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The role of the dynein light intermediate chain in retrograde IFT and flagellar function in Chlamydomonas
The assembly of cilia and flagella depends on the activity of two microtubule motor complexes, kinesin-2 and dynein-2/1b, but the specific functions of the different subunits are poorly defined. Here we analyze Chlamydomonas strains expressing different amounts of the dynein 1b light intermediate ch...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The American Society for Cell Biology
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4966982/ https://www.ncbi.nlm.nih.gov/pubmed/27251063 http://dx.doi.org/10.1091/mbc.E16-03-0191 |
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author | Reck, Jaimee Schauer, Alexandria M. VanderWaal Mills, Kristyn Bower, Raqual Tritschler, Douglas Perrone, Catherine A. Porter, Mary E. |
author_facet | Reck, Jaimee Schauer, Alexandria M. VanderWaal Mills, Kristyn Bower, Raqual Tritschler, Douglas Perrone, Catherine A. Porter, Mary E. |
author_sort | Reck, Jaimee |
collection | PubMed |
description | The assembly of cilia and flagella depends on the activity of two microtubule motor complexes, kinesin-2 and dynein-2/1b, but the specific functions of the different subunits are poorly defined. Here we analyze Chlamydomonas strains expressing different amounts of the dynein 1b light intermediate chain (D1bLIC). Disruption of D1bLIC alters the stability of the dynein 1b complex and reduces both the frequency and velocity of retrograde intraflagellar transport (IFT), but it does not eliminate retrograde IFT. Flagellar assembly, motility, gliding, and mating are altered in a dose-dependent manner. iTRAQ-based proteomics identifies a small subset of proteins that are significantly reduced or elevated in d1blic flagella. Transformation with D1bLIC-GFP rescues the mutant phenotypes, and D1bLIC-GFP assembles into the dynein 1b complex at wild-type levels. D1bLIC-GFP is transported with anterograde IFT particles to the flagellar tip, dissociates into smaller particles, and begins processive retrograde IFT in <2 s. These studies demonstrate the role of D1bLIC in facilitating the recycling of IFT subunits and other proteins, identify new components potentially involved in the regulation of IFT, flagellar assembly, and flagellar signaling, and provide insight into the role of D1bLIC and retrograde IFT in other organisms. |
format | Online Article Text |
id | pubmed-4966982 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | The American Society for Cell Biology |
record_format | MEDLINE/PubMed |
spelling | pubmed-49669822016-10-16 The role of the dynein light intermediate chain in retrograde IFT and flagellar function in Chlamydomonas Reck, Jaimee Schauer, Alexandria M. VanderWaal Mills, Kristyn Bower, Raqual Tritschler, Douglas Perrone, Catherine A. Porter, Mary E. Mol Biol Cell Articles The assembly of cilia and flagella depends on the activity of two microtubule motor complexes, kinesin-2 and dynein-2/1b, but the specific functions of the different subunits are poorly defined. Here we analyze Chlamydomonas strains expressing different amounts of the dynein 1b light intermediate chain (D1bLIC). Disruption of D1bLIC alters the stability of the dynein 1b complex and reduces both the frequency and velocity of retrograde intraflagellar transport (IFT), but it does not eliminate retrograde IFT. Flagellar assembly, motility, gliding, and mating are altered in a dose-dependent manner. iTRAQ-based proteomics identifies a small subset of proteins that are significantly reduced or elevated in d1blic flagella. Transformation with D1bLIC-GFP rescues the mutant phenotypes, and D1bLIC-GFP assembles into the dynein 1b complex at wild-type levels. D1bLIC-GFP is transported with anterograde IFT particles to the flagellar tip, dissociates into smaller particles, and begins processive retrograde IFT in <2 s. These studies demonstrate the role of D1bLIC in facilitating the recycling of IFT subunits and other proteins, identify new components potentially involved in the regulation of IFT, flagellar assembly, and flagellar signaling, and provide insight into the role of D1bLIC and retrograde IFT in other organisms. The American Society for Cell Biology 2016-08-01 /pmc/articles/PMC4966982/ /pubmed/27251063 http://dx.doi.org/10.1091/mbc.E16-03-0191 Text en © 2016 Reck et al. This article is distributed by The American Society for Cell Biology under license from the author(s). Two months after publication it is available to the public under an Attribution–Noncommercial–Share Alike 3.0 Unported Creative Commons License (http://creativecommons.org/licenses/by-nc-sa/3.0). “ASCB®,” “The American Society for Cell Biology®,” and “Molecular Biology of the Cell®” are registered trademarks of The American Society for Cell Biology. |
spellingShingle | Articles Reck, Jaimee Schauer, Alexandria M. VanderWaal Mills, Kristyn Bower, Raqual Tritschler, Douglas Perrone, Catherine A. Porter, Mary E. The role of the dynein light intermediate chain in retrograde IFT and flagellar function in Chlamydomonas |
title | The role of the dynein light intermediate chain in retrograde IFT and flagellar function in Chlamydomonas |
title_full | The role of the dynein light intermediate chain in retrograde IFT and flagellar function in Chlamydomonas |
title_fullStr | The role of the dynein light intermediate chain in retrograde IFT and flagellar function in Chlamydomonas |
title_full_unstemmed | The role of the dynein light intermediate chain in retrograde IFT and flagellar function in Chlamydomonas |
title_short | The role of the dynein light intermediate chain in retrograde IFT and flagellar function in Chlamydomonas |
title_sort | role of the dynein light intermediate chain in retrograde ift and flagellar function in chlamydomonas |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4966982/ https://www.ncbi.nlm.nih.gov/pubmed/27251063 http://dx.doi.org/10.1091/mbc.E16-03-0191 |
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