Cargando…
SNX19 restricts endolysosome motility through contacts with the endoplasmic reticulum
The ability of endolysosomal organelles to move within the cytoplasm is essential for the performance of their functions. Long-range movement involves coupling of the endolysosomes to motor proteins that carry them along microtubule tracks. This movement is influenced by interactions with other orga...
Autores principales: | , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8316374/ https://www.ncbi.nlm.nih.gov/pubmed/34315878 http://dx.doi.org/10.1038/s41467-021-24709-1 |
_version_ | 1783729845629353984 |
---|---|
author | Saric, Amra Freeman, Spencer A. Williamson, Chad D. Jarnik, Michal Guardia, Carlos M. Fernandopulle, Michael S. Gershlick, David C. Bonifacino, Juan S. |
author_facet | Saric, Amra Freeman, Spencer A. Williamson, Chad D. Jarnik, Michal Guardia, Carlos M. Fernandopulle, Michael S. Gershlick, David C. Bonifacino, Juan S. |
author_sort | Saric, Amra |
collection | PubMed |
description | The ability of endolysosomal organelles to move within the cytoplasm is essential for the performance of their functions. Long-range movement involves coupling of the endolysosomes to motor proteins that carry them along microtubule tracks. This movement is influenced by interactions with other organelles, but the mechanisms involved are incompletely understood. Herein we show that the sorting nexin SNX19 tethers endolysosomes to the endoplasmic reticulum (ER), decreasing their motility and contributing to their concentration in the perinuclear area of the cell. Tethering depends on two N-terminal transmembrane domains that anchor SNX19 to the ER, and a PX domain that binds to phosphatidylinositol 3-phosphate on the endolysosomal membrane. Two other domains named PXA and PXC negatively regulate the interaction of SNX19 with endolysosomes. These studies thus identify a mechanism for controlling the motility and positioning of endolysosomes that involves tethering to the ER by a sorting nexin. |
format | Online Article Text |
id | pubmed-8316374 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-83163742021-08-03 SNX19 restricts endolysosome motility through contacts with the endoplasmic reticulum Saric, Amra Freeman, Spencer A. Williamson, Chad D. Jarnik, Michal Guardia, Carlos M. Fernandopulle, Michael S. Gershlick, David C. Bonifacino, Juan S. Nat Commun Article The ability of endolysosomal organelles to move within the cytoplasm is essential for the performance of their functions. Long-range movement involves coupling of the endolysosomes to motor proteins that carry them along microtubule tracks. This movement is influenced by interactions with other organelles, but the mechanisms involved are incompletely understood. Herein we show that the sorting nexin SNX19 tethers endolysosomes to the endoplasmic reticulum (ER), decreasing their motility and contributing to their concentration in the perinuclear area of the cell. Tethering depends on two N-terminal transmembrane domains that anchor SNX19 to the ER, and a PX domain that binds to phosphatidylinositol 3-phosphate on the endolysosomal membrane. Two other domains named PXA and PXC negatively regulate the interaction of SNX19 with endolysosomes. These studies thus identify a mechanism for controlling the motility and positioning of endolysosomes that involves tethering to the ER by a sorting nexin. Nature Publishing Group UK 2021-07-27 /pmc/articles/PMC8316374/ /pubmed/34315878 http://dx.doi.org/10.1038/s41467-021-24709-1 Text en © This is a U.S. Government work and not under copyright protection in the US; foreign copyright protection may apply 2021 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 Saric, Amra Freeman, Spencer A. Williamson, Chad D. Jarnik, Michal Guardia, Carlos M. Fernandopulle, Michael S. Gershlick, David C. Bonifacino, Juan S. SNX19 restricts endolysosome motility through contacts with the endoplasmic reticulum |
title | SNX19 restricts endolysosome motility through contacts with the endoplasmic reticulum |
title_full | SNX19 restricts endolysosome motility through contacts with the endoplasmic reticulum |
title_fullStr | SNX19 restricts endolysosome motility through contacts with the endoplasmic reticulum |
title_full_unstemmed | SNX19 restricts endolysosome motility through contacts with the endoplasmic reticulum |
title_short | SNX19 restricts endolysosome motility through contacts with the endoplasmic reticulum |
title_sort | snx19 restricts endolysosome motility through contacts with the endoplasmic reticulum |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8316374/ https://www.ncbi.nlm.nih.gov/pubmed/34315878 http://dx.doi.org/10.1038/s41467-021-24709-1 |
work_keys_str_mv | AT saricamra snx19restrictsendolysosomemotilitythroughcontactswiththeendoplasmicreticulum AT freemanspencera snx19restrictsendolysosomemotilitythroughcontactswiththeendoplasmicreticulum AT williamsonchadd snx19restrictsendolysosomemotilitythroughcontactswiththeendoplasmicreticulum AT jarnikmichal snx19restrictsendolysosomemotilitythroughcontactswiththeendoplasmicreticulum AT guardiacarlosm snx19restrictsendolysosomemotilitythroughcontactswiththeendoplasmicreticulum AT fernandopullemichaels snx19restrictsendolysosomemotilitythroughcontactswiththeendoplasmicreticulum AT gershlickdavidc snx19restrictsendolysosomemotilitythroughcontactswiththeendoplasmicreticulum AT bonifacinojuans snx19restrictsendolysosomemotilitythroughcontactswiththeendoplasmicreticulum |