A lack of genetic linkage of renin gene restriction fragment length polymorphisms with human hypertension.
- 1 December 1989
- journal article
- research article
- Published by Wolters Kluwer Health in Hypertension
- Vol. 14 (6) , 614-618
- https://doi.org/10.1161/01.hyp.14.6.614
Abstract
Because renin is an important enzyme in blood pressure regulation, we studied the possibility that an alteration in the structure of the human renin gene is genetically linked to human essential hypertension or associated with levels of plasma renin activity or blood pressure. By using specific DNA probes, we have identified four polymorphisms in the human renin gene with the restriction enzymes Taq I, HindIII, Bgl I, and Bgl II. The gene location of all of these polymorphisms except for the Bgl II polymorphism has been determined, and their frequencies were initially estimated in a population of 50 random subjects. To test the clinical significance of these polymorphisms, we studied 68 persons from a large Utah pedigree with a high incidence of hypertension. Among nine relatives with hypertension, genetic linkage without recombination was ruled out by observing several obligate recombinants. We also found no significant association of the restriction fragment length polymorphisms with quantitative measur...This publication has 22 references indexed in Scilit:
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