z-logo
open-access-imgOpen Access
Genetic Analysis of Rat Chromosome 1 and the Sa Gene in Spontaneous Hypertension
Author(s) -
Elizabeth St. Lezin,
Weizhong Liu,
Jiaming Wang,
Ying Yang,
Nianning Qi,
Vladimı́r Křen,
Václav Zı́dek,
Theodore W. Kurtz,
Michal Pravenec
Publication year - 2000
Publication title -
hypertension
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.986
H-Index - 265
eISSN - 1524-4563
pISSN - 0194-911X
DOI - 10.1161/01.hyp.35.1.225
Subject(s) - congenic , locus (genetics) , spontaneously hypertensive rat , chromosome 4 , chromosome , genetics , biology , gene , quantitative trait locus , candidate gene , chromosome 3 , chromosome 15 , chromosome 18 , genetic linkage , gene map , chromosome regions , chromosome 16 , blood pressure , chromosome 12 , chromosome 17 (human) , gene mapping , endocrinology
Linkage studies in segregating populations derived from the spontaneously hypertensive rat (SHR) indicate that a blood pressure quantitative trait locus exists on rat chromosome 1 in the vicinity of the Sa gene. On the basis of these findings and the observation of increased renal expression of the Sa gene in SHR versus normotensive rats, the Sa gene has been proposed as a candidate gene for spontaneous hypertension. In SHR congenic strains, we and others have found that replacement of a segment of SHR chromosome 1 that contains the Sa gene with the corresponding chromosome segment from a normotensive Brown Norway (BN) rat or Wistar-Kyoto rat can reduce blood pressure. To test whether the Sa gene is necessary for the effect of this region of chromosome 1 on blood pressure, we studied a new SHR congenic subline that harbors a smaller segment of BN chromosome 1 that does not include the Sa gene. Transfer of this subregion of chromosome 1 from the BN rat onto the SHR background was associated with significant reductions in blood pressure comparable to those previously observed on transfer of a larger region of chromosome 1 that included the Sa gene. Thus, in the SHR-BN model of hypertension, the results of these mapping studies (1) demonstrate that molecular variation in the Sa gene is not required for the effect of this region of chromosome 1 on blood pressure and (2) should direct attention toward other candidate genes within the differential chromosome segment of the new congenic subline.

The content you want is available to Zendy users.

Already have an account? Click here to sign in.
Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom