PUBLICATION

Comparative 3D genome analysis between neural retina and retinal pigment epithelium reveals differential cis-regulatory interactions at retinal disease loci

Authors
D'haene, E., López-Soriano, V., Martínez-García, P.M., Kalayanamontri, S., Rey, A.D., Sousa-Ortega, A., Naranjo, S., Van de Sompele, S., Vantomme, L., Mahieu, Q., Vergult, S., Neto, A., Gómez-Skarmeta, J.L., Martínez-Morales, J.R., Bauwens, M., Tena, J.J., De Baere, E.
ID
ZDB-PUB-240518-10
Date
2024
Source
Genome biology   25: 123123 (Journal)
Registered Authors
Gómez-Skarmeta, José Luis, Martinez-Morales, Juan R., Naranjo, Silvia, Neto, Ana, Tena, Juan
Keywords
ABCA4, Cis-regulatory element (CRE), 3D genome structure, Enhancer assay, Hi-C, HiChIP, Inherited retinal disease (IRD), Neural retina, Retinal pigment epithelium (RPE), UMI-4C
MeSH Terms
  • ATP-Binding Cassette Transporters/genetics
  • ATP-Binding Cassette Transporters/metabolism
  • Animals
  • Chromatin*/metabolism
  • Genetic Loci
  • Genome, Human
  • Humans
  • Promoter Regions, Genetic
  • Regulatory Sequences, Nucleic Acid
  • Retina*/metabolism
  • Retinal Diseases*/genetics
  • Retinal Diseases*/metabolism
  • Retinal Pigment Epithelium*/metabolism
  • Zebrafish/genetics
PubMed
38760655 Full text @ Genome Biol.
Abstract
Vision depends on the interplay between photoreceptor cells of the neural retina and the underlying retinal pigment epithelium (RPE). Most genes involved in inherited retinal diseases display specific spatiotemporal expression within these interconnected retinal components through the local recruitment of cis-regulatory elements (CREs) in 3D nuclear space.
To understand the role of differential chromatin architecture in establishing tissue-specific expression at inherited retinal disease loci, we mapped genome-wide chromatin interactions using in situ Hi-C and H3K4me3 HiChIP on neural retina and RPE/choroid from human adult donor eyes. We observed chromatin looping between active promoters and 32,425 and 8060 candidate CREs in the neural retina and RPE/choroid, respectively. A comparative 3D genome analysis between these two retinal tissues revealed that 56% of 290 known inherited retinal disease genes were marked by differential chromatin interactions. One of these was ABCA4, which is implicated in the most common autosomal recessive inherited retinal disease. We zoomed in on retina- and RPE-specific cis-regulatory interactions at the ABCA4 locus using high-resolution UMI-4C. Integration with bulk and single-cell epigenomic datasets and in vivo enhancer assays in zebrafish revealed tissue-specific CREs interacting with ABCA4.
Through comparative 3D genome mapping, based on genome-wide, promoter-centric, and locus-specific assays of human neural retina and RPE, we have shown that gene regulation at key inherited retinal disease loci is likely mediated by tissue-specific chromatin interactions. These findings do not only provide insight into tissue-specific regulatory landscapes at retinal disease loci, but also delineate the search space for non-coding genomic variation underlying unsolved inherited retinal diseases.
Genes / Markers
Figures
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Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Antibodies
Orthology
Engineered Foreign Genes
Mapping