CLONING AND EXPRESSION OF 3 ISOFORMS OF THE HUMAN EP(3) PROSTANOID RECEPTOR

被引:115
作者
ADAM, M [1 ]
BOIE, Y [1 ]
RUSHMORE, TH [1 ]
MULLER, G [1 ]
BASTIEN, L [1 ]
MCKEE, KT [1 ]
METTERS, KM [1 ]
ABRAMOVITZ, M [1 ]
机构
[1] MERCK FROSST CTR THERAPEUT RES,DEPT BIOCHEM & MOLEC BIOL,POINTE CLAIRE H9R 4P8,PQ,CANADA
关键词
PROSTAGLANDIN E(2); PROSTANOID RECEPTOR; EP(3) CDNA; RECEPTOR BINDING;
D O I
10.1016/0014-5793(94)80358-7
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
Functional cDNA clones coding for three isoforms of the human prostaglandin E receptor EP, subtype have been isolated from kidney and uterus cDNA libraries. The three isoforms, designated hEP(3.I), hEP(3.II), and hEP(3.III), have open reading frames corresponding to 390, 388 and 365 amino acids, respectively. They differ only in the length and amino acid composition of their carboxy-terminal regions, beginning at position 360. The human EP, receptor has seven predicted transmembrane spanning domains and therefore belongs to the G-protein-coupled receptor family. The rank order of potency for prostaglandins and related analogs in competition for [H-3]PGE, specific binding to membranes prepared from transfected COS cells was comparable for all three isoforms, and as predicted for the EP(3) receptor, with PGE(2) = PGE(1) >> PGF(2 alpha) = iloprost > PGD(2) >> U44619. In addition, the EP(3)-selective agonist MB28767 was a potent competing ligand with an IC50 value of 0.3 nM, whereas the EP(1)-selective antagonist AH6909 gave IC50 values of 2-7 mu M and the EP(2)-selective agonist butaprost was inactive. In summary, we have cloned three isoforms of the human EP(3) receptor having comparable ligand binding properties.
引用
收藏
页码:170 / 174
页数:5
相关论文
共 18 条
  • [1] ABRAMOVITZ M, 1994, IN PRESS J BIOL CHEM
  • [2] CLONING AND EXPRESSION OF THE EP2 SUBTYPE OF HUMAN RECEPTORS FOR PROSTAGLANDIN-E2
    AN, SZ
    YANG, JH
    XIA, MH
    GOETZL, EJ
    [J]. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1993, 197 (01) : 263 - 270
  • [3] COLEMAN RA, 1989, COMPREHENSIVE MED CH, V3, P643
  • [4] DAVIES P, 1992, INFLAMMATION BASIC P, P123
  • [5] CHARACTERIZATION OF THE LEUKOTRIENE D4 RECEPTOR IN DIMETHYLSULFOXIDE-DIFFERENTIATED-U937 CELLS - COMPARISON WITH THE LEUKOTRIENE-D4 RECEPTOR IN HUMAN LUNG AND GUINEA-PIG LUNG
    FREY, EA
    NICHOLSON, DW
    METTERS, KM
    [J]. EUROPEAN JOURNAL OF PHARMACOLOGY-MOLECULAR PHARMACOLOGY SECTION, 1993, 244 (03): : 239 - 250
  • [6] FUNK CD, 1993, J BIOL CHEM, V268, P26767
  • [7] CLONING AND EXPRESSION OF CDNA FOR A HUMAN THROMBOXANE-A2 RECEPTOR
    HIRATA, M
    HAYASHI, Y
    USHIKUBI, F
    YOKOTA, Y
    KAGEYAMA, R
    NAKANISHI, S
    NARUMIYA, S
    [J]. NATURE, 1991, 349 (6310) : 617 - 620
  • [8] HONDA A, 1993, J BIOL CHEM, V268, P7759
  • [9] 3RD ISOFORM OF THE PROSTAGLANDIN-E-RECEPTOR EP3 SUBTYPE WITH DIFFERENT C-TERMINAL TAIL COUPLING TO BOTH STIMULATION AND INHIBITION OF ADENYLATE-CYCLASE
    IRIE, A
    SUGIMOTO, Y
    NAMBA, T
    HARAZONO, A
    HONDA, A
    WATABE, A
    NEGISHI, M
    NARUMIYA, S
    ICHIKAWA, A
    [J]. EUROPEAN JOURNAL OF BIOCHEMISTRY, 1993, 217 (01): : 313 - 318
  • [10] A SIMPLE METHOD FOR DISPLAYING THE HYDROPATHIC CHARACTER OF A PROTEIN
    KYTE, J
    DOOLITTLE, RF
    [J]. JOURNAL OF MOLECULAR BIOLOGY, 1982, 157 (01) : 105 - 132