Stewart Alan J, Mukherjee Joy, Roberts Scott J, Lester Douglas, Farquharson Colin
Division of Gene Function and Development, Roslin Institute, Roslin, Midlothian EH25 9PS, UK.
Int J Mol Med. 2005 Jan;15(1):117-21.
Phosphoinositol (PhoIns)-specific phospholipase C enzymes (PLCs) are central to the inositol lipid signaling pathways and contribute to intracellular Ca2+ release and protein kinase C activation. Five distinct classes of PhoIns-specific PLCs are known to exist in mammals, which are activated by membrane receptor-mediated events. Here we have identified a sixth class of PhoIns-specific PLC with a novel domain structure, which we have termed PLC-eta. Two putative PLC-eta enzymes were identified in humans and in mice. Sequence analysis revealed that residues implicated in substrate binding and catalysis from other PhoIns-specific PLCs are conserved in the novel enzymes. PLC-eta enzymes are most closely related to the PLC-delta class and share a close evolutionary relationship with other PLC isozymes. EST analysis and RT-PCR data suggest that PLC-eta enzymes are expressed in several cell types and, by analogy with other mammalian PhoIns-specific PLCs, are likely to be involved in signal transduction pathways.
磷酸肌醇(PhoIns)特异性磷脂酶C(PLCs)是肌醇脂质信号通路的核心,有助于细胞内Ca2+释放和蛋白激酶C激活。已知哺乳动物中存在五种不同类型的PhoIns特异性PLCs,它们由膜受体介导的事件激活。在此,我们鉴定出了具有新型结构域结构的第六类PhoIns特异性PLC,我们将其命名为PLC-η。在人和小鼠中鉴定出了两种推定的PLC-η酶。序列分析表明,与其他PhoIns特异性PLCs中参与底物结合和催化的残基在这些新型酶中是保守的。PLC-η酶与PLC-δ类关系最为密切,与其他PLC同工酶有着密切的进化关系。EST分析和RT-PCR数据表明,PLC-η酶在多种细胞类型中表达,并且与其他哺乳动物PhoIns特异性PLCs类似,可能参与信号转导通路。