Evidence map›Paper›PMID 40054857›Full record

ArticleJournal of proteome research2025

Coupling Proximity Biotinylation with Genomic Targeting to Characterize Locus-Specific Changes in Chromatin Environments.

Pata-Eting Kougnassoukou Tchara, Jérémy Loehr, Jean-Philippe Lambert

Abstract read
In one paragraph

Article in Journal of proteome research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. A chemical epigenetic tool to probe site-specific DNA-binding protein complexes.Proceedings of the National Academy of Sciences of the United States of America · 2025
    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

3 authors.

Pata-Eting Kougnassoukou TcharaDepartment of Molecular Medicine and Cancer Research Centre, Université Laval, Quebec, QC G1V 0A6, Canada.ORCID 0000-0003-3524-7225
Jérémy LoehrDepartment of Molecular Medicine and Cancer Research Centre, Université Laval, Quebec, QC G1V 0A6, Canada.ORCID 0000-0002-9746-800X
Jean-Philippe LambertDepartment of Molecular Medicine and Cancer Research Centre, Université Laval, Quebec, QC G1V 0A6, Canada.ORCID 0000-0002-0833-1221

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Regulating gene expression involves significant changes in the chromatin environment at the locus level, especially at regulatory sequences. However, their modulation following pharmacological treatments or pathological conditions remain mostly undetermined. Here, we report versatile locus-specific proteomics tools to address this knowledge gap, which combine the targeting ability of the CRISPR/Cas9 system and the protein-labeling capability of the highly reactive biotin ligases TurboID (in CasTurbo) and UltraID (in CasUltra). CasTurbo and CasUltra enabled rapid chromatin protein labeling at repetitive sequences like centromeres and telomeres, as well as nonamplified genes. We applied CasUltra to A375 melanoma cell lines to decipher the protein environment of the

Indexed as

ChromatinProteomicsAzepinesBiotinylationBromodomain Containing ProteinsCell Line, TumorCRISPR-Cas SystemsGenetic LociHumansMelanomaPromoter Regions, GeneticProteinsProto-Oncogene Proteins c-mycTriazolesAzepinesbromodomain and extra-terminal domain protein, humanBromodomain Containing ProteinsChromatin(+)-JQ1 compoundProteinsProto-Oncogene Proteins c-mycTriazolesBET inhibitorsbromodomainchromatinhistone acetylationMYCproteomics

Identifiers

PMID40054857
PMCPMC11976867

What OpenQuestion holds

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LicenceCC BY-NC-ND
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.