LINKAGE OF 11-BETA-HYDROXYLASE MUTATIONS WITH ALTERED STEROID-BIOSYNTHESIS AND BLOOD-PRESSURE IN THE DAHL RAT

被引:140
作者
CICILA, GT
RAPP, JP
WANG, JM
STLEZIN, E
NG, SC
KURTZ, TW
机构
[1] UNIV CALIF SAN FRANCISCO,DEPT LAB MED,SAN FRANCISCO,CA 94143
[2] BRISTOL MYERS SQUIBB PHARMACEUT RES INST,DEPT MACROMOLEC BIOCHEM,PRINCETON,NJ 08543
[3] PRINCETON UNIV,DEPT BIOL,PRINCETON,NJ 08544
[4] MED COLL OHIO,DEPT MED,TOLEDO,OH 43699
关键词
D O I
10.1038/ng0493-346
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
In Dahl salt-hypertension sensitive (S) and resistant (R) strains fed a high NaCl diet, 11beta-hydroxylase polymorphisms cosegregate with the adrenal capacity to synthesize 18-hydroxy-11-deoxycorticosterone (18-OH-DOC) and blood pressure. The R rat carries an 11beta-hydroxylase allele that: (i) differs from those of 12 other rat strains; (ii) is associated with a uniquely reduced capacity to synthesize 18-OH-DOC; and (iii) encodes 5 amino acid substitutions in the 11beta-hydroxylase protein. The robust salt-resistance of the Dahl R rat may be due in part to reduced synthesis of the mineralocorticoid 18-OH-DOC stemming from mutations in the 11beta-hydroxylase gene. 11beta-hydroxylase, located on rat chromosome 7, is the first candidate gene identified in an animal model in which coding sequence mutations have been linked to the regulation of blood pressure.
引用
收藏
页码:346 / 353
页数:8
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