Evidence map›Paper›PMID 37173345›Full record

ArticleScientific reports2023

Prediction of mammalian tissue-specific CLOCK-BMAL1 binding to E-box DNA motifs.

Daniel Marri, David Filipovic, Omar Kana, Shelley Tischkau, Sudin Bhattacharya

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
3.5field-weighted citation impact, top 7% of its field
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

14 citing papers in PubMed, 23 citations in OpenAlex.

  1. Review
  2. CircadianiScience · 2026
    Article
  3. Review
  4. Review
  5. Research Progress of BMAL1 in Heart Failure.Journal of the American Heart Association · 2025
    Review
  6. bioRxiv : the preprint server for biology · 2025
    Article
  7. Review
  8. Article
  9. Review
  10. Article
  11. Circadian immunity from bench to bedside: a practical guide.The Journal of clinical investigation · 2024
    Review
  12. Clock gene Per2 modulates epidermal tissue repair in vivo.Journal of cellular biochemistry · 2024
    Article
  13. Article
  14. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors at 2 institutions in 1 country.

Daniel MarriDepartment of Biomedical Engineering, Michigan State University, East Lansing, MI, USA.ORCID 0000-0002-7109-1566
David FilipovicDepartment of Biomedical Engineering, Michigan State University, East Lansing, MI, USA.ORCID 0000-0003-4421-1654
Omar KanaInstitute for Quantitative Health Science and Engineering, Michigan State University, East Lansing, MI, USA.ORCID 0000-0002-7772-4694
Shelley TischkauDepartment of Pharmacology, Southern Illinois University School of Medicine, Springfield, IL, USA.ORCID 0000-0002-8016-6398
Sudin BhattacharyaDepartment of Biomedical Engineering, Michigan State University, East Lansing, MI, USA. sbhattac@msu.edu.ORCID 0000-0002-2360-1672
Michigan State University · USSouthern Illinois University School of Medicine · US

Funding

Integrative transcriptional and epigenomic modeling of xenobiotic-activated gene regulatory networksR01ES031937 · NIEHS · MICHIGAN STATE UNIVERSITY · PI BHATTACHARYA, SUDIN, CUDDAPAH, SURESH · 2020 to 2024
$2.4M
NIEHS NIH HHS R01 ES031937
6 · The paper itself

Abstract

The Brain and Muscle ARNTL-Like 1 protein (BMAL1) forms a heterodimer with either Circadian Locomotor Output Cycles Kaput (CLOCK) or Neuronal PAS domain protein 2 (NPAS2) to act as a master regulator of the mammalian circadian clock gene network. The dimer binds to E-box gene regulatory elements on DNA, activating downstream transcription of clock genes. Identification of transcription factor binding sites and genomic features that correlate to DNA binding by BMAL1 is a challenging problem, given that CLOCK-BMAL1 or NPAS2-BMAL1 bind to several distinct binding motifs (CANNTG) on DNA. Using three different types of tissue-specific machine learning models with features based on (1) DNA sequence, (2) DNA sequence plus DNA shape, and (3) DNA sequence and shape plus histone modifications, we developed an interpretable predictive model of genome-wide BMAL1 binding to E-box motifs and dissected the mechanisms underlying BMAL1-DNA binding. Our results indicated that histone modifications, the local shape of the DNA, and the flanking sequence of the E-box motif are sufficient predictive features for BMAL1-DNA binding. Our models also provide mechanistic insights into tissue specificity of DNA binding by BMAL1.

Indexed as

ARNTL Transcription FactorsE-Box ElementsAnimalsBasic Helix-Loop-Helix ProteinsCircadian RhythmCLOCK ProteinsDNAMammalsNucleotide MotifsProtein BindingARNTL Transcription FactorsBasic Helix-Loop-Helix ProteinsCLOCK ProteinsDNA

Identifiers

PMID37173345
PMCPMC10182026
OpenAlexW4376274485

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.