Spiegel Allen M, Weinstein Lee S
National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, Maryland 20892, USA.
Annu Rev Med. 2004;55:27-39. doi: 10.1146/annurev.med.55.091902.103843.
Heterotrimeric G proteins couple seven-transmembrane receptors for diverse extracellular signals to effectors that generate intracellular signals altering cell function. Mutations in the gene encoding the alpha subunit of the G protein-coupling receptors to stimulation of adenylyl cyclase cause developmental abnormalities of bone, as well as hormone resistance (pseudohypoparathyroidism caused by loss-of-function mutations) and hormone hypersecretion (McCune-Albright syndrome caused by gain-of-function mutations). Loss- and gain-of-function mutations in genes encoding G protein-coupled receptors (GPCRs) have been identified as the cause of an increasing number of retinal, endocrine, metabolic, and developmental disorders. GPCRs comprise an evolutionarily conserved gene superfamily ( 1 ). By coupling to heterotrimeric G proteins, GPCRs transduce a wide variety of extracellular signals including monoamine, amino acid, and nucleoside neurotransmitters, as well as photons, chemical odorants, divalent cations, hormones, lipids, peptides and proteins. Following a brief overview of G protein-coupled signal transduction, we review the growing body of evidence that mutations in genes encoding GPCRs and G proteins are an important cause of human disease.
异源三聚体G蛋白将用于多种细胞外信号的七跨膜受体与效应器偶联,效应器产生改变细胞功能的细胞内信号。编码G蛋白偶联受体α亚基的基因发生突变,导致对腺苷酸环化酶刺激产生反应异常,会引起骨骼发育异常以及激素抵抗(功能丧失性突变导致的假性甲状旁腺功能减退)和激素分泌过多(功能获得性突变导致的McCune-Albright综合征)。已确定编码G蛋白偶联受体(GPCR)的基因中的功能丧失和功能获得性突变是越来越多视网膜、内分泌、代谢和发育障碍的病因。GPCR构成一个进化上保守的基因超家族(1)。通过与异源三聚体G蛋白偶联,GPCR转导多种细胞外信号,包括单胺、氨基酸和核苷神经递质,以及光子、化学气味剂、二价阳离子、激素、脂质、肽和蛋白质。在简要概述G蛋白偶联信号转导之后,我们回顾了越来越多的证据,即编码GPCR和G蛋白的基因中的突变是人类疾病的重要原因。