Pex13p is an SH3 protein of the peroxisome membrane and a docking factor for the predominantly cytoplasmic PTS1 receptor

被引:207
|
作者
Gould, SJ
Kalish, JE
Morrell, JC
Bjorkman, J
Urquhart, AJ
Crane, DI
机构
[1] JOHNS HOPKINS UNIV,SCH MED,DEPT CELL BIOL & ANAT,BALTIMORE,MD 21205
[2] KENNEDY KRIEGER INST,BALTIMORE,MD 21205
[3] GRIFFITH UNIV,SCH BIOMOL & BIOMED SCI,BRISBANE,QLD 4111,AUSTRALIA
来源
JOURNAL OF CELL BIOLOGY | 1996年 / 135卷 / 01期
关键词
D O I
10.1083/jcb.135.1.85
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Import of newly synthesized PTS1 proteins into the peroxisome requires the PTS1 receptor (Pex5p), a predominantly cytoplasmic protein that cycles between the cytoplasm and peroxisome. We have identified Pex13p, a novel integral peroxisomal membrane from both yeast and humans that binds the PTS1 receptor via a cytoplasmically oriented SH3 domain. Although only a small amount of Pex5p is bound to peroxisomes at steady state (<5%), loss of Pex13p further reduces the amount of peroxisome-associated Pex5p by similar to 40-fold. Furthermore, loss of Pex13p eliminates import of peroxisomal matrix proteins that contain either the type-1 or type-2 peroxisomal targeting signal but does not affect targeting and insertion of integral peroxisomal membrane proteins. We conclude that Pex13p functions as a docking factor for the predominantly cytoplasmic PTS1 receptor.
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页码:85 / 95
页数:11
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