Publication:
Analysis of gene network bifurcation during optic cup morphogenesis in zebrafish.

dc.contributor.authorBuono, Lorena
dc.contributor.authorCorbacho, Jorge
dc.contributor.authorNaranjo, Silvia
dc.contributor.authorAlmuedo-Castillo, María
dc.contributor.authorMoreno-Marmol, Tania
dc.contributor.authorde la Cerda, Berta
dc.contributor.authorSanabria-Reinoso, Estefanía
dc.contributor.authorPolvillo, Rocío
dc.contributor.authorDíaz-Corrales, Francisco-Javier
dc.contributor.authorBogdanovic, Ozren
dc.contributor.authorBovolenta, Paola
dc.contributor.authorMartínez-Morales, Juan-Ramón
dc.date.accessioned2023-02-09T11:40:56Z
dc.date.available2023-02-09T11:40:56Z
dc.date.issued2021-06-23
dc.description.abstractSight depends on the tight cooperation between photoreceptors and pigmented cells, which derive from common progenitors through the bifurcation of a single gene regulatory network into the neural retina (NR) and retinal-pigmented epithelium (RPE) programs. Although genetic studies have identified upstream nodes controlling these networks, their regulatory logic remains poorly investigated. Here, we characterize transcriptome dynamics and chromatin accessibility in segregating NR/RPE populations in zebrafish. We analyze cis-regulatory modules and enriched transcription factor motives to show extensive network redundancy and context-dependent activity. We identify downstream targets, highlighting an early recruitment of desmosomal genes in the flattening RPE and revealing Tead factors as upstream regulators. We investigate the RPE specification network dynamics to uncover an unexpected sequence of transcription factors recruitment, which is conserved in humans. This systematic interrogation of the NR/RPE bifurcation should improve both genetic counseling for eye disorders and hiPSCs-to-RPE differentiation protocols for cell-replacement therapies in degenerative diseases.
dc.identifier.doi10.1038/s41467-021-24169-7
dc.identifier.essn2041-1723
dc.identifier.pmcPMC8222258
dc.identifier.pmid34162866
dc.identifier.pubmedURLhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8222258/pdf
dc.identifier.unpaywallURLhttps://www.nature.com/articles/s41467-021-24169-7.pdf
dc.identifier.urihttp://hdl.handle.net/10668/18035
dc.issue.number1
dc.journal.titleNature communications
dc.journal.titleabbreviationNat Commun
dc.language.isoen
dc.organizationCentro Andaluz de Biología Molecular y Medicina Regenerativa-CABIMER
dc.page.number3866
dc.pubmedtypeJournal Article
dc.pubmedtypeResearch Support, Non-U.S. Gov't
dc.rightsAttribution 4.0 International
dc.rights.accessRightsopen access
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.subject.meshAnimals
dc.subject.meshAnimals, Genetically Modified
dc.subject.meshChromatin Immunoprecipitation Sequencing
dc.subject.meshCluster Analysis
dc.subject.meshGene Expression Profiling
dc.subject.meshGene Expression Regulation, Developmental
dc.subject.meshGene Regulatory Networks
dc.subject.meshHumans
dc.subject.meshInduced Pluripotent Stem Cells
dc.subject.meshMorphogenesis
dc.subject.meshRNA-Seq
dc.subject.meshRetinal Pigment Epithelium
dc.subject.meshReverse Transcriptase Polymerase Chain Reaction
dc.subject.meshTranscription Factors
dc.subject.meshZebrafish
dc.titleAnalysis of gene network bifurcation during optic cup morphogenesis in zebrafish.
dc.typeresearch article
dc.type.hasVersionVoR
dc.volume.number12
dspace.entity.typePublication

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