降级(电信)
泛素连接酶
蛋白质降解
单纯疱疹病毒
着丝粒
泛素
化学
分子生物学
蛋白酶体
病毒
细胞生物学
生物
生物化学
病毒学
基因
电信
计算机科学
染色体
作者
Patrick Lomonte,Eric Morency
出处
期刊:FEBS Letters
[Wiley]
日期:2007-01-19
卷期号:581 (4): 658-662
被引量:59
标识
DOI:10.1016/j.febslet.2007.01.027
摘要
The ICP0 protein of herpes simplex virus type 1 (HSV‐1) is a nuclear protein that possesses a well‐characterized E3 ubiquitin ligase activity. This activity is responsible for the proteasomal‐dependent degradation of several cellular proteins. This study shows that ICP0 induces the proteasomal‐dependent degradation of the centromeric protein CENP‐B in infected as well as ICP0‐expressing cells. It is also shown that the ICP0‐induced CENP‐B degradation occurs as efficiently in human and mouse cells. CENP‐B is one of the major proteins of centromeres and its degradation is likely to contribute to the severe damage induced to centromeres by ICP0.
科研通智能强力驱动
Strongly Powered by AbleSci AI