TY - JOUR
T1 - GPR56, a novel secretin-like human G-protein-coupled receptor gene
AU - Liu, Marjorie
AU - Parker, Rachel M.C.
AU - Darby, Karen
AU - Eyre, Helen J.
AU - Copeland, Neal G.
AU - Crawford, Joanna
AU - Gilbert, Debra J.
AU - Sutherland, Grant R.
AU - Jenkins, Nancy A.
AU - Herzog, Herbert
N1 - Funding Information:
We thank Andreé Reuss for excellent technical assistance. This research was supported by Bristol-Myers Squibb, the J. H. and J. D. Gunn Medical Research Foundation, the National Health and Medical Research Council of Australia, and in part, by the National Cancer Institute, DHHS, under contract with ABL.
Copyright:
Copyright 2017 Elsevier B.V., All rights reserved.
PY - 1999/2/1
Y1 - 1999/2/1
N2 - A novel gene product, GPR56, with homology to the seven transmembrane- domain receptor superfamily, has been cloned by PCR amplification using degenerate oligonucleotide primers and subsequent screening of a human heart cDNA library. The isolated 2.8-kb cDNA clone encodes a protein of 693 amino acids that shows highest identity (32%) to HE6, a member of a subclass of the class B secretin-like G-protein-coupled receptors. Northern analysis of various human tissues revealed a wide distribution of the transcript with highest levels found in thyroid gland, brain, and heart. In situ hybridization analysis of human thyroid gland as well as rat heart and brain tissue confirms these results and identifies the hippocampus and hypothalamic nuclei as brain areas with particularly high expression of GPR56 mRNA. The high level of mRNA expression, its wide distribution, and the mucin-like extracellular domain of the receptor protein suggest a possible role for this receptor in cell-cell interaction processes. The human gene for GPR56 has been isolated and its exon-intron structure determined. The total length of the human GPR56 gene is approximately 15 kb, and it consists of 13 exons. Fluorescence in situ hybridization, PCR analysis of somatic cell hybrids, and interspecific mouse backcross mapping have localized the genes to human chromosome 16q13 and mouse chromosome 8.
AB - A novel gene product, GPR56, with homology to the seven transmembrane- domain receptor superfamily, has been cloned by PCR amplification using degenerate oligonucleotide primers and subsequent screening of a human heart cDNA library. The isolated 2.8-kb cDNA clone encodes a protein of 693 amino acids that shows highest identity (32%) to HE6, a member of a subclass of the class B secretin-like G-protein-coupled receptors. Northern analysis of various human tissues revealed a wide distribution of the transcript with highest levels found in thyroid gland, brain, and heart. In situ hybridization analysis of human thyroid gland as well as rat heart and brain tissue confirms these results and identifies the hippocampus and hypothalamic nuclei as brain areas with particularly high expression of GPR56 mRNA. The high level of mRNA expression, its wide distribution, and the mucin-like extracellular domain of the receptor protein suggest a possible role for this receptor in cell-cell interaction processes. The human gene for GPR56 has been isolated and its exon-intron structure determined. The total length of the human GPR56 gene is approximately 15 kb, and it consists of 13 exons. Fluorescence in situ hybridization, PCR analysis of somatic cell hybrids, and interspecific mouse backcross mapping have localized the genes to human chromosome 16q13 and mouse chromosome 8.
UR - http://www.scopus.com/inward/record.url?scp=0033082960&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=0033082960&partnerID=8YFLogxK
U2 - 10.1006/geno.1998.5644
DO - 10.1006/geno.1998.5644
M3 - Article
C2 - 10049584
AN - SCOPUS:0033082960
SN - 0888-7543
VL - 55
SP - 296
EP - 305
JO - Genomics
JF - Genomics
IS - 3
ER -