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RUFY3 and RUFY4 are ARL8 effectors that promote coupling of endolysosomes to dynein-dynactin
The small GTPase ARL8 associates with endolysosomes, leading to the recruitment of several effectors that couple endolysosomes to kinesins for anterograde transport along microtubules, and to tethering factors for eventual fusion with other organelles. Herein we report the identification of the RUN-...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8938451/ https://www.ncbi.nlm.nih.gov/pubmed/35314674 http://dx.doi.org/10.1038/s41467-022-28952-y |
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author | Keren-Kaplan, Tal Sarić, Amra Ghosh, Saikat Williamson, Chad D. Jia, Rui Li, Yan Bonifacino, Juan S. |
author_facet | Keren-Kaplan, Tal Sarić, Amra Ghosh, Saikat Williamson, Chad D. Jia, Rui Li, Yan Bonifacino, Juan S. |
author_sort | Keren-Kaplan, Tal |
collection | PubMed |
description | The small GTPase ARL8 associates with endolysosomes, leading to the recruitment of several effectors that couple endolysosomes to kinesins for anterograde transport along microtubules, and to tethering factors for eventual fusion with other organelles. Herein we report the identification of the RUN- and FYVE-domain-containing proteins RUFY3 and RUFY4 as ARL8 effectors that promote coupling of endolysosomes to dynein-dynactin for retrograde transport along microtubules. Using various methodologies, we find that RUFY3 and RUFY4 interact with both GTP-bound ARL8 and dynein-dynactin. In addition, we show that RUFY3 and RUFY4 promote concentration of endolysosomes in the juxtanuclear area of non-neuronal cells, and drive redistribution of endolysosomes from the axon to the soma in hippocampal neurons. The function of RUFY3 in retrograde transport contributes to the juxtanuclear redistribution of endolysosomes upon cytosol alkalinization. These studies thus identify RUFY3 and RUFY4 as ARL8-dependent, dynein-dynactin adaptors or regulators, and highlight the role of ARL8 in the control of both anterograde and retrograde endolysosome transport. |
format | Online Article Text |
id | pubmed-8938451 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-89384512022-04-08 RUFY3 and RUFY4 are ARL8 effectors that promote coupling of endolysosomes to dynein-dynactin Keren-Kaplan, Tal Sarić, Amra Ghosh, Saikat Williamson, Chad D. Jia, Rui Li, Yan Bonifacino, Juan S. Nat Commun Article The small GTPase ARL8 associates with endolysosomes, leading to the recruitment of several effectors that couple endolysosomes to kinesins for anterograde transport along microtubules, and to tethering factors for eventual fusion with other organelles. Herein we report the identification of the RUN- and FYVE-domain-containing proteins RUFY3 and RUFY4 as ARL8 effectors that promote coupling of endolysosomes to dynein-dynactin for retrograde transport along microtubules. Using various methodologies, we find that RUFY3 and RUFY4 interact with both GTP-bound ARL8 and dynein-dynactin. In addition, we show that RUFY3 and RUFY4 promote concentration of endolysosomes in the juxtanuclear area of non-neuronal cells, and drive redistribution of endolysosomes from the axon to the soma in hippocampal neurons. The function of RUFY3 in retrograde transport contributes to the juxtanuclear redistribution of endolysosomes upon cytosol alkalinization. These studies thus identify RUFY3 and RUFY4 as ARL8-dependent, dynein-dynactin adaptors or regulators, and highlight the role of ARL8 in the control of both anterograde and retrograde endolysosome transport. Nature Publishing Group UK 2022-03-21 /pmc/articles/PMC8938451/ /pubmed/35314674 http://dx.doi.org/10.1038/s41467-022-28952-y Text en © This is a U.S. Government work and not under copyright protection in the US; foreign copyright protection may apply 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Keren-Kaplan, Tal Sarić, Amra Ghosh, Saikat Williamson, Chad D. Jia, Rui Li, Yan Bonifacino, Juan S. RUFY3 and RUFY4 are ARL8 effectors that promote coupling of endolysosomes to dynein-dynactin |
title | RUFY3 and RUFY4 are ARL8 effectors that promote coupling of endolysosomes to dynein-dynactin |
title_full | RUFY3 and RUFY4 are ARL8 effectors that promote coupling of endolysosomes to dynein-dynactin |
title_fullStr | RUFY3 and RUFY4 are ARL8 effectors that promote coupling of endolysosomes to dynein-dynactin |
title_full_unstemmed | RUFY3 and RUFY4 are ARL8 effectors that promote coupling of endolysosomes to dynein-dynactin |
title_short | RUFY3 and RUFY4 are ARL8 effectors that promote coupling of endolysosomes to dynein-dynactin |
title_sort | rufy3 and rufy4 are arl8 effectors that promote coupling of endolysosomes to dynein-dynactin |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8938451/ https://www.ncbi.nlm.nih.gov/pubmed/35314674 http://dx.doi.org/10.1038/s41467-022-28952-y |
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