
Comparative 3D genome analysis between neural retina and RPE reveals differential cis-regulatory interactions at retinal disease loci
(2023)
- Author
- Eva D'haene (UGent) , Victor Lopez Soriano (UGent) , Pedro Manuel Martínez-García, Soraya Kalayanamontri, Alfredo Dueñas Rey (UGent) , Ana Sousa-Ortega, Silvia Naranjo, Stijn Van de Sompele (UGent) , Lies Vantomme (UGent) , Quinten Mahieu (UGent) , Sarah Vergult (UGent) , Ana Bastos Neto, José Luis Gómez-Skarmeta, Juan R. Martínez-Morales, Miriam Bauwens (UGent) , Juan J. Tena and Elfride De Baere (UGent)
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- Abstract
- <jats:title>ABSTRACT</jats:title><jats:p>Vision depends on the functional interplay between the photoreceptor cells of the neural retina and the supporting cells of the underlying retinal pigment epithelium (RPE). Most genes involved in inherited retinal diseases (IRD) display highly specific spatiotemporal expression within these interconnected retinal components through the local recruitment of<jats:italic>cis</jats:italic>-regulatory elements (CREs) in 3D nuclear space.</jats:p><jats:p>To understand the role of differential chromatin architecture in establishing tissue-specific expression patterns at IRD loci in the human neural retina and the RPE, we mapped genome-wide chromatin interactions by applying<jats:italic>in situ</jats:italic>Hi-C and H3K4me3 HiChIP to human adult post-mortem donor retinas. A comparative 3D genome analysis between neural retina and RPE/choroid revealed that almost 60% of 290 known IRD genes were marked by differential 3D genome structure and/or<jats:italic>cis</jats:italic>-regulatory interactions. One of these genes was<jats:italic>ABCA4</jats:italic>, which is implicated in the most common autosomal recessive IRD. We zoomed in on tissue-specific chromatin interactions at the<jats:italic>ABCA4</jats:italic>locus using high-resolution UMI-4C assays. Upon integration with bulk and single-cell epigenomic datasets and<jats:italic>in vivo</jats:italic>enhancer assays in zebrafish, we revealed tissue-specific CREs interacting with<jats:italic>ABCA4</jats:italic>.</jats:p><jats:p>In summary, through extensive comparative 3D genome mapping, based on genome-wide (Hi-C), promoter-centric (HiChIP) and locus-specific (UMI-4C) assays of human neural retina and RPE, we have shown that gene regulation at key IRD loci is likely mediated by tissue-specific chromatin interactions. These findings do not only provide insight into tissue-specific regulatory landscapes of IRD genes, but also delineate the search space for non-coding genomic variation underlying unsolved IRD.</jats:p><jats:sec><jats:title>Abstract Figure</jats:title><jats:fig id="ufig1" position="float" fig-type="figure" orientation="portrait"><jats:graphic xmlns:xlink="http://www.w3.org/1999/xlink" xlink:href="543842v1_ufig1" position="float" orientation="portrait" /></jats:fig></jats:sec>
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Please use this url to cite or link to this publication: http://hdl.handle.net/1854/LU-01HHCDHBAPMEKP57JXAFEGY2EV
- MLA
- D’haene, Eva, et al. Comparative 3D Genome Analysis between Neural Retina and RPE Reveals Differential Cis-Regulatory Interactions at Retinal Disease Loci. Cold Spring Harbor Laboratory, 2023, doi:10.1101/2023.06.20.543842.
- APA
- D’haene, E., Lopez Soriano, V., Martínez-García, P. M., Kalayanamontri, S., Dueñas Rey, A., Sousa-Ortega, A., … De Baere, E. (2023). Comparative 3D genome analysis between neural retina and RPE reveals differential cis-regulatory interactions at retinal disease loci. https://doi.org/10.1101/2023.06.20.543842
- Chicago author-date
- D’haene, Eva, Victor Lopez Soriano, Pedro Manuel Martínez-García, Soraya Kalayanamontri, Alfredo Dueñas Rey, Ana Sousa-Ortega, Silvia Naranjo, et al. 2023. “Comparative 3D Genome Analysis between Neural Retina and RPE Reveals Differential Cis-Regulatory Interactions at Retinal Disease Loci.” Cold Spring Harbor Laboratory. https://doi.org/10.1101/2023.06.20.543842.
