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The Bif-1-Dynamin 2 membrane fission machinery regulates Atg9-containing vesicle generation at the Rab11-positive reservoirs

Atg9 is a multispanning transmembrane protein that is required for autophagosome formation. During autophagy, vesicles containing Atg9 are generated through an unknown mechanism and delivered to the autophagosome formation sites. We have previously reported that Atg9-containing membranes undergo con...

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Autores principales: Takahashi, Yoshinori, Tsotakos, Nikolaos, Liu, Ying, Young, Megan M., Serfass, Jacob, Tang, Zhenyuan, Abraham, Thomas, Wang, Hong-Gang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4991497/
https://www.ncbi.nlm.nih.gov/pubmed/26980706
http://dx.doi.org/10.18632/oncotarget.8028
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author Takahashi, Yoshinori
Tsotakos, Nikolaos
Liu, Ying
Young, Megan M.
Serfass, Jacob
Tang, Zhenyuan
Abraham, Thomas
Wang, Hong-Gang
author_facet Takahashi, Yoshinori
Tsotakos, Nikolaos
Liu, Ying
Young, Megan M.
Serfass, Jacob
Tang, Zhenyuan
Abraham, Thomas
Wang, Hong-Gang
author_sort Takahashi, Yoshinori
collection PubMed
description Atg9 is a multispanning transmembrane protein that is required for autophagosome formation. During autophagy, vesicles containing Atg9 are generated through an unknown mechanism and delivered to the autophagosome formation sites. We have previously reported that Atg9-containing membranes undergo continuous tubulation and fission during nutrient starvation in a manner dependent on the curvature-inducing protein Bif-1/Sh3glb1. Here, we identify Dynamin 2 (DNM2) as a Bif-1-interacting protein that mediates the fission of Atg9-containing membranes during autophagy. The interaction of Bif-1 and DNM2 is enhanced upon nutrient starvation, and Bif-1 and DNM2 cooperatively induce the generation of Atg9-containing vesicles. Inhibition of the GTPase activity of DNM2 results in the accumulation of Atg9-positive tubular structures that originate from a Rab11-positive reservoir. Although Atg9 seems to be constitutively trafficked to the reservoir regardless of Bif-1 expression, membrane tubulation from the Atg9 reservoir is dependent on Bif-1 and is strongly induced upon nutrient starvation. These findings suggest that the generation of Atg9 vesicles from a Rab11-positive reservoir is tightly controlled by the Bif-1-DNM2 membrane fission machinery in response to cellular demand for autophagy.
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spelling pubmed-49914972016-09-01 The Bif-1-Dynamin 2 membrane fission machinery regulates Atg9-containing vesicle generation at the Rab11-positive reservoirs Takahashi, Yoshinori Tsotakos, Nikolaos Liu, Ying Young, Megan M. Serfass, Jacob Tang, Zhenyuan Abraham, Thomas Wang, Hong-Gang Oncotarget Research Paper Atg9 is a multispanning transmembrane protein that is required for autophagosome formation. During autophagy, vesicles containing Atg9 are generated through an unknown mechanism and delivered to the autophagosome formation sites. We have previously reported that Atg9-containing membranes undergo continuous tubulation and fission during nutrient starvation in a manner dependent on the curvature-inducing protein Bif-1/Sh3glb1. Here, we identify Dynamin 2 (DNM2) as a Bif-1-interacting protein that mediates the fission of Atg9-containing membranes during autophagy. The interaction of Bif-1 and DNM2 is enhanced upon nutrient starvation, and Bif-1 and DNM2 cooperatively induce the generation of Atg9-containing vesicles. Inhibition of the GTPase activity of DNM2 results in the accumulation of Atg9-positive tubular structures that originate from a Rab11-positive reservoir. Although Atg9 seems to be constitutively trafficked to the reservoir regardless of Bif-1 expression, membrane tubulation from the Atg9 reservoir is dependent on Bif-1 and is strongly induced upon nutrient starvation. These findings suggest that the generation of Atg9 vesicles from a Rab11-positive reservoir is tightly controlled by the Bif-1-DNM2 membrane fission machinery in response to cellular demand for autophagy. Impact Journals LLC 2016-03-10 /pmc/articles/PMC4991497/ /pubmed/26980706 http://dx.doi.org/10.18632/oncotarget.8028 Text en Copyright: © 2016 Takahashi et al. http://creativecommons.org/licenses/by/2.5/ 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 author and source are credited.
spellingShingle Research Paper
Takahashi, Yoshinori
Tsotakos, Nikolaos
Liu, Ying
Young, Megan M.
Serfass, Jacob
Tang, Zhenyuan
Abraham, Thomas
Wang, Hong-Gang
The Bif-1-Dynamin 2 membrane fission machinery regulates Atg9-containing vesicle generation at the Rab11-positive reservoirs
title The Bif-1-Dynamin 2 membrane fission machinery regulates Atg9-containing vesicle generation at the Rab11-positive reservoirs
title_full The Bif-1-Dynamin 2 membrane fission machinery regulates Atg9-containing vesicle generation at the Rab11-positive reservoirs
title_fullStr The Bif-1-Dynamin 2 membrane fission machinery regulates Atg9-containing vesicle generation at the Rab11-positive reservoirs
title_full_unstemmed The Bif-1-Dynamin 2 membrane fission machinery regulates Atg9-containing vesicle generation at the Rab11-positive reservoirs
title_short The Bif-1-Dynamin 2 membrane fission machinery regulates Atg9-containing vesicle generation at the Rab11-positive reservoirs
title_sort bif-1-dynamin 2 membrane fission machinery regulates atg9-containing vesicle generation at the rab11-positive reservoirs
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4991497/
https://www.ncbi.nlm.nih.gov/pubmed/26980706
http://dx.doi.org/10.18632/oncotarget.8028
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