TY - JOUR
T1 - Identification, chromosomal location, and genome organization of mammalian g-protein-coupled receptors
AU - Wilkie, Thomas M.
AU - Chen, Yan
AU - Gilbert, Debra J.
AU - Moore, Karen J.
AU - Yu, Lei
AU - Simon, Melvin I.
AU - Copeland, Neal G.
AU - Jenkins, Nancy A.
N1 - Copyright:
Copyright 2017 Elsevier B.V., All rights reserved.
PY - 1993/11
Y1 - 1993/11
N2 - Vertebrate G-protein-coupled receptors are encoded by a diverse multigene family. Thirteen distinct G-protein-coupled receptors (Gpcr) were cloned from mouse germline cDNA following amplification in the polymerase chain reaction (PCR) with degenerate oligonucleotide primers complementary to the third and sixth transmembrane domains. Eleven Gpcr clones were mapped to single sites in the mouse genome following interspecific backcross analysis. One clone was mapped to two sites and another was not polymorphic in the cross and could not be mapped. Gpcr loci were well dispersed throughout the mouse genome and mapped to chromosomes 1, 2, 3, 4, 5, 8, 9, 10, 13, 17, and 18. Six Gpcr clones likely represent mouse homologs of already identified receptors, one Gpcr clone may identify a third type of IL-8 receptor, and three Gpcr clones appear to encode novel G-protein-coupled receptors. Further, three factor crosses and Southern blot analyses demonstrated that Gpcr 16 maps proximally within the Sp deletion on mouse chromosome 1, near the Vil and Beg loci. Human chromosomal locations for most Gpcr loci could be predicted based on linkage homologies that have been identified between human and mouse. Mapping additional G-protein-coupled receptors against the panel of murine interspecific backcrosses should expand our understanding of mammalian Gpcr gene evolution and genome organization.
AB - Vertebrate G-protein-coupled receptors are encoded by a diverse multigene family. Thirteen distinct G-protein-coupled receptors (Gpcr) were cloned from mouse germline cDNA following amplification in the polymerase chain reaction (PCR) with degenerate oligonucleotide primers complementary to the third and sixth transmembrane domains. Eleven Gpcr clones were mapped to single sites in the mouse genome following interspecific backcross analysis. One clone was mapped to two sites and another was not polymorphic in the cross and could not be mapped. Gpcr loci were well dispersed throughout the mouse genome and mapped to chromosomes 1, 2, 3, 4, 5, 8, 9, 10, 13, 17, and 18. Six Gpcr clones likely represent mouse homologs of already identified receptors, one Gpcr clone may identify a third type of IL-8 receptor, and three Gpcr clones appear to encode novel G-protein-coupled receptors. Further, three factor crosses and Southern blot analyses demonstrated that Gpcr 16 maps proximally within the Sp deletion on mouse chromosome 1, near the Vil and Beg loci. Human chromosomal locations for most Gpcr loci could be predicted based on linkage homologies that have been identified between human and mouse. Mapping additional G-protein-coupled receptors against the panel of murine interspecific backcrosses should expand our understanding of mammalian Gpcr gene evolution and genome organization.
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U2 - 10.1006/geno.1993.1452
DO - 10.1006/geno.1993.1452
M3 - Article
C2 - 8288218
AN - SCOPUS:0027440482
SN - 0888-7543
VL - 18
SP - 175
EP - 184
JO - Genomics
JF - Genomics
IS - 2
ER -