Literature DB >> 26554015

Circadian and feeding rhythms differentially affect rhythmic mRNA transcription and translation in mouse liver.

Florian Atger1, Cédric Gobet2, Julien Marquis3, Eva Martin4, Jingkui Wang5, Benjamin Weger4, Grégory Lefebvre3, Patrick Descombes6, Felix Naef7, Frédéric Gachon8.   

Abstract

Diurnal oscillations of gene expression are a hallmark of rhythmic physiology across most living organisms. Such oscillations are controlled by the interplay between the circadian clock and feeding rhythms. Although rhythmic mRNA accumulation has been extensively studied, comparatively less is known about their transcription and translation. Here, we quantified simultaneously temporal transcription, accumulation, and translation of mouse liver mRNAs under physiological light-dark conditions and ad libitum or night-restricted feeding in WT and brain and muscle Arnt-like 1 (Bmal1)-deficient animals. We found that rhythmic transcription predominantly drives rhythmic mRNA accumulation and translation for a majority of genes. Comparison of wild-type and Bmal1 KO mice shows that circadian clock and feeding rhythms have broad impact on rhythmic gene expression, Bmal1 deletion affecting surprisingly both transcriptional and posttranscriptional levels. Translation efficiency is differentially regulated during the diurnal cycle for genes with 5'-Terminal Oligo Pyrimidine tract (5'-TOP) sequences and for genes involved in mitochondrial activity, many harboring a Translation Initiator of Short 5'-UTR (TISU) motif. The increased translation efficiency of 5'-TOP and TISU genes is mainly driven by feeding rhythms but Bmal1 deletion also affects amplitude and phase of translation, including TISU genes. Together this study emphasizes the complex interconnections between circadian and feeding rhythms at several steps ultimately determining rhythmic gene expression and translation.

Entities:  

Keywords:  5′-TOP sequences; TISU motifs; circadian rhythms; mRNA translation; ribosome profiling

Mesh:

Substances:

Year:  2015        PMID: 26554015      PMCID: PMC4664316          DOI: 10.1073/pnas.1515308112

Source DB:  PubMed          Journal:  Proc Natl Acad Sci U S A        ISSN: 0027-8424            Impact factor:   11.205


  81 in total

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6.  Genome-wide analysis in vivo of translation with nucleotide resolution using ribosome profiling.

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Journal:  Science       Date:  2009-02-12       Impact factor: 47.728

7.  Circadian clocks and feeding time regulate the oscillations and levels of hepatic triglycerides.

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Journal:  Cell Metab       Date:  2014-02-04       Impact factor: 27.287

8.  Circadian clock feedback cycle through NAMPT-mediated NAD+ biosynthesis.

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9.  Genome-wide RNA polymerase II profiles and RNA accumulation reveal kinetics of transcription and associated epigenetic changes during diurnal cycles.

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Journal:  PLoS Biol       Date:  2012-11-27       Impact factor: 8.029

10.  Quantitative profiling of initiating ribosomes in vivo.

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Journal:  Nat Methods       Date:  2014-12-08       Impact factor: 28.547

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  93 in total

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Review 6.  Signaling to and from the RNA Polymerase III Transcription and Processing Machinery.

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Review 9.  New insights into non-transcriptional regulation of mammalian core clock proteins.

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10.  Circadian clock regulation of mRNA translation through eukaryotic elongation factor eEF-2.

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