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Comparative analysis of three murine G-protein coupled receptors activated by sphingosine-1-phosphate
Journal article   Peer reviewed

Comparative analysis of three murine G-protein coupled receptors activated by sphingosine-1-phosphate

Guangfa Zhang, James J.A Contos, Joshua A Weiner, Nobuyuki Fukushima and Jerold Chun
Gene, Vol.227(1), pp.89-99
1999
DOI: 10.1016/S0378-1119(98)00589-7
PMID: 9931453

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Abstract

The cloning and analysis of the first identified lysophosphatidic acid (LPA) receptor gene, lp A1 (also referred to as vzg-1 or edg-2), led us to identify homologous murine genes that might also encode receptors for related lysophospholipid ligands. Three murine genomic clones (designated lp B1, lp B2, and lp B3) were isolated, corresponding to human/rat Edg-1, rat H218/AGR16, and human edg-3, respectively. Based on the amino acid similarities of their predicted proteins (44–52% identical), the three lp B genes could be grouped into a separate G-protein coupled receptor subfamily, distinct from that containing the LPA receptor genes lp A1 and lp A2. Unlike lp A1 and lp A2, which contain multiple coding exons, all lp B members contained a single coding exon. Heterologous expression of individual lp B members in a hepatoma cell line (RH7777), followed by 35S-GTPγS incorporation assays demonstrated that each of the three LP B receptors conferred sphingosine-1-phosphate-dependent, but not lysophosphatidic acid-dependent, G-protein activation. Northern blot and in situ hybridization analyses revealed overlapping as well as distinct expression patterns in both embryonic and adult tissues. This comparative characterization of multiple sphingosine-1-phosphate receptor genes and their spatiotemporal expression patterns will aid in understanding the biological roles of this enlarging lysophospholipid receptor family.
Lysophospholipid edg GPCR Lysophosphatidic acid

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