Evidence map›Paper›PMID 38994775›Full record

ArticleDevelopment (Cambridge, England)2024

Evolutionary conservation of VSX2 super-enhancer modules in retinal development.

Victoria Honnell, Shannon Sweeney, Jackie Norrie, Madison Parks, Cody Ramirez, Asha Jacob Jannu, Beisi Xu, Brett Teubner, Ah Young Lee, Claire Bell and 1 more

Abstract read
In one paragraph

Article in Development (Cambridge, England), 2024. 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. Article
  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

11 authors.

Victoria HonnellDepartment of Developmental Neurobiology at St. Jude Children's Research Hospital, Memphis, TN 38105, USA.ORCID 0000-0003-2742-2951
Shannon SweeneyDepartment of Developmental Neurobiology at St. Jude Children's Research Hospital, Memphis, TN 38105, USA.
Jackie NorrieDepartment of Developmental Neurobiology at St. Jude Children's Research Hospital, Memphis, TN 38105, USA.ORCID 0000-0002-1021-0306
Madison ParksDepartment of Developmental Neurobiology at St. Jude Children's Research Hospital, Memphis, TN 38105, USA.
Cody RamirezDepartment of Developmental Neurobiology at St. Jude Children's Research Hospital, Memphis, TN 38105, USA.ORCID 0000-0001-5598-0876
Asha Jacob JannuDepartment of Developmental Neurobiology at St. Jude Children's Research Hospital, Memphis, TN 38105, USA.
Beisi XuCenter for Applied Bioinformatics at St. Jude Children's Research Hospital, Memphis, TN 38105, USA.ORCID 0000-0003-0099-858X
Brett TeubnerDepartment of Developmental Neurobiology at St. Jude Children's Research Hospital, Memphis, TN 38105, USA.
Ah Young LeeWilmer Eye Institute, Johns Hopkins University School of Medicine, Baltimore, MD 21231, USA.
Claire BellWilmer Eye Institute, Johns Hopkins University School of Medicine, Baltimore, MD 21231, USA.
Michael A DyerDepartment of Developmental Neurobiology at St. Jude Children's Research Hospital, Memphis, TN 38105, USA.ORCID 0000-0003-4027-4850

Funding

Cell-type– and developmental stage–specific regulation of gene expression in the retinaR01EY030180 · NEI · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI DYER, MICHAEL A · 2020 to 2023
$1.8M
Characterizing enhancers regulating transcription factor expression for cell-type specification across neurodevelopmentF99NS125819 · NINDS · ST. JUDE CHILDREN'S RESEARCH HOSPITAL GRADUATE SCHOOL OF BIOMEDICAL SCIENCES, LLC · PI HONNELL, VICTORIA · 2021 to 2022
$87k
Alex's Lemonade Stand Foundation for Childhood CancerAmerican Lebanese Syrian Associated CharitiesNEI NIH HHS R01 EY030180NIH HHS R01EY030180NINDS NIH HHS F99 NS125819Peter G. Peterson FoundationTully Family Foundation
6 · The paper itself

Abstract

Super-enhancers (SEs) are expansive regions of genomic DNA that regulate the expression of genes involved in cell identity and cell fate. We recently identified developmental stage- and cell type-specific modules within the murine Vsx2 SE. Here, we show that the human VSX2 SE modules have similar developmental stage- and cell type-specific activity in reporter gene assays. By inserting the human sequence of one VSX2 SE module into a mouse with microphthalmia, eye size was rescued. To understand the function of these SE modules during human retinal development, we deleted individual modules in human embryonic stem cells and generated retinal organoids. Deleting one module results in small organoids, recapitulating the small-eyed phenotype of mice with microphthalmia, while deletion of the other module led to disruptions in bipolar neuron development. This prototypical SE serves as a model for understanding developmental stage- and cell type-specific effects of neurogenic transcription factors with complex expression patterns. Moreover, by elucidating the gene regulatory mechanisms, we can begin to examine how dysregulation of these mechanisms contributes to phenotypic diversity and disease.

Indexed as

Enhancer Elements, GeneticGene Expression Regulation, DevelopmentalHomeodomain ProteinsRetinaTranscription FactorsAnimalsEvolution, MolecularHuman Embryonic Stem CellsHumansMiceMicrophthalmosNeurogenesisOrganoidsHomeodomain ProteinsTranscription FactorsVSX2 protein, humanVsx2 protein, mouseOrganoidRetinaRetinal developmentSuper-enhancer

Identifiers

PMID38994775
PMCPMC11266796

What Socratic holds

Textmetadata
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 Socratic graph.