Medical Scientist Training Program, University of California San Francisco, San Francisco, CA 94143-0662, USA.
Trends Cell Biol. 2010 Apr;20(4):205-13. doi: 10.1016/j.tcb.2010.01.002. Epub 2010 Feb 1.
Ubiquitin was first described as a tag allowing cells to degrade and recycle their own proteins. Recent research has shown ubiquitin to be central for immune system recognition of invading bacteria. This review describes a set of complex host-pathogen interactions that are dependent on ubiquitination. From the host perspective, ubiquitin-dependent activation of inflammation and degradation of bacterial effectors is protective. Several pathogens become ubiquitinated in the host cell cytosol, and recent research suggests that this could trigger a form of autophagy, increasingly recognized as an important mechanism for the control of infection by a variety of human pathogens. Meanwhile, bacteria have developed mechanisms to evade or exploit the fundamental processes activated by ubiquitination, producing both ubiquitin ligases and deubiquitinases that modulate host responses.
泛素最初被描述为一种标签,允许细胞降解和回收自身的蛋白质。最近的研究表明,泛素对于免疫系统识别入侵的细菌至关重要。这篇综述描述了一组依赖于泛素化的复杂的宿主-病原体相互作用。从宿主的角度来看,泛素依赖性的炎症激活和细菌效应物的降解是具有保护作用的。一些病原体在宿主细胞胞质溶胶中被泛素化,最近的研究表明,这可能会引发一种自噬,越来越多的研究认为自噬是控制多种人类病原体感染的重要机制。与此同时,细菌已经发展出逃避或利用泛素化激活的基本过程的机制,产生了泛素连接酶和去泛素化酶,这些酶调节宿主的反应。