Relationships between circadian rhythms and modulation of gene expression by glucocorticoids in skeletal muscle.

The existence and maintenance of biological rhythms linked to the 24-h light-dark cycle are essential to the health and functioning of an organism. Although much is known concerning central clock mechanisms, much less is known about control in peripheral tissues. In this study, circadian regulation of gene expression was examined in rat skeletal muscle. A rich time series involving 54 animals euthanized at 18 distinct time points within the 24-h cycle was performed, and mRNA expression in gastrocnemius muscles was examined using Affymetrix gene arrays. Data mining identified 109 genes that were expressed rhythmically, which could be grouped into eight distinct temporal clusters within the 24-h cycle. These genes were placed into 11 functional categories, which were examined within the context of temporal expression. Transcription factors involved in the regulation of central rhythms were examined, and eight were found to be rhythmically expressed in muscle. Because endogenous glucocorticoids are a major effector of circadian rhythms, genes identified here were compared with those identified in previous studies as glucocorticoid regulated. Of the 109 genes identified here as circadian rhythm regulated, only 55 were also glucocorticoid regulated. Examination of transcription factors involved in circadian control suggests that corticosterone may be the initiator of their rhythmic expression patterns in skeletal muscle.

[1]  Phillip D. Zamore,et al.  Modular Recognition of RNA by a Human Pumilio-Homology Domain , 2002, Cell.

[2]  D. DuBois,et al.  Corticosteroid effects in skeletal muscle: Gene induction/receptor autoregulation , 1997, Muscle & nerve.

[3]  Richard R Almon,et al.  Temporal profiling of the transcriptional basis for the development of corticosteroid-induced insulin resistance in rat muscle. , 2005, The Journal of endocrinology.

[4]  Robert V Farese,et al.  Increased lipid accumulation and insulin resistance in transgenic mice expressing DGAT2 in glycolytic (type II) muscle. , 2007, American journal of physiology. Endocrinology and metabolism.

[5]  E. Maywood,et al.  Circadian clocks: regulators of endocrine and metabolic rhythms. , 2007, The Journal of endocrinology.

[6]  P. Murphy,et al.  Regulation of glucocorticoid receptor steroid binding and trafficking by the hsp90/hsp70-based chaperone machinery: implications for clinical intervention , 2005, Leukemia.

[7]  H. Koistinen,et al.  Regulation of glucose transport in human skeletal muscle , 2002, Annals of medicine.

[8]  S. G. Rønn,et al.  Diabetes and Suppressors of Cytokine Signaling Proteins , 2007, Diabetes.

[9]  Jason P. DeBruyne,et al.  A Clock Shock: Mouse CLOCK Is Not Required for Circadian Oscillator Function , 2006, Neuron.

[10]  M. Bevan,et al.  The extracellular matrix protein mindin is a pattern-recognition molecule for microbial pathogens , 2004, Nature Immunology.

[11]  C. Graff,et al.  Synchronization of the Molecular Clockwork by Light- and Food-Related Cues in Mammals , 2003, Biological chemistry.

[12]  A. B. Reddy,et al.  Circadian clocks: neural and peripheral pacemakers that impact upon the cell division cycle. , 2005, Mutation research.

[13]  D. P. King,et al.  Molecular cloning and characterization of the human CLOCK gene: expression in the suprachiasmatic nuclei. , 1999, Genomics.

[14]  C. Levenson,et al.  Expression profiling of p53-target genes in copper-mediated neuronal apoptosis , 2007, NeuroMolecular Medicine.

[15]  Erin L. McDearmon,et al.  Identification of the circadian transcriptome in adult mouse skeletal muscle. , 2007, Physiological genomics.

[16]  Kenny K. Wong,et al.  Inhibition of cardiac lipoprotein utilization by transgenic overexpression of Angptl4 in the heart. , 2005, Proceedings of the National Academy of Sciences of the United States of America.

[17]  Isaac S Kohane,et al.  Expression profiling reveals altered satellite cell numbers and glycolytic enzyme transcription in nemaline myopathy muscle , 2003, Proceedings of the National Academy of Sciences of the United States of America.

