Key result
Introgressing Lewis QTL alleles on chromosomes 1, 5, and 10 lowers blood pressure in Dahl S rats.
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An F2 population (n = 151) derived from Dahl salt-sensitive (S) and Lewis rats was raised on a 8% NaCl diet for 9 weeks and analyzed for blood pressure quantitative trait loci (QTL) by use of a whole genome scan. Chromosomes 5 and 10 yielded lod scores for linkage to blood pressure that were significant; chromosomes 1, 2, 3, 8, 16, 17, and 18 gave lod scores suggestive for linkage. Chromosome 7 gave a significant signal for heart weight with a lesser effect on blood pressure. Congenic strains were constructed by introgressing Lewis low-blood-pressure QTL alleles for chromosomes 1, 5, 10, and 17 into the S genetic background. Congenic strains for chromosomes 1, 5, and 10 had significantly lower blood pressure than S, proving the existence of QTL on these chromosomes, but the chromosome 17 congenic strain failed to trap a contrasting QTL allele. The QTL allele increasing blood pressure originated from S rats for all QTL except those on chromosomes 2 and 7 in which the Lewis allele increased blood pressure. Interactions between each QTL and every other locus in the genome scan yielded significant interactions between chromosomes 10 and 4, and between chromosomes 2 and 3.
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Garrett et al. (1998) studied Blood pressure quantitative trait loci (n=151). Congenic strains with introgressed Lewis low-blood-pressure QTL alleles (chromosomes 1, 5, 10, and 17) vs. Dahl salt-sensitive (S) genetic background was evaluated on Blood pressure quantitative trait loci (QTL) and blood pressure levels. Congenic strains with introgressed Lewis QTL alleles for chromosomes 1, 5, and 10 had significantly lower blood pressure than Dahl S rats, confirming QTL existence on these chromosomes.
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