Complex haplotypes of the PGC-1α gene are associated with carbohydrate metabolism and type 2 diabetes

被引:81
作者
Oberkofler, H
Linnemayr, V
Weitgasser, R
Klein, K
Xie, MQ
Iglseder, B
Krempler, F
Paulweber, B
Patsch, W
机构
[1] Landesklin & Paracelsus Private Med Univ Salzburg, Dept Lab Med, A-5020 Salzburg, Austria
[2] Landesklin & Paracelsus Private Med Univ Salzburg, Dept Internal Med, A-5020 Salzburg, Austria
[3] Landesklin & Paracelsus Private Med Univ Salzburg, Dept Neurol, A-5020 Salzburg, Austria
[4] Hosp Hallein, Dept Internal Med, Hallein, Austria
关键词
D O I
10.2337/diabetes.53.5.1385
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Peroxisome proliferator-activated receptor coactivator-1alpha (PGC-1alpha) is a transcriptional coactivator implicated in transcriptional programs of hepatic gluconeogenesis, oxidative phosphorylation, and insulin release by beta-cells. To study associations of the PGC-1alpha gene locus with carbohydrate metabolism and type 2 diabetes in humans, we identified several polymorphisms in the promoter region that were located in a haplotype block distinct from a second haplotype block containing part of intron 2 and extending beyond exon 13. Each block contained five common haplotypes. Oral glucose tolerance testing revealed associations of promoter haplotype combinations with 30- and 60-min postload plasma glucose levels, whereas haplotypes in both blocks were associated with indexes of beta-cell function. The associations of promoter haplotypes are supported by functional studies showing that some polymorphisms are located in transcription factor binding sites and affect transactivation in an allele-specific manner. By comparing patients with type 2 diabetes and control subjects, we observed borderline significant differences of four-loci haplotype distributions in the downstream haplotype block. Moreover, the haplotype that was associated with the strongest insulin response to glucose conferred the lowest risk of type 2 diabetes (P < 0.01). Thus, the PGC-1alpha gene locus influences carbohydrate metabolism and contributes to type 2 diabetes in the population studied.
引用
收藏
页码:1385 / 1393
页数:9
相关论文
共 42 条
[1]  
Andersen G, 2002, DIABETES, V51, pA49
[2]   Adaptations of skeletal muscle to exercise: rapid increase in the transcriptional coactivator PGC-1 [J].
Baar, K ;
Wende, AR ;
Jones, TE ;
Marison, M ;
Nolte, LA ;
Chen, M ;
Kelly, DP ;
Holloszy, JO .
FASEB JOURNAL, 2002, 16 (14) :1879-1886
[3]   Minimal model-based insulin sensitivity has greater heritability and a different genetic basis than homeostasis model assessment or fasting insulin [J].
Bergman, RN ;
Zaccaro, DJ ;
Watanabe, RM ;
Haffner, SM ;
Saad, MF ;
Norris, JM ;
Wagenknecht, LE ;
Hokanson, JE ;
Rotter, JI ;
Rich, SS .
DIABETES, 2003, 52 (08) :2168-2174
[4]  
CHIU KC, 2000, J CLIN ENDOCR METAB, V85, P2718
[5]  
CZURYT MP, 2003, P NATL ACAD SCI USA, V100, P1711
[6]   High-resolution haplotype structure in the human genome [J].
Daly, MJ ;
Rioux, JD ;
Schaffner, SE ;
Hudson, TJ ;
Lander, ES .
NATURE GENETICS, 2001, 29 (02) :229-232
[7]   Mutation analysis of peroxisome proliferator-activated receptor-γ coactivator-1 (PGC-1) and relationships of identified amino acid polymorphisms to Type II diabetes mellitus [J].
Ek, J ;
Andersen, G ;
Urhammer, SA ;
Gæde, PH ;
Drivsholm, T ;
Borch-Johnsen, K ;
Hansen, T ;
Pedersen, O .
DIABETOLOGIA, 2001, 44 (12) :2220-2226
[8]   A common polymorphism in the promoter of UCP2 is associated with decreased risk of obesity in middle-aged humans [J].
Esterbauer, H ;
Schneitler, C ;
Oberkofler, H ;
Ebenbichler, C ;
Paulweber, B ;
Sandhofer, F ;
Ladurner, G ;
Hell, E ;
Strosberg, AD ;
Patsch, JR ;
Krempler, F ;
Patsch, W .
NATURE GENETICS, 2001, 28 (02) :178-183
[9]   Mechanisms of disease: Molecular mechanisms and clinical pathophysiology of maturity-onset diabetes of the young. [J].
Fajans, SS ;
Bell, GI ;
Polonsky, KS .
NEW ENGLAND JOURNAL OF MEDICINE, 2001, 345 (13) :971-980
[10]   An autoregulatory loop controls peroxisome proliferator-activated receptor γ coactivator 1α expression in muscle [J].
Handschin, C ;
Rhee, J ;
Lin, JD ;
Tarr, PT ;
Spiegelman, BM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (12) :7111-7116