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      The calcineurin-NFAT pathway controls activity-dependent circadian gene expression in slow skeletal muscle

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          Abstract

          Objective

          Physical activity and circadian rhythms are well-established determinants of human health and disease, but the relationship between muscle activity and the circadian regulation of muscle genes is a relatively new area of research. It is unknown whether muscle activity and muscle clock rhythms are coupled together, nor whether activity rhythms can drive circadian gene expression in skeletal muscle.

          Methods

          We compared the circadian transcriptomes of two mouse hindlimb muscles with vastly different circadian activity patterns, the continuously active slow soleus and the sporadically active fast tibialis anterior, in the presence or absence of a functional skeletal muscle clock (skeletal muscle-specific Bmal1 KO). In addition, we compared the effect of denervation on muscle circadian gene expression.

          Results

          We found that different skeletal muscles exhibit major differences in their circadian transcriptomes, yet core clock gene oscillations were essentially identical in fast and slow muscles. Furthermore, denervation caused relatively minor changes in circadian expression of most core clock genes, yet major differences in expression level, phase and amplitude of many muscle circadian genes.

          Conclusions

          We report that activity controls the oscillation of around 15% of skeletal muscle circadian genes independently of the core muscle clock, and we have identified the Ca 2+-dependent calcineurin-NFAT pathway as an important mediator of activity-dependent circadian gene expression, showing that circadian locomotor activity rhythms drive circadian rhythms of NFAT nuclear translocation and target gene expression.

          Highlights

          • Activity is a major extrinsic factor driving ∼15% of muscle circadian genes.

          • Calcineurin-NFAT drives activity-dependent circadian gene expression in muscle.

          • The majority of skeletal muscle circadian genes are muscle type-specific.

          • A common set of skeletal muscle circadian genes are clock-dependent.

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          Most cited references40

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          Coordinated transcription of key pathways in the mouse by the circadian clock.

          In mammals, circadian control of physiology and behavior is driven by a master pacemaker located in the suprachiasmatic nuclei (SCN) of the hypothalamus. We have used gene expression profiling to identify cycling transcripts in the SCN and in the liver. Our analysis revealed approximately 650 cycling transcripts and showed that the majority of these were specific to either the SCN or the liver. Genetic and genomic analysis suggests that a relatively small number of output genes are directly regulated by core oscillator components. Major processes regulated by the SCN and liver were found to be under circadian regulation. Importantly, rate-limiting steps in these various pathways were key sites of circadian control, highlighting the fundamental role that circadian clocks play in cellular and organismal physiology.
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            Early aging and age-related pathologies in mice deficient in BMAL1, the core componentof the circadian clock.

            Mice deficient in the circadian transcription factor BMAL1 (brain and muscle ARNT-like protein) have impaired circadian behavior and demonstrate loss of rhythmicity in the expression of target genes. Here we report that Bmal1(-/-) mice have reduced lifespans and display various symptoms of premature aging including sarcopenia, cataracts, less subcutaneous fat, organ shrinkage, and others. The early aging phenotype correlates with increased levels of reactive oxygen species in some tissues of the Bmal1(-/- )animals. These findings, together with data on CLOCK/BMAL1-dependent control of stress responses, may provide a mechanistic explanation for the early onset of age-related pathologies in the absence of BMAL1.
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              Extensive and divergent circadian gene expression in liver and heart.

              Many mammalian peripheral tissues have circadian clocks; endogenous oscillators that generate transcriptional rhythms thought to be important for the daily timing of physiological processes. The extent of circadian gene regulation in peripheral tissues is unclear, and to what degree circadian regulation in different tissues involves common or specialized pathways is unknown. Here we report a comparative analysis of circadian gene expression in vivo in mouse liver and heart using oligonucleotide arrays representing 12,488 genes. We find that peripheral circadian gene regulation is extensive (> or = 8-10% of the genes expressed in each tissue), that the distributions of circadian phases in the two tissues are markedly different, and that very few genes show circadian regulation in both tissues. This specificity of circadian regulation cannot be accounted for by tissue-specific gene expression. Despite this divergence, the clock-regulated genes in liver and heart participate in overlapping, extremely diverse processes. A core set of 37 genes with similar circadian regulation in both tissues includes candidates for new clock genes and output genes, and it contains genes responsive to circulating factors with circadian or diurnal rhythms.
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                Author and article information

                Contributors
                Journal
                Mol Metab
                Mol Metab
                Molecular Metabolism
                Elsevier
                2212-8778
                25 September 2015
                November 2015
                25 September 2015
                : 4
                : 11
                : 823-833
                Affiliations
                [1 ]Venetian Institute of Molecular Medicine (VIMM), Padova, Italy
                [2 ]Center for Genome Research, Department of Life Sciences, University of Modena and Reggio Emilia, Modena, Italy
                [3 ]Department of Biomedical Sciences, University of Padova, Italy
                [4 ]Institute of Neurosciences, Consiglio Nazionale delle Ricerche (CNR), Padova, Italy
                [5 ]Institute for Medical Informatics, Statistics and Epidemiology, University of Leipzig, Germany
                [6 ]Istituto Nazionale Genetica Molecolare ‘Romeo ed Enrica Invernizzi’, Via F. Sforza 35, 20122 Milan, Italy
                Author notes
                []Corresponding author. Institute for Diabetes and Obesity, Helmholtz Zentrum München, Parkring 13, 85748 Garching, Germany. kenneth.dyar@ 123456helmholtz-muenchen.de
                [∗∗ ]Corresponding author. Venetian Institute of Molecular Medicine (VIMM), Via Orus 2, 35129 Padova, Italy. bert.blaauw@ 123456unipd.it
                [7]

                Present address: Molecular Endocrinology, Institute for Diabetes and Obesity, Helmholtz Zentrum München, Germany.

                Article
                S2212-8778(15)00174-X
                10.1016/j.molmet.2015.09.004
                4632177
                26629406
                a5fdec2d-2eae-42cc-a18d-f1d1b9452f74
                © 2015 The Authors

                This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).

                History
                : 4 September 2015
                : 15 September 2015
                Categories
                Original Article

                skeletal muscle,circadian,activity,nfat
                skeletal muscle, circadian, activity, nfat

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