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RAB2 regulates the formation of autophagosome and autolysosome in mammalian cells

Multiple sources contribute membrane and protein machineries to construct functional macroautophagic/autophagic structures. However, the underlying molecular mechanisms remain elusive. Here, we show that RAB2 connects the Golgi network to autophagy pathway by delivering membrane and by sequentially...

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Autores principales: Ding, Xianming, Jiang, Xiao, Tian, Rui, Zhao, Pengwei, Li, Lin, Wang, Xinyi, Chen, She, Zhu, Yushan, Mei, Mei, Bao, Shilai, Liu, Wei, Tang, Zaiming, Sun, Qiming
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6735470/
https://www.ncbi.nlm.nih.gov/pubmed/30957628
http://dx.doi.org/10.1080/15548627.2019.1596478
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author Ding, Xianming
Jiang, Xiao
Tian, Rui
Zhao, Pengwei
Li, Lin
Wang, Xinyi
Chen, She
Zhu, Yushan
Mei, Mei
Bao, Shilai
Liu, Wei
Tang, Zaiming
Sun, Qiming
author_facet Ding, Xianming
Jiang, Xiao
Tian, Rui
Zhao, Pengwei
Li, Lin
Wang, Xinyi
Chen, She
Zhu, Yushan
Mei, Mei
Bao, Shilai
Liu, Wei
Tang, Zaiming
Sun, Qiming
author_sort Ding, Xianming
collection PubMed
description Multiple sources contribute membrane and protein machineries to construct functional macroautophagic/autophagic structures. However, the underlying molecular mechanisms remain elusive. Here, we show that RAB2 connects the Golgi network to autophagy pathway by delivering membrane and by sequentially engaging distinct autophagy machineries. In unstressed cells, RAB2 resides primarily in the Golgi apparatus, as evidenced by its interaction and colocalization with GOLGA2/GM130. Importantly, autophagy stimuli dissociate RAB2 from GOLGA2 to interact with ULK1 complex, which facilitates the recruitment of ULK1 complex to form phagophores. Intriguingly, RAB2 appears to modulate ULK1 kinase activity to propagate signals for autophagosome formation. Subsequently, RAB2 switches to interact with autophagosomal RUBCNL/PACER and STX17 to further specify the recruitment of HOPS complex for autolysosome formation. Together, our study reveals a multivalent pathway in bulk autophagy regulation, and provides mechanistic insights into how the Golgi apparatus contributes to the formation of different autophagic structures. Abbreviations: ACTB: actin beta; ATG9: autophagy related 9A; ATG14: autophagy related 14; ATG16L1: autophagy related 16 like 1; BCAP31: B cell receptor associated protein 31; BECN1: beclin 1; Ctrl: control; CQ: chloroquine; CTSD: cathepsin D; DMSO: dimethyl sulfoxide; EBSS: Earle’s balanced salt solution; EEA1: early endosome antigen 1; GDI: guanine nucleotide dissociation inhibitor; GFP: green fluorescent protein; GOLGA2: golgin A2; HOPS: homotypic fusion and protein sorting complex; IP: immunoprecipitation; KD: knockdown; KO: knockout; LAMP1: lysosomal associated membrane protein 1; LC3: microtubule-associated protein 1 light chain 3; OE: overexpression; PtdIns3K: class III phosphatidylinositol 3-kinase; SQSTM1/p62: sequestosome 1; RAB2: RAB2A, member RAS oncogene family; RAB7: RAB7A, member RAS oncogene family; RAB11: RAB11A, member RAS oncogene family; RUBCNL/PACER: rubicon like autophagy enhancer; STX17: syntaxin 17; TBC1D14: TBC1 domain family member 14; TFRC: transferrin receptor; TGOLN2: trans-golgi network protein 2; TUBB: tubulin beta class I; ULK1: unc-51 like autophagy activating kinase 1; VPS41: VPS41, HOPS complex subunit; WB: western blot; WT: wild type; YPT1: GTP-binding protein YPT1.
