Evidence map›Paper›PMID 36745553›Full record

ArticleeLife2023

Transcription factors underlying photoreceptor diversity.

Juan M Angueyra, Vincent P Kunze, Laura K Patak, Hailey Kim, Katie Kindt, Wei Li

Open access · goldAbstract read
In one paragraph

Article in eLife, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
2.9field-weighted citation impact, top 9% of its field
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

11 citing papers in PubMed, 19 citations in OpenAlex.

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  8. Proceedings of the National Academy of Sciences of the United States of America · 2024
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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

6 authors at 2 institutions in 1 country.

Juan M AngueyraUnit of Retinal Neurophysiology, National Eye Institute, National Institutes of Health, Bethesda, United States.ORCID 0000-0002-9217-3069
Vincent P KunzeUnit of Retinal Neurophysiology, National Eye Institute, National Institutes of Health, Bethesda, United States.ORCID 0000-0002-7869-9793
Laura K PatakUnit of Retinal Neurophysiology, National Eye Institute, National Institutes of Health, Bethesda, United States.
Hailey KimUnit of Retinal Neurophysiology, National Eye Institute, National Institutes of Health, Bethesda, United States.
Katie KindtSection on Sensory Cell Development and Function, National Institute on Deafness and Other Communication Disorders, National Institutes of Health, Bethesda, United States.ORCID 0000-0002-1065-8215
Wei LiUnit of Retinal Neurophysiology, National Eye Institute, National Institutes of Health, Bethesda, United States.ORCID 0000-0002-2897-649X
National Institutes of Health · USNational Institute on Deafness and Other Communication Disorders · US

Funding

In vivo investigation of sensory hair cell function and developmentZIADC000085 · NIDCD · NATIONAL INSTITUTE ON DEAFNESS AND OTHER COMMUNICATION DISORDERS · PI KINDT, KATIE · 2014 to 2025
$21.4M
Organization and development of the S-cone systemZIAEY000502 · NEI · NATIONAL EYE INSTITUTE · PI LI, WEI · 2010 to 2025
$12.6M
Identification of genes involved in photoreceptor recognition and synapse formationR00EY030144 · NEI · UNIV OF MARYLAND, COLLEGE PARK · PI ANGUEYRA, JUAN · 2023 to 2025
$738k
Intramural NIH HHS ZIA DC000085NEI NIH HHS R00 EY030144
6 · The paper itself

Abstract

During development, retinal progenitors navigate a complex landscape of fate decisions to generate the major cell classes necessary for proper vision. Transcriptional regulation is critical to generate diversity within these major cell classes. Here, we aim to provide the resources and techniques required to identify transcription factors necessary to generate and maintain diversity in photoreceptor subtypes, which are critical for vision. First, we generate a key resource: a high-quality and deep transcriptomic profile of each photoreceptor subtype in adult zebrafish. We make this resource openly accessible, easy to explore, and have integrated it with other currently available photoreceptor transcriptomic datasets. Second, using our transcriptomic profiles, we derive an in-depth map of expression of transcription factors in photoreceptors. Third, we use efficient CRISPR-Cas9 based mutagenesis to screen for null phenotypes in F0 larvae (F0 screening) as a fast, efficient, and versatile technique to assess the involvement of candidate transcription factors in the generation of photoreceptor subtypes. We first show that known phenotypes can be easily replicated using this method: loss of S cones in

Indexed as

Transcription FactorsZebrafishAnimalsCell DifferentiationReceptors, Cytoplasmic and NuclearRetinaRetinal Cone Photoreceptor CellsZebrafish ProteinsNr2e3 protein, zebrafishReceptors, Cytoplasmic and NuclearTranscription FactorsZebrafish Proteinscone subtypesdevelopmental biologyneurosciencephotoreceptor fateretinatranscription factortranscriptomicszebrafish

Identifiers

PMID36745553
PMCPMC9901936
OpenAlexW4319294725

What OpenQuestion holds

Textmetadata
LicenceCC0
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.