Quintana Ariel, Rajanikanth Vangipurapu, Farber-Katz Suzette, Gudlur Aparna, Zhang Chen, Jing Ji, Zhou Yubin, Rao Anjana, Hogan Patrick G
Division of Signalling and Gene Expression, La Jolla Institute for Allergy and Immunology, La Jolla, CA 92037;
Center for Translational Cancer Research, Institute of Biosciences and Technology, Texas A&M University Health Science Center, Houston, TX 77030;
Proc Natl Acad Sci U S A. 2015 Dec 22;112(51):E7083-92. doi: 10.1073/pnas.1521924112. Epub 2015 Dec 7.
The stromal interaction molecule (STIM)-ORAI calcium release-activated calcium modulator (ORAI) pathway controls store-dependent calcium entry, a major mechanism of physiological calcium signaling in mammalian cells. The core elements of the pathway are the regulatory protein STIM1, located in the endoplasmic reticulum (ER) membrane, the calcium channel ORAI1 in the plasma membrane, and sites of close contact between the ER and the plasma membrane that permit the two proteins to interact. Research on calcium signaling has centered on STIM1, ORAI1, and a few proteins that directly modulate STIM-ORAI function. However, little is known about proteins that organize ER-plasma membrane junctions for STIM-ORAI-dependent calcium signaling. Here, we report that an ER-resident membrane protein identified in a previous genome-wide RNAi screen, transmembrane protein 110 (TMEM110), regulates the long-term maintenance of ER-plasma membrane junctions and the short-term physiological remodeling of the junctions during store-dependent calcium signaling.
基质相互作用分子(STIM)-钙释放激活钙调蛋白(ORAI)途径控制储存依赖性钙内流,这是哺乳动物细胞中生理钙信号传导的主要机制。该途径的核心元件包括位于内质网(ER)膜上的调节蛋白STIM1、质膜中的钙通道ORAI1以及ER与质膜之间紧密接触的位点,这些位点允许这两种蛋白质相互作用。钙信号传导的研究主要集中在STIM1、ORAI1以及一些直接调节STIM-ORAI功能的蛋白质上。然而,对于为STIM-ORAI依赖性钙信号传导组织ER-质膜连接的蛋白质知之甚少。在这里,我们报告称,在先前全基因组RNA干扰筛选中鉴定出的一种内质网驻留膜蛋白,即跨膜蛋白110(TMEM110),在储存依赖性钙信号传导过程中调节ER-质膜连接的长期维持以及连接的短期生理重塑。