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Regulation of branched versus linear Arp2/3‐generated actin filaments
Activation of the Arp2/3 complex by VCA‐motif‐bearing actin nucleation‐promoting factors results in the formation of “daughter” actin filaments branching off the sides of pre‐existing “mother” filaments. Alternatively, when stimulated by SPIN90, Arp2/3 directly nucleates “linear” actin filaments. Un...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10152144/ https://www.ncbi.nlm.nih.gov/pubmed/36939020 http://dx.doi.org/10.15252/embj.2022113008 |
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author | Cao, Luyan Ghasemi, Foad Way, Michael Jégou, Antoine Romet‐Lemonne, Guillaume |
author_facet | Cao, Luyan Ghasemi, Foad Way, Michael Jégou, Antoine Romet‐Lemonne, Guillaume |
author_sort | Cao, Luyan |
collection | PubMed |
description | Activation of the Arp2/3 complex by VCA‐motif‐bearing actin nucleation‐promoting factors results in the formation of “daughter” actin filaments branching off the sides of pre‐existing “mother” filaments. Alternatively, when stimulated by SPIN90, Arp2/3 directly nucleates “linear” actin filaments. Uncovering the similarities and differences between these two mechanisms is fundamental to understanding how actin cytoskeleton dynamics are regulated. Here, analysis of individual filaments reveals that, unexpectedly, the VCA motifs of WASP, N‐WASP, and WASH destabilize existing branches, as well as SPIN90‐Arp2/3 at linear filament ends. Furthermore, branch stabilizer cortactin and destabilizer GMF each have a similar impact on SPIN90‐activated Arp2/3. However, unlike branch junctions, SPIN90‐Arp2/3 at the ends of linear filaments is not destabilized by piconewton forces and does not become less stable with time. It thus appears that linear and branched Arp2/3‐generated filaments respond similarly to the regulatory proteins we have tested, albeit with some differences, but significantly differ in their responses to aging and mechanical stress. These kinetic differences likely reflect the small conformational differences recently reported between Arp2/3 in branch junctions and linear filaments and suggest that their turnover in cells may be differently regulated. |
format | Online Article Text |
id | pubmed-10152144 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-101521442023-05-03 Regulation of branched versus linear Arp2/3‐generated actin filaments Cao, Luyan Ghasemi, Foad Way, Michael Jégou, Antoine Romet‐Lemonne, Guillaume EMBO J Articles Activation of the Arp2/3 complex by VCA‐motif‐bearing actin nucleation‐promoting factors results in the formation of “daughter” actin filaments branching off the sides of pre‐existing “mother” filaments. Alternatively, when stimulated by SPIN90, Arp2/3 directly nucleates “linear” actin filaments. Uncovering the similarities and differences between these two mechanisms is fundamental to understanding how actin cytoskeleton dynamics are regulated. Here, analysis of individual filaments reveals that, unexpectedly, the VCA motifs of WASP, N‐WASP, and WASH destabilize existing branches, as well as SPIN90‐Arp2/3 at linear filament ends. Furthermore, branch stabilizer cortactin and destabilizer GMF each have a similar impact on SPIN90‐activated Arp2/3. However, unlike branch junctions, SPIN90‐Arp2/3 at the ends of linear filaments is not destabilized by piconewton forces and does not become less stable with time. It thus appears that linear and branched Arp2/3‐generated filaments respond similarly to the regulatory proteins we have tested, albeit with some differences, but significantly differ in their responses to aging and mechanical stress. These kinetic differences likely reflect the small conformational differences recently reported between Arp2/3 in branch junctions and linear filaments and suggest that their turnover in cells may be differently regulated. John Wiley and Sons Inc. 2023-03-20 /pmc/articles/PMC10152144/ /pubmed/36939020 http://dx.doi.org/10.15252/embj.2022113008 Text en © 2023 The Authors. Published under the terms of the CC BY 4.0 license https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Articles Cao, Luyan Ghasemi, Foad Way, Michael Jégou, Antoine Romet‐Lemonne, Guillaume Regulation of branched versus linear Arp2/3‐generated actin filaments |
title | Regulation of branched versus linear Arp2/3‐generated actin filaments |
title_full | Regulation of branched versus linear Arp2/3‐generated actin filaments |
title_fullStr | Regulation of branched versus linear Arp2/3‐generated actin filaments |
title_full_unstemmed | Regulation of branched versus linear Arp2/3‐generated actin filaments |
title_short | Regulation of branched versus linear Arp2/3‐generated actin filaments |
title_sort | regulation of branched versus linear arp2/3‐generated actin filaments |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10152144/ https://www.ncbi.nlm.nih.gov/pubmed/36939020 http://dx.doi.org/10.15252/embj.2022113008 |
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