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Motor axon navigation relies on Fidgetin-like 1–driven microtubule plus end dynamics
During neural circuit assembly, extrinsic signals are integrated into changes in growth cone (GC) cytoskeleton underlying axon guidance decisions. Microtubules (MTs) were shown to play an instructive role in GC steering. However, the numerous actors required for MT remodeling during axon navigation...
Autores principales: | , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Rockefeller University Press
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5940295/ https://www.ncbi.nlm.nih.gov/pubmed/29535193 http://dx.doi.org/10.1083/jcb.201604108 |
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author | Fassier, Coralie Fréal, Amélie Gasmi, Laïla Delphin, Christian Ten Martin, Daniel De Gois, Stéphanie Tambalo, Monica Bosc, Christophe Mailly, Philippe Revenu, Céline Peris, Leticia Bolte, Susanne Schneider-Maunoury, Sylvie Houart, Corinne Nothias, Fatiha Larcher, Jean-Christophe Andrieux, Annie Hazan, Jamilé |
author_facet | Fassier, Coralie Fréal, Amélie Gasmi, Laïla Delphin, Christian Ten Martin, Daniel De Gois, Stéphanie Tambalo, Monica Bosc, Christophe Mailly, Philippe Revenu, Céline Peris, Leticia Bolte, Susanne Schneider-Maunoury, Sylvie Houart, Corinne Nothias, Fatiha Larcher, Jean-Christophe Andrieux, Annie Hazan, Jamilé |
author_sort | Fassier, Coralie |
collection | PubMed |
description | During neural circuit assembly, extrinsic signals are integrated into changes in growth cone (GC) cytoskeleton underlying axon guidance decisions. Microtubules (MTs) were shown to play an instructive role in GC steering. However, the numerous actors required for MT remodeling during axon navigation and their precise mode of action are far from being deciphered. Using loss- and gain-of-function analyses during zebrafish development, we identify in this study the meiotic clade adenosine triphosphatase Fidgetin-like 1 (Fignl1) as a key GC-enriched MT-interacting protein in motor circuit wiring and larval locomotion. We show that Fignl1 controls GC morphology and behavior at intermediate targets by regulating MT plus end dynamics and growth directionality. We further reveal that alternative translation of Fignl1 transcript is a sophisticated mechanism modulating MT dynamics: a full-length isoform regulates MT plus end–tracking protein binding at plus ends, whereas shorter isoforms promote their depolymerization beneath the cell cortex. Our study thus pinpoints Fignl1 as a multifaceted key player in MT remodeling underlying motor circuit connectivity. |
format | Online Article Text |
id | pubmed-5940295 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-59402952018-11-07 Motor axon navigation relies on Fidgetin-like 1–driven microtubule plus end dynamics Fassier, Coralie Fréal, Amélie Gasmi, Laïla Delphin, Christian Ten Martin, Daniel De Gois, Stéphanie Tambalo, Monica Bosc, Christophe Mailly, Philippe Revenu, Céline Peris, Leticia Bolte, Susanne Schneider-Maunoury, Sylvie Houart, Corinne Nothias, Fatiha Larcher, Jean-Christophe Andrieux, Annie Hazan, Jamilé J Cell Biol Research Articles During neural circuit assembly, extrinsic signals are integrated into changes in growth cone (GC) cytoskeleton underlying axon guidance decisions. Microtubules (MTs) were shown to play an instructive role in GC steering. However, the numerous actors required for MT remodeling during axon navigation and their precise mode of action are far from being deciphered. Using loss- and gain-of-function analyses during zebrafish development, we identify in this study the meiotic clade adenosine triphosphatase Fidgetin-like 1 (Fignl1) as a key GC-enriched MT-interacting protein in motor circuit wiring and larval locomotion. We show that Fignl1 controls GC morphology and behavior at intermediate targets by regulating MT plus end dynamics and growth directionality. We further reveal that alternative translation of Fignl1 transcript is a sophisticated mechanism modulating MT dynamics: a full-length isoform regulates MT plus end–tracking protein binding at plus ends, whereas shorter isoforms promote their depolymerization beneath the cell cortex. Our study thus pinpoints Fignl1 as a multifaceted key player in MT remodeling underlying motor circuit connectivity. Rockefeller University Press 2018-05-07 /pmc/articles/PMC5940295/ /pubmed/29535193 http://dx.doi.org/10.1083/jcb.201604108 Text en © 2018 Fassier et al. http://www.rupress.org/terms/https://creativecommons.org/licenses/by-nc-sa/4.0/This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms/). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 International license, as described at https://creativecommons.org/licenses/by-nc-sa/4.0/). |
spellingShingle | Research Articles Fassier, Coralie Fréal, Amélie Gasmi, Laïla Delphin, Christian Ten Martin, Daniel De Gois, Stéphanie Tambalo, Monica Bosc, Christophe Mailly, Philippe Revenu, Céline Peris, Leticia Bolte, Susanne Schneider-Maunoury, Sylvie Houart, Corinne Nothias, Fatiha Larcher, Jean-Christophe Andrieux, Annie Hazan, Jamilé Motor axon navigation relies on Fidgetin-like 1–driven microtubule plus end dynamics |
title | Motor axon navigation relies on Fidgetin-like 1–driven microtubule plus end dynamics |
title_full | Motor axon navigation relies on Fidgetin-like 1–driven microtubule plus end dynamics |
title_fullStr | Motor axon navigation relies on Fidgetin-like 1–driven microtubule plus end dynamics |
title_full_unstemmed | Motor axon navigation relies on Fidgetin-like 1–driven microtubule plus end dynamics |
title_short | Motor axon navigation relies on Fidgetin-like 1–driven microtubule plus end dynamics |
title_sort | motor axon navigation relies on fidgetin-like 1–driven microtubule plus end dynamics |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5940295/ https://www.ncbi.nlm.nih.gov/pubmed/29535193 http://dx.doi.org/10.1083/jcb.201604108 |
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