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Phylogenetic profiling and cellular analyses of ARL16 reveal roles in traffic of IFT140 and INPP5E
The ARF family of regulatory GTPases is ancient, with 16 members predicted to have been present in the last eukaryotic common ancestor. Our phylogenetic profiling of paralogues in diverse species identified four family members whose presence correlates with that of a cilium/flagellum: ARL3, ARL6, AR...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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The American Society for Cell Biology
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9250359/ https://www.ncbi.nlm.nih.gov/pubmed/35196065 http://dx.doi.org/10.1091/mbc.E21-10-0509-T |
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author | Dewees, Skylar I. Vargová, Romana Hardin, Katherine R. Turn, Rachel E. Devi, Saroja Linnert, Joshua Wolfrum, Uwe Caspary, Tamara Eliáš, Marek Kahn, Richard A. |
author_facet | Dewees, Skylar I. Vargová, Romana Hardin, Katherine R. Turn, Rachel E. Devi, Saroja Linnert, Joshua Wolfrum, Uwe Caspary, Tamara Eliáš, Marek Kahn, Richard A. |
author_sort | Dewees, Skylar I. |
collection | PubMed |
description | The ARF family of regulatory GTPases is ancient, with 16 members predicted to have been present in the last eukaryotic common ancestor. Our phylogenetic profiling of paralogues in diverse species identified four family members whose presence correlates with that of a cilium/flagellum: ARL3, ARL6, ARL13, and ARL16. No prior evidence links ARL16 to cilia or other cell functions, despite its presence throughout eukaryotes. Deletion of ARL16 in mouse embryonic fibroblasts (MEFs) results in decreased ciliogenesis yet increased ciliary length. We also found Arl16 knockout (KO) in MEFs to alter ciliary protein content, including loss of ARL13B, ARL3, INPP5E, and the IFT-A core component IFT140. Instead, both INPP5E and IFT140 accumulate at the Golgi in Arl16 KO lines, while other intraflagellar transport (IFT) proteins do not, suggesting a specific defect in traffic from Golgi to cilia. We propose that ARL16 regulates a Golgi–cilia traffic pathway and is required specifically in the export of IFT140 and INPP5E from the Golgi. |
format | Online Article Text |
id | pubmed-9250359 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | The American Society for Cell Biology |
record_format | MEDLINE/PubMed |
spelling | pubmed-92503592022-07-07 Phylogenetic profiling and cellular analyses of ARL16 reveal roles in traffic of IFT140 and INPP5E Dewees, Skylar I. Vargová, Romana Hardin, Katherine R. Turn, Rachel E. Devi, Saroja Linnert, Joshua Wolfrum, Uwe Caspary, Tamara Eliáš, Marek Kahn, Richard A. Mol Biol Cell Articles The ARF family of regulatory GTPases is ancient, with 16 members predicted to have been present in the last eukaryotic common ancestor. Our phylogenetic profiling of paralogues in diverse species identified four family members whose presence correlates with that of a cilium/flagellum: ARL3, ARL6, ARL13, and ARL16. No prior evidence links ARL16 to cilia or other cell functions, despite its presence throughout eukaryotes. Deletion of ARL16 in mouse embryonic fibroblasts (MEFs) results in decreased ciliogenesis yet increased ciliary length. We also found Arl16 knockout (KO) in MEFs to alter ciliary protein content, including loss of ARL13B, ARL3, INPP5E, and the IFT-A core component IFT140. Instead, both INPP5E and IFT140 accumulate at the Golgi in Arl16 KO lines, while other intraflagellar transport (IFT) proteins do not, suggesting a specific defect in traffic from Golgi to cilia. We propose that ARL16 regulates a Golgi–cilia traffic pathway and is required specifically in the export of IFT140 and INPP5E from the Golgi. The American Society for Cell Biology 2022-03-17 /pmc/articles/PMC9250359/ /pubmed/35196065 http://dx.doi.org/10.1091/mbc.E21-10-0509-T Text en © 2022 Dewees et al. “ASCB®,” “The American Society for Cell Biology®,” and “Molecular Biology of the Cell®” are registered trademarks of The American Society for Cell Biology. https://creativecommons.org/licenses/by-nc-sa/4.0/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 4.0 International Creative Commons License. |
spellingShingle | Articles Dewees, Skylar I. Vargová, Romana Hardin, Katherine R. Turn, Rachel E. Devi, Saroja Linnert, Joshua Wolfrum, Uwe Caspary, Tamara Eliáš, Marek Kahn, Richard A. Phylogenetic profiling and cellular analyses of ARL16 reveal roles in traffic of IFT140 and INPP5E |
title | Phylogenetic profiling and cellular analyses of ARL16 reveal roles in traffic of IFT140 and INPP5E |
title_full | Phylogenetic profiling and cellular analyses of ARL16 reveal roles in traffic of IFT140 and INPP5E |
title_fullStr | Phylogenetic profiling and cellular analyses of ARL16 reveal roles in traffic of IFT140 and INPP5E |
title_full_unstemmed | Phylogenetic profiling and cellular analyses of ARL16 reveal roles in traffic of IFT140 and INPP5E |
title_short | Phylogenetic profiling and cellular analyses of ARL16 reveal roles in traffic of IFT140 and INPP5E |
title_sort | phylogenetic profiling and cellular analyses of arl16 reveal roles in traffic of ift140 and inpp5e |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9250359/ https://www.ncbi.nlm.nih.gov/pubmed/35196065 http://dx.doi.org/10.1091/mbc.E21-10-0509-T |
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