Department of Molecular, Cellular, and Developmental Biology and the Neuroscience Research Institute, University of California, Santa Barbara, California 93106.
Department of Molecular, Cellular, and Developmental Biology and the Neuroscience Research Institute, University of California, Santa Barbara, California 93106
Genetics. 2020 Jul;215(3):713-728. doi: 10.1534/genetics.120.303268. Epub 2020 May 20.
TRP channels function in many types of sensory receptor cells. Despite extensive analyses, an open question is whether there exists a family of auxiliary subunits, which could influence localization, trafficking, and function of TRP channels. Here, using , we reveal a previously unknown TRP interacting protein, INAF-C, which is expressed exclusively in the ultraviolet-sensing R7 photoreceptor cells. INAF-C is encoded by an unusual locus comprised of four distinct coding regions, which give rise to four unique single-transmembrane-containing proteins. With the exception of INAF-B, roles for the other INAF proteins were unknown. We found that both INAF-B and INAF-C are required for TRP stability and localization in R7 cells. Conversely, loss of just INAF-B greatly reduced TRP from other types of photoreceptor cells, but not R7. The requirements for TRP and INAF are reciprocal, since loss of TRP decreased the concentrations of both INAF-B and INAF-C. INAF-A, which is not normally expressed in photoreceptor cells, can functionally substitute for INAF-B, indicating that it is a third TRP auxiliary protein. Reminiscent of the structural requirements between K channels and KCNE auxiliary subunits, the codependencies of TRP and INAF depended on several transmembrane domains (TMDs) in TRP, and the TMD and the C-terminus of INAF-B. Our studies support a model in which the locus encodes a family of at least three TRP auxiliary subunits.
TRP 通道在多种感觉受体细胞中发挥作用。尽管进行了广泛的分析,但仍有一个悬而未决的问题,即是否存在一类辅助亚基,它们可以影响 TRP 通道的定位、运输和功能。在这里,我们使用 ,揭示了一个以前未知的与 TRP 相互作用的蛋白 INAF-C,它只在紫外线感应的 R7 光感受器细胞中表达。INAFC 由一个不寻常的基因座编码,该基因座由四个不同的编码区组成,产生四个独特的单跨膜含蛋白。除了 INAF-B 之外,其他 INAF 蛋白的作用是未知的。我们发现,INAF-B 和 INAF-C 都需要 TRP 在 R7 细胞中的稳定性和定位。相反,仅缺失 INAF-B 就会大大减少其他类型光感受器细胞中的 TRP,但不会减少 R7 细胞中的 TRP。TRP 和 INAF 的需求是相互的,因为 TRP 的缺失降低了 INAF-B 和 INAF-C 的浓度。通常不在光感受器细胞中表达的 INAF-A 可以功能性地替代 INAF-B,表明它是第三种 TRP 辅助蛋白。类似于 K 通道和 KCNE 辅助亚基之间的结构要求,TRP 和 INAF 的相互依赖取决于 TRP 中的几个跨膜结构域(TMDs),以及 INAF-B 的 TMD 和 C 末端。我们的研究支持这样一种模型,即 基因座编码至少三种 TRP 辅助亚基家族。