Evidence map›Paper›PMID 42397899›Full record

ArticleScience advances2026

Real-time imaging of transcriptional feedback in nonsense-mediated mRNA decay.

Md Dobirul Islam, Tamoghna Das, Robert H Singer, Hanae Sato

Abstract read
In one paragraph

Article in Science advances, 2026. 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
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1 · What the graph read from it

What it found

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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

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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

5 · Who and what money

Authors and funding

4 authors.

Md Dobirul IslamWPI Nano Life Science Institute (NanoLSI), Kanazawa University, Kanazawa, Ishikawa, Japan.ORCID 0000-0003-1568-5500
Tamoghna DasWPI Nano Life Science Institute (NanoLSI), Kanazawa University, Kanazawa, Ishikawa, Japan.ORCID 0000-0001-7112-2820
Robert H SingerDepartment of Cell Biology, Albert Einstein College of Medicine, 1300 Morris Park Ave, Bronx, NY 10451, USA.ORCID 0000-0002-6725-0093
Hanae SatoWPI Nano Life Science Institute (NanoLSI), Kanazawa University, Kanazawa, Ishikawa, Japan.ORCID 0000-0002-7953-5643

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Nonsense-mediated mRNA decay (NMD) is a translation-coupled mRNA decay pathway triggered by a premature termination codon (PTC). While in-frame stop codons are typically defined by cytoplasmic ribosomes, unexpected changes in transcription have been reported in genes containing PTCs. This observation suggests the possibility of PTC detection at the transcription site (TS), which has not been thoroughly investigated with high temporal and spatial resolution. Here, we use a real-time imaging approach to simultaneously detecting transcription sites (TSs) expressing wild-type or NMD-targeted β-globin reporter genes in the same cell. Our data indicate a dynamic change in the transcription of PTC-containing β-globin mRNA that depends on translation, NMD, and nuclear protein import, supporting the existence of rapid transcriptional feedback following NMD in the cytoplasm. This study establishes a robust temporal link between cytoplasmic mRNA decay and nuclear transcription.

Indexed as

Feedback, PhysiologicalNonsense Mediated mRNA DecayRNA, MessengerTranscription, Geneticbeta-GlobinsCell NucleusCodon, NonsenseCytoplasmGenes, ReporterHumansProtein Biosynthesisbeta-GlobinsCodon, NonsenseRNA, Messenger

Identifiers

PMID42397899
PMCPMC13330901

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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.