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Cross-linker design determines microtubule network organization by opposing motors
During cell division, cross-linking motors determine the architecture of the spindle, a dynamic microtubule network that segregates the chromosomes in eukaryotes. It is unclear how motors with opposite directionality coordinate to drive both contractile and extensile behaviors in the spindle. Partic...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
National Academy of Sciences
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9388136/ https://www.ncbi.nlm.nih.gov/pubmed/35960844 http://dx.doi.org/10.1073/pnas.2206398119 |
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author | Henkin, Gil Chew, Wei-Xiang Nédélec, François Surrey, Thomas |
author_facet | Henkin, Gil Chew, Wei-Xiang Nédélec, François Surrey, Thomas |
author_sort | Henkin, Gil |
collection | PubMed |
description | During cell division, cross-linking motors determine the architecture of the spindle, a dynamic microtubule network that segregates the chromosomes in eukaryotes. It is unclear how motors with opposite directionality coordinate to drive both contractile and extensile behaviors in the spindle. Particularly, the impact of different cross-linker designs on network self-organization is not understood, limiting our understanding of self-organizing structures in cells but also our ability to engineer new active materials. Here, we use experiment and theory to examine active microtubule networks driven by mixtures of motors with opposite directionality and different cross-linker design. We find that although the kinesin-14 HSET causes network contraction when dominant, it can also assist the opposing kinesin-5 KIF11 to generate extensile networks. This bifunctionality results from HSET’s asymmetric design, distinct from symmetric KIF11. These findings expand the set of rules underlying patterning of active microtubule assemblies and allow a better understanding of motor cooperation in the spindle. |
format | Online Article Text |
id | pubmed-9388136 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | National Academy of Sciences |
record_format | MEDLINE/PubMed |
spelling | pubmed-93881362022-08-19 Cross-linker design determines microtubule network organization by opposing motors Henkin, Gil Chew, Wei-Xiang Nédélec, François Surrey, Thomas Proc Natl Acad Sci U S A Biological Sciences During cell division, cross-linking motors determine the architecture of the spindle, a dynamic microtubule network that segregates the chromosomes in eukaryotes. It is unclear how motors with opposite directionality coordinate to drive both contractile and extensile behaviors in the spindle. Particularly, the impact of different cross-linker designs on network self-organization is not understood, limiting our understanding of self-organizing structures in cells but also our ability to engineer new active materials. Here, we use experiment and theory to examine active microtubule networks driven by mixtures of motors with opposite directionality and different cross-linker design. We find that although the kinesin-14 HSET causes network contraction when dominant, it can also assist the opposing kinesin-5 KIF11 to generate extensile networks. This bifunctionality results from HSET’s asymmetric design, distinct from symmetric KIF11. These findings expand the set of rules underlying patterning of active microtubule assemblies and allow a better understanding of motor cooperation in the spindle. National Academy of Sciences 2022-08-12 2022-08-16 /pmc/articles/PMC9388136/ /pubmed/35960844 http://dx.doi.org/10.1073/pnas.2206398119 Text en Copyright © 2022 the Author(s). Published by PNAS. https://creativecommons.org/licenses/by/4.0/This open access article is distributed under Creative Commons Attribution License 4.0 (CC BY) (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Biological Sciences Henkin, Gil Chew, Wei-Xiang Nédélec, François Surrey, Thomas Cross-linker design determines microtubule network organization by opposing motors |
title | Cross-linker design determines microtubule network organization by opposing motors |
title_full | Cross-linker design determines microtubule network organization by opposing motors |
title_fullStr | Cross-linker design determines microtubule network organization by opposing motors |
title_full_unstemmed | Cross-linker design determines microtubule network organization by opposing motors |
title_short | Cross-linker design determines microtubule network organization by opposing motors |
title_sort | cross-linker design determines microtubule network organization by opposing motors |
topic | Biological Sciences |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9388136/ https://www.ncbi.nlm.nih.gov/pubmed/35960844 http://dx.doi.org/10.1073/pnas.2206398119 |
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