Bunney Tom D, Katan Matilda
Cancer Research UK Centre for Cell and Molecular Biology, Chester Beatty Laboratories, The Institute of Cancer Research, Fulham Road, London SW3 6JB, UK.
Trends Cell Biol. 2006 Dec;16(12):640-8. doi: 10.1016/j.tcb.2006.10.007. Epub 2006 Nov 7.
Although several observations over the years suggested a link between the Ras superfamily of GTPases and second messengers generated by the isoforms of phospholipase C, such links had not been substantiated at the molecular level until recently. In particular, identification of a novel phospholipase C isoform, PLC epsilon, which also incorporates domains for guanine nucleotide exchange and Ras binding, have prompted an interest in the interplay between small GTPases and phospholipase C and possible significance of these interconnectivities. Research that followed suggests that activation of each of the major classes of phospholipase C by small GTPases could have a different mechanism and different function, and also that phospholipase C enzymes in turn control Ras GTPases through regulatory proteins that respond directly to second messengers.
多年来的多项观察表明,GTP酶的Ras超家族与磷脂酶C同工型产生的第二信使之间存在联系,但直到最近,这种联系在分子水平上仍未得到证实。特别是,一种新型磷脂酶C同工型——磷脂酶Cε的鉴定,它还包含鸟嘌呤核苷酸交换和Ras结合结构域,引发了人们对小GTP酶与磷脂酶C之间相互作用以及这些相互联系可能具有的意义的兴趣。随后的研究表明,小GTP酶对磷脂酶C各主要类别激活的机制和功能可能不同,而且磷脂酶C酶反过来通过直接响应第二信使的调节蛋白来控制Ras GTP酶。