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      Regulation of muscle GLUT-4 transcription by AMP-activated protein kinase.

      Journal of Applied Physiology
      AMP-Activated Protein Kinases, Aminoimidazole Carboxamide, analogs & derivatives, pharmacology, Animals, DNA-Binding Proteins, metabolism, Enzyme Activation, drug effects, Gene Expression Regulation, physiology, Glucose Transporter Type 4, Humans, Hypoglycemic Agents, MEF2 Transcription Factors, Male, Mice, Mice, Transgenic, Monosaccharide Transport Proteins, genetics, Multienzyme Complexes, Muscle Fibers, Skeletal, Muscle Proteins, Muscle, Skeletal, cytology, Myogenic Regulatory Factors, Promoter Regions, Genetic, Protein-Serine-Threonine Kinases, RNA, Messenger, analysis, Rats, Rats, Sprague-Dawley, Ribonucleotides, Transcription Factors, Transcriptional Activation

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          Abstract

          Skeletal muscle GLUT-4 transcription in response to treatment with 5-aminoimidazole-4-carboxamide-1-beta-D-ribofuranoside (AICAR), a known activator of AMP-activated protein kinase (AMPK), was studied in rats and mice. The increase in GLUT-4 mRNA levels in response to a single subcutaneous injection of AICAR, peaked at 13 h in white and red quadriceps muscles but not in the soleus muscle. The mRNA level of chloramphenicol acyltransferase reporter gene which is driven by 1,154 or 895 bp of the human GLUT-4 proximal promoter was increased in AICAR-treated transgenic mice, demonstrating the transcriptional upregulation of the GLUT-4 gene by AICAR. However, this induction of transcription was not apparent with 730 bp of the promoter. In addition, nuclear extracts from AICAR-treated mice bound to the consensus sequence of myocyte enhancer factor-2 (from -473 to -464) to a greater extent than from saline-injected mice. Thus AMP-activated protein kinase activation by AICAR increases GLUT-4 transcription by a mechanism that requires response elements within 895 bp of human GLUT-4 proximal promoter and that may be cooperatively mediated by myocyte enhancer factor-2.

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