Protein quality control in the secretory pathway

被引:279
作者
Sun, Zhihao [1 ]
Brodsky, Jeffrey L. [1 ]
机构
[1] Univ Pittsburgh, Dept Biol Sci, Pittsburgh, PA 15260 USA
基金
美国国家卫生研究院;
关键词
RETICULUM-ASSOCIATED DEGRADATION; ER-ASSOCIATED DEGRADATION; PLASMA-MEMBRANE ATPASE; UBIQUITIN LIGASE DOA10; I HEAVY-CHAINS; ENDOPLASMIC-RETICULUM; MISFOLDED PROTEINS; SACCHAROMYCES-CEREVISIAE; MOLECULAR CHAPERONES; SORTING RECEPTOR;
D O I
10.1083/jcb.201906047
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Protein folding is inherently error prone, especially in the endoplasmic reticulum (ER). Even with an elaborate network of molecular chaperones and protein folding facilitators, misfolding can occur quite frequently. To maintain protein homeostasis, eukaryotes have evolved a series of protein quality-control checkpoints. When secretory pathway quality-control pathways fail, stress response pathways, such as the unfolded protein response (UPR), are induced. In addition, the ER, which is the initial hub of protein biogenesis in the secretory pathway, triages misfolded proteins by delivering substrates to the proteasome or to the lysosome/vacuole through ER-associated degradation (ERAD) or ER-phagy. Some misfolded proteins escape the ER and are instead selected for Golgi quality control. These substrates are targeted for degradation after retrieval to the ER or delivery to the lysosome/vacuole. Here, we discuss how these guardian pathways function, how their activities intersect upon induction of the UPR, and how decisions are made to dispose of misfolded proteins in the secretory pathway.
引用
收藏
页码:3171 / 3187
页数:17
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