A family of membrane-shaping proteins at ER subdomains regulates pre-peroxisomal vesicle biogenesis

被引:70
作者
Joshi, Amit S. [1 ]
Huang, Xiaofang [2 ,3 ]
Choudhary, Vineet [1 ]
Levine, Tim P. [4 ]
Hu, Junjie [2 ,3 ,5 ]
Prinz, William A. [1 ]
机构
[1] NIDDK, Lab Cell & Mol Biol, NIH, Bethesda, MD 20892 USA
[2] Nankai Univ, Dept Genet & Cell Biol, Coll Life Sci, Tianjin 300071, Peoples R China
[3] Nankai Univ, Tianjin Key Lab Prot Sci, Tianjin 300071, Peoples R China
[4] UCL, Inst Ophthalmol, London EC1V 9EL, England
[5] Chinese Acad Sci, Inst Biophys, Natl Lab Macromol, Beijing 100101, Peoples R China
基金
中国国家自然科学基金; 英国生物技术与生命科学研究理事会; 瑞士国家科学基金会;
关键词
TUBULAR ENDOPLASMIC-RETICULUM; SACCHAROMYCES-CEREVISIAE; NUCLEAR-ENVELOPE; SELECTIVE AUTOPHAGY; NETWORK FORMATION; S; CEREVISIAE; GTPASE SEY1P; CELLS; FORM; MECHANISMS;
D O I
10.1083/jcb.201602064
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Saccharomyces cerevisiae contains three conserved reticulon and reticulon-like proteins that help maintain ER structure by stabilizing high membrane curvature in ER tubules and the edges of ER sheets. A mutant lacking all three proteins has dramatically altered ER morphology. We found that ER shape is restored in this mutant when Pex30p or its homologue Pex31p is overexpressed. Pex30p can tubulate membranes both in cells and when reconstituted into proteoliposomes, indicating that Pex30p is a novel ER-shaping protein. In contrast to the reticulons, Pex30p is low abundance, and we found that it localizes to subdomains in the ER. We show that these ER subdomains are the sites where most preperoxisomal vesicles (PPVs) are generated. In addition, overproduction or deletion of Pex30p or Pex31p alters the size, shape, and number of PPVs. Our findings suggest that Pex30p and Pex31p help shape and generate regions of the ER where PPV biogenesis occurs.
引用
收藏
页码:515 / 529
页数:15
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共 50 条
[1]   De novo peroxisome biogenesis: Evolving concepts and conundrums [J].
Agrawal, Gaurav ;
Subramani, Suresh .
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH, 2016, 1863 (05) :892-901
[2]   Distinct requirements for intra-ER sorting and budding of peroxisomal membrane proteins from the ER [J].
Agrawal, Gaurav ;
Fassas, Scott N. ;
Xia, Zhi-Jie ;
Subramani, Suresh .
JOURNAL OF CELL BIOLOGY, 2016, 212 (03) :335-348
[3]   Cell-free sorting of peroxisomal membrane proteins from the endoplasmic reticulum [J].
Agrawal, Gaurav ;
Joshi, Saurabh ;
Subramani, Suresh .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2011, 108 (22) :9113-9118
[4]   The dynamin-like GTPase Sey1p mediates homotypic ER fusion in S. cerevisiae [J].
Anwar, Kamran ;
Klemm, Robin W. ;
Condon, Amanda ;
Severin, Katharina N. ;
Zhang, Miao ;
Ghirlando, Rodolfo ;
Hu, Junjie ;
Rapoport, Tom A. ;
Prinz, William A. .
JOURNAL OF CELL BIOLOGY, 2012, 197 (02) :209-217
[5]  
BARTLETT GR, 1959, J BIOL CHEM, V234, P466
[6]   Removal of Pex3p is an important initial stage in selective peroxisome degradation in Hansenula polymorpha [J].
Bellu, AR ;
Salomons, FA ;
Kiel, JAKW ;
Veenhuis, M ;
van der Klei, IJ .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (45) :42875-42880
[7]   Yeast nuclear envelope subdomains with distinct abilities to resist membrane expansion [J].
Campbell, JL ;
Lorenz, A ;
Witkin, KL ;
Hays, T ;
Loidl, L ;
Cohen-Fix, O .
MOLECULAR BIOLOGY OF THE CELL, 2006, 17 (04) :1768-1778
[8]   Lunapark stabilizes nascent three-way junctions in the endoplasmic reticulum [J].
Chen, Shuliang ;
Desai, Tanvi ;
McNew, James A. ;
Gerard, Patrick ;
Novick, Peter J. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2015, 112 (02) :418-423
[9]   ER network formation requires a balance of the dynamin-like GTPase Sey1p and the Lunapark family member Lnp1p [J].
Chen, Shuliang ;
Novick, Peter ;
Ferro-Novick, Susan .
NATURE CELL BIOLOGY, 2012, 14 (07) :707-716
[10]   A conserved family of proteins facilitates nascent lipid droplet budding from the ER [J].
Choudhary, Vineet ;
Ojha, Namrata ;
Golden, Andy ;
Prinz, William A. .
JOURNAL OF CELL BIOLOGY, 2015, 211 (02) :261-271