Evidence map›Paper›PMID 42578585›Full record

ArticleInvestigative ophthalmology & visual science2026

Off-Target Retinal Pigment Epithelium (RPE) Expression of Cre in the Rhodopsin-iCre75 Mouse Line.

David G Ball, Eleanor Ostafin, William J Spencer

Abstract read
In one paragraph

Article in Investigative ophthalmology & visual science, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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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

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.

David G BallOphthalmology and Visual Sciences, SUNY Upstate Medical University, Syracuse, New York, United States.
Eleanor OstafinOphthalmology and Visual Sciences, SUNY Upstate Medical University, Syracuse, New York, United States.
William J SpencerOphthalmology and Visual Sciences, SUNY Upstate Medical University, Syracuse, New York, United States.

Funding

Training Program in Molecular and Translational Visual SciencesT32EY037212 · NEI · UPSTATE MEDICAL UNIVERSITY · PI WILLIAM J BRUNKEN · 2025 to 2026
$439k
NEI NIH HHS T32 EY037212
6 · The paper itself

Abstract

Purpose: Cre mouse lines are an important tool to manipulate gene expression in specific cell types and at distinct developmental timepoints. Overlooked and off-target expression of Cre is a common issue with transgenic Cre lines that has confounded the interpretation of many studies. The rhodopsin-iCre75 mouse line expresses Cre behind a rod opsin promoter and has been the most widely used line for targeting rod photoreceptor cells over the past two decades. Here, we re-evaluated the specificity of the rhodopsin-iCre75 mouse line for rod photoreceptors. Methods: We crossed the rhodopsin-iCre75 mouse line with the fluorescent Cre reporter strain, Ai14, which expresses tdTomato in Cre-lox recombined cells. We identified recombined cells in mouse eye tissues by confocal microscopy. Independent of this reporter strain and as validation, we detected the presence of Cre protein by western blotting. Results: We report that Cre expression in the rhodopsin-iCre75 mouse line is unexpectedly not rod photoreceptor specific. We show that Cre is expressed in approximately 6% ± 2% (mean ± SD) of retinal pigment epithelium (RPE) cells by postnatal day 4, a timepoint preceding rhodopsin expression in rods. Recombined RPE cells are found in patches and are concentrated centrally where approximately 17% ± 6% (mean ± SD) of RPE cells are Cre positive. Conclusions: These findings indicate that the rhodopsin-iCre75 line has unintended Cre recombination in RPE cells providing important implications for the interpretation of prior and future studies using this line.

Indexed as

IntegrasesRetinal Pigment EpitheliumRetinal Rod Photoreceptor CellsRhodopsinAnimalsBlotting, WesternMiceMice, Inbred C57BLMice, TransgenicMicroscopy, ConfocalCre recombinaseIntegrasesRhodopsin

Identifiers

PMID42578585
PMCPMC13480038

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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.