W. Filipowicz, Mechanisms of post-transcriptional regulation by 361 microRNAs: are the answers in sight, Nat Rev Genet, vol.9, issue.2, pp.102-114, 2008.

T. Glisovic, RNA-binding proteins and post-transcriptional gene regulation, FEBS Letters, vol.433, issue.14, pp.1977-1986, 2008.
DOI : 10.1016/j.febslet.2008.03.004

URL : http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2858862

J. D. Keene, Minireview: Global Regulation and Dynamics of Ribonucleic Acid, Endocrinology, vol.151, issue.4, pp.1391-1397, 2010.
DOI : 10.1210/en.2009-1250

W. V. So and M. Rosbash, Post-transcriptional regulation contributes to Drosophila clock gene mRNA cycling, The EMBO Journal, vol.16, issue.23, pp.7146-7155, 1997.
DOI : 10.1093/emboj/16.23.7146

URL : http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1170315

K. C. Woo, Mouse period 2 mRNA circadian oscillation is modulated by PTB-mediated rhythmic mRNA degradation, Nucleic Acids Research, vol.37, issue.1, pp.26-37, 2009.
DOI : 10.1093/nar/gkn893

K. C. Woo, Circadian Amplitude of Cryptochrome 1 Is Modulated by mRNA Stability Regulation via Cytoplasmic hnRNP D Oscillation, Molecular and Cellular Biology, vol.30, issue.1, pp.197-205, 2010.
DOI : 10.1128/MCB.01154-09

S. Kojima, LARK activates posttranscriptional expression of an essential mammalian clock protein, PERIOD1, Proceedings of the National Academy of Sciences, vol.104, issue.6, pp.1859-1864, 2007.
DOI : 10.1073/pnas.0607567104

Y. Huang, Altered LARK expression perturbs development and physiology of the Drosophila PDF clock neurons, Molecular and Cellular Neuroscience, vol.41, issue.2, pp.196-205, 2009.
DOI : 10.1016/j.mcn.2009.02.013

D. P. Bartel, MicroRNAs: Target Recognition and Regulatory Functions, Cell, vol.136, issue.2, pp.378-215, 2009.
DOI : 10.1016/j.cell.2009.01.002

H. Y. Cheng, microRNA Modulation of Circadian-Clock Period and Entrainment, Neuron, vol.54, issue.5, pp.813-829, 2007.
DOI : 10.1016/j.neuron.2007.05.017

T. D. Kim, Rhythmic Serotonin N-Acetyltransferase mRNA Degradation Is Essential for the Maintenance of Its Circadian Oscillation, Molecular and Cellular Biology, vol.25, issue.8, pp.3232-383, 2005.
DOI : 10.1128/MCB.25.8.3232-3246.2005

T. D. Kim, Rhythmic control of AANAT translation by hnRNP Q in circadian melatonin production, Genes & Development, vol.21, issue.7, pp.797-810, 2007.
DOI : 10.1101/gad.1519507

B. Kornmann, System-Driven and Oscillator-Dependent Circadian Transcription in Mice with a Conditionally Active Liver Clock, PLoS Biology, vol.6, issue.2, pp.34-388, 2007.
DOI : 10.1371/journal.pbio.0050034.st001

M. E. Hughes, Harmonics of Circadian Gene Transcription in Mammals, PLoS Genetics, vol.153, issue.2, p.389, 2009.
DOI : 10.1371/journal.pgen.1000442.s019

P. Lidder, Circadian Control of Messenger RNA Stability. Association with a Sequence-Specific Messenger RNA Decay Pathway, PLANT PHYSIOLOGY, vol.138, issue.4, pp.2374-392, 2005.
DOI : 10.1104/pp.105.060368

C. Sire, microRNAs, miR167, miR168, miR171 and miR398, FEBS Letters, vol.394, issue.6, pp.1039-1044, 2009.
DOI : 10.1016/j.febslet.2009.02.024

M. Yang, Circadian regulation of a limited set of conserved microRNAs in Drosophila, BMC Genomics, vol.9, issue.1, p.83, 2008.
DOI : 10.1186/1471-2164-9-83

S. Xu, MicroRNA (miRNA) Transcriptome of Mouse Retina and Identification of a Sensory Organ-specific miRNA Cluster, Journal of Biological Chemistry, vol.282, issue.34, pp.25053-25066, 2007.
DOI : 10.1074/jbc.M700501200

M. Mittag, Circadian expression of the luciferin-binding protein 401 correlates with the binding of a protein to the 3' untranslated region of its mRNA, Proc, vol.402, 1994.

