Molecular cloning and functional expression of the alpha 1A-adrenoceptor of Medaka fish, Oryzias latipes

被引:16
作者
Yasuoka, A [1 ]
Abe, K [1 ]
Arai, S [1 ]
Emori, Y [1 ]
机构
[1] UNIV TOKYO,DEPT APPL BIOL CHEM,DIV AGR & AGR LIFE SCI,TOKYO,JAPAN
来源
EUROPEAN JOURNAL OF BIOCHEMISTRY | 1996年 / 235卷 / 03期
关键词
alpha; 1A-adrenoceptor; gene structure; Xenopus oocyte; Ca2+-dependent Cl- current; Oryzias latipes;
D O I
10.1111/j.1432-1033.1996.00501.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
A genomic DNA encoding a subtype adrenoceptor (AR) was cloned from Medaka fish, Oryzias latipes, using an oligonucleotide probe corresponding to the consensus sequence of mammalian alpha-AR and beta-AR. The gene spans at least 9 kbp, and the coding region consists of two exons split by an intron of 7.2 kbp located at the same position as those of mammalian alpha 1B-AR genes. The gene encodes 470 amino acid residues, the sequence of which shows the highest similarity to that of mammalian alpha 1A-AR (61 %) and significant but lower similarities to other alpha-AR and beta-AR proteins (31-45 %), indicating that the gene encodes a Medaka homolog of alpha 1A-AR. To characterize the encoded protein, the mRNA was synthesized in vitro, and injected into Xenopus oocytes. As a result, the oocytes responded to 100 nM epinephrine evoking a Ca2+-dependent Cl- current in the order of microamperes, which was not observed for oocytes injected with water alone. The response was reversibly inhibited by an alpha 1-selective antagonist, WB4101 (2-([2,6-dimethoxyphenoxyethyl]aminomethyl)-1,4-benzodioxane). Similar experiments using several adrenergic agonists revealed that Medaka alpha 1A-AR responds to the following agonists in the order: epinephrine greater than or equal to (-)norepinephrine > oxymetazoline greater than or equal to methoxamine, which is similar to the responses of rat alpha 1A receptor expressed in COS cells. The results indicate that fish contains adrenoceptor systems similar to those of mammals in terms of primary structure and pharmacological properties.
引用
收藏
页码:501 / 507
页数:7
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