[18]  A. Goldberg,et al.  Patterns of gene expression in atrophying skeletal muscles: response to food deprivation , 2002, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

[19]  K. Kadota,et al.  Genome-wide Expression Analysis of Mouse Liver Reveals CLOCK-regulated Circadian Output Genes* , 2003, Journal of Biological Chemistry.

[20]  U. Schibler,et al.  Glucocorticoid hormones inhibit food‐induced phase‐shifting of peripheral circadian oscillators , 2001, The EMBO journal.

[21]  J. Sanes,et al.  Expression of zfh‐4, a new member of the zinc finger‐homeodomain family, in developing brain and muscle , 1995, Developmental dynamics : an official publication of the American Association of Anatomists.

[22]  Debra C DuBois,et al.  Pharmacodynamics and pharmacogenomics of methylprednisolone during 7-day infusions in rats. , 2002, The Journal of pharmacology and experimental therapeutics.

[23]  F. Foufelle,et al.  SREBP transcription factors: master regulators of lipid homeostasis. , 2004, Biochimie.

[24]  S. Bhasin,et al.  Characterization of 5'-regulatory region of human myostatin gene: regulation by dexamethasone in vitro. , 2001, American journal of physiology. Endocrinology and metabolism.

[25]  P. Pévet,et al.  Phenotype of Per1- and Per2-expressing neurons in the suprachiasmatic nucleus of a diurnal rodent (Arvicanthis ansorgei): comparison with a nocturnal species, the rat , 2002, Cell and Tissue Research.

[26]  D. DuBois,et al.  Pharmacokinetic/Pharmacodynamic models for corticosteroid receptor down-regulation and glutamine synthetase induction in rat skeletal muscle by a Receptor/Gene-mediated mechanism. , 1999, The Journal of pharmacology and experimental therapeutics.

[27]  W. Jusko,et al.  Analysis of methylprednisolone, methylprednisone and corticosterone for assessment of methylprednisolone disposition in the rat. , 1988, Journal of chromatography.

[28]  Eric P Hoffman,et al.  Microarray analysis of the temporal response of skeletal muscle to methylprednisolone: comparative analysis of two dosing regimens. , 2007, Physiological genomics.

[29]  Richard R. Almon,et al.  Modeling Circadian Rhythms of Glucocorticoid Receptor and Glutamine Synthetase Expression in Rat Skeletal Muscle , 2006, Pharmaceutical Research.

[30]  H. Aasheim,et al.  The human solute carrier SLC41A1 belongs to a novel eukaryotic subfamily with homology to prokaryotic MgtE Mg2+ transporters. , 2003, Biochemical and biophysical research communications.

[31]  D. Virshup,et al.  The B56 Family of Protein Phosphatase 2A (PP2A) Regulatory Subunits Encodes Differentiation-induced Phosphoproteins That Target PP2A to Both Nucleus and Cytoplasm* , 1996, The Journal of Biological Chemistry.

[32]  C. Badiu Genetic clock of biologic rhythms , 2003, Journal of cellular and molecular medicine.

[33]  B. Roozendaal,et al.  Do Corticosteroids Damage the Brain? , 2006, Journal of neuroendocrinology.

[34]  Nathan Salomonis,et al.  Time- and exercise-dependent gene regulation in human skeletal muscle , 2003, Genome Biology.

[35]  Christopher M. Adams,et al.  Cholesterol and 25-Hydroxycholesterol Inhibit Activation of SREBPs by Different Mechanisms, Both Involving SCAP and Insigs* , 2004, Journal of Biological Chemistry.

[36]  H. Heng,et al.  Tissue distribution, genomic structure, and chromosome mapping of mouse and human eukaryotic initiation factor 4E-binding proteins 1 and 2. , 1996, Genomics.

[37]  R. Coleman,et al.  Rat long-chain acyl-CoA synthetase mRNA, protein, and activity vary in tissue distribution and in response to diet Published, JLR Papers in Press, June 13, 2006. , 2006, Journal of Lipid Research.

[38]  Masamitsu Iino,et al.  System-level identification of transcriptional circuits underlying mammalian circadian clocks , 2005, Nature Genetics.

[39]  Joseph Fogerty,et al.  Loss of Nocturnin, a circadian deadenylase, confers resistance to hepatic steatosis and diet-induced obesity , 2007, Proceedings of the National Academy of Sciences.