D. Iliev, A Heteromeric RNA-Binding Protein Is Involved in Maintaining Acrophase and Period of the Circadian Clock, PLANT PHYSIOLOGY, vol.142, issue.2, pp.797-806, 2006.
DOI : 10.1104/pp.106.085944

O. Voytsekh, Both Subunits of the Circadian RNA-Binding Protein CHLAMY1 Can Integrate Temperature Information, PLANT PHYSIOLOGY, vol.147, issue.4, pp.2179-2193, 2008.
DOI : 10.1104/pp.108.118570

J. S. Kim, Muscleblind-like 2: circadian expression in the mammalian pineal gland is controlled by an adrenergic-cAMP mechanism, Journal of Neurochemistry, vol.13, issue.2, pp.756-764, 2009.
DOI : 10.1111/j.1471-4159.2009.06184.x

J. Baggs and C. Green, Nocturnin, a Deadenylase in Xenopus laevis Retina. A 411 Mechanism for Posttranscriptional Control of Circadian-Related mRNA, Curr Biol, vol.13, issue.3, pp.412-189, 2003.

C. B. Green, Loss of Nocturnin, a circadian deadenylase, confers 414 resistance to hepatic steatosis and diet-induced obesity, Proc Natl Acad Sci U S A, vol.104, issue.23, pp.415-9888, 2007.

A. B. Reddy, Circadian Orchestration of the Hepatic Proteome, Current Biology, vol.16, issue.11, pp.16-1107, 2006.
DOI : 10.1016/j.cub.2006.04.026

J. Houseley, RNA-quality control by the exosome, Nature Reviews Molecular Cell Biology, vol.126, issue.7, pp.7-529, 2006.
DOI : 10.1038/nrm1964

J. Guo, The Exosome Regulates Circadian Gene Expression in a Posttranscriptional Negative Feedback Loop, Cell, vol.138, issue.6, pp.1236-1246, 2009.
DOI : 10.1016/j.cell.2009.06.043

C. Heintzen, AtGRP7, a nuclear RNA-binding protein as a component of 423 a circadian-regulated negative feedback loop in Arabidopsis thaliana, Proc Natl Acad, p.424, 1997.

J. C. Schoning, GRP7 and regulation of its targets is impaired by a single RNA recognition motif point mutation, The Plant Journal, vol.31, issue.6, pp.1119-1130, 2007.
DOI : 10.1111/j.1365-313X.2007.03302.x

J. C. Schoning, Reciprocal regulation of glycine-rich RNA-binding proteins via an interlocked feedback loop coupling alternative splicing to nonsense-mediated decay in Arabidopsis, Nucleic Acids Research, vol.36, issue.22, pp.6977-6987, 2008.
DOI : 10.1093/nar/gkn847

M. C. Wollerton, Autoregulation of Polypyrimidine Tract Binding Protein by Alternative Splicing Leading to Nonsense-Mediated Decay, Molecular Cell, vol.13, issue.1, pp.91-100, 2004.
DOI : 10.1016/S1097-2765(03)00502-1

L. Rahman, Alternative Splicing of Brain-Specific PTB Defines a Tissue-Specific Isoform Pattern That Predicts Distinct Functional Roles, Genomics, vol.80, issue.3, pp.245-435, 2002.
DOI : 10.1006/geno.2002.6826

R. Spellman, Crossregulation and Functional Redundancy between the Splicing Regulator PTB and Its Paralogs nPTB and ROD1, Molecular Cell, vol.27, issue.3, pp.420-434, 2007.
DOI : 10.1016/j.molcel.2007.06.016

P. L. Boutz, A post-transcriptional regulatory switch in polypyrimidine 439 tract-binding proteins reprograms alternative splicing in developing neurons, Genes, vol.440, issue.13, pp.21-1636, 2007.

