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STIM1 carboxyl-terminus activates native SOC, Icrac and TRPC1 channels

Authors
 Guo N. Huang  ;  Weizhong Zeng  ;  Joo Young Kim  ;  Joseph P. Yuan  ;  Linhuang Han  ;  Shmuel Muallem  ;  Paul F. Worley 
Citation
 Nature Cell Biology, Vol.8(9) : 1003-1010, 2006 
Journal Title
 Nature Cell Biology 
ISSN
 1465-7392 
Issue Date
2006
MeSH
Amino Acid Sequence ; Calcium Channels/physiology* ; Calcium Signaling/physiology* ; Cell Line ; Cell Nucleus/metabolism ; Humans ; Ion Channel Gating ; Membrane Proteins/genetics ; Membrane Proteins/physiology* ; Molecular Sequence Data ; Mutation ; Neoplasm Proteins/genetics ; Neoplasm Proteins/physiology* ; Protein Binding ; Protein Transport ; Stromal Interaction Molecule 1 ; TRPC Cation Channels/genetics ; TRPC Cation Channels/physiology*
Abstract
Receptor-evoked Ca2+ signalling involves Ca2+ release from the endoplasmic reticulum, followed by Ca2+ influx across the plasma membrane. Ca2+ influx is essential for many cellular functions, from secretion to transcription, and is mediated by Ca2+-release activated Ca2+ (I(crac)) channels and store-operated calcium entry (SOC) channels. Although the molecular identity and regulation of I(crac) and SOC channels have not been precisely determined, notable recent findings are the identification of STIM1, which has been indicated to regulate SOC and I(crac) channels by functioning as an endoplasmic reticulum Ca2+ sensor, and ORAI1 (ref. 7) or CRACM1 (ref. 8)--both of which may function as I(crac) channels or as an I(crac) 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 I(crac) 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, I(crac) 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 STIM1(D76A) yields dominant-negative mutants that block native SOC channels, expressed TRPC1 in HEK293 cells and I(crac) in Jurkat cells. These observations implicate STIM1 as a key regulator of activity rather than a channel component, and reveal similar regulation of SOC, I(crac) and TRPC channel activation by STIM1.
Full Text
http://www.nature.com/ncb/journal/v8/n9/full/ncb1454.html
DOI
10.1038/ncb1454
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Pharmacology (약리학교실) > 1. Journal Papers
Yonsei Authors
Kim, Joo Young(김주영) ORCID logo https://orcid.org/0000-0003-2623-1491
URI
https://ir.ymlib.yonsei.ac.kr/handle/22282913/111032
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