Novel, Universally Active C-terminal Protein Degradation Signal Generated by Alternative Splicing

被引:4
|
作者
Peter, Stephen A. [1 ]
Isaac, Jessica S. [1 ]
Narberhaus, Franz [2 ]
Weigand, Julia E. [1 ]
机构
[1] Tech Univ Darmstadt, Dept Biol, D-64287 Darmstadt, Germany
[2] Ruhr Univ Bochum, Microbial Biol, D-44780 Bochum, Germany
关键词
protein surveillance; C-degron; alternative splicing; hypoxia; MAX; MISFOLDED PROTEINS; HALF-LIFE; PROTEASOME; TRANSLATION; EXPRESSION; PATHWAYS; LON; MAX; PROTEOLYSIS; INHIBITORS;
D O I
10.1016/j.jmb.2021.166890
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
Proteome integrity is crucial for cellular homeostasis and adaptation to stress conditions such as hypoxia. One mechanism for rapid adaptation of the proteome in response to changing environmental signals is alternative splicing. In addition to generating different protein isoforms, alternative splicing is also capable of controlling total protein levels by the regulated synthesis of non-productive mRNA isoforms. The hypoxia-induced isoform E of the tumor suppressor MAX is produced by retention and translation of the last intron. This leads to an alternative C-terminus that harbors a potent C-degron, the isoE degron. Strikingly, the isoE degron represents a universal protein degradation signal that is not only functional in mammalian cells, but also in yeast and even in bacteria. Essential for efficient protein decay is a conserved (F/W)xxW motif. Degradation of isoE tagged proteins is mediated by the proteasome in eukaryotes and Lon protease in bacteria. Thus, the isoE degron is a broadly applicable and highly efficient tool in protein analyses. (C) 2021 Elsevier Ltd. All rights reserved.
引用
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页数:11
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