Evidence map›Paper›PMID 40917896›Full record

ArticleMolecular therapy. Nucleic acids2025

Human opsin restoration by histone methylation using methyltransferase fusion protein SETD7-dCas9.

Na Ly Tran, Yoo Eun Kang, Hyeyeon Jeong, Yeojin Kim, Sang Chul Shin, Sang-Heon Kim, Byeongho Park, Seung Ja Oh

Abstract read
In one paragraph

Article in Molecular therapy. Nucleic acids, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

8 authors.

Na Ly TranDepartment of Genetics and Biotechnology, College of Life Sciences, Kyung Hee University, Yongin-si, Gyeonggi-do 17104, Republic of Korea.
Yoo Eun KangGraduate School of Biotechnology, Kyung Hee University, Yongin-si, Gyeonggi-do 17104, Republic of Korea.
Hyeyeon JeongDepartment of Genetics and Biotechnology, College of Life Sciences, Kyung Hee University, Yongin-si, Gyeonggi-do 17104, Republic of Korea.
Yeojin KimGraduate School of Biotechnology, Kyung Hee University, Yongin-si, Gyeonggi-do 17104, Republic of Korea.
Sang Chul ShinKorea Institute of Science and Technology (KIST), Seoul 02792, Korea.
Sang-Heon KimKorea Institute of Science and Technology (KIST), Seoul 02792, Korea.
Byeongho ParkKorea Institute of Science and Technology (KIST), Seoul 02792, Korea.
Seung Ja OhDepartment of Genetics and Biotechnology, College of Life Sciences, Kyung Hee University, Yongin-si, Gyeonggi-do 17104, Republic of Korea.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Epigenetic modulation enables precise gene regulation without altering DNA sequences. While histone acetylation has been widely utilized for gene activation, the therapeutic potential of histone methylation remains underexplored. In this study, we developed a new epigenetic activator by fusing the histone methyltransferase SETD7 to deactivated Cas9 (dCas9). The optimized SETD7-dCas9 fusion protein successfully induced H3K4 mono-methylation and activated transcription at multiple target loci. We further established a prediction model using promoter CpG methylation status to identify genes most responsive to SETD7-dCas9-mediated activation. To evaluate therapeutic relevance, we targeted the medium-wavelength-sensitive opsin gene (

Indexed as

CpG epigenome engineeringCpG methylationepigenetic regulationMT: RNA/DNA Editingopsinretinitis pigmentosaSET domain-containing 7

Identifiers

PMID40917896
PMCPMC12410342

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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.