期刊
FEBS LETTERS
卷 584, 期 22, 页码 4570-4574出版社
ELSEVIER SCIENCE BV
DOI: 10.1016/j.febslet.2010.10.052
关键词
G-protein coupled receptor; Regulator of G-protein signaling 4; Proteasome degradation; Palmitoylation; DHHC acyltransferases; alpha(1A)-Adrenergic receptor
资金
- National Institute of Health [R011CA125661]
- Nebraska State
- National Basic Research Program of China [2004CB720000]
- National Natural Science Foundation of China [30900246]
Regulator of G-protein signaling 4 (RGS4), an intracellular modulator of G-protein coupled receptor (GPCR)-mediated signaling, is regulated by multiple processes including palmitoylation and proteasome degradation. We found that co-expression of DHHC acyltransferases (DHHC3 or DHHC7), but not their acyltransferase-inactive mutants, increased expression levels of RGS4 but not its Cys2 to Ser mutant (RGS4C2S). DHHC3 interacts with and palmitoylates RGS4 but not RGS4C2S in vivo. Palmitoylation prolongs the half-life of RGS4 by over 8-fold and palmitoylated RGS4 blocked alpha(1A)-adrenergic receptor-stimulated intracellular Ca(2+) mobilization. Together, our findings revealed that DHHC proteins could regulate GPCR-mediated signaling by increasing RGS4 stability. Structured summary: MINT-8049215: Rgs4 (uniprotkb:P49799) physically interacts (MI:0915) with DHHC3 (uniprotkb:Q8R173) by anti-tag coimmunoprecipitation (MI: 0007) (C) 2010 Federation of European Biochemical Societies. Published by Elsevier B. V. All rights reserved.
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