Literature DB >> 15710778

Combined genealogical, mapping, and expression approaches to identify spontaneously hypertensive rat hypertension candidate genes.

Cruz A Hinojos1, Eric Boerwinkle, Myriam Fornage, Peter A Doris.   

Abstract

Allelic expression in genes has become recognized as a heritable trait by which phenotypes are generated. We have examined gene expression in the rat kidney using genome-wide microarray technology (Affymetrix). Gene expression was determined across 4 rat strains, 3 hypertensive spontaneously hypertensive rat (SHR) substrains (SHR-A3, SHR-B2, and SHR-C), and a normotensive strain (Wistar-Kyoto [WKY]). Expression measurements were made in multiple animals from all strains at 4 time points (4 weeks, 8 weeks, 12 weeks, and 18 weeks of age), covering the prehypertensive period in SHR (4 weeks), and the period of rapidly rising blood pressure (8 and 12 weeks) and of sustained hypertension (18 weeks). Regression analysis revealed a close relationship across all strains during the first 3 time points, after which SHR-A3 became a substantial outlier. SHR-B2 and SHR-C demonstrated a very close relationship in gene expression at all times but also showed increased differences compared with the other strains at 18 weeks of age. We identified genes that were consistently different in expression, comparing all SHR substrains at each time point with WKY. The resulting list of genes was compared with blood pressure quantitative trait loci reported for SHR to refine a number of genes consistently differentially expressed between SHR substrains and WKY, persistently differentially expressed across multiple time points, and located in SHR blood pressure-determinative regions of the genome. Genealogical relationships and SHR substrain intercrosses suggest that genes responsible for heritable hypertension in SHR are shared across SHR substrains. The present approach identifies a number of genes that may influence blood pressure in SHR by virtue of allelic effects on gene expression.

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Year:  2005        PMID: 15710778     DOI: 10.1161/01.HYP.0000156498.78896.37

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


  9 in total

1.  Fine-mapping and comprehensive transcript analysis reveals nonsynonymous variants within a novel 1.17 Mb blood pressure QTL region on rat chromosome 10.

Authors:  Yasser Saad; Michael R Garrett; Ezhilarasi Manickavasagam; Shane Yerga-Woolwine; Phyllis Farms; Tracy Radecki; Bina Joe
Journal:  Genomics       Date:  2007-01-10       Impact factor: 5.736

2.  Genetic architecture of Wistar-Kyoto rat and spontaneously hypertensive rat substrains from different sources.

Authors:  Yanli Zhang-James; Frank A Middleton; Stephen V Faraone
Journal:  Physiol Genomics       Date:  2013-05-14       Impact factor: 3.107

3.  Hepatocyte nuclear factor 1 and hypertensive nephropathy.

Authors:  Renata I Dmitrieva; Cruz A Hinojos; Eric Boerwinkle; Michael C Braun; Myriam Fornage; Peter A Doris
Journal:  Hypertension       Date:  2008-04-28       Impact factor: 10.190

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

5.  Genetic dissection of a blood pressure quantitative trait locus on rat chromosome 1 and gene expression analysis identifies SPON1 as a novel candidate hypertension gene.

Authors:  Jenny-Rebecca Clemitson; Richard J Dixon; Steve Haines; Andrew J Bingham; Bhakti R Patel; Laurence Hall; Ming Lo; Jean Sassard; Fadi J Charchar; Nilesh J Samani
Journal:  Circ Res       Date:  2007-03-01       Impact factor: 17.367

6.  Gene expression suggests spontaneously hypertensive rats may have altered metabolism and reduced hypoxic tolerance.

Authors:  Marie-Françoise Ritz; Caspar Grond-Ginsbach; Stefan Engelter; Philippe Lyrer
Journal:  Curr Neurovasc Res       Date:  2012-02       Impact factor: 1.990

7.  Characterization of cognitive deficits in spontaneously hypertensive rats, accompanied by brain insulin receptor dysfunction.

Authors:  Edna Grünblatt; Jasmin Bartl; Diana-Iulia Iuhos; Ana Knezovic; Vladimir Trkulja; Peter Riederer; Susanne Walitza; Melita Salkovic-Petrisic
Journal:  J Mol Psychiatry       Date:  2015-06-04

8.  Heterogeneity in arterial remodeling among sublines of spontaneously hypertensive rats.

Authors:  Erik N T P Bakker; Gergely Groma; Léon J A Spijkers; Judith de Vos; Angela van Weert; Henk van Veen; Vincent Everts; Silvia M Arribas; Ed VanBavel
Journal:  PLoS One       Date:  2014-09-24       Impact factor: 3.240

9.  Consequences of perinatal treatment with L-arginine and antioxidants for the renal transcriptome in spontaneously hypertensive rats.

Authors:  Sebastiaan Wesseling; Maarten P Koeners; Farid Kantouh; Jaap A Joles; Branko Braam
Journal:  Pflugers Arch       Date:  2009-02-03       Impact factor: 3.657

  9 in total

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