J. A. Dembowski and P. J. Grabowski, The CUGBP2 Splicing Factor Regulates an Ensemble of Branchpoints from Perimeter Binding Sites with Implications for Autoregulation, PLoS Genetics, vol.6, issue.8, pp.1000595-444, 2009.
DOI : 10.1371/journal.pgen.1000595.s008

M. L. Dequeant, A Complex Oscillating Network of Signaling Genes Underlies the Mouse Segmentation Clock, Science, vol.314, issue.5805, pp.1595-1598, 2006.
DOI : 10.1126/science.1133141

A. Morales, Periodic Lunatic fringe expression is controlled during 447 segmentation by a cyclic transcriptional enhancer responsive to notch signaling, Dev 448 Cell, pp.63-74, 2002.

M. Gajewski, Anterior and posterior waves of cyclic her1 gene 450 expression are differentially regulated in the presomitic mesoderm of zebrafish, Development, vol.451, issue.13018, pp.4269-4278, 2003.

R. Davis, Molecular Targets of Vertebrate Segmentation, Developmental Cell, vol.1, issue.4, pp.553-565, 2001.
DOI : 10.1016/S1534-5807(01)00054-5

K. Hitachi, Tbx6, Thylacine1, and E47 synergistically activate bowline expression in Xenopus somitogenesis, Developmental Biology, vol.313, issue.2, pp.816-828, 2008.
DOI : 10.1016/j.ydbio.2007.10.015

V. Hilgers, In vivo analysis of mRNA stability using the Tet-Off system in the chicken embryo, Developmental Biology, vol.284, issue.2, pp.292-300, 2005.
DOI : 10.1016/j.ydbio.2005.05.021

J. Lewis, Autoinhibition with Transcriptional Delay, Current Biology, vol.13, issue.16, pp.1398-1408, 2003.
DOI : 10.1016/S0960-9822(03)00534-7

URL : http://doi.org/10.1016/s0960-9822(03)00534-7

K. K. Dill and S. L. Amacher, tortuga refines Notch pathway gene expression in the zebrafish presomitic mesoderm at the post-transcriptional level, Developmental Biology, vol.287, issue.2, pp.225-236, 2005.
DOI : 10.1016/j.ydbio.2005.07.032

C. Gautier-courteille, EDEN-BP-dependent post-transcriptional 465 regulation of gene expression in Xenopus somitic segmentation, Development, vol.131, issue.24, pp.466-6107, 2004.

M. E. Huot, The RNA-binding Protein Fragile X-related 1 Regulates Somite Formation in Xenopus laevis, Molecular Biology of the Cell, vol.16, issue.9, pp.4350-4361, 2005.
DOI : 10.1091/mbc.E05-04-0304

M. Cibois, A strategy to analyze the phenotypic consequences of 470 inhibiting the association of an RNA-binding protein with a specific RNA, Rna, vol.16, issue.1, pp.471-481, 2010.

R. Nagel, The miRNA-192/194 cluster regulates the Period gene family and the circadian clock, FEBS Journal, vol.93, issue.19, pp.5447-5455, 2009.
DOI : 10.1111/j.1742-4658.2009.07229.x

D. Gatfield, Integration of microRNA miR-122 in hepatic circadian gene expression, Genes & Development, vol.23, issue.11, pp.1313-1326, 2009.
DOI : 10.1101/gad.1781009

S. Kadener, A role for microRNAs in the Drosophila circadian clock, Genes & Development, vol.23, issue.18, p.477, 2009.
DOI : 10.1101/gad.1819509

E. Kwak, Essential Role of 3'-Untranslated Region-mediated mRNA Decay in Circadian Oscillations of Mouse Period3 mRNA, Journal of Biological Chemistry, vol.281, issue.28, pp.19100-480, 2006.
DOI : 10.1074/jbc.M511927200

L. D. Wilsbacher, Photic and circadian expression of luciferase in mPeriod1-luc transgenic mice in vivo, Proceedings of the National Academy of Sciences, vol.99, issue.1, pp.489-494, 2002.
DOI : 10.1073/pnas.012248599

D. O. Wang, Spatially restricting gene expression by local translation at synapses, Trends in Neurosciences, vol.33, issue.4, pp.173-182, 2010.
DOI : 10.1016/j.tins.2010.01.005

P. F. Giampietro, Progress in the Understanding of the Genetic Etiology of Vertebral Segmentation Disorders in Humans, Annals of the New York Academy of Sciences, vol.18, issue.1, pp.38-67, 2009.
DOI : 10.1111/j.1749-6632.2008.03452.x

