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Rod genesis driven by mafba in an nrl knockout zebrafish model with altered photoreceptor composition and progressive retinal degeneration

Neural retina leucine zipper (NRL) is an essential gene for the fate determination and differentiation of the precursor cells into rod photoreceptors in mammals. Mutations in NRL are associated with the autosomal recessive enhanced S-cone syndrome and autosomal dominant retinitis pigmentosa. However...

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Autores principales: Liu, Fei, Qin, Yayun, Huang, Yuwen, Gao, Pan, Li, Jingzhen, Yu, Shanshan, Jia, Danna, Chen, Xiang, Lv, Yuexia, Tu, Jiayi, Sun, Kui, Han, Yunqiao, Reilly, James, Shu, Xinhua, Lu, Qunwei, Tang, Zhaohui, Xu, Chengqi, Luo, Daji, Liu, Mugen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8926279/
https://www.ncbi.nlm.nih.gov/pubmed/35245286
http://dx.doi.org/10.1371/journal.pgen.1009841
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author Liu, Fei
Qin, Yayun
Huang, Yuwen
Gao, Pan
Li, Jingzhen
Yu, Shanshan
Jia, Danna
Chen, Xiang
Lv, Yuexia
Tu, Jiayi
Sun, Kui
Han, Yunqiao
Reilly, James
Shu, Xinhua
Lu, Qunwei
Tang, Zhaohui
Xu, Chengqi
Luo, Daji
Liu, Mugen
author_facet Liu, Fei
Qin, Yayun
Huang, Yuwen
Gao, Pan
Li, Jingzhen
Yu, Shanshan
Jia, Danna
Chen, Xiang
Lv, Yuexia
Tu, Jiayi
Sun, Kui
Han, Yunqiao
Reilly, James
Shu, Xinhua
Lu, Qunwei
Tang, Zhaohui
Xu, Chengqi
Luo, Daji
Liu, Mugen
author_sort Liu, Fei
collection PubMed
description Neural retina leucine zipper (NRL) is an essential gene for the fate determination and differentiation of the precursor cells into rod photoreceptors in mammals. Mutations in NRL are associated with the autosomal recessive enhanced S-cone syndrome and autosomal dominant retinitis pigmentosa. However, the exact role of Nrl in regulating the development and maintenance of photoreceptors in the zebrafish (Danio rerio), a popular animal model used for retinal degeneration and regeneration studies, has not been fully determined. In this study, we generated an nrl knockout zebrafish model via the CRISPR-Cas9 technology and observed a surprising phenotype characterized by a reduced number, but not the total loss, of rods and over-growth of green cones. We discovered two waves of rod genesis, nrl-dependent and -independent at the embryonic and post-embryonic stages, respectively, in zebrafish by monitoring the rod development. Through bulk and single-cell RNA sequencing, we characterized the gene expression profiles of the whole retina and each retinal cell type from the wild type and nrl knockout zebrafish. The over-growth of green cones and mis-expression of green-cone-specific genes in rods in nrl mutants suggested that there are rod/green-cone bipotent precursors, whose fate choice between rod versus green-cone is controlled by nrl. Besides, we identified the mafba gene as a novel regulator of the nrl-independent rod development, based on the cell-type-specific expression patterns and the retinal phenotype of nrl/mafba double-knockout zebrafish. Gene collinearity analysis revealed the evolutionary origin of mafba and suggested that the function of mafba in rod development is specific to modern fishes. Furthermore, the altered photoreceptor composition and abnormal gene expression in nrl mutants caused progressive retinal degeneration and subsequent regeneration. Accordingly, this study revealed a novel function of the mafba gene in rod development and established a working model for the developmental and regulatory mechanisms regarding the rod and green-cone photoreceptors in zebrafish.
