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Roles of protrudin at interorganelle membrane contact sites

Intracellular organelles were long viewed as isolated compartments floating in the cytosol. However, this view has been radically changed within the last decade by the discovery that most organelles communicate with the endoplasmic reticulum (ER) network via membrane contact sites (MCSs) that are es...

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Autor principal: SHIRANE, Michiko
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Japan Academy 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6766452/
https://www.ncbi.nlm.nih.gov/pubmed/31406056
http://dx.doi.org/10.2183/pjab.95.023
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author SHIRANE, Michiko
author_facet SHIRANE, Michiko
author_sort SHIRANE, Michiko
collection PubMed
description Intracellular organelles were long viewed as isolated compartments floating in the cytosol. However, this view has been radically changed within the last decade by the discovery that most organelles communicate with the endoplasmic reticulum (ER) network via membrane contact sites (MCSs) that are essential for intracellular homeostasis. Protrudin is an ER resident protein that was originally shown to regulate neurite formation by promoting endosome trafficking. More recently, however, protrudin has been found to serve as a tethering factor at MCSs. The roles performed by protrudin at MCSs are mediated by its various domains, including inactivation of the small GTPase Rab11, bending of the ER membrane, and functional interactions with other molecules such as the motor protein KIF5 and the ER protein VAP. Mutations in the protrudin gene (ZFYVE27) are associated with hereditary spastic paraplegia, an axonopathy that results from defective ER structure. This review, examines the pleiotropic molecular functions of protrudin and its role in interorganellar communication.
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spelling pubmed-67664522019-10-02 Roles of protrudin at interorganelle membrane contact sites SHIRANE, Michiko Proc Jpn Acad Ser B Phys Biol Sci Review Intracellular organelles were long viewed as isolated compartments floating in the cytosol. However, this view has been radically changed within the last decade by the discovery that most organelles communicate with the endoplasmic reticulum (ER) network via membrane contact sites (MCSs) that are essential for intracellular homeostasis. Protrudin is an ER resident protein that was originally shown to regulate neurite formation by promoting endosome trafficking. More recently, however, protrudin has been found to serve as a tethering factor at MCSs. The roles performed by protrudin at MCSs are mediated by its various domains, including inactivation of the small GTPase Rab11, bending of the ER membrane, and functional interactions with other molecules such as the motor protein KIF5 and the ER protein VAP. Mutations in the protrudin gene (ZFYVE27) are associated with hereditary spastic paraplegia, an axonopathy that results from defective ER structure. This review, examines the pleiotropic molecular functions of protrudin and its role in interorganellar communication. The Japan Academy 2019-07-31 /pmc/articles/PMC6766452/ /pubmed/31406056 http://dx.doi.org/10.2183/pjab.95.023 Text en © 2019 The Japan Academy This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review
SHIRANE, Michiko
Roles of protrudin at interorganelle membrane contact sites
title Roles of protrudin at interorganelle membrane contact sites
title_full Roles of protrudin at interorganelle membrane contact sites
title_fullStr Roles of protrudin at interorganelle membrane contact sites
title_full_unstemmed Roles of protrudin at interorganelle membrane contact sites
title_short Roles of protrudin at interorganelle membrane contact sites
title_sort roles of protrudin at interorganelle membrane contact sites
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6766452/
https://www.ncbi.nlm.nih.gov/pubmed/31406056
http://dx.doi.org/10.2183/pjab.95.023
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