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Microtubule motors mediate endosomal sorting by maintaining functional domain organization
Many microtubule motors have been shown to couple to endosomal membranes. These motors include dynein in addition to many different kinesin family members. Sorting nexins (SNXs) are central to the organization and function of endosomes. These proteins can actively shape endosomal membranes and coupl...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Company of Biologists
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3679488/ https://www.ncbi.nlm.nih.gov/pubmed/23549789 http://dx.doi.org/10.1242/jcs.122317 |
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author | Hunt, Sylvie D. Townley, Anna K. Danson, Chris M. Cullen, Peter J. Stephens, David J. |
author_facet | Hunt, Sylvie D. Townley, Anna K. Danson, Chris M. Cullen, Peter J. Stephens, David J. |
author_sort | Hunt, Sylvie D. |
collection | PubMed |
description | Many microtubule motors have been shown to couple to endosomal membranes. These motors include dynein in addition to many different kinesin family members. Sorting nexins (SNXs) are central to the organization and function of endosomes. These proteins can actively shape endosomal membranes and couple directly or indirectly to the minus-end microtubule motor dynein. Motor proteins acting on endosomes drive their motility, dictate their morphology and affect cargo segregation. We have used well-characterized members of the SNX family to elucidate motor coupling using high-resolution light microscopy coupled with depletion of specific microtubule motors. Endosomal domains labelled with SNX1, SNX4 and SNX8 couple to discrete combinations of dynein and kinesin motors. These specific combinations govern the structure and motility of each SNX-coated membrane in addition to the segregation of distinct functional endosomal subdomains. Taken together, our data show that these key features of endosome dynamics are governed by the same set of opposing microtubule motors. Thus, microtubule motors help to define the mosaic layout of endosomes that underpins cargo sorting. |
format | Online Article Text |
id | pubmed-3679488 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | The Company of Biologists |
record_format | MEDLINE/PubMed |
spelling | pubmed-36794882013-06-25 Microtubule motors mediate endosomal sorting by maintaining functional domain organization Hunt, Sylvie D. Townley, Anna K. Danson, Chris M. Cullen, Peter J. Stephens, David J. J Cell Sci Research Article Many microtubule motors have been shown to couple to endosomal membranes. These motors include dynein in addition to many different kinesin family members. Sorting nexins (SNXs) are central to the organization and function of endosomes. These proteins can actively shape endosomal membranes and couple directly or indirectly to the minus-end microtubule motor dynein. Motor proteins acting on endosomes drive their motility, dictate their morphology and affect cargo segregation. We have used well-characterized members of the SNX family to elucidate motor coupling using high-resolution light microscopy coupled with depletion of specific microtubule motors. Endosomal domains labelled with SNX1, SNX4 and SNX8 couple to discrete combinations of dynein and kinesin motors. These specific combinations govern the structure and motility of each SNX-coated membrane in addition to the segregation of distinct functional endosomal subdomains. Taken together, our data show that these key features of endosome dynamics are governed by the same set of opposing microtubule motors. Thus, microtubule motors help to define the mosaic layout of endosomes that underpins cargo sorting. The Company of Biologists 2013-06-01 /pmc/articles/PMC3679488/ /pubmed/23549789 http://dx.doi.org/10.1242/jcs.122317 Text en © 2013. Published by The Company of Biologists Ltd http://creativecommons.org/licenses/by-nc-sa/3.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial Share Alike License (http://creativecommons.org/licenses/by-nc-sa/3.0/), which permits unrestricted non-commercial use, distribution and reproduction in any medium provided that the original work is properly cited and all further distributions of the work or adaptation are subject to the same Creative Commons License terms. |
spellingShingle | Research Article Hunt, Sylvie D. Townley, Anna K. Danson, Chris M. Cullen, Peter J. Stephens, David J. Microtubule motors mediate endosomal sorting by maintaining functional domain organization |
title | Microtubule motors mediate endosomal sorting by maintaining functional domain organization |
title_full | Microtubule motors mediate endosomal sorting by maintaining functional domain organization |
title_fullStr | Microtubule motors mediate endosomal sorting by maintaining functional domain organization |
title_full_unstemmed | Microtubule motors mediate endosomal sorting by maintaining functional domain organization |
title_short | Microtubule motors mediate endosomal sorting by maintaining functional domain organization |
title_sort | microtubule motors mediate endosomal sorting by maintaining functional domain organization |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3679488/ https://www.ncbi.nlm.nih.gov/pubmed/23549789 http://dx.doi.org/10.1242/jcs.122317 |
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