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Physiol. Genomics 22: 70-75, 2005. First published April 12, 2005; doi:10.1152/physiolgenomics.00019.2005
1094-8341/05 $8.00
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Received 21 January 2005; accepted in final form 6 April 2005.
Physiological Genomics 22:70-75 (2005)
1094-8341/05 $8.00 © 2005 American Physiological Society

Severe hypertension caused by alleles from normotensive Lewis for a quantitative trait locus on chromosome 2

Vasiliki Eliopoulos 1, Julie Dutil 1, Yishu Deng 2, Myrian Grondin 1 and Alan Y. Deng 1

1 Research Centre-Centre Hospitalier de l'Université de Montréal (CHUM), Hôtel Dieu, Montreal, Quebec, Canada
2 Third People's Hospital of Yunann, Kunming, Yunnan, China

Pursuing fully a suggestion from linkage analysis that there might be a quantitative trait locus (QTL) for blood pressure (BP) in a chromosome (Chr) 2 region of the Dahl salt-sensitive rat (DSS), four congenic strains were made by replacing various fragments of DSS Chr 2 with those of Lewis (LEW). Consequently, a BP QTL was localized to a segment of around 3 cM or near 3 Mb on Chr 2 by comparative congenics. The BP-augmenting alleles of this QTL originated from the LEW rat, a normotensive strain compared with DSS. The dissection of a QTL with such a paradoxical effect illustrated the power of congenics in unearthing a gene hidden in the context of the whole animal system, presumably by interactions with other genes. The locus for the angiotensin II receptor AT-1B (Agtr1b) is not supported as a candidate gene for the QTL because a congenic strain harboring it did not have an effect on BP. There are ~19 known and unknown genes present in the QTL interval. Among them, no standout candidate genes are reputed to affect BP. Thus the QTL will likely represent a novel gene for BP regulation.

comparative congenics; functional genomics; blood pressure; fine mapping




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