MOLECULAR-CLONING OF THE MURINE SUBSTANCE-K AND SUBSTANCE-P RECEPTOR GENES

被引:44
|
作者
SUNDELIN, JB
PROVVEDINI, DM
WAHLESTEDT, CR
LAURELL, H
POHL, JS
PETERSON, PA
机构
[1] Scripps Res Inst, RES INST, DEPT IMMUNOL, LA JOLLA, CA 92037 USA
[2] CORNELL UNIV, MED CTR, COLL MED, DIV NEUROL, NEW YORK, NY 10021 USA
来源
EUROPEAN JOURNAL OF BIOCHEMISTRY | 1992年 / 203卷 / 03期
关键词
D O I
10.1111/j.1432-1033.1992.tb16592.x
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The peptides substance K and substance P evoke a variety of biological responses via distinct, guanosine-nucleotide-binding-regulatory-protein-coupled receptors. We have screened a murine genomic cosmid library using oligonucleotide probes and have isolated, cloned and characterized the substance K receptor and the substance P receptor genes. The coding portion of the substance K receptor gene consists of five exons distributed over 13 kbp. The substance P receptor gene is considerably larger than that of substance K (more than 30 kbp), however, the bundaries of the four exons that have been characterized in the substance P receptor gene correspond exactly to the homologous exons in the substance K receptor gene. To verify the identity of the isolated genes, we have cloned the corresponding cDNA by means of the polymerase chain reaction and we have expressed these cDNA species in Xenopus laevis oocytes. The ligand binding characteristics determined in this system pharmacologically confirm the identity of the two receptors. The deduced amino acid sequence of the mouse substance K receptor is 94% identical to the rat sequence and 85% identical to the bovine and human sequences. The mouse substance P receptor amino acid sequence is 99% identical to the rat sequence. The cloning of the murine substance K and substance P receptor genes should contribute substantially to the generation of in vivo models for the detailed analysis of the functional significance of these receptors.
引用
收藏
页码:625 / 631
页数:7
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