A design principle underlying the paradoxical roles of E3 ubiquitin ligases

被引:9
|
作者
Lee, Daewon [1 ]
Kim, Minjin [1 ]
Cho, Kwang-Hyun [1 ]
机构
[1] Korea Adv Inst Sci & Technol, Dept Bio & Brain Engn, Taejon 305701, South Korea
来源
SCIENTIFIC REPORTS | 2014年 / 4卷
基金
新加坡国家研究基金会;
关键词
SMAD4 PROTEIN STABILITY; KAPPA-B-ALPHA; PROTEASOME SYSTEM; BETA-TRCP; TRANSCRIPTIONAL REPRESSION; DEPENDENT REGULATION; CELL-PROLIFERATION; GENETIC REDUNDANCY; C-MYC; CANCER;
D O I
10.1038/srep05573
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
E3 ubiquitin ligases are important cellular components that determine the specificity of proteolysis in the ubiquitin-proteasome system. However, an increasing number of studies have indicated that E3 ubiquitin ligases also participate in transcription. Intrigued by the apparently paradoxical functions of E3 ubiquitin ligases in both proteolysis and transcriptional activation, we investigated the underlying design principles using mathematical modeling. We found that the antagonistic functions integrated in E3 ubiquitin ligases can prevent any undesirable sustained activation of downstream genes when E3 ubiquitin ligases are destabilized by unexpected perturbations. Interestingly, this design principle of the system is similar to the operational principle of a safety interlock device in engineering systems, which prevents a system from abnormal operation unless stability is guaranteed.
引用
收藏
页数:13
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