Cargando…
Vertebrate Fidgetin Restrains Axonal Growth by Severing Labile Domains of Microtubules
Individual microtubules (MTs) in the axon consist of a stable domain that is highly acetylated and a labile domain that is not. Traditional MT-severing proteins preferentially cut the MT in the stable domain. In Drosophila, fidgetin behaves in this fashion, with targeted knockdown resulting in neuro...
Autores principales: | , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2015
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4837332/ https://www.ncbi.nlm.nih.gov/pubmed/26344772 http://dx.doi.org/10.1016/j.celrep.2015.08.017 |
_version_ | 1782427837007921152 |
---|---|
author | Leo, Lanfranco Yu, Wenqian D’Rozario, Mitchell Waddell, Edward A. Marenda, Daniel R. Baird, Michelle A. Davidson, Michael W. Zhou, Bin Wu, Bingro Baker, Lisa Sharp, David J. Baas, Peter W. |
author_facet | Leo, Lanfranco Yu, Wenqian D’Rozario, Mitchell Waddell, Edward A. Marenda, Daniel R. Baird, Michelle A. Davidson, Michael W. Zhou, Bin Wu, Bingro Baker, Lisa Sharp, David J. Baas, Peter W. |
author_sort | Leo, Lanfranco |
collection | PubMed |
description | Individual microtubules (MTs) in the axon consist of a stable domain that is highly acetylated and a labile domain that is not. Traditional MT-severing proteins preferentially cut the MT in the stable domain. In Drosophila, fidgetin behaves in this fashion, with targeted knockdown resulting in neurons with a higher fraction of acetylated (stable) MT mass in their axons. Conversely, in a fidgetin knockout mouse, the fraction of MT mass that is acetylated is lower than in the control animal. When fidgetin is depleted from cultured rodent neurons, there is a 62% increase in axonal MT mass, all of which is labile. Concomitantly, there are more minor processes and a longer axon. Together with experimental data showing that vertebrate fidgetin targets unacetylated tubulin, these results indicate that vertebrate fidgetin (unlike its fly ortholog) regulates neuronal development by tamping back the expansion of the labile domains of MTs. |
format | Online Article Text |
id | pubmed-4837332 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
record_format | MEDLINE/PubMed |
spelling | pubmed-48373322016-04-20 Vertebrate Fidgetin Restrains Axonal Growth by Severing Labile Domains of Microtubules Leo, Lanfranco Yu, Wenqian D’Rozario, Mitchell Waddell, Edward A. Marenda, Daniel R. Baird, Michelle A. Davidson, Michael W. Zhou, Bin Wu, Bingro Baker, Lisa Sharp, David J. Baas, Peter W. Cell Rep Article Individual microtubules (MTs) in the axon consist of a stable domain that is highly acetylated and a labile domain that is not. Traditional MT-severing proteins preferentially cut the MT in the stable domain. In Drosophila, fidgetin behaves in this fashion, with targeted knockdown resulting in neurons with a higher fraction of acetylated (stable) MT mass in their axons. Conversely, in a fidgetin knockout mouse, the fraction of MT mass that is acetylated is lower than in the control animal. When fidgetin is depleted from cultured rodent neurons, there is a 62% increase in axonal MT mass, all of which is labile. Concomitantly, there are more minor processes and a longer axon. Together with experimental data showing that vertebrate fidgetin targets unacetylated tubulin, these results indicate that vertebrate fidgetin (unlike its fly ortholog) regulates neuronal development by tamping back the expansion of the labile domains of MTs. 2015-09-03 2015-09-22 /pmc/articles/PMC4837332/ /pubmed/26344772 http://dx.doi.org/10.1016/j.celrep.2015.08.017 Text en This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Leo, Lanfranco Yu, Wenqian D’Rozario, Mitchell Waddell, Edward A. Marenda, Daniel R. Baird, Michelle A. Davidson, Michael W. Zhou, Bin Wu, Bingro Baker, Lisa Sharp, David J. Baas, Peter W. Vertebrate Fidgetin Restrains Axonal Growth by Severing Labile Domains of Microtubules |
title | Vertebrate Fidgetin Restrains Axonal Growth by Severing Labile Domains of Microtubules |
title_full | Vertebrate Fidgetin Restrains Axonal Growth by Severing Labile Domains of Microtubules |
title_fullStr | Vertebrate Fidgetin Restrains Axonal Growth by Severing Labile Domains of Microtubules |
title_full_unstemmed | Vertebrate Fidgetin Restrains Axonal Growth by Severing Labile Domains of Microtubules |
title_short | Vertebrate Fidgetin Restrains Axonal Growth by Severing Labile Domains of Microtubules |
title_sort | vertebrate fidgetin restrains axonal growth by severing labile domains of microtubules |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4837332/ https://www.ncbi.nlm.nih.gov/pubmed/26344772 http://dx.doi.org/10.1016/j.celrep.2015.08.017 |
work_keys_str_mv | AT leolanfranco vertebratefidgetinrestrainsaxonalgrowthbyseveringlabiledomainsofmicrotubules AT yuwenqian vertebratefidgetinrestrainsaxonalgrowthbyseveringlabiledomainsofmicrotubules AT drozariomitchell vertebratefidgetinrestrainsaxonalgrowthbyseveringlabiledomainsofmicrotubules AT waddelledwarda vertebratefidgetinrestrainsaxonalgrowthbyseveringlabiledomainsofmicrotubules AT marendadanielr vertebratefidgetinrestrainsaxonalgrowthbyseveringlabiledomainsofmicrotubules AT bairdmichellea vertebratefidgetinrestrainsaxonalgrowthbyseveringlabiledomainsofmicrotubules AT davidsonmichaelw vertebratefidgetinrestrainsaxonalgrowthbyseveringlabiledomainsofmicrotubules AT zhoubin vertebratefidgetinrestrainsaxonalgrowthbyseveringlabiledomainsofmicrotubules AT wubingro vertebratefidgetinrestrainsaxonalgrowthbyseveringlabiledomainsofmicrotubules AT bakerlisa vertebratefidgetinrestrainsaxonalgrowthbyseveringlabiledomainsofmicrotubules AT sharpdavidj vertebratefidgetinrestrainsaxonalgrowthbyseveringlabiledomainsofmicrotubules AT baaspeterw vertebratefidgetinrestrainsaxonalgrowthbyseveringlabiledomainsofmicrotubules |