Clk post-transcriptional control denoises circadian transcription both temporally and spatially.
basic_science · Level V
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- Record sourced from PubMed, PMID 25952406.
- Also identified by DOI 10.1038/ncomms8056 and PMC identifier 4915573.
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Abstract
The transcription factor CLOCK (CLK) is essential for the development and maintenance of circadian rhythms in Drosophila. However, little is known about how CLK levels are controlled. Here we show that Clk mRNA is strongly regulated post-transcriptionally through its 3' UTR. Flies expressing Clk transgenes without normal 3' UTR exhibit variable CLK-driven transcription and circadian behaviour as well as ectopic expression of CLK-target genes in the brain. In these flies, the number of the key circadian neurons differs stochastically between individuals and within the two hemispheres of the same brain. Moreover, flies carrying Clk transgenes with deletions in the binding sites for the miRNA bantam have stochastic number of pacemaker neurons, suggesting that this miRNA mediates the deterministic expression of CLK. Overall our results demonstrate a key role of Clk post-transcriptional control in stabilizing circadian transcription, which is essential for proper development and maintenance of circadian rhythms in Drosophila.
Medical subject headings
- CLOCK Proteins
- Circadian Rhythm
- Drosophila Proteins
- Drosophila melanogaster
- Gene Expression Regulation
- Transcription, Genetic