4.8 Article

Systematic analysis of differential rhythmic liver gene expression mediated by the circadian clock and feeding rhythms

Publisher

NATL ACAD SCIENCES
DOI: 10.1073/pnas.2015803118

Keywords

circadian clock; feeding-fasting cycle; liver metabolism; transcriptomics; differential rhythmicity analysis

Funding

  1. European Research Council [ERC-2010-StG-260988]
  2. Institute for Molecular Bioscience, The University of Queensland
  3. Swiss National Science Foundation [310030_173079]
  4. Ecole Polytechnique Federale de Lausanne (EPFL)
  5. Swiss National Science Foundation (SNF) [310030_173079] Funding Source: Swiss National Science Foundation (SNF)

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The study investigated the roles of the circadian clock and feeding rhythms in regulating rhythmic gene expression in the liver, highlighting their importance and differential contributions. Both feeding patterns and the circadian clock influence gene expression rhythms, with distinct amplitudes. By analyzing multiple core clock regulators, the research revealed their varying impacts on liver gene expression regulation.
The circadian clock and feeding rhythms are both important regulators of rhythmic gene expression in the liver. To further dissect the respective contributions of feeding and the clock, we analyzed differential rhythmicity of liver tissue samples across several conditions. We developed a statistical method tailored to compare rhythmic liver messenger RNA (mRNA) expression in mouse knockout models of multiple clock genes, as well as PARbZip output transcription factors (Hlf/Dbp/Tef). Mice were exposed to ad libitum or night-restricted feeding under regular light-dark cycles. During ad libitum feeding, genetic ablation of the core clock attenuated rhythmic-feeding patterns, which could be restored by the night-restricted feeding regimen. High-amplitude mRNA expression rhythms in wild-type livers were driven by the circadian clock, but rhythmic feeding also contributed to rhythmic gene expression, albeit with significantly lower amplitudes. We observed that Bmal1 and Cry1/2 knockouts differed in their residual rhythmic gene expression. Differences in mean expression levels between wild types and knockouts correlated with rhythmic gene expression in wild type. Surprisingly, in PARbZip knockout mice, the mean expression levels of PARbZip targets were more strongly impacted than their rhythms, potentially due to the rhythmic activity of the D-box-repressor NFIL3. Genes that lost rhythmicity in PARbZip knockouts were identified to be indirect targets. Our findings provide insights into the diurnal transcriptome in mouse liver as we identified the differential contributions of several core clock regulators. In addition, we gained more insights on the specific effects of the feeding-fasting cycle.

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