Evidence map›Paper›PMID 42268918›Full record

ArticlePLoS genetics2026

The regulation of Xrp1 expression by uORFs and main ORF sequences and its function in Drosophila disease models.

Hidetaka Katow, Thao Nguyen, Sarah Hyunsoh Park, Hyung Don Ryoo

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In one paragraph

Article in PLoS genetics, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

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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

4 authors.

Hidetaka KatowDepartment of Cell Biology, NYU Grossman School of Medicine, New York, New York, United States of America.ORCID https://orcid.org/0009-0005-0449-230X
Thao NguyenDepartment of Cell Biology, NYU Grossman School of Medicine, New York, New York, United States of America.
Sarah Hyunsoh ParkDepartment of Cell Biology, NYU Grossman School of Medicine, New York, New York, United States of America.
Hyung Don RyooDepartment of Cell Biology, NYU Grossman School of Medicine, New York, New York, United States of America.ORCID https://orcid.org/0000-0002-1046-535X

Funding

Unfolded Protein Response in Eye Development and DiseaseR01EY020866 · NEI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI HYUNG D RYOO · 2010 to 2026
$6.9M
Translational control of stress response signaling - Equipment SupplementR35GM148357 · NIGMS · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI HYUNG D RYOO · 2023 to 2026
$1.7M
NEI NIH HHS R01 EY020866NIGMS NIH HHS R35 GM148357
6 · The paper itself

Abstract

The Integrated Stress Response (ISR) mediates cellular adaptation to endoplasmic reticulum (ER) stress, amino acid deprivation, and mitochondrial dysfunction. The ISR regulates gene expression in part by preferentially translating the transcription factor ATF4, a process regulated by upstream open reading frames (uORFs) in its 5' leader. In Drosophila, Xrp1 is another transcription factor induced during the ISR, but the precise underlying mechanism remains unclear. Here, we report that Xrp1 induction in response to ER stress is regulated by both its uORFs and the main ORF sequence. Xrp1 has seven splice isoforms, and the two predominant transcripts expressed in eye imaginal discs contain uORFs. Expressing the ER stress-imposing ninaEG69D transgene in this tissue induced Xrp1 expression without significantly changing the Xrp1 splice isoform composition. The uORF-containing 5' leaders, particularly the AUG codon of the second uORF, inhibited DsRed expression when placed upstream of the reporter. Unlike ATF4, the uORF-containing 5' leader alone was insufficient to mediate the main ORF induction, but Xrp1 induction occurred in ninaEG69D-expressing discs when Xrp1's 5' leader and the main ORF sequence were both present. Functionally, Xrp1 was required to maintain the integrity of Drosophila photoreceptors exposed to constant light. In a different disease model, parkin mutants activated Xrp1 target gene expression in specific tissues and Xrp1 loss enhanced the viability of parkin mutant flies during adult eclosion. These results provide molecular and pathological insights into Xrp1 regulation and function in disease models.

Indexed as

DNA-Binding ProteinsDrosophila ProteinsIntegrated Stress ResponseOpen Reading FramesActivating Transcription Factor 4AnimalsDisease Models, AnimalDrosophila melanogasterGene Expression RegulationImaginal DiscsProtein IsoformsActivating Transcription Factor 4DNA-Binding ProteinsDrosophila ProteinsProtein IsoformsXrp1 protein, Drosophila

Identifiers

PMID42268918
PMCPMC13268129

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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.