Quantitative trait loci that regulate plasma lipid concentration in hereditary obese KK and KK-Ay mice

被引:42
作者
Suto, J [1 ]
Matsuura, S [1 ]
Yamanaka, H [1 ]
Sekikawa, K [1 ]
机构
[1] Natl Inst Anim Hlth, Dept Immunol, Ibaraki, Osaka 3050856, Japan
来源
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE | 1999年 / 1453卷 / 03期
关键词
quantitative trait locus; plasma lipid; obese mouse; KK mouse; A(y) allele;
D O I
10.1016/S0925-4439(99)00013-7
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
To identify quantitative trait loci (QTLs) responsible for regulating plasma lipid concentration associated with obesity, linkage analysis was carried out on the 190 F-2 progeny of a cross between C57BL/6J female and KK-A(y) (A(y) allele at the agouti locus congenic) male. In F-2 a/a (agouti locus genotype) mice, two QTLs were identified on chromosome 1 and a QTL on chromosome 3 for total-cholesterol. A QTL for HDL-cholesterol was identified on chromosome 1 and a QTL for NEFA on chromosome 9. In F-2 A(y)/a mice, two QTLs for HDL-cholesterol were found on chromosome 1. Loci for other lipids with suggestive linkage were also identified. In both F-2 mice, one QTL on chromosome 1 for total- and HDL-cholesterol was mapped near D1Mit150, in the vicinity of the apolipoprotein A-II (Apoa2) locus. Seven nucleotide substitutions out of 309 nucleotide apolipoprotein A-II cDNA sequences were identified between KK and C57BL/6J. The AY allele may be an indication of the plasma lipid levels, but its influence was less apparent than in the case of weight control. The loci for lipids were not on identical chromosomes with those previously identified for obesity, suggesting that hyperlipidemia in KK does not coincidentally occur with obesity. (C) 1999 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:385 / 395
页数:11
相关论文
共 26 条
[1]  
DIETRICH W, 1992, GENETICS, V131, P423
[2]  
DOOLITTLE DP, 1996, GENETIC VARIANTS STR, V1
[3]  
DOOLITTLE MH, 1990, J BIOL CHEM, V265, P16380
[4]   Role of melanocortinergic neurons in feeding and the agouti obesity syndrome [J].
Fan, W ;
Boston, BA ;
Kesterson, RA ;
Hruby, VJ ;
Cone, RD .
NATURE, 1997, 385 (6612) :165-168
[5]   MORBIDITY AND MORTALITY IN DIABETICS IN FRAMINGHAM POPULATION - 16-YEAR FOLLOW-UP STUDY [J].
GARCIA, MJ ;
MCNAMARA, PM ;
GORDON, T ;
KANNELL, WB .
DIABETES, 1974, 23 (02) :105-111
[6]  
HEDRICK CC, 1993, J BIOL CHEM, V268, P20676
[7]  
Hill JO, 1994, GENETIC DETERMINANTS, P35
[8]   Targeted disruption of the melanocortin-4 receptor results in obesity in mice [J].
Huszar, D ;
Lynch, CA ;
FairchildHuntress, V ;
Dunmore, JH ;
Fang, Q ;
Berkemeier, LR ;
Gu, W ;
Kesterson, RA ;
Boston, BA ;
Cone, RD ;
Smith, FJ ;
Campfield, LA ;
Burn, P ;
Lee, F .
CELL, 1997, 88 (01) :131-141
[9]  
IWATSUKA H, 1970, ENDOCRINOL JAPON, V17, P23
[10]   GENETIC-MAPPING OF 40 CDNA CLONES ON THE MOUSE GENOME BY PCR [J].
KO, MSH ;
WANG, X ;
HORTON, JH ;
HAGEN, MD ;
TAKAHASHI, N ;
MAEZAKI, Y ;
NADEAU, JH .
MAMMALIAN GENOME, 1994, 5 (06) :349-355