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The role of retrograde intraflagellar transport in flagellar assembly, maintenance, and function
The maintenance of flagellar length is believed to require both anterograde and retrograde intraflagellar transport (IFT). However, it is difficult to uncouple the functions of retrograde transport from anterograde, as null mutants in dynein heavy chain 1b (DHC1b) have stumpy flagella, demonstrating...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Rockefeller University Press
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3461521/ https://www.ncbi.nlm.nih.gov/pubmed/23027906 http://dx.doi.org/10.1083/jcb.201206068 |
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author | Engel, Benjamin D. Ishikawa, Hiroaki Wemmer, Kimberly A. Geimer, Stefan Wakabayashi, Ken-ichi Hirono, Masafumi Craige, Branch Pazour, Gregory J. Witman, George B. Kamiya, Ritsu Marshall, Wallace F. |
author_facet | Engel, Benjamin D. Ishikawa, Hiroaki Wemmer, Kimberly A. Geimer, Stefan Wakabayashi, Ken-ichi Hirono, Masafumi Craige, Branch Pazour, Gregory J. Witman, George B. Kamiya, Ritsu Marshall, Wallace F. |
author_sort | Engel, Benjamin D. |
collection | PubMed |
description | The maintenance of flagellar length is believed to require both anterograde and retrograde intraflagellar transport (IFT). However, it is difficult to uncouple the functions of retrograde transport from anterograde, as null mutants in dynein heavy chain 1b (DHC1b) have stumpy flagella, demonstrating solely that retrograde IFT is required for flagellar assembly. We isolated a Chlamydomonas reinhardtii mutant (dhc1b-3) with a temperature-sensitive defect in DHC1b, enabling inducible inhibition of retrograde IFT in full-length flagella. Although dhc1b-3 flagella at the nonpermissive temperature (34°C) showed a dramatic reduction of retrograde IFT, they remained nearly full-length for many hours. However, dhc1b-3 cells at 34°C had strong defects in flagellar assembly after cell division or pH shock. Furthermore, dhc1b-3 cells displayed altered phototaxis and flagellar beat. Thus, robust retrograde IFT is required for flagellar assembly and function but is dispensable for the maintenance of flagellar length. Proteomic analysis of dhc1b-3 flagella revealed distinct classes of proteins that change in abundance when retrograde IFT is inhibited. |
format | Online Article Text |
id | pubmed-3461521 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-34615212013-04-01 The role of retrograde intraflagellar transport in flagellar assembly, maintenance, and function Engel, Benjamin D. Ishikawa, Hiroaki Wemmer, Kimberly A. Geimer, Stefan Wakabayashi, Ken-ichi Hirono, Masafumi Craige, Branch Pazour, Gregory J. Witman, George B. Kamiya, Ritsu Marshall, Wallace F. J Cell Biol Research Articles The maintenance of flagellar length is believed to require both anterograde and retrograde intraflagellar transport (IFT). However, it is difficult to uncouple the functions of retrograde transport from anterograde, as null mutants in dynein heavy chain 1b (DHC1b) have stumpy flagella, demonstrating solely that retrograde IFT is required for flagellar assembly. We isolated a Chlamydomonas reinhardtii mutant (dhc1b-3) with a temperature-sensitive defect in DHC1b, enabling inducible inhibition of retrograde IFT in full-length flagella. Although dhc1b-3 flagella at the nonpermissive temperature (34°C) showed a dramatic reduction of retrograde IFT, they remained nearly full-length for many hours. However, dhc1b-3 cells at 34°C had strong defects in flagellar assembly after cell division or pH shock. Furthermore, dhc1b-3 cells displayed altered phototaxis and flagellar beat. Thus, robust retrograde IFT is required for flagellar assembly and function but is dispensable for the maintenance of flagellar length. Proteomic analysis of dhc1b-3 flagella revealed distinct classes of proteins that change in abundance when retrograde IFT is inhibited. The Rockefeller University Press 2012-10-01 /pmc/articles/PMC3461521/ /pubmed/23027906 http://dx.doi.org/10.1083/jcb.201206068 Text en © 2012 Engel et al. 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 3.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/3.0/). |
spellingShingle | Research Articles Engel, Benjamin D. Ishikawa, Hiroaki Wemmer, Kimberly A. Geimer, Stefan Wakabayashi, Ken-ichi Hirono, Masafumi Craige, Branch Pazour, Gregory J. Witman, George B. Kamiya, Ritsu Marshall, Wallace F. The role of retrograde intraflagellar transport in flagellar assembly, maintenance, and function |
title | The role of retrograde intraflagellar transport in flagellar assembly, maintenance, and function |
title_full | The role of retrograde intraflagellar transport in flagellar assembly, maintenance, and function |
title_fullStr | The role of retrograde intraflagellar transport in flagellar assembly, maintenance, and function |
title_full_unstemmed | The role of retrograde intraflagellar transport in flagellar assembly, maintenance, and function |
title_short | The role of retrograde intraflagellar transport in flagellar assembly, maintenance, and function |
title_sort | role of retrograde intraflagellar transport in flagellar assembly, maintenance, and function |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3461521/ https://www.ncbi.nlm.nih.gov/pubmed/23027906 http://dx.doi.org/10.1083/jcb.201206068 |
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