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spelling pubmed-67354702019-09-16 RAB2 regulates the formation of autophagosome and autolysosome in mammalian cells Ding, Xianming Jiang, Xiao Tian, Rui Zhao, Pengwei Li, Lin Wang, Xinyi Chen, She Zhu, Yushan Mei, Mei Bao, Shilai Liu, Wei Tang, Zaiming Sun, Qiming Autophagy Research Paper Multiple sources contribute membrane and protein machineries to construct functional macroautophagic/autophagic structures. However, the underlying molecular mechanisms remain elusive. Here, we show that RAB2 connects the Golgi network to autophagy pathway by delivering membrane and by sequentially engaging distinct autophagy machineries. In unstressed cells, RAB2 resides primarily in the Golgi apparatus, as evidenced by its interaction and colocalization with GOLGA2/GM130. Importantly, autophagy stimuli dissociate RAB2 from GOLGA2 to interact with ULK1 complex, which facilitates the recruitment of ULK1 complex to form phagophores. Intriguingly, RAB2 appears to modulate ULK1 kinase activity to propagate signals for autophagosome formation. Subsequently, RAB2 switches to interact with autophagosomal RUBCNL/PACER and STX17 to further specify the recruitment of HOPS complex for autolysosome formation. Together, our study reveals a multivalent pathway in bulk autophagy regulation, and provides mechanistic insights into how the Golgi apparatus contributes to the formation of different autophagic structures. Abbreviations: ACTB: actin beta; ATG9: autophagy related 9A; ATG14: autophagy related 14; ATG16L1: autophagy related 16 like 1; BCAP31: B cell receptor associated protein 31; BECN1: beclin 1; Ctrl: control; CQ: chloroquine; CTSD: cathepsin D; DMSO: dimethyl sulfoxide; EBSS: Earle’s balanced salt solution; EEA1: early endosome antigen 1; GDI: guanine nucleotide dissociation inhibitor; GFP: green fluorescent protein; GOLGA2: golgin A2; HOPS: homotypic fusion and protein sorting complex; IP: immunoprecipitation; KD: knockdown; KO: knockout; LAMP1: lysosomal associated membrane protein 1; LC3: microtubule-associated protein 1 light chain 3; OE: overexpression; PtdIns3K: class III phosphatidylinositol 3-kinase; SQSTM1/p62: sequestosome 1; RAB2: RAB2A, member RAS oncogene family; RAB7: RAB7A, member RAS oncogene family; RAB11: RAB11A, member RAS oncogene family; RUBCNL/PACER: rubicon like autophagy enhancer; STX17: syntaxin 17; TBC1D14: TBC1 domain family member 14; TFRC: transferrin receptor; TGOLN2: trans-golgi network protein 2; TUBB: tubulin beta class I; ULK1: unc-51 like autophagy activating kinase 1; VPS41: VPS41, HOPS complex subunit; WB: western blot; WT: wild type; YPT1: GTP-binding protein YPT1. Taylor & Francis 2019-04-06 /pmc/articles/PMC6735470/ /pubmed/30957628 http://dx.doi.org/10.1080/15548627.2019.1596478 Text en © 2019 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives License (http://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited, and is not altered, transformed, or built upon in any way.
spellingShingle Research Paper
Ding, Xianming
Jiang, Xiao
Tian, Rui
Zhao, Pengwei
Li, Lin
Wang, Xinyi
Chen, She
Zhu, Yushan
Mei, Mei
Bao, Shilai
Liu, Wei
Tang, Zaiming
Sun, Qiming
RAB2 regulates the formation of autophagosome and autolysosome in mammalian cells
title RAB2 regulates the formation of autophagosome and autolysosome in mammalian cells
title_full RAB2 regulates the formation of autophagosome and autolysosome in mammalian cells
title_fullStr RAB2 regulates the formation of autophagosome and autolysosome in mammalian cells
title_full_unstemmed RAB2 regulates the formation of autophagosome and autolysosome in mammalian cells
title_short RAB2 regulates the formation of autophagosome and autolysosome in mammalian cells
title_sort rab2 regulates the formation of autophagosome and autolysosome in mammalian cells
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6735470/
https://www.ncbi.nlm.nih.gov/pubmed/30957628
http://dx.doi.org/10.1080/15548627.2019.1596478
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