The N-End Rule Pathway

被引:292
作者
Tasaki, Takafumi [1 ,2 ]
Sriram, Shashikanth M. [1 ,2 ]
Park, Kyong Soo [3 ,4 ]
Kwon, Yong Tae [1 ,2 ,3 ]
机构
[1] Univ Pittsburgh, Sch Pharm, Ctr Pharmacogenet, Pittsburgh, PA 15261 USA
[2] Univ Pittsburgh, Sch Pharm, Dept Pharmaceut Sci, Pittsburgh, PA 15261 USA
[3] Seoul Natl Univ, World Class Univ Program, Dept Mol Med & Biopharmaceut Sci, Grad Sch Convergence Sci & Technol, Seoul 110799, South Korea
[4] Seoul Natl Univ, Coll Med, Dept Internal Med, Seoul 110799, South Korea
来源
ANNUAL REVIEW OF BIOCHEMISTRY, VOL 81 | 2012年 / 81卷
关键词
N-degron; arginylation; ubiquitin; proteolysis; RNA-PROTEIN TRANSFERASE; E3 UBIQUITIN LIGASES; HEAT-INDUCIBLE DEGRON; TERMINAL ACETYLATION; MICE LACKING; RECOGNITION COMPONENT; ESCHERICHIA-COLI; STRUCTURAL BASIS; ENZYMATIC MODIFICATION; SUBSTRATE RECOGNITION;
D O I
10.1146/annurev-biochem-051710-093308
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
The N-end rule pathway is a proteolytic system in which N-terminal residues of short-lived proteins are recognized by recognition components (N-recognins) as essential components of degrons, called N-degrons. Known N-recognins in eukaryotes mediate protein ubiquitylation and selective proteolysis by the 26S proteasome. Substrates of N-recognins can be generated when normally embedded destabilizing residues are exposed at the N terminus by proteolytic cleavage. N-degrons can also be generated through modifications of posttranslationally exposed pro-N-degrons of otherwise stable proteins; such modifications include oxidation, arginylation, leucylation, phenylalanylation, and acetylation. Although there are variations in components, degrons, and hierarchical structures, the proteolytic systems based on generation and recognition of N-degrons have been observed in all eukaryotes and prokaryotes examined thus far. The N-end rule pathway regulates homeostasis of various physiological processes, in part, through interaction with small molecules. Here, we review the biochemical mechanisms, structures, physiological functions, and small-molecule-mediated regulation of the N-end rule pathway.
引用
收藏
页码:261 / 289
页数:29
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