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.
Biochem J. 2005 Nov 1;391(Pt 3):e7-9. doi: 10.1042/BJ20051506.
A study in this issue of the Biochemical Journal by Harden and colleagues, in association with one published in the Biochemical Journal very recently [Hwang, Oh, Shin, Kim, Ryu and Suh (2005) Biochem. J. 389, 181-186], have defined a new member of the superfamily of PLC (phosphoinositide-specific phospholipase C) enzymes, PLCeta. Two isoforms, PLCeta1 and PLCeta2, and their splice variants add to the molecular diversity of PLC enzymes. The studies of PLCeta regulation suggest that at least some splice variants of PLCeta2 could be regulated by the G-protein subunits Gbetagamma. As two other families, PLCbeta and PLC, are also regulated through heterotrimeric G-proteins, this finding reveals further complexity and possible interplay between different PLC families and their regulatory networks. At this point, when it is likely that the PLCeta family completes the effort of identifying new members of this related group of PLC enzymes, I also discuss some more general concepts of PLC regulation and catalysis, and challenges awaiting their further studies.
哈登及其同事在本期《生物化学杂志》上发表的一项研究,与最近发表在《生物化学杂志》上的一项研究 [黄、吴、申、金、柳和徐(2005年),《生物化学杂志》389卷,第181 - 186页] 共同确定了磷脂酰肌醇特异性磷脂酶C(PLC)超家族的一个新成员,即PLCη。两种同工型,PLCη1和PLCη2,以及它们的剪接变体增加了PLC酶的分子多样性。对PLCη调节的研究表明,PLCη2的至少一些剪接变体可能受G蛋白亚基Gβγ调节。由于另外两个家族,PLCβ和PLCγ,也通过异源三聚体G蛋白进行调节,这一发现揭示了不同PLC家族及其调节网络之间进一步的复杂性和可能的相互作用。此时,当PLCη家族可能完成了识别这一相关PLC酶组新成员的工作时,我也讨论了一些关于PLC调节和催化的更一般概念,以及等待它们进一步研究的挑战。