Xu X Z, Chien F, Butler A, Salkoff L, Montell C
Department of Biological Chemistry and Neuroscience, The Johns Hopkins University School of Medicine, Baltimore, Maryland 21205, USA.
Neuron. 2000 Jun;26(3):647-57. doi: 10.1016/s0896-6273(00)81201-5.
TRP and TRPL are two light-sensitive cation channel subunits required for the Drosophila photoresponse; however, our understanding of the identities, subunit composition, and function of the light-responsive channels is incomplete. To explain the residual photoresponse that remains in the trp mutant, a third TRP-related subunit has previously been proposed to function with TRPL. Here, we identify such a subunit, TRPgamma. We show that TRPgamma is highly enriched in photoreceptor cells and preferentially heteromultimerizes with TRPL in vitro and in vivo. The N-terminal domain of TRPgamma dominantly suppressed the TRPL-dependent photoresponse, indicating that TRPgamma-TRPL heteromultimers contribute to the photoresponse. While TRPL and TRPgamma homomultimers are constitutively active, we demonstrate that TRPL-TRPgamma heteromultimers form a regulated phospholipase C- (PLC-) stimulated channel.
TRP和TRPL是果蝇光反应所需的两个光敏感阳离子通道亚基;然而,我们对光反应通道的特性、亚基组成和功能的了解并不完整。为了解释trp突变体中残留的光反应,先前有人提出第三个与TRP相关的亚基与TRPL共同发挥作用。在这里,我们鉴定出了这样一个亚基,即TRPγ。我们发现TRPγ在光感受器细胞中高度富集,并且在体外和体内优先与TRPL形成异源多聚体。TRPγ的N端结构域显著抑制了依赖TRPL的光反应,表明TRPγ-TRPL异源多聚体参与了光反应。虽然TRPL和TRPγ同源多聚体具有组成性活性,但我们证明TRPL-TRPγ异源多聚体形成了一种受调节的磷脂酶C(PLC)刺激通道。