Evidence map›Paper›PMID 38361031›Full record

ArticleNature genetics2024

Genome-wide ATAC-see screening identifies TFDP1 as a modulator of global chromatin accessibility.

Satoko Ishii, Taishi Kakizuka, Sung-Joon Park, Ayako Tagawa, Chiaki Sanbo, Hideyuki Tanabe, Yasuyuki Ohkawa, Mahito Nakanishi, Kenta Nakai, Yusuke Miyanari

Abstract read
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In one paragraph

Article in Nature genetics, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
4.9field-weighted citation impact, top 4% 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

20 citing papers in PubMed, 21 citations in OpenAlex.

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  11. Functional Genomics: Principles and Methods.Advances in experimental medicine and biology · 2026
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  14. Engineered histones reshape chromatin in human cells.bioRxiv : the preprint server for biology · 2025
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  16. Multi-omics profile of exceptional long-term survivors of AJCC stage III triple-negative breast cancer.Chinese journal of cancer research = Chung-kuo yen cheng yen chiu · 2025
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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

10 authors at 6 institutions in 1 country.

Satoko IshiiThe Graduate University for Advanced Studies, SOKENDAI, Okazaki, Japan.ORCID http://orcid.org/0000-0003-0116-6275
Taishi KakizukaGraduate School of Frontier Biosciences, Osaka University, Suita, Japan.
Sung-Joon ParkHuman Genome Center, The Institute of Medical Science, The University of Tokyo, Tokyo, Japan.ORCID http://orcid.org/0000-0002-1774-9590
Ayako TagawaWPI Nano Life Science Institute, Kanazawa University, Kanazawa, Japan.
Chiaki SanboNational Institute for Basic Biology, National Institutes of Natural Sciences, Okazaki, Japan.
Hideyuki TanabeResearch Center for Integrative Evolutionary Science, SOKENDAI, Hayama, Japan.
Yasuyuki OhkawaDivision of Transcriptomics, Medical Institute of Bioregulation, Kyushu University, Fukuoka, Japan.
Mahito NakanishiTOKIWA-Bio Inc., Tsukuba, Japan.
Kenta NakaiHuman Genome Center, The Institute of Medical Science, The University of Tokyo, Tokyo, Japan.
Yusuke MiyanariWPI Nano Life Science Institute, Kanazawa University, Kanazawa, Japan. miyanari@staff.kanazawa-u.ac.jp.ORCID http://orcid.org/0000-0002-8641-6466
Kanazawa University · JPNational Institute for Basic Biology · JPThe University of Tokyo · JPKyushu University · JPThe Graduate University for Advanced Studies, SOKENDAI · JPThe University of Osaka · JP

Funding

MEXT | Japan Society for the Promotion of Science (JSPS) 18J15182MEXT | Japan Society for the Promotion of Science (JSPS) 21H04765MEXT | Japan Society for the Promotion of Science (JSPS) 22H04688
6 · The paper itself

Abstract

Chromatin accessibility is a hallmark of active regulatory regions and is functionally linked to transcriptional networks and cell identity. However, the molecular mechanisms and networks that govern chromatin accessibility have not been thoroughly studied. Here we conducted a genome-wide CRISPR screening combined with an optimized ATAC-see protocol to identify genes that modulate global chromatin accessibility. In addition to known chromatin regulators like CREBBP and EP400, we discovered a number of previously unrecognized proteins that modulate chromatin accessibility, including TFDP1, HNRNPU, EIF3D and THAP11 belonging to diverse biological pathways. ATAC-seq analysis upon their knockouts revealed their distinct and specific effects on chromatin accessibility. Remarkably, we found that TFDP1, a transcription factor, modulates global chromatin accessibility through transcriptional regulation of canonical histones. In addition, our findings highlight the manipulation of chromatin accessibility as an approach to enhance various cell engineering applications, including genome editing and induced pluripotent stem cell reprogramming.

Indexed as

ChromatinHigh-Throughput Nucleotide SequencingGene Regulatory NetworksHistonesTranscription FactorsChromatinHistonesTranscription Factors

Identifiers

PMID38361031
OpenAlexW4391843347

What OpenQuestion holds

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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.