Evidence map›Paper›PMID 39127768›Full record

ArticleNature communications2024

Quantitative analysis of cis-regulatory elements in transcription with KAS-ATAC-seq.

Ruitu Lyu, Yun Gao, Tong Wu, Chang Ye, Pingluan Wang, Chuan He

Abstract read
In one paragraph

Article in Nature communications, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. KAS-CUT&Tag for direct mapping of transcription bubbles.bioRxiv : the preprint server for biology · 2026
    Article
  2. Review
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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

6 authors.

Ruitu Lyu *Department of Chemistry, The University of Chicago, Chicago, IL, 60637, USA. lvruitu@uchicago.edu.ORCID http://orcid.org/0000-0003-4597-1604
Yun Gao *Department of Chemistry, The University of Chicago, Chicago, IL, 60637, USA.
Tong Wu *Department of Chemistry, The University of Chicago, Chicago, IL, 60637, USA.ORCID http://orcid.org/0000-0001-9968-9909
Chang YeDepartment of Chemistry, The University of Chicago, Chicago, IL, 60637, USA.ORCID http://orcid.org/0000-0003-0236-5671
Pingluan WangDepartment of Chemistry, The University of Chicago, Chicago, IL, 60637, USA.
Chuan HeDepartment of Chemistry, The University of Chicago, Chicago, IL, 60637, USA. chuanhe@uchicago.edu.ORCID http://orcid.org/0000-0003-4319-7424

Funding

Transcriptome-wide base-resolution sequencing of pseudouridine in human normal and AD brain tissues-CEGS Admin supplement 2020-2021RM1HG008935 · NHGRI · UNIVERSITY OF CHICAGO · PI HE, CHUAN · 2016 to 2025
$24.4M
Labeling and sequencing of 5hmC and 5mC in DNA-RenewalR01HG006827 · NHGRI · UNIVERSITY OF CHICAGO · PI HE, CHUAN · 2012 to 2025
$7.2M
Targets and functions of the mammalian snoRNAomeR01HG012780 · NHGRI · UNIVERSITY OF CHICAGO · PI HE, CHUAN, PAN, TAO · 2022 to 2025
$2.8M
NHGRI NIH HHS R01 HG006827NHGRI NIH HHS R01 HG012780NHGRI NIH HHS RM1 HG008935U.S. Department of Health & Human Services | National Institutes of Health (NIH) R01HG012780U.S. Department of Health & Human Services | National Institutes of Health (NIH) RM1HG008935
6 · The paper itself

Abstract

Cis-regulatory elements (CREs) are pivotal in orchestrating gene expression throughout diverse biological systems. Accurate identification and in-depth characterization of functional CREs are crucial for decoding gene regulation networks during cellular processes. In this study, we develop Kethoxal-Assisted Single-stranded DNA Assay for Transposase-Accessible Chromatin with Sequencing (KAS-ATAC-seq) to quantitatively analyze the transcriptional activity of CREs. A main advantage of KAS-ATAC-seq lies in its precise measurement of ssDNA levels within both proximal and distal ATAC-seq peaks, enabling the identification of transcriptional regulatory sequences. This feature is particularly adept at defining Single-Stranded Transcribing Enhancers (SSTEs). SSTEs are highly enriched with nascent RNAs and specific transcription factors (TFs) binding sites that define cellular identity. Moreover, KAS-ATAC-seq provides a detailed characterization and functional implications of various SSTE subtypes. Our analysis of CREs during mouse neural differentiation demonstrates that KAS-ATAC-seq can effectively identify immediate-early activated CREs in response to retinoic acid (RA) treatment. Our findings indicate that KAS-ATAC-seq provides more precise annotation of functional CREs in transcription. Future applications of KAS-ATAC-seq would help elucidate the intricate dynamics of gene regulation in diverse biological processes.

Indexed as

Transcription FactorsAnimalsBinding SitesCell DifferentiationChromatinChromatin Immunoprecipitation SequencingDNA, Single-StrandedEnhancer Elements, GeneticGene Expression RegulationHumansMiceRegulatory Elements, TranscriptionalRegulatory Sequences, Nucleic AcidSequence Analysis, DNATranscription, GeneticTransposasesChromatinDNA, Single-StrandedTranscription FactorsTransposasesTretinoin

Identifiers

PMID39127768
PMCPMC11316786

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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.