E. L. Gould, Melatonin profiles and sleep characteristics in boys with fragile X syndrome: A preliminary study, American Journal of Medical Genetics, vol.19, issue.4, pp.307-315, 2000.
DOI : 10.1002/1096-8628(20001211)95:4<307::AID-AJMG3>3.0.CO;2-3

J. Zhang, Fragile X-Related Proteins Regulate Mammalian Circadian Behavioral Rhythms, The American Journal of Human Genetics, vol.83, issue.1, pp.43-52, 2008.
DOI : 10.1016/j.ajhg.2008.06.003

J. Ule, CLIP Identifies Nova-Regulated RNA Networks in the Brain, Science, vol.302, issue.5648, pp.1212-1215, 2003.
DOI : 10.1126/science.1090095

D. D. Licatalosi, HITS-CLIP yields genome-wide insights into brain alternative RNA processing, Nature, vol.8, issue.7221, pp.464-469, 2008.
DOI : 10.1038/nature07488

J. R. Sanford, Splicing factor SFRS1 recognizes a functionally diverse landscape of RNA transcripts, Genome Research, vol.19, issue.3, pp.381-394, 2009.
DOI : 10.1101/gr.082503.108

G. W. Yeo, An RNA code for the FOX2 splicing regulator revealed by mapping RNA-protein interactions in stem cells, Nature Structural & Molecular Biology, vol.66, issue.2, pp.130-137, 2009.
DOI : 10.1038/nsmb.1545

S. W. Chi, Argonaute HITS-CLIP decodes microRNA-mRNA interaction 500 maps, Nature, vol.460, issue.7254, pp.479-486, 2009.

D. G. Zisoulis, Comprehensive discovery of endogenous Argonaute binding sites in Caenorhabditis elegans, Nature Structural & Molecular Biology, vol.460, issue.2, pp.173-179, 2010.
DOI : 10.1101/gr.3715005

J. B. Robertson, Real-time luminescence monitoring of cell-cycle and respiratory oscillations in yeast, Proceedings of the National Academy of Sciences, vol.105, issue.46, pp.17988-17993, 2008.
DOI : 10.1073/pnas.0809482105

J. D. Veldhuis, Spectrum of the Pulsatile Characteristics of LH Release in Normal Men, Journal of Andrology, vol.109, issue.2, pp.83-92, 1986.
DOI : 10.1002/j.1939-4640.1986.tb00885.x

J. E. Knight, mRNA Stability and Polysome Loss in Hibernating Arctic Ground Squirrels (Spermophilus parryii), Molecular and Cellular Biology, vol.20, issue.17, pp.6374-6379, 2000.
DOI : 10.1128/MCB.20.17.6374-6379.2000

F. C. Hoppensteadt and J. B. Keller, Synchronization of periodical cicada emergences, Science, vol.194, issue.4262, pp.335-337, 1976.
DOI : 10.1126/science.987617

A. Kawamura, Zebrafish Hairy/Enhancer of split protein links FGF signaling to cyclic gene expression in the periodic segmentation of somites, Genes & Development, vol.19, issue.10, pp.1156-1161, 2005.
DOI : 10.1101/gad.1291205

S. Kuersten and E. B. Goodwin, The power of the 3??? UTR: translational control and development, Nature Reviews Genetics, vol.4, issue.8, pp.626-637, 2003.
DOI : 10.1038/nrg1125

F. Mauxion, BTG/TOB factors impact deadenylases, Trends in Biochemical Sciences, vol.34, issue.12, pp.34-640, 2009.
DOI : 10.1016/j.tibs.2009.07.008

URL : http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2787745

N. Y. Garceau, Alternative initiation of translation and time-specific 519 phosphorylation yield multiple forms of the essential clock protein FREQUENCY, Cell, vol.520, issue.893, pp.469-476, 1997.

L. Hir, H. Seraphin, and B. , EJCs at the heart of translational control, Cell, vol.133, issue.2, pp.522-213, 2008.

R. Kamath, Systematic functional analysis of the Caenorhabditis elegans genome using RNAi, Nature, vol.421, issue.6920, pp.231-237, 2003.
DOI : 10.1038/nature01278

G. Dietzl, A genome-wide transgenic RNAi library for conditional gene inactivation in Drosophila, Nature, vol.39, issue.7150, pp.151-156, 2007.
DOI : 10.1038/nature05954