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spelling pubmed-89262792022-03-17 Rod genesis driven by mafba in an nrl knockout zebrafish model with altered photoreceptor composition and progressive retinal degeneration Liu, Fei Qin, Yayun Huang, Yuwen Gao, Pan Li, Jingzhen Yu, Shanshan Jia, Danna Chen, Xiang Lv, Yuexia Tu, Jiayi Sun, Kui Han, Yunqiao Reilly, James Shu, Xinhua Lu, Qunwei Tang, Zhaohui Xu, Chengqi Luo, Daji Liu, Mugen PLoS Genet Research Article Neural retina leucine zipper (NRL) is an essential gene for the fate determination and differentiation of the precursor cells into rod photoreceptors in mammals. Mutations in NRL are associated with the autosomal recessive enhanced S-cone syndrome and autosomal dominant retinitis pigmentosa. However, the exact role of Nrl in regulating the development and maintenance of photoreceptors in the zebrafish (Danio rerio), a popular animal model used for retinal degeneration and regeneration studies, has not been fully determined. In this study, we generated an nrl knockout zebrafish model via the CRISPR-Cas9 technology and observed a surprising phenotype characterized by a reduced number, but not the total loss, of rods and over-growth of green cones. We discovered two waves of rod genesis, nrl-dependent and -independent at the embryonic and post-embryonic stages, respectively, in zebrafish by monitoring the rod development. Through bulk and single-cell RNA sequencing, we characterized the gene expression profiles of the whole retina and each retinal cell type from the wild type and nrl knockout zebrafish. The over-growth of green cones and mis-expression of green-cone-specific genes in rods in nrl mutants suggested that there are rod/green-cone bipotent precursors, whose fate choice between rod versus green-cone is controlled by nrl. Besides, we identified the mafba gene as a novel regulator of the nrl-independent rod development, based on the cell-type-specific expression patterns and the retinal phenotype of nrl/mafba double-knockout zebrafish. Gene collinearity analysis revealed the evolutionary origin of mafba and suggested that the function of mafba in rod development is specific to modern fishes. Furthermore, the altered photoreceptor composition and abnormal gene expression in nrl mutants caused progressive retinal degeneration and subsequent regeneration. Accordingly, this study revealed a novel function of the mafba gene in rod development and established a working model for the developmental and regulatory mechanisms regarding the rod and green-cone photoreceptors in zebrafish. Public Library of Science 2022-03-04 /pmc/articles/PMC8926279/ /pubmed/35245286 http://dx.doi.org/10.1371/journal.pgen.1009841 Text en © 2022 Liu et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Liu, Fei
Qin, Yayun
Huang, Yuwen
Gao, Pan
Li, Jingzhen
Yu, Shanshan
Jia, Danna
Chen, Xiang
Lv, Yuexia
Tu, Jiayi
Sun, Kui
Han, Yunqiao
Reilly, James
Shu, Xinhua
Lu, Qunwei
Tang, Zhaohui
Xu, Chengqi
Luo, Daji
Liu, Mugen
Rod genesis driven by mafba in an nrl knockout zebrafish model with altered photoreceptor composition and progressive retinal degeneration
title Rod genesis driven by mafba in an nrl knockout zebrafish model with altered photoreceptor composition and progressive retinal degeneration
title_full Rod genesis driven by mafba in an nrl knockout zebrafish model with altered photoreceptor composition and progressive retinal degeneration
title_fullStr Rod genesis driven by mafba in an nrl knockout zebrafish model with altered photoreceptor composition and progressive retinal degeneration
title_full_unstemmed Rod genesis driven by mafba in an nrl knockout zebrafish model with altered photoreceptor composition and progressive retinal degeneration
title_short Rod genesis driven by mafba in an nrl knockout zebrafish model with altered photoreceptor composition and progressive retinal degeneration
title_sort rod genesis driven by mafba in an nrl knockout zebrafish model with altered photoreceptor composition and progressive retinal degeneration
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8926279/
https://www.ncbi.nlm.nih.gov/pubmed/35245286
http://dx.doi.org/10.1371/journal.pgen.1009841
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