Zagotta W N, Siegelbaum S A
Department of Physiology and Biophysics, Howard Hughes Medical Institute, University of Washington School of Medicine, Seattle, Washington 98195-7370, USA.
Annu Rev Neurosci. 1996;19:235-63. doi: 10.1146/annurev.ne.19.030196.001315.
Cyclic nucleotide-gated (CNG) channels play important roles in both visual (Yau & Baylor 1989) and olfactory (Zufall et al 1994) signal transduction. The cloning of the gene coding for a rod photoreceptor channel (Kaupp et al 1989) and the subsequent cloning of related genes from olfactory neurons (Dhallan et al 1990, Ludwig et al 1990, Goulding et al 1992) has sparked much progress over the past several years in elucidating the structural bases for the function of the CNG channels. One of the surprising features to emerge from these cloning studies was that the CNG channels are structurally homologous to the voltage-gated channels (Jan & Jan 1990) despite the fact that the CNG channels are gated by the binding of a ligand-cAMP or cGMP-and not by voltage. In this review we focus on recent studies of the relationship between the structure and function of the CNG channels. Given the homology between CNG channels and voltage-gated channels, such studies are likely to provide important general information about the structure and function of a wide variety of channel types.
环核苷酸门控(CNG)通道在视觉(Yau和Baylor,1989年)和嗅觉(Zufall等人,1994年)信号转导中均发挥着重要作用。编码视杆光感受器通道的基因的克隆(Kaupp等人,1989年)以及随后从嗅觉神经元中克隆相关基因(Dhallan等人,1990年;Ludwig等人,1990年;Goulding等人,1992年)在过去几年中引发了在阐明CNG通道功能的结构基础方面的诸多进展。这些克隆研究中出现的一个令人惊讶的特征是,尽管CNG通道是由配体(cAMP或cGMP)结合而非电压门控,但它们在结构上与电压门控通道同源(Jan和Jan,1990年)。在本综述中,我们聚焦于近期关于CNG通道结构与功能关系的研究。鉴于CNG通道与电压门控通道之间的同源性,此类研究可能会提供关于多种通道类型的结构与功能的重要通用信息。