Involvement of members of the Rab family and related small GTPases in autophagosome formation and maturation

被引:94
作者
Chua, Christelle En Lin [1 ]
Gan, Bin Qi [1 ]
Tang, Bor Luen [1 ]
机构
[1] Natl Univ Singapore, Natl Univ Hlth Syst, Yong Loo Lin Sch Med, Dept Biochem, Singapore 117597, Singapore
关键词
Autophagy; Autophagosome; Parkinson's disease; Rab; RalB; PICK-C DISEASE; ENDOPLASMIC-RETICULUM; MULTIVESICULAR BODIES; PARKINSONS-DISEASE; NEURODEGENERATIVE DISORDERS; SACCHAROMYCES-CEREVISIAE; REGULATE AUTOPHAGY; VESICLE TRANSPORT; GOLGI TRANSPORT; TRAPP COMPLEXES;
D O I
10.1007/s00018-011-0748-9
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
Macroautophagy, the process by which cytosolic components and organelles are engulfed and degraded by a double-membrane structure, could be viewed as a specialized, multistep membrane transport process. As such, it intersects with the exocytic and endocytic membrane trafficking pathways. A number of Rab GTPases which regulate secretory and endocytic membrane traffic have been shown to play either critical or accessory roles in autophagy. The biogenesis of the pre-autophagosomal isolation membrane (or phagophore) is dependent on the functionality of Rab1. A non-canonical, Atg5/Atg7-independent mode of autophagosome generation from the trans-Golgi or endosome requires Rab9. Other Rabs, such as Rab5, Rab24, Rab33, and Rab7 have all been shown to be required, or involved at various stages of autophagosomal genesis and maturation. Another small GTPase, RalB, was very recently demonstrated to induce isolation membrane formation and maturation via its engagement of the exocyst complex, a known Rab effector. We summarize here what is now known about the involvement of Rabs in autophagy, and discuss plausible mechanisms with future perspectives.
引用
收藏
页码:3349 / 3358
页数:10
相关论文
共 93 条
[1]
α-Synuclein: Membrane Interactions and Toxicity in Parkinson's Disease [J].
Auluck, Pavan K. ;
Caraveo, Gabriela ;
Lindquist, Susan .
ANNUAL REVIEW OF CELL AND DEVELOPMENTAL BIOLOGY, VOL 26, 2010, 26 :211-233
[2]
Autophagosome formation from membrane compartments enriched in phosphatidylinositol 3-phosphate and dynamically connected to the endoplasmic reticulum [J].
Axe, Elizabeth L. ;
Walker, Simon A. ;
Manifava, Maria ;
Chandra, Priya ;
Roderick, H. Llewelyn ;
Habermann, Anja ;
Griffiths, Gareth ;
Ktistakis, Nicholas T. .
JOURNAL OF CELL BIOLOGY, 2008, 182 (04) :685-701
[3]
Autophagy in neurodegenerative disorders: pathogenic roles and therapeutic implications [J].
Banerjee, Rebecca ;
Beal, M. Flint ;
Thomas, Bobby .
TRENDS IN NEUROSCIENCES, 2010, 33 (12) :541-549
[4]
Getting into the Golgi [J].
Bannykh, SI ;
Nishimura, N ;
Balch, WE .
TRENDS IN CELL BIOLOGY, 1998, 8 (01) :21-25
[5]
Visualization of Rab9-mediated vesicle transport from endosomes to the trans-Golgi in living cells [J].
Barbero, P ;
Bittova, L ;
Pfeffer, SR .
JOURNAL OF CELL BIOLOGY, 2002, 156 (03) :511-518
[6]
TRAPP complexes in membrane traffic: convergence through a common Rab [J].
Barrowman, Jemima ;
Bhandari, Deepali ;
Reinisch, Karin ;
Ferro-Novick, Susan .
NATURE REVIEWS MOLECULAR CELL BIOLOGY, 2010, 11 (11) :759-763
[7]
Autophagosomes and human diseases [J].
Beau, Isabelle ;
Mehrpour, Maryam ;
Codogno, Patrice .
INTERNATIONAL JOURNAL OF BIOCHEMISTRY & CELL BIOLOGY, 2011, 43 (04) :460-464
[8]
Network organization of the human autophagy system [J].
Behrends, Christian ;
Sowa, Mathew E. ;
Gygi, Steven P. ;
Harper, J. Wade .
NATURE, 2010, 466 (7302) :68-U84
[9]
Ral GTPases and cancer: linchpin support of the tumorigenic platform [J].
Bodemann, Brian O. ;
White, Michael A. .
NATURE REVIEWS CANCER, 2008, 8 (02) :133-140
[10]
RalB and the Exocyst Mediate the Cellular Starvation Response by Direct Activation of Autophagosome Assembly [J].
Bodemann, Brian O. ;
Orvedahl, Anthony ;
Cheng, Tzuling ;
Ram, Rosalyn R. ;
Ou, Yi-Hung ;
Formstecher, Etienne ;
Maiti, Mekhala ;
Hazelett, C. Clayton ;
Wauson, Eric M. ;
Balakireva, Maria ;
Camonis, Jacques H. ;
Yeaman, Charles ;
Levine, Beth ;
White, Michael A. .
CELL, 2011, 144 (02) :253-267