Mao, Ying Lu, Haojie Hu, Weiguo Lei, Qun-Ying Li, Zhouhua Zhang, Mingjie Cai, Yu Wen, Wenyu |
author_sort | Liu, Ziheng |
collection | PubMed |
description | The evolutionarily conserved Par3/Par6/aPKC complex regulates the polarity establishment of diverse cell types and distinct polarity-driven functions. However, how the Par complex is concentrated beneath the membrane to initiate cell polarization remains unclear. Here we show that the Par complex exhibits cell cycle-dependent condensation in Drosophila neuroblasts, driven by liquid–liquid phase separation. The open conformation of Par3 undergoes autonomous phase separation likely due to its NTD-mediated oligomerization. Par6, via C-terminal tail binding to Par3 PDZ3, can be enriched to Par3 condensates and in return dramatically promote Par3 phase separation. aPKC can also be concentrated to the Par3N/Par6 condensates as a client. Interestingly, activated aPKC can disperse the Par3/Par6 condensates via phosphorylation of Par3. Perturbations of Par3/Par6 phase separation impair the establishment of apical–basal polarity during neuroblast asymmetric divisions and lead to defective lineage development. We propose that phase separation may be a common mechanism for localized cortical condensation of cell polarity complexes. |
format | Online Article Text |
id | pubmed-7211019 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-72110192020-05-13 Par complex cluster formation mediated by phase separation Liu, Ziheng Yang, Ying Gu, Aihong Xu, Jiawen Mao, Ying Lu, Haojie Hu, Weiguo Lei, Qun-Ying Li, Zhouhua Zhang, Mingjie Cai, Yu Wen, Wenyu Nat Commun Article The evolutionarily conserved Par3/Par6/aPKC complex regulates the polarity establishment of diverse cell types and distinct polarity-driven functions. However, how the Par complex is concentrated beneath the membrane to initiate cell polarization remains unclear. Here we show that the Par complex exhibits cell cycle-dependent condensation in Drosophila neuroblasts, driven by liquid–liquid phase separation. The open conformation of Par3 undergoes autonomous phase separation likely due to its NTD-mediated oligomerization. Par6, via C-terminal tail binding to Par3 PDZ3, can be enriched to Par3 condensates and in return dramatically promote Par3 phase separation. aPKC can also be concentrated to the Par3N/Par6 condensates as a client. Interestingly, activated aPKC can disperse the Par3/Par6 condensates via phosphorylation of Par3. Perturbations of Par3/Par6 phase separation impair the establishment of apical–basal polarity during neuroblast asymmetric divisions and lead to defective lineage development. We propose that phase separation may be a common mechanism for localized cortical condensation of cell polarity complexes. Nature Publishing Group UK 2020-05-08 /pmc/articles/PMC7211019/ /pubmed/32385244 http://dx.doi.org/10.1038/s41467-020-16135-6 Text en © The Author(s) 2020 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/. |
spellingShingle | Article Liu, Ziheng Yang, Ying Gu, Aihong Xu, Jiawen Mao, Ying Lu, Haojie Hu, Weiguo Lei, Qun-Ying Li, Zhouhua Zhang, Mingjie Cai, Yu Wen, Wenyu Par complex cluster formation mediated by phase separation |
title | Par complex cluster formation mediated by phase separation |
title_full | Par complex cluster formation mediated by phase separation |
title_fullStr | Par complex cluster formation mediated by phase separation |
title_full_unstemmed | Par complex cluster formation mediated by phase separation |
title_short | Par complex cluster formation mediated by phase separation |
title_sort | par complex cluster formation mediated by phase separation |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7211019/ https://www.ncbi.nlm.nih.gov/pubmed/32385244 http://dx.doi.org/10.1038/s41467-020-16135-6 |
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