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Gata2a Mutation Causes Progressive Microphthalmia and Blindness in Nile Tilapia
The normal development of lens fiber cells plays a critical role in lens morphogenesis and maintaining transparency. Factors involved in the development of lens fiber cells are largely unknown in vertebrates. In this study, we reported that GATA2 is essential for lens morphogenesis in Nile tilapia (...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9958714/ https://www.ncbi.nlm.nih.gov/pubmed/36834978 http://dx.doi.org/10.3390/ijms24043567 |
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author | Liu, Xingyong Zhou, Li Li, Wenbo Wu, Jiahong Wang, Deshou |
author_facet | Liu, Xingyong Zhou, Li Li, Wenbo Wu, Jiahong Wang, Deshou |
author_sort | Liu, Xingyong |
collection | PubMed |
description | The normal development of lens fiber cells plays a critical role in lens morphogenesis and maintaining transparency. Factors involved in the development of lens fiber cells are largely unknown in vertebrates. In this study, we reported that GATA2 is essential for lens morphogenesis in Nile tilapia (Oreochromis niloticus). In this study, Gata2a was detected in the primary and secondary lens fiber cells, with the highest expression in primary fiber cells. gata2a homozygous mutants of tilapia were obtained using CRISPR/Cas9. Different from fetal lethality caused by Gata2/gata2a mutation in mice and zebrafish, some gata2a homozygous mutants of tilapia are viable, which provides a good model for studying the role of gata2 in non-hematopoietic organs. Our data showed that gata2a mutation caused extensive degeneration and apoptosis of primary lens fiber cells. The mutants exhibited progressive microphthalmia and blindness in adulthood. Transcriptome analysis of the eyes showed that the expression levels of almost all genes encoding crystallin were significantly down-regulated, while the expression levels of genes involved in visual perception and metal ion binding were significantly up-regulated after gata2a mutation. Altogether, our findings indicate that gata2a is required for the survival of lens fiber cells and provide insights into transcriptional regulation underlying lens morphogenesis in teleost fish. |
format | Online Article Text |
id | pubmed-9958714 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-99587142023-02-26 Gata2a Mutation Causes Progressive Microphthalmia and Blindness in Nile Tilapia Liu, Xingyong Zhou, Li Li, Wenbo Wu, Jiahong Wang, Deshou Int J Mol Sci Article The normal development of lens fiber cells plays a critical role in lens morphogenesis and maintaining transparency. Factors involved in the development of lens fiber cells are largely unknown in vertebrates. In this study, we reported that GATA2 is essential for lens morphogenesis in Nile tilapia (Oreochromis niloticus). In this study, Gata2a was detected in the primary and secondary lens fiber cells, with the highest expression in primary fiber cells. gata2a homozygous mutants of tilapia were obtained using CRISPR/Cas9. Different from fetal lethality caused by Gata2/gata2a mutation in mice and zebrafish, some gata2a homozygous mutants of tilapia are viable, which provides a good model for studying the role of gata2 in non-hematopoietic organs. Our data showed that gata2a mutation caused extensive degeneration and apoptosis of primary lens fiber cells. The mutants exhibited progressive microphthalmia and blindness in adulthood. Transcriptome analysis of the eyes showed that the expression levels of almost all genes encoding crystallin were significantly down-regulated, while the expression levels of genes involved in visual perception and metal ion binding were significantly up-regulated after gata2a mutation. Altogether, our findings indicate that gata2a is required for the survival of lens fiber cells and provide insights into transcriptional regulation underlying lens morphogenesis in teleost fish. MDPI 2023-02-10 /pmc/articles/PMC9958714/ /pubmed/36834978 http://dx.doi.org/10.3390/ijms24043567 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Liu, Xingyong Zhou, Li Li, Wenbo Wu, Jiahong Wang, Deshou Gata2a Mutation Causes Progressive Microphthalmia and Blindness in Nile Tilapia |
title | Gata2a Mutation Causes Progressive Microphthalmia and Blindness in Nile Tilapia |
title_full | Gata2a Mutation Causes Progressive Microphthalmia and Blindness in Nile Tilapia |
title_fullStr | Gata2a Mutation Causes Progressive Microphthalmia and Blindness in Nile Tilapia |
title_full_unstemmed | Gata2a Mutation Causes Progressive Microphthalmia and Blindness in Nile Tilapia |
title_short | Gata2a Mutation Causes Progressive Microphthalmia and Blindness in Nile Tilapia |
title_sort | gata2a mutation causes progressive microphthalmia and blindness in nile tilapia |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9958714/ https://www.ncbi.nlm.nih.gov/pubmed/36834978 http://dx.doi.org/10.3390/ijms24043567 |
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