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Clock-dependent Chromatin Accessibility Rhythms Regulate Circadian Transcription

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Journal PLoS Genet
Specialty Genetics
Date 2024 May 28
PMID 38805552
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Abstract

Chromatin organization plays a crucial role in gene regulation by controlling the accessibility of DNA to transcription machinery. While significant progress has been made in understanding the regulatory role of clock proteins in circadian rhythms, how chromatin organization affects circadian rhythms remains poorly understood. Here, we employed ATAC-seq (Assay for Transposase-Accessible Chromatin with Sequencing) on FAC-sorted Drosophila clock neurons to assess genome-wide chromatin accessibility at dawn and dusk over the circadian cycle. We observed significant oscillations in chromatin accessibility at promoter and enhancer regions of hundreds of genes, with enhanced accessibility either at dusk or dawn, which correlated with their peak transcriptional activity. Notably, genes with enhanced accessibility at dusk were enriched with E-box motifs, while those more accessible at dawn were enriched with VRI/PDP1-box motifs, indicating that they are regulated by the core circadian feedback loops, PER/CLK and VRI/PDP1, respectively. Further, we observed a complete loss of chromatin accessibility rhythms in per01 null mutants, with chromatin consistently accessible at both dawn and dusk, underscoring the critical role of Period protein in driving chromatin compaction during the repression phase at dawn. Together, this study demonstrates the significant role of chromatin organization in circadian regulation, revealing how the interplay between clock proteins and chromatin structure orchestrates the precise timing of biological processes throughout the day. This work further implies that variations in chromatin accessibility might play a central role in the generation of diverse circadian gene expression patterns in clock neurons.

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References
1.
Kim J, Kwak P, Weitz C . Specificity in circadian clock feedback from targeted reconstitution of the NuRD corepressor. Mol Cell. 2014; 56(6):738-48. DOI: 10.1016/j.molcel.2014.10.017. View

2.
Bell-Pedersen D, Cassone V, Earnest D, Golden S, Hardin P, Thomas T . Circadian rhythms from multiple oscillators: lessons from diverse organisms. Nat Rev Genet. 2005; 6(7):544-56. PMC: 2735866. DOI: 10.1038/nrg1633. View

3.
Etchegaray J, Lee C, Wade P, Reppert S . Rhythmic histone acetylation underlies transcription in the mammalian circadian clock. Nature. 2002; 421(6919):177-82. DOI: 10.1038/nature01314. View

4.
Shulga Y, Topham M, Epand R . Regulation and functions of diacylglycerol kinases. Chem Rev. 2011; 111(10):6186-208. DOI: 10.1021/cr1004106. View

5.
Thurman R, Rynes E, Humbert R, Vierstra J, Maurano M, Haugen E . The accessible chromatin landscape of the human genome. Nature. 2012; 489(7414):75-82. PMC: 3721348. DOI: 10.1038/nature11232. View