Evidence map›Paper›PMID 38805552›Full record

ArticlePLoS genetics2024

Clock-dependent chromatin accessibility rhythms regulate circadian transcription.

Ye Yuan, Qianqian Chen, Margarita Brovkina, E Josephine Clowney, Swathi Yadlapalli

Abstract read
In one paragraph

Article in PLoS genetics, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

16 citing papers in PubMed.

  1. Review
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  6. Article
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  10. Single-Cell Multiomic Analysis of Circadian Rhythmicity in Mouse Liver.bioRxiv : the preprint server for biology · 2025
    Article
  11. Article
  12. Article
  13. Mineralocorticoid Receptor and Sleep Quality in Chronic Kidney Disease.International journal of molecular sciences · 2024
    Review
  14. Review
  15. Review
  16. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors.

Ye YuanCellular and Molecular Biology Program, University of Michigan, Ann Arbor, Michigan, United States of America.ORCID 0000-0001-9641-9102
Qianqian ChenDepartment of Cell and Developmental Biology, University of Michigan, Ann Arbor, Michigan, United States of America.
Margarita BrovkinaCellular and Molecular Biology Program, University of Michigan, Ann Arbor, Michigan, United States of America.
E Josephine ClowneyCellular and Molecular Biology Program, University of Michigan, Ann Arbor, Michigan, United States of America.
Swathi YadlapalliCellular and Molecular Biology Program, University of Michigan, Ann Arbor, Michigan, United States of America.ORCID 0000-0001-5870-341X

Funding

CELLULAR AND MOLECULAR BIOLOGY AT MICHIGANT32GM007315 · NIGMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI PUTHENVEEDU, MANOJKUMAR A · 1985 to 2021
$12.8M
Spatiotemporal mechanisms controlling circadian rhythmsR35GM133737 · NIGMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Swathi Yadlapalli · 2019 to 2026
$3.4M
Chromatin-based encoding of sex differentiation of neuronsF31NS127484 · NINDS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI BROVKINA, MARGARITA · 2023 to 2024
$72k
NIGMS NIH HHS R35 GM133737NIGMS NIH HHS T32 GM007315NINDS NIH HHS F31 NS127484
6 · The paper itself

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.

Indexed as

ChromatinCircadian RhythmDrosophila melanogasterDrosophila ProteinsAnimalsBasic-Leucine Zipper Transcription FactorsCircadian ClocksCLOCK ProteinsDrosophilaEnhancer Elements, GeneticGene Expression RegulationNeuronsPeriod Circadian ProteinsPromoter Regions, GeneticTranscription, GeneticBasic-Leucine Zipper Transcription FactorsChromatinClk protein, DrosophilaCLOCK ProteinsDrosophila ProteinsPDP1 protein, DrosophilaPeriod Circadian ProteinsPER protein, Drosophila

Identifiers

PMID38805552
PMCPMC11161047

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.