THE MOLECULAR EVOLUTION OF G-PROTEIN-COUPLED RECEPTORS - FOCUS ON 5-HYDROXYTRYPTAMINE RECEPTORS

被引:130
作者
PEROUTKA, SJ
HOWELL, TA
机构
[1] Palo Alto Institute for Molecular Medicine, Hillsborough, CA 94010
关键词
5-HYDROXYTRYPTAMINE RECEPTORS; EVOLUTION; G-PROTEIN COUPLED; MOLECULAR EVOLUTION ANALYSIS;
D O I
10.1016/0028-3908(94)90060-4
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Phylogenetic comparisons between homologous proteins can provide information on the rates of molecular evolution of the proteins. G protein-coupled receptors are a ''superfamily'' of proteins which exist in species ranging from yeast to man. Based on an analysis of the percentage of amino acid homology between various species, the rate of molecular evolution of G protein-coupled receptors can be estimated at approx 1% per 10 million years. Based on this assumption, the primordial 5-HT receptor must have evolved more than 700-800 million years ago since the 3 major classes of G protein-coupled 5-HT receptors (i.e. 5-HT1, 5-HT2 and 5-HT6 receptors) are less than 25% homologous. 5-HT5, 5-HT7, 5-HTsnail, 5-HTdro, and 5-HT1A receptors differentiated approx 600-700 million years ago, the time period during which vertebrates diverged from invertebrates. The mammalian 5-HT receptor subtypes have differentiated over the past 90 million years. Thus, although a recent flurry of ''new'' 5-HT receptors have appeared in the literature, the first ''primordial'' 5-HT receptor evolved over 750 million years ago, a date which likely predates the evolution of muscarinic, dopaminergic and adrenergic receptor systems. This analysis also predicts that a significant number of both mammalian and invertebrate G protein-coupled 5-HT receptor subtypes remain to be identified.
引用
收藏
页码:319 / 324
页数:6
相关论文
共 18 条
[1]  
[Anonymous], 1990, INVERTEBRATES
[2]  
COLBERT EH, 1991, EVOLUTION VERTEBRATE, V4
[3]  
Doolittle R., 1990, METHOD ENZYMOL, V183, P303
[4]   2 MEMBERS OF A DISTINCT SUBFAMILY OF 5-HYDROXYTRYPTAMINE RECEPTORS DIFFERENTIALLY EXPRESSED IN RAT-BRAIN [J].
ERLANDER, MG ;
LOVENBERG, TW ;
BARON, BM ;
DELECEA, L ;
DANIELSON, PE ;
RACKE, M ;
SLONE, AL ;
SIEGEL, BW ;
FOYE, PE ;
CANNON, K ;
BURNS, JE ;
SUTCLIFFE, JG .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (08) :3452-3456
[5]  
GUAN X, 1994, HDB RECEPTORS CHANNE, V1, P299
[6]  
KRAUSE JE, 1994, HDB RECEPTORS CHANNE, V1, P277
[7]  
MATTHES H, 1993, MOL PHARMACOL, V43, P313
[8]   AN ALU SEQUENCE INTERRUPTS A HUMAN 5-HYDROXYTRYPTAMINE(1D) RECEPTOR PSEUDOGENE [J].
NGUYEN, T ;
MARCHESE, A ;
KENNEDY, JL ;
PETRONIS, A ;
PEROUTKA, SJ ;
WU, PH ;
ODOWD, BF .
GENE, 1993, 124 (02) :295-301
[9]  
PEROUTKA SJ, 1994, HBK REC CH, V1, P209
[10]  
PEROUTKA SJ, 1994, HDB RECEPTORS CHANNE, V1