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Chlamydomonas DYX1C1/PF23 is essential for axonemal assembly and proper morphology of inner dynein arms

Cytoplasmic assembly of ciliary dyneins, a process known as preassembly, requires numerous non-dynein proteins, but the identities and functions of these proteins are not fully elucidated. Here, we show that the classical Chlamydomonas motility mutant pf23 is defective in the Chlamydomonas homolog o...

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Autores principales: Yamamoto, Ryosuke, Obbineni, Jagan M., Alford, Lea M., Ide, Takahiro, Owa, Mikito, Hwang, Juyeon, Kon, Takahide, Inaba, Kazuo, James, Noliyanda, King, Stephen M., Ishikawa, Takashi, Sale, Winfield S., Dutcher, Susan K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5608425/
https://www.ncbi.nlm.nih.gov/pubmed/28892495
http://dx.doi.org/10.1371/journal.pgen.1006996
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author Yamamoto, Ryosuke
Obbineni, Jagan M.
Alford, Lea M.
Ide, Takahiro
Owa, Mikito
Hwang, Juyeon
Kon, Takahide
Inaba, Kazuo
James, Noliyanda
King, Stephen M.
Ishikawa, Takashi
Sale, Winfield S.
Dutcher, Susan K.
author_facet Yamamoto, Ryosuke
Obbineni, Jagan M.
Alford, Lea M.
Ide, Takahiro
Owa, Mikito
Hwang, Juyeon
Kon, Takahide
Inaba, Kazuo
James, Noliyanda
King, Stephen M.
Ishikawa, Takashi
Sale, Winfield S.
Dutcher, Susan K.
author_sort Yamamoto, Ryosuke
collection PubMed
description Cytoplasmic assembly of ciliary dyneins, a process known as preassembly, requires numerous non-dynein proteins, but the identities and functions of these proteins are not fully elucidated. Here, we show that the classical Chlamydomonas motility mutant pf23 is defective in the Chlamydomonas homolog of DYX1C1. The pf23 mutant has a 494 bp deletion in the DYX1C1 gene and expresses a shorter DYX1C1 protein in the cytoplasm. Structural analyses, using cryo-ET, reveal that pf23 axonemes lack most of the inner dynein arms. Spectral counting confirms that DYX1C1 is essential for the assembly of the majority of ciliary inner dynein arms (IDA) as well as a fraction of the outer dynein arms (ODA). A C-terminal truncation of DYX1C1 shows a reduction in a subset of these ciliary IDAs. Sucrose gradients of cytoplasmic extracts show that preassembled ciliary dyneins are reduced compared to wild-type, which suggests an important role in dynein complex stability. The role of PF23/DYX1C1 remains unknown, but we suggest that DYX1C1 could provide a scaffold for macromolecular assembly.
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spelling pubmed-56084252017-10-09 Chlamydomonas DYX1C1/PF23 is essential for axonemal assembly and proper morphology of inner dynein arms Yamamoto, Ryosuke Obbineni, Jagan M. Alford, Lea M. Ide, Takahiro Owa, Mikito Hwang, Juyeon Kon, Takahide Inaba, Kazuo James, Noliyanda King, Stephen M. Ishikawa, Takashi Sale, Winfield S. Dutcher, Susan K. PLoS Genet Research Article Cytoplasmic assembly of ciliary dyneins, a process known as preassembly, requires numerous non-dynein proteins, but the identities and functions of these proteins are not fully elucidated. Here, we show that the classical Chlamydomonas motility mutant pf23 is defective in the Chlamydomonas homolog of DYX1C1. The pf23 mutant has a 494 bp deletion in the DYX1C1 gene and expresses a shorter DYX1C1 protein in the cytoplasm. Structural analyses, using cryo-ET, reveal that pf23 axonemes lack most of the inner dynein arms. Spectral counting confirms that DYX1C1 is essential for the assembly of the majority of ciliary inner dynein arms (IDA) as well as a fraction of the outer dynein arms (ODA). A C-terminal truncation of DYX1C1 shows a reduction in a subset of these ciliary IDAs. Sucrose gradients of cytoplasmic extracts show that preassembled ciliary dyneins are reduced compared to wild-type, which suggests an important role in dynein complex stability. The role of PF23/DYX1C1 remains unknown, but we suggest that DYX1C1 could provide a scaffold for macromolecular assembly. Public Library of Science 2017-09-11 /pmc/articles/PMC5608425/ /pubmed/28892495 http://dx.doi.org/10.1371/journal.pgen.1006996 Text en © 2017 Yamamoto et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Yamamoto, Ryosuke
Obbineni, Jagan M.
Alford, Lea M.
Ide, Takahiro
Owa, Mikito
Hwang, Juyeon
Kon, Takahide
Inaba, Kazuo
James, Noliyanda
King, Stephen M.
Ishikawa, Takashi
Sale, Winfield S.
Dutcher, Susan K.
Chlamydomonas DYX1C1/PF23 is essential for axonemal assembly and proper morphology of inner dynein arms
title Chlamydomonas DYX1C1/PF23 is essential for axonemal assembly and proper morphology of inner dynein arms
title_full Chlamydomonas DYX1C1/PF23 is essential for axonemal assembly and proper morphology of inner dynein arms
title_fullStr Chlamydomonas DYX1C1/PF23 is essential for axonemal assembly and proper morphology of inner dynein arms
title_full_unstemmed Chlamydomonas DYX1C1/PF23 is essential for axonemal assembly and proper morphology of inner dynein arms
title_short Chlamydomonas DYX1C1/PF23 is essential for axonemal assembly and proper morphology of inner dynein arms
title_sort chlamydomonas dyx1c1/pf23 is essential for axonemal assembly and proper morphology of inner dynein arms
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5608425/
https://www.ncbi.nlm.nih.gov/pubmed/28892495
http://dx.doi.org/10.1371/journal.pgen.1006996
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