TY - JOUR
T1 - STIM1 carboxyl-terminus activates native SOC, Icrac and TRPC1 channels
AU - Huang, Guo N.
AU - Zeng, Weizhong
AU - Kim, Joo Young
AU - Yuan, Joseph P.
AU - Han, Linhuang
AU - Muallem, Shmuel
AU - Worley, Paul F.
N1 - Funding Information:
We thank J. Liu (Johns Hopkins University) for the plasmids NFAT1–GFP (HA– mNFAT1(1–460)–GFP), pNFAT-luc, pAP1-luc and pSV40-β-galactosidase; and T. Meyer (Stanford University) for the plasmid YFP–STIM1. Research was supported by grants from the National Institute on Drug Abuse (NIDA; DA00266, DA10309) and the National Institute of Mental Health (NIMH; MH068830) to P.F.W., and the National Institute of Dental and Craniofacial Research (NIDCR) and National Institute of Diabetes, Digestive and Kidney Diseases (NIDDK) to S.M.
PY - 2006/9
Y1 - 2006/9
N2 - Receptor-evoked Ca2+ signalling involves Ca2+ release from the endoplasmic reticulum, followed by Ca2+ influx across the plasma membrane1. Ca2+ influx is essential for many cellular functions, from secretion to transcription, and is mediated by Ca2+-release activated Ca2+ (Icrac) channels and store-operated calcium entry (SOC) channels. Although the molecular identity and regulation of Icrac and SOC channels have not been precisely determined, notable recent findings are the identification of STIM1, which has been indicated to regulate SOC and Icrac channels by functioning as an endoplasmic reticulum Ca2+ sensor3-6), and ORAI1 (ref. 7) or CRACM1 (ref. 8) - both of which may function as Icrac channels or as an Icrac subunit. How STIM1 activates the Ca2+ influx channels and whether STIM1 contributes to the channel pore remains unknown. Here, we identify the structural features that are essential for STIM1-dependent activation of SOC and Icrac channels, and demonstrate that they are identical to those involved in the binding and activation of TRPC1. Notably, the cytosolic carboxyl terminus of STIM1 is sufficient to activate SOC, Icrac and TRPC1 channels even when native STIM1 is depleted by small interfering RNA. Activity of STIM1 requires an ERM domain, which mediates the selective binding of STIM1 to TRPC1, 2 and 4, but not to TRPC3, 6 or 7, and a cationic lysine-rich region, which is essential for gating of TRPC1. Deletion of either region in the constitutively active STIM1D76A yields dominant-negative mutants that block native SOC channels, expressed TRPC1 in HEK293 cells and Icrac in Jurkat cells. These observations implicate STIM1 as a key regulator of activity rather than a channel component, and reveal similar regulation of SOC, Icrac and TRPC channel activation by STIM1.
AB - Receptor-evoked Ca2+ signalling involves Ca2+ release from the endoplasmic reticulum, followed by Ca2+ influx across the plasma membrane1. Ca2+ influx is essential for many cellular functions, from secretion to transcription, and is mediated by Ca2+-release activated Ca2+ (Icrac) channels and store-operated calcium entry (SOC) channels. Although the molecular identity and regulation of Icrac and SOC channels have not been precisely determined, notable recent findings are the identification of STIM1, which has been indicated to regulate SOC and Icrac channels by functioning as an endoplasmic reticulum Ca2+ sensor3-6), and ORAI1 (ref. 7) or CRACM1 (ref. 8) - both of which may function as Icrac channels or as an Icrac subunit. How STIM1 activates the Ca2+ influx channels and whether STIM1 contributes to the channel pore remains unknown. Here, we identify the structural features that are essential for STIM1-dependent activation of SOC and Icrac channels, and demonstrate that they are identical to those involved in the binding and activation of TRPC1. Notably, the cytosolic carboxyl terminus of STIM1 is sufficient to activate SOC, Icrac and TRPC1 channels even when native STIM1 is depleted by small interfering RNA. Activity of STIM1 requires an ERM domain, which mediates the selective binding of STIM1 to TRPC1, 2 and 4, but not to TRPC3, 6 or 7, and a cationic lysine-rich region, which is essential for gating of TRPC1. Deletion of either region in the constitutively active STIM1D76A yields dominant-negative mutants that block native SOC channels, expressed TRPC1 in HEK293 cells and Icrac in Jurkat cells. These observations implicate STIM1 as a key regulator of activity rather than a channel component, and reveal similar regulation of SOC, Icrac and TRPC channel activation by STIM1.
UR - http://www.scopus.com/inward/record.url?scp=33748136477&partnerID=8YFLogxK
U2 - 10.1038/ncb1454
DO - 10.1038/ncb1454
M3 - Article
C2 - 16906149
AN - SCOPUS:33748136477
SN - 1465-7392
VL - 8
SP - 1003
EP - 1010
JO - Nature Cell Biology
JF - Nature Cell Biology
IS - 9
ER -