Evidence map›Paper›PMID 41258079›Full record

ReviewExperimental & molecular medicine2025

The multiple layers of RNA response in double-strand break repair.

Yilin Lu, Francesca Storici, Youngkyu Jeon

Abstract readReview
In one paragraph

Review in Experimental & molecular medicine, 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. Mechanisms and disease relevance of DNA break repair pathway choice.Nature reviews. Molecular cell biology · 2026
    Review
  2. 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.

Yilin LuSchool of Biological Sciences, Georgia Institute of Technology, Atlanta, GA, USA.
Francesca StoriciSchool of Biological Sciences, Georgia Institute of Technology, Atlanta, GA, USA. fracesca.storici@biosci.gatech.edu.
Youngkyu JeonSchool of Biological Sciences, Georgia Institute of Technology, Atlanta, GA, USA. youngkyu.jeon@nih.gov.ORCID http://orcid.org/0000-0002-6223-2187

Funding

Interrogation of Genetic Dependencies in Renal Cell Carcinomas.ZIABC012099 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI AREGGER, MICHAEL · 2022 to 2025
$1.8M
RNA-mediated DNA break repairR01GM115927 · NIGMS · GEORGIA INSTITUTE OF TECHNOLOGY · PI STORICI, FRANCESCA · 2015 to 2018
$1.2M
Howard Hughes Medical Institute (HHMI) 55108574Intramural NIH HHS ZIA BC012099National Science Foundation (NSF) DMS-1764406National Science Foundation (NSF) MCB-1615335NIGMS NIH HHS R01 GM115927Simons Foundation 594594U.S. Department of Health & Human Services | NIH | National Cancer Institute (NCI) Project ZIA BC 012099U.S. Department of Health & Human Services | NIH | National Institute of General Medical Sciences (NIGMS) GM115927
6 · The paper itself

Abstract

RNA molecules are now recognized as active regulators of DNA double-strand break repair. In end-joining pathways, nascent transcripts promote repair through RNA:DNA hybrids, end bridging and RNA-templated synthesis. In homologous recombination, RNA:DNA hybrids modulate DNA end resection, recruit repair factors and enable RNA-templated repair, with DNA polymerase ζ emerging as a key reverse transcriptase in this process. Transcription at double-strand break sites generates regulatory RNAs that further influence pathway choice and repair fidelity. Long noncoding RNAs, RNA-binding proteins and RNA modifications add additional control layers. Advances in genomic mapping, reporter assays and in vitro methods are now dissecting these complex RNA-mediated processes, although important challenges remain in capturing their full kinetics and contributions. Finally, RNA-templated genome editing platforms, such as prime editing, harness these principles for precise, programmable DNA repair. Together, these findings position RNA as a multifunctional player in genome maintenance and engineering.

Indexed as

DNA Breaks, Double-StrandedDNA RepairRNAAnimalsDNA End-Joining RepairGene EditingHumansRNA

Identifiers

PMID41258079
PMCPMC12686478

What OpenQuestion holds

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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.