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

被引:36
作者
Clemitson, Jenny-Rebecca
Dixon, Richard J.
Haines, Steve
Bingham, Andrew J.
Patel, Bhakti R.
Hall, Laurence
Lo, Ming
Sassard, Jean
Charchar, Fadi J.
Samani, Nilesh J. [1 ]
机构
[1] Univ Leicester, Glenfield Hosp, Dept Cardiovasc Sci, Leicester LE3 9QP, Leics, England
[2] Fac Pharm Lyon, Dept Physiol & Pharmacol Clin, F-69008 Lyon, France
基金
英国惠康基金;
关键词
hypertension; genetics; rats; gene expression; quantitative trait locus;
D O I
10.1161/01.RES.0000261961.41889.9c
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
A region with a major effect on blood pressure (BP) is located on rat chromosome 1. We have previously isolated this region in reciprocal congenic strains (WKY.SHR-Sa and SHR.WKY-Sa) derived from a cross of the spontaneously hypertensive rat (SHR) with the Wistar-Kyoto rat (WKY) and shown that there are 2 distinct BP quantitative trait loci, BP1 and BP2, in this region. Sisa1, a congenic substrain from the SHR.WKY-Sa animals carrying an introgressed segment of 4.3Mb, contains BP1. Here, we report further dissection of BP1 by the creation of 2 new mutually exclusive congenic substrains (Sisa1a and Sisa1b) and interrogation of candidate genes by expression profiling and targeted transcript sequencing. Only 1 of the substrains (Sisa1a) continued to demonstrate a BP difference but with a reduced introgressed segment of 3Mb. Exonic sequencing of the 20 genes located in the Sisa1a region did not identify any major differences between SHR and WKY. However, microarray expression profiling of whole kidney samples and subsequent quantitative RT-PCR identified a single gene, Spon1 that exhibited significant differential expression between the WKY and SHR genotypes at both 6 and 24 weeks of age. Western blot analysis confirmed an increased level of the Spon1 gene product in SHR kidneys. Spon1 belongs to a family of genes with antiangiogenic properties. These findings justify further investigation of this novel positional candidate gene in BP control in hypertensive rat models and humans.
引用
收藏
页码:992 / 999
页数:8
相关论文
共 19 条
[1]   Identification of Cd36 (Fat) as an insulin-resistance gene causing defective fatty acid and glucose metabolism in hypertensive rats [J].
Aitman, TJ ;
Glazier, AM ;
Wallace, CA ;
Cooper, LD ;
Norsworthy, PJ ;
Wahid, FN ;
Al-Majali, KM ;
Trembling, PM ;
Mann, CJ ;
Shoulders, CC ;
Graf, D ;
St Lezin, E ;
Kurtz, TW ;
Kren, V ;
Pravenec, M ;
Ibrahimi, A ;
Abumrad, NA ;
Stanton, LW ;
Scott, J .
NATURE GENETICS, 1999, 21 (01) :76-83
[2]   Tandem repeats finder: a program to analyze DNA sequences [J].
Benson, G .
NUCLEIC ACIDS RESEARCH, 1999, 27 (02) :573-580
[3]   Kidney specificity of rat chromosome 1 blood pressure quantitative trait locus region [J].
Clemitson, JR ;
Pratt, JR ;
Frantz, S ;
Sacks, S ;
Samani, NJ .
HYPERTENSION, 2002, 40 (03) :292-297
[4]   Thrombospondins and tumor angiogenesis [J].
de Fraipont, F ;
Nicholson, AC ;
Feige, JJ ;
Van Meir, EG .
TRENDS IN MOLECULAR MEDICINE, 2001, 7 (09) :401-407
[5]   Genetic dissection of region around the Sa gene on rat chromosome 1 - Evidence for multiple loci affecting blood pressure [J].
Frantz, S ;
Clemitson, JR ;
Bihoreau, MT ;
Gauguier, D ;
Samani, NJ .
HYPERTENSION, 2001, 38 (02) :216-221
[6]   Successful isolation of a rat chromosome 1 blood pressure quantitative trait locus in reciprocal congenic strains [J].
Frantz, SA ;
Kaiser, M ;
Gardiner, SM ;
Gauguier, D ;
Vincent, M ;
Thompson, JR ;
Bennett, T ;
Samani, NJ .
HYPERTENSION, 1998, 32 (04) :639-646
[7]   AN ARGININE TO HISTIDINE MUTATION IN CODON 311 OF THE C-ERBA-BETA GENE RESULTS IN A MUTANT THYROID-HORMONE RECEPTOR THAT DOES NOT MEDIATE A DOMINANT NEGATIVE PHENOTYPE [J].
GEFFNER, ME ;
SU, F ;
ROSS, NS ;
HERSHMAN, JM ;
VANDOP, C ;
MENKE, JB ;
HAO, E ;
STANZAK, RK ;
EATON, T ;
SAMUELS, HH ;
USALA, SJ .
JOURNAL OF CLINICAL INVESTIGATION, 1993, 91 (02) :538-546
[8]   Combined genealogical, mapping, and expression approaches to identify spontaneously hypertensive rat hypertension candidate genes [J].
Hinojos, CA ;
Boerwinkle, E ;
Fornage, M ;
Doris, PA .
HYPERTENSION, 2005, 45 (04) :698-704
[9]   Integrated transcriptional profiling and linkage analysis for identification of genes underlying disease [J].
Hubner, N ;
Wallace, CA ;
Zimdahl, H ;
Petretto, E ;
Schulz, H ;
Maciver, F ;
Mueller, M ;
Hummel, O ;
Monti, J ;
Zidek, V ;
Musilova, A ;
Kren, V ;
Causton, H ;
Game, L ;
Born, G ;
Schmidt, S ;
Müller, A ;
Cook, SA ;
Kurtz, TW ;
Whittaker, J ;
Pravenec, M ;
Aitman, TJ .
NATURE GENETICS, 2005, 37 (03) :243-253
[10]   Novel members of the Vesl/Homer family of PDZ proteins that bind metabotropic glutamate receptors [J].
Kato, A ;
Ozawa, F ;
Saitoh, Y ;
Fukazawa, Y ;
Sugiyama, H ;
Inokuchi, K .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (37) :23969-23975