MAPPING OF THE GENES ENCODING MOUSE THROMBOXANE A(2) RECEPTOR AND PROSTAGLANDIN-E RECEPTOR SUBTYPES EP(2) AND EP(3)

被引:21
作者
TAKETO, M
ROCHELLE, JM
SUGIMOTO, Y
NAMBA, T
HONDA, A
NEGISHI, M
ICHIKAWA, A
NARUMIYA, S
SELDIN, MF
机构
[1] DUKE UNIV,MED CTR,DEPT MED,DURHAM,NC 27710
[2] BANYU TSUKUBA RES INST MERCK,TSUKUBA,IBARAKI 30033,JAPAN
[3] KYOTO UNIV,FAC PHARMACEUT SCI,DEPT PHYSIOL CHEM,KYOTO 606,JAPAN
[4] KYOTO UNIV,FAC MED,DEPT PHARMACOL,KYOTO 606,JAPAN
关键词
D O I
10.1006/geno.1994.1113
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Thromboxane A(2) (TXA(2)) and prostaglandin E(2) (PGE(2)) are two of the most representative eicosanoids that are formed from arachidonic acid. They produce a broad spectrum of biological effects mediated through specific cell surface receptors. We have mapped genetic loci for TXA(2) receptor, Tbxa2r, and for PGE(2) receptor subtypes EP(2) and EP(3), Ptgerep2 and Ptgerep3, respectively, using restriction fragment length variants in interspecific backcross mice. None of the three loci cosegregated with each other. Tbxa2r mapped to Chr 10, Ptgerep2 mapped to the centromeric region of Chr 15, and Ptgerep3 mapped to the distal end of Chr 3. Possible human loci for these receptors are predicted based on the homology between mouse and human chromosomes. (C) 1994 Academic Press, Inc.
引用
收藏
页码:585 / 588
页数:4
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