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Abstract
Approximately 30% of circadian transcripts in mouse liver and Drosophila heads may be influenced by rhythmic posttranscriptional regulation.
- Circadian cellular outputs impact thousands of genes across various cell types.
- Transcript peak abundances do not consistently align with gene-expression activity peaks.
- Circadian degradation of mRNAs and proteins may critically influence the timing of their peaks.
- A theoretical framework was developed to describe the amplitudes and phases of biomolecules with circadian half-lives.
- The framework successfully explains both transcriptome and proteome studies, including unexpected timing of transcript and protein appearances.
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