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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...

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Autores principales: Reck, Jaimee, Schauer, Alexandria M., VanderWaal Mills, Kristyn, Bower, Raqual, Tritschler, Douglas, Perrone, Catherine A., Porter, Mary E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The American Society for Cell Biology 2016
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.
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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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