Dissection of a quantitative trait locus for genetic hypertension on rat chromosome 10.

We have previously identified a locus on rat chromosome 10 as carrying a major hypertension gene, BP/SP-1. The 100:1 odds support interval for this gene extended over a 35-centimorgan (cM) region of the chromosome that included the angiotensin I-converting enzyme (ACE) locus as demonstrated in a cro...

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Main Authors: Kreutz, R, Hübner, N, James, MR, Bihoreau, M, Gauguier, D, Lathrop, G, Ganten, D, Lindpaintner, K
Format: Journal article
Language:English
Published: 1995
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author Kreutz, R
Hübner, N
James, MR
Bihoreau, M
Gauguier, D
Lathrop, G
Ganten, D
Lindpaintner, K
author_facet Kreutz, R
Hübner, N
James, MR
Bihoreau, M
Gauguier, D
Lathrop, G
Ganten, D
Lindpaintner, K
author_sort Kreutz, R
collection OXFORD
description We have previously identified a locus on rat chromosome 10 as carrying a major hypertension gene, BP/SP-1. The 100:1 odds support interval for this gene extended over a 35-centimorgan (cM) region of the chromosome that included the angiotensin I-converting enzyme (ACE) locus as demonstrated in a cross between the stroke-prone spontaneously hypertensive rat (SHRSPHD) and the normotensive Wistar-Kyoto (WKY-0HD) rat. Here we report on the further characterization of BP/SP-1, using a congenic strain, WKY-1HD. WKY-1HD animals carry a 6-cM chromosomal fragment genotypically identical with SHRSPHD on chromosome 10, 26 cM away from the ACE locus. Higher blood pressures in the WKY-1HD strain compared with the WKY-0HD strain, as well as absence of linkage of the chromosome 10 region to blood pressure in an F2 (WKY-1HD x SHRSPHD) population suggested the existence of a quantitative trait locus, termed BP/SP-1a, that lies within the SHRSP-congenic region in WKY-1HD. Linkage analysis in the F2 (WKY-0HD x SHRSPHD) cross revealed that BP/SP-1a is linked to basal blood pressure, whereas a second locus on chromosome 10, termed BP/SP-1b, that maps closer to the ACE locus cosegregates predominantly with blood pressure after exposure to excess dietary NaCl. Thus, we hypothesize that the previously reported effect of BP/SP-1 represents a composite phenotype that can be dissected into at least two specific components on the basis of linkage data and congenic experimentation. One of the loci identified, BP/SP-1a, represents the most precisely mapped locus affecting blood pressure that has so far been characterized by random-marker genome screening.
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spelling oxford-uuid:e92724ae-b655-448b-8447-5e6119e3694d2022-03-27T10:52:10ZDissection of a quantitative trait locus for genetic hypertension on rat chromosome 10.Journal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:e92724ae-b655-448b-8447-5e6119e3694dEnglishSymplectic Elements at Oxford1995Kreutz, RHübner, NJames, MRBihoreau, MGauguier, DLathrop, GGanten, DLindpaintner, KWe have previously identified a locus on rat chromosome 10 as carrying a major hypertension gene, BP/SP-1. The 100:1 odds support interval for this gene extended over a 35-centimorgan (cM) region of the chromosome that included the angiotensin I-converting enzyme (ACE) locus as demonstrated in a cross between the stroke-prone spontaneously hypertensive rat (SHRSPHD) and the normotensive Wistar-Kyoto (WKY-0HD) rat. Here we report on the further characterization of BP/SP-1, using a congenic strain, WKY-1HD. WKY-1HD animals carry a 6-cM chromosomal fragment genotypically identical with SHRSPHD on chromosome 10, 26 cM away from the ACE locus. Higher blood pressures in the WKY-1HD strain compared with the WKY-0HD strain, as well as absence of linkage of the chromosome 10 region to blood pressure in an F2 (WKY-1HD x SHRSPHD) population suggested the existence of a quantitative trait locus, termed BP/SP-1a, that lies within the SHRSP-congenic region in WKY-1HD. Linkage analysis in the F2 (WKY-0HD x SHRSPHD) cross revealed that BP/SP-1a is linked to basal blood pressure, whereas a second locus on chromosome 10, termed BP/SP-1b, that maps closer to the ACE locus cosegregates predominantly with blood pressure after exposure to excess dietary NaCl. Thus, we hypothesize that the previously reported effect of BP/SP-1 represents a composite phenotype that can be dissected into at least two specific components on the basis of linkage data and congenic experimentation. One of the loci identified, BP/SP-1a, represents the most precisely mapped locus affecting blood pressure that has so far been characterized by random-marker genome screening.
spellingShingle Kreutz, R
Hübner, N
James, MR
Bihoreau, M
Gauguier, D
Lathrop, G
Ganten, D
Lindpaintner, K
Dissection of a quantitative trait locus for genetic hypertension on rat chromosome 10.
title Dissection of a quantitative trait locus for genetic hypertension on rat chromosome 10.
title_full Dissection of a quantitative trait locus for genetic hypertension on rat chromosome 10.
title_fullStr Dissection of a quantitative trait locus for genetic hypertension on rat chromosome 10.
title_full_unstemmed Dissection of a quantitative trait locus for genetic hypertension on rat chromosome 10.
title_short Dissection of a quantitative trait locus for genetic hypertension on rat chromosome 10.
title_sort dissection of a quantitative trait locus for genetic hypertension on rat chromosome 10
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