- Chicago author-date (all authors)
- D’haene, Eva, Victor Lopez Soriano, Pedro Manuel Martínez-García, Soraya Kalayanamontri, Alfredo Dueñas Rey, Ana Sousa-Ortega, Silvia Naranjo, Stijn Van de Sompele, Lies Vantomme, Quinten Mahieu, Sarah Vergult, Ana Bastos Neto, José Luis Gómez-Skarmeta, Juan R. Martínez-Morales, Miriam Bauwens, Juan J. Tena, and Elfride De Baere. 2023. “Comparative 3D Genome Analysis between Neural Retina and RPE Reveals Differential Cis-Regulatory Interactions at Retinal Disease Loci.” Cold Spring Harbor Laboratory. doi:10.1101/2023.06.20.543842.
- Vancouver
- 1.D’haene E, Lopez Soriano V, Martínez-García PM, Kalayanamontri S, Dueñas Rey A, Sousa-Ortega A, et al. Comparative 3D genome analysis between neural retina and RPE reveals differential cis-regulatory interactions at retinal disease loci. Cold Spring Harbor Laboratory; 2023.
- IEEE
- [1]E. D’haene et al., “Comparative 3D genome analysis between neural retina and RPE reveals differential cis-regulatory interactions at retinal disease loci.” Cold Spring Harbor Laboratory, 2023.
@misc{01HHCDHBAPMEKP57JXAFEGY2EV, abstract = {{<jats:title>ABSTRACT</jats:title><jats:p>Vision depends on the functional interplay between the photoreceptor cells of the neural retina and the supporting cells of the underlying retinal pigment epithelium (RPE). Most genes involved in inherited retinal diseases (IRD) display highly specific spatiotemporal expression within these interconnected retinal components through the local recruitment of<jats:italic>cis</jats:italic>-regulatory elements (CREs) in 3D nuclear space.</jats:p><jats:p>To understand the role of differential chromatin architecture in establishing tissue-specific expression patterns at IRD loci in the human neural retina and the RPE, we mapped genome-wide chromatin interactions by applying<jats:italic>in situ</jats:italic>Hi-C and H3K4me3 HiChIP to human adult post-mortem donor retinas. A comparative 3D genome analysis between neural retina and RPE/choroid revealed that almost 60% of 290 known IRD genes were marked by differential 3D genome structure and/or<jats:italic>cis</jats:italic>-regulatory interactions. One of these genes was<jats:italic>ABCA4</jats:italic>, which is implicated in the most common autosomal recessive IRD. We zoomed in on tissue-specific chromatin interactions at the<jats:italic>ABCA4</jats:italic>locus using high-resolution UMI-4C assays. Upon integration with bulk and single-cell epigenomic datasets and<jats:italic>in vivo</jats:italic>enhancer assays in zebrafish, we revealed tissue-specific CREs interacting with<jats:italic>ABCA4</jats:italic>.</jats:p><jats:p>In summary, through extensive comparative 3D genome mapping, based on genome-wide (Hi-C), promoter-centric (HiChIP) and locus-specific (UMI-4C) assays of human neural retina and RPE, we have shown that gene regulation at key IRD loci is likely mediated by tissue-specific chromatin interactions. These findings do not only provide insight into tissue-specific regulatory landscapes of IRD genes, but also delineate the search space for non-coding genomic variation underlying unsolved IRD.</jats:p><jats:sec><jats:title>Abstract Figure</jats:title><jats:fig id="ufig1" position="float" fig-type="figure" orientation="portrait"><jats:graphic xmlns:xlink="http://www.w3.org/1999/xlink" xlink:href="543842v1_ufig1" position="float" orientation="portrait" /></jats:fig></jats:sec>}}, author = {{D'haene, Eva and Lopez Soriano, Victor and Martínez-García, Pedro Manuel and Kalayanamontri, Soraya and Dueñas Rey, Alfredo and Sousa-Ortega, Ana and Naranjo, Silvia and Van de Sompele, Stijn and Vantomme, Lies and Mahieu, Quinten and Vergult, Sarah and Neto, Ana Bastos and Gómez-Skarmeta, José Luis and Martínez-Morales, Juan R. and Bauwens, Miriam and Tena, Juan J. and De Baere, Elfride}}, language = {{und}}, publisher = {{Cold Spring Harbor Laboratory}}, title = {{Comparative 3D genome analysis between neural retina and RPE reveals differential cis-regulatory interactions at retinal disease loci}}, url = {{http://doi.org/10.1101/2023.06.20.543842}}, year = {{2023}}, }
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