Literature DB >> 15080379

Combining congenic coverage with gene profiling in search of candidates for blood pressure quantitative trait loci in Dahl rats.

Myriam Moujahidine1, Raphaelle Lambert, Julie Dutil, Ana Palijan, Zsuzsa Sivo, Anita Ariyarajah, Alan Y Deng.   

Abstract

Chromosomes (Chr) 10 and 16 of the Dahl salt-sensitive (S) rat harbor quantitative trait loci (QTLs) for blood pressure (BP). To facilitate gene discovery of these QTLs, gene profiling based on microarrays was combined with fine QTL mapping to identify potential candidate genes that are differentially expressed. First, the region harboring the BP QTL on Chr 16 was narrowed by comparative congenic mapping. In this endeavor, a number of new chromosome markers were generated and used to physically define the chromosome interval in question. Second, in an effort to minimize the costs of gene profiling without sacrificing the chance of gene discovery, a combination congenic strain was produced by replacing one segment of Chr 10 along with one segment of Chr 16 of the hypertensive S rat by those of the normotensive Lewis (LEW) rat. Both of these regions are known to contain BP QTLs. Third, kidneys of this combination congenic strain and the S strain were employed for expression profiling studies. Finally, a comparison between the two strains yielded a number of potentially differentially expressed candidates. Six Established Sequence Tags (ESTs)/genes among them were located in Chr 10 regions and 1 was found in a Chr 16 region, and the genetic make-ups of all these regions were shown to be different between S and LEW. However, none of these ESTs/genes identified by gene profiling were located in an interval containing a QTL. Thus, the present study highlights the importance of correlating the results of gene expression profiling with fine congenic mapping.

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Year:  2004        PMID: 15080379     DOI: 10.1291/hypres.27.203

Source DB:  PubMed          Journal:  Hypertens Res        ISSN: 0916-9636            Impact factor:   3.872


  8 in total

1.  Serious limitations of the QTL/microarray approach for QTL gene discovery.

Authors:  Ricardo A Verdugo; Charles R Farber; Craig H Warden; Juan F Medrano
Journal:  BMC Biol       Date:  2010-07-12       Impact factor: 7.431

2.  Substitution of Brown Norway chromosome 16 preserves cardiac function with aging in a salt-sensitive Dahl consomic rat.

Authors:  A J Kriegel; A S Greene
Journal:  Physiol Genomics       Date:  2008-10-21       Impact factor: 3.107

3.  High-resolution mapping of a novel rat blood pressure locus on chromosome 9 to a region containing the Spp2 gene and colocalization of a QTL for bone mass.

Authors:  Ying Nie; Sivarajan Kumarasamy; Harshal Waghulde; Xi Cheng; Blair Mell; Piotr J Czernik; Beata Lecka-Czernik; Bina Joe
Journal:  Physiol Genomics       Date:  2016-04-25       Impact factor: 3.107

4.  Genome-wide identification of allelic expression in hypertensive rats.

Authors:  Renata I Dmitrieva; Cruz A Hinojos; Megan L Grove; Rebecca J Bell; Eric Boerwinkle; Myriam Fornage; Peter A Doris
Journal:  Circ Cardiovasc Genet       Date:  2009-02-12

Review 5.  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

Review 6.  Integrated gene expression profiling and linkage analysis in the rat.

Authors:  Enrico Petretto; Jonathan Mangion; Michal Pravanec; Norbert Hubner; Timothy J Aitman
Journal:  Mamm Genome       Date:  2006-06-12       Impact factor: 2.957

7.  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

8.  Isolation of a Genomic Region Affecting Most Components of Metabolic Syndrome in a Chromosome-16 Congenic Rat Model.

Authors:  Lucie Šedová; Michal Pravenec; Drahomíra Křenová; Ludmila Kazdová; Václav Zídek; Michaela Krupková; František Liška; Vladimír Křen; Ondřej Šeda
Journal:  PLoS One       Date:  2016-03-31       Impact factor: 3.240

  8 in total

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