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Physiol. Genomics 21: 112-116, 2005. First published January 4, 2005; doi:10.1152/physiolgenomics.00275.2004
1094-8341/05 $8.00
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Received 18 November 2004; accepted in final form 18 December 2004.
Physiological Genomics 21:112-116 (2005)
1094-8341/05 $8.00 © 2005 American Physiological Society

Complete and overlapping congenics proving the existence of a quantitative trait locus for blood pressure on Dahl rat chromosome 17

Myrian Grondin 1, Vasiliki Eliopoulos 1, Raphaelle Lambert 1, Yishu Deng 2, Anita Ariyarajah 1, Myriam Moujahidine 1, Julie Dutil 1, Sophie Charron 1 and Alan Y. Deng 1

1 Research Centre, Centre Hospitalier de l’Universite de Montréal (CHUM), Montréal, Québec, Canada
2 Number Three People’s Hospital of Yunnan, Kunming, Yunnan, China

Linkage studies suggested that a quantitative trait locus (QTL) for blood pressure (BP) was present in a region on chromosome 17 (Chr 17) of Dahl salt-sensitive (DSS) rats. A subsequent congenic strain targeting this QTL, however, could not confirm it. These conflicting results called into question the validity of localization of a QTL by linkage followed by the use of a congenic strain made with an incomplete chromosome coverage. To resolve this issue, we constructed five new congenic strains, designated C17S.L1 to C17S.L5, that completely spanned the ±2 LOD confidence interval supposedly containing the QTL. Each congenic strain was made by replacing a segment of the DSS rat by that of the normotensive Lewis (LEW) rat. The only section to be LL homozygous is the region on Chr 17 specified in a congenic strain, as evidenced by a total genome scan. The results showed that BPs of C17S.L1 and C17S.L2 were lower (P < 0.04) than that of DSS rats. In contrast, BPs of C17S.L3, C17S.L4, and C17S.L5 were not different (P > 0.6) from that of DSS rats. Consequently, a BP QTL must be located in an interval of ~15 cM shared between C17S.L1 and C17S.L2 and unique to them both, as opposed to C17S.L3, C17S.L4, and C17S.L5. The present study illustrates the importance of thorough chromosome coverage, the necessity for a genome-wide screening, and the use of "negative" controls in physically mapping a QTL by congenic strains.

Dahl salt-sensitive rat; normotensive Lewis rat; congenic strain; congenic substrain




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