Literature DB >> 10642295

Applicability of a "speed" congenic strategy to dissect blood pressure quantitative trait loci on rat chromosome 2.

B Jeffs1, C D Negrin, D Graham, J S Clark, N H Anderson, D Gauguier, A F Dominiczak.   

Abstract

The identification of any quantitative trait locus (QTL) via a genome scan is only the first step toward the ultimate goal of gene identification. The next step is the production of congenic strains by which the existence of a QTL may be verified and the implicated chromosomal region be reduced to a size applicable to positional cloning of the causal gene. We used a speed congenic breeding protocol previously verified in mice for 2 blood pressure QTLs on rat chromosome 2. Four congenic strains were produced through introgression of various segments of chromosome 2 from Wistar-Kyoto rats from Glasgow colonies [WKY((Gla)) rats] into the recipient stroke-prone spontaneously hypertensive rats from Glasgow colonies [SHRSP((Gla))], and vice versa. The number of backcross generations required for each strain to achieve complete homozygosity at 83 background genetic markers in a "best" male varied between 3 and 4. Transfer of the region of rat chromosome 2 containing both QTLs from WKY((Gla)) into an SHRSP((Gla)) genetic background lowered both baseline and salt-loaded systolic blood pressure by approximately 20 and approximately 40 mm Hg in male congenic rats compared with the SHRSP parental strain (F=53.4, P<0.005; F=28.0, P< 0.0005, respectively). In contrast, control animals for stowaway heterozygosity presented no deviation from the blood pressure values recorded for the SHRSP((Gla)), indicating that if such heterozygosity exists, its effect on blood pressure is negligible. A reciprocal strategy in which 1 or both QTLs on rat chromosome 2 were transferred from SHRSP((Gla)) into a WKY((Gla)) genetic background resulted in statistically significant but smaller blood pressure increases for 1 of these QTLs. These results confirm the existence of blood pressure QTLs on rat chromosome 2 and demonstrate the applicability of a speed congenic strategy in the rat and emphasize the important role of the genetic background.

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Year:  2000        PMID: 10642295     DOI: 10.1161/01.hyp.35.1.179

Source DB:  PubMed          Journal:  Hypertension        ISSN: 0194-911X            Impact factor:   10.190


  15 in total

Review 1.  Functional genomics in rodent models of hypertension.

Authors:  Martin W McBride; Fadi J Charchar; Delyth Graham; William H Miller; Pamela Strahorn; Fiona J Carr; Anna F Dominiczak
Journal:  J Physiol       Date:  2004-01-01       Impact factor: 5.182

2.  Marker-assisted congenic screening (MACS): a database tool for the efficient production and characterization of congenic lines.

Authors:  Stephan C Collins; Robert H Wallis; Karin Wallace; Marie Thérèse Bihoreau; Dominique Gauguier
Journal:  Mamm Genome       Date:  2003-05       Impact factor: 2.957

3.  Single and multiple congenic strains for hydrocephalus in the H-Tx rat.

Authors:  Hazel C Jones; Gin-Fu Chen; Baligh R Yehia; Barbara J Carter; Elizabeth J Akins; Logan C Wolpin
Journal:  Mamm Genome       Date:  2005-04       Impact factor: 2.957

4.  Congenic mapping of a blood pressure QTL on chromosome 16 of Dahl rats.

Authors:  Myriam Moujahidine; Julie Dutil; Pavel Hamet; Alan Y Deng
Journal:  Mamm Genome       Date:  2002-03       Impact factor: 2.957

5.  Predictive response-relevant clustering of expression data provides insights into disease processes.

Authors:  Lisa E M Hopcroft; Martin W McBride; Keith J Harris; Amanda K Sampson; John D McClure; Delyth Graham; Graham Young; Tessa L Holyoake; Mark A Girolami; Anna F Dominiczak
Journal:  Nucleic Acids Res       Date:  2010-06-22       Impact factor: 16.971

Review 6.  Application of chromosomal substitution techniques in gene-function discovery.

Authors:  Allen W Cowley; Richard J Roman; Howard J Jacob
Journal:  J Physiol       Date:  2004-01-01       Impact factor: 5.182

7.  Genetically hypertensive Brown Norway congenic rat strains suggest intermediate traits underlying genetic hypertension.

Authors:  Marijo Bilusić; Carol Moreno; Nadia E Barreto; Michael R Tschannen; Eugenie L Harris; William K Porteous; Caryn M Thompson; Murray R Grigor; Alan Weder; Eric Boerwinkle; Steven C Hunt; J David Curb; Howard J Jacob; Anne E Kwitek
Journal:  Croat Med J       Date:  2008-10       Impact factor: 1.351

8.  Genetics of hypertension: discoveries from the bench to human populations.

Authors:  Nora Franceschini; Thu H Le
Journal:  Am J Physiol Renal Physiol       Date:  2013-10-16

9.  Distinct quantitative trait loci for kidney, cardiac, and aortic mass dissociated from and associated with blood pressure in Dahl congenic rats.

Authors:  Chenda Duong; Sophie Charron; Chunjie Xiao; Pavel Hamet; Annie Ménard; Julie Roy; Alan Y Deng
Journal:  Mamm Genome       Date:  2006-12-01       Impact factor: 3.224

Review 10.  Genetics of hypertension: from experimental animals to humans.

Authors:  Christian Delles; Martin W McBride; Delyth Graham; Sandosh Padmanabhan; Anna F Dominiczak
Journal:  Biochim Biophys Acta       Date:  2009-12-24
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