Quantitative trait loci influencing cholesterol and phospholipid phenotypes map to chromosomes that contain genes regulating blood pressure in the spontaneously hypertensive rat

被引:78
作者
Bottger, A
vanLith, HA
Kren, V
Krenova, D
Bila, V
Vorlicek, J
Zidek, V
Musilova, A
Zdobinska, M
Wang, JM
vanZutphen, BFM
Kurtz, TW
Pravenec, M
机构
[1] ACAD SCI CZECH REPUBL, INST PHYSIOL, PRAGUE 14220 4, CZECH REPUBLIC
[2] UNIV UTRECHT, FAC VET, DEPT LAB ANIM SCI, NL-3508 TD UTRECHT, NETHERLANDS
[3] CHARLES UNIV, FAC MED 1, DEPT BIOL, PRAGUE 12800, CZECH REPUBLIC
[4] UNIV CALIF SAN FRANCISCO, DEPT LAB MED, SAN FRANCISCO, CA 94143 USA
关键词
rat; genetics; dyslipidemia; hypertension; quantitative trait loci;
D O I
10.1172/JCI118858
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
The frequent coincidence of hypertension and dyslipidemia suggests that related genetic factors might underlie these common risk factors for cardiovascular disease. To investigate whether quantitative trait loci (QTLs) regulating lipid levels map to chromosomes known to contain genes regulating blood pressure, we used a genome scanning approach to map QTLs influencing cholesterol and phospholipid phenotypes in a large set of recombinant inbred strains and in congenic strains derived from the spontaneously hypertensive rat and normotensive Brown-Norway (BN.Lx) rat fed normal and high cholesterol diets. QTLs regulating lipid phenotypes were mapped by scanning the genome with 534 genetic markers. A significant relationship (P <0.00006) was found between basal HDL2 cholesterol levels and the D19Mit2 marker on chromosome 19. Analysis of congenic strains of spontaneously hypertensive rat indicated that QTLs regulating postdietary lipid phenotypes exist also on chromosomes 8 and 20. Previous studies in the recombinant inbred and congenic strains have demonstrated the presence of blood pressure regulatory genes in corresponding segments of chromosomes 8, 19, and 20. These findings provide support for the hypothesis that blood pressure and certain lipid subfractions can be modulated by linked genes or perhaps even the same genes.
引用
收藏
页码:856 / 862
页数:7
相关论文
共 44 条
[1]   THE STRUCTURAL GENE FOR LECITHIN - CHOLESTEROL ACYL TRANSFERASE (LCAT) MAPS TO 16Q22 [J].
AZOULAY, M ;
HENRY, I ;
TATA, F ;
WEIL, D ;
GRZESCHIK, KH ;
CHAVES, ME ;
MCINTYRE, N ;
WILLIAMSON, R ;
HUMPHRIES, SE ;
JUNIEN, C .
ANNALS OF HUMAN GENETICS, 1987, 51 :129-136
[2]   EMPIRICAL ESTIMATES OF BONFERRONI CORRECTIONS FOR USE IN CHROMOSOME MAPPING STUDIES WITH THE BXD RECOMBINANT INBRED STRAINS [J].
BELKNAP, JK .
BEHAVIOR GENETICS, 1992, 22 (06) :677-684
[3]   Strain-specific response to hypercholesterolaemic diets in the rat [J].
Bottger, AE ;
denBieman, M ;
Lankhorst, AE ;
vanLith, HA ;
vanZutphen, LFM .
LABORATORY ANIMALS, 1996, 30 (02) :149-157
[4]   SEQUENCE OF RAT LIPOPROTEIN LIPASE-ENCODING CDNA [J].
BRAULT, D ;
NOE, L ;
ETIENNE, J ;
HAMELIN, J ;
RAISONNIER, A ;
SOULI, A ;
CHUAT, JC ;
DUGAIL, I ;
QUIGNARDBOULANGE, A ;
LAVAU, M ;
GALIBERT, F .
GENE, 1992, 121 (02) :237-246
[5]   EXPRESSION OF THE HUMAN APOLIPOPROTEIN-A-I GENE IN TRANSGENIC MICE ALTERS HIGH-DENSITY-LIPOPROTEIN (HDL) PARTICLE-SIZE DISTRIBUTION AND DIMINISHES SELECTIVE UPTAKE OF HDL CHOLESTERYL ESTERS [J].
CHAJEKSHAUL, T ;
HAYEK, T ;
WALSH, A ;
BRESLOW, JL .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (15) :6731-6735
[6]   VARIATION AT THE HEPATIC LIPASE AND APOLIPOPROTEIN AI/CIII/AIV LOCI IS A MAJOR CAUSE OF GENETICALLY-DETERMINED VARIATION IN PLASMA HDL CHOLESTEROL LEVELS [J].
COHEN, JC ;
WANG, ZF ;
GRUNDY, SM ;
STOESZ, MR ;
GUERRA, R .
JOURNAL OF CLINICAL INVESTIGATION, 1994, 94 (06) :2377-2384
[7]   ABNORMALITIES OF INSULIN AND LIPID-METABOLISM IN MILAN HYPERTENSIVE RATS [J].
DALLAGLIO, E ;
TOSINI, P ;
FERRARI, P ;
ZAVARONI, I ;
PASSERI, M ;
REAVEN, GM .
AMERICAN JOURNAL OF HYPERTENSION, 1991, 4 (09) :773-775
[8]  
DARVASI A, 1995, GENETICS, V141, P1199
[9]   PANCREATIC COLIPASE - STRUCTURAL AND PHYSIOLOGICAL-ASPECTS [J].
ERLANSONALBERTSSON, C .
BIOCHIMICA ET BIOPHYSICA ACTA, 1992, 1125 (01) :1-7
[10]   MILD DYSLIPIDEMIA IN MICE FOLLOWING TARGETED INACTIVATION OF THE HEPATIC LIPASE GENE [J].
HOMANICS, GE ;
DESILVA, HV ;
OSADA, J ;
ZHANG, SH ;
WONG, H ;
BORENSZTAJN, J ;
MAEDA, N .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (07) :2974-2980