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

被引:66
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
英国生物技术与生命科学研究理事会; 中国国家自然科学基金; 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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