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Msp1-mediated proofreading mechanism for localization of tail-anchored membrane proteins
被引:1
|作者:
Matsumoto, Shunsuke
[1
]
机构:
[1] Kyushu Univ, Grad Sch Bioresource & Bioenvironm Sci, Dept Biosci & Biotechnol, Motooka 744,Nishi Ku, Fukuoka 8190395, Japan
来源:
关键词:
GET pathway;
mislocalization;
Msp1;
proofreading;
TA protein;
QUALITY-CONTROL;
TARGETING FACTOR;
STRUCTURAL BASIS;
ATPASE MSP1;
COMPLEX;
RETICULUM;
INSERTION;
DEGRADATION;
CHAPERONE;
RECRUITS;
D O I:
10.1093/jb/mvad025
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
Protein targeting to organelles has been thought to be a very precise process, and proteins that fail to localize correctly are rapidly degraded. Tail-anchored proteins are posttranslationally targeted to the endoplasmic reticulum membrane via guided entry of tail-anchored (TA) proteins pathway. However, these proteins can be mislocalized to the mitochondrial outer membrane. We found that the AAA-ATPase Msp1 on the mitochondrial outer membrane extracts mislocalized TA proteins to the cytosol, passing them to the guided entry of the TA proteins pathway to facilitate their transfer to the endoplasmic reticulum membrane. After the transfer to the endoplasmic reticulum, such TA proteins are directed to degradation if they are recognized by the quality control system on the endoplasmic reticulum. If not recognized, they are retargeted to their original destination along the secretory pathway. Thus, we have identified an intracellular proofreading system that corrects the localization of TA proteins.
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页码:13 / 20
页数:8
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