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TBC1D14 sets the TRAPP for ATG9

Amino acid withdrawal induces the formation of autophagosomes, which results in dozens of these large double-membrane vesicles appearing in the starved cell within 10–15 min, and the initiation of autophagy. This vesicle-mediated response clearly requires an adequate supply of membrane and a tight m...

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Autores principales: Lamb, Christopher A., Tooze, Sharon A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4990985/
https://www.ncbi.nlm.nih.gov/pubmed/27171758
http://dx.doi.org/10.1080/15548627.2016.1177696
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author Lamb, Christopher A.
Tooze, Sharon A.
author_facet Lamb, Christopher A.
Tooze, Sharon A.
author_sort Lamb, Christopher A.
collection PubMed
description Amino acid withdrawal induces the formation of autophagosomes, which results in dozens of these large double-membrane vesicles appearing in the starved cell within 10–15 min, and the initiation of autophagy. This vesicle-mediated response clearly requires an adequate supply of membrane and a tight molecular regulation creating a substantial challenge for the cell in terms of vesicle trafficking pathways. Several membrane sources, which contribute to autophagosome initiation and formation, have been identified including the ER, Golgi, plasma membrane, mitochondria and recycling endosomes. How contributions from these organelles are regulated is an intensive area of study. Members of several families of membrane traffic regulators, including small GTPases, such as RAB proteins, and their regulators, SNARE proteins and BAR domain-containing proteins, have recently been shown to support autophagosome formation.
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spelling pubmed-49909852016-08-25 TBC1D14 sets the TRAPP for ATG9 Lamb, Christopher A. Tooze, Sharon A. Autophagy Autophagic Puncta Amino acid withdrawal induces the formation of autophagosomes, which results in dozens of these large double-membrane vesicles appearing in the starved cell within 10–15 min, and the initiation of autophagy. This vesicle-mediated response clearly requires an adequate supply of membrane and a tight molecular regulation creating a substantial challenge for the cell in terms of vesicle trafficking pathways. Several membrane sources, which contribute to autophagosome initiation and formation, have been identified including the ER, Golgi, plasma membrane, mitochondria and recycling endosomes. How contributions from these organelles are regulated is an intensive area of study. Members of several families of membrane traffic regulators, including small GTPases, such as RAB proteins, and their regulators, SNARE proteins and BAR domain-containing proteins, have recently been shown to support autophagosome formation. Taylor & Francis 2016-05-12 /pmc/articles/PMC4990985/ /pubmed/27171758 http://dx.doi.org/10.1080/15548627.2016.1177696 Text en © 2016 The Author(s). Published with license by Taylor & Francis. http://creativecommons.org/licenses/by/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The moral rights of the named author(s) have been asserted.
spellingShingle Autophagic Puncta
Lamb, Christopher A.
Tooze, Sharon A.
TBC1D14 sets the TRAPP for ATG9
title TBC1D14 sets the TRAPP for ATG9
title_full TBC1D14 sets the TRAPP for ATG9
title_fullStr TBC1D14 sets the TRAPP for ATG9
title_full_unstemmed TBC1D14 sets the TRAPP for ATG9
title_short TBC1D14 sets the TRAPP for ATG9
title_sort tbc1d14 sets the trapp for atg9
topic Autophagic Puncta
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4990985/
https://www.ncbi.nlm.nih.gov/pubmed/27171758
http://dx.doi.org/10.1080/15548627.2016.1177696
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