Microarray profiling of human skeletal muscle reveals that insulin regulates ≁800 genes during a hyperinsulinemic clamp

被引:154
作者
Rome, S
Clément, K
Rabasa-Lhoret, R
Loizon, E
Poitou, C
Barsh, GS
Riou, JP
Laville, M
Vidal, H
机构
[1] Fac Med R Laennec, INSERM, U449, F-69372 Lyon 08, France
[2] Fac Med R Laennec, Human Nutr Res Ctr, F-69372 Lyon 08, France
[3] Univ Paris 06, Dept Nutr, Hotel Dieu, EA3502, F-75004 Paris, France
[4] Stanford Univ, Sch Med, Beckman Ctr, Howard Hughes Med Inst,Dept Pediat & Genet, Stanford, CA 94305 USA
关键词
D O I
10.1074/jbc.M300293200
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
Insulin action in target tissues involved precise regulation of gene expression. To define the set of insulin-regulated genes in human skeletal muscle, we analyzed the global changes in mRNA levels during a 3-h hyperinsulinemic euglycemic clamp in vastus lateralis muscle of six healthy subjects. Using 29,308 cDNA element microarrays, we found that the mRNA expression of 762 genes, including 353 expressed sequence tags, was significantly modified during insulin infusion. 478 were up-regulated and 284 down-regulated. Most of the genes with known function are novel targets of insulin. They are involved in the transcriptional and translational regulation (29%), intermediary and energy metabolisms (14%), intracellular signaling (12%), and cytoskeleton and vesicle traffic (9%). Other categories consisted of genes coding for receptors, carriers, and transporters (8%), components of the ubiquitin/proteasome pathways (7%) and elements of the immune response (5.5%). These results thus define a transcriptional signature of insulin action in human skeletal muscle. They will help to better define the mechanisms involved in the reduction of insulin effectiveness in pathologies such as type 2 diabetes mellitus, a disease characterized by defective regulation of gene expression in response to insulin.
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收藏
页码:18063 / 18068
页数:6
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