Literature DB >> 15632271

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

Myrian Grondin1, Vasiliki Eliopoulos, Raphaelle Lambert, Yishu Deng, Anita Ariyarajah, Myriam Moujahidine, Julie Dutil, Sophie Charron, Alan Y Deng.   

Abstract

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 approximately 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.

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Year:  2005        PMID: 15632271     DOI: 10.1152/physiolgenomics.00275.2004

Source DB:  PubMed          Journal:  Physiol Genomics        ISSN: 1094-8341            Impact factor:   3.107


  5 in total

1.  Vascular responses in aortic rings of a consomic rat panel derived from the Fawn Hooded Hypertensive strain.

Authors:  Mary Pat Kunert; Melinda R Dwinell; Julian H Lombard
Journal:  Physiol Genomics       Date:  2010-09-14       Impact factor: 3.107

Review 2.  Towards Precision Medicine for Hypertension: A Review of Genomic, Epigenomic, and Microbiomic Effects on Blood Pressure in Experimental Rat Models and Humans.

Authors:  Sandosh Padmanabhan; Bina Joe
Journal:  Physiol Rev       Date:  2017-10-01       Impact factor: 37.312

3.  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

4.  Contribution of independent and pleiotropic genetic effects in the metabolic syndrome in a hypertensive rat.

Authors:  Man Chun John Ma; Janette M Pettus; Jessica A Jakoubek; Matthew G Traxler; Karen C Clark; Amanda K Mennie; Anne E Kwitek
Journal:  PLoS One       Date:  2017-08-08       Impact factor: 3.240

Review 5.  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
  5 in total

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