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Functional Role of the RNA-Binding Protein Rbm24a and Its Target sox2 in Microphthalmia
Congenital eye defects represent a large class of disorders affecting roughly 21 million children worldwide. Microphthalmia and anophthalmia are relatively common congenital defects, with approximately 20% of human cases caused by mutations in SOX2. Recently, we identified the RNA-binding motif prot...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7909789/ https://www.ncbi.nlm.nih.gov/pubmed/33494192 http://dx.doi.org/10.3390/biomedicines9020100 |
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author | Brastrom, Lindy K. Scott, C. Anthony Wang, Kai Slusarski, Diane C. |
author_facet | Brastrom, Lindy K. Scott, C. Anthony Wang, Kai Slusarski, Diane C. |
author_sort | Brastrom, Lindy K. |
collection | PubMed |
description | Congenital eye defects represent a large class of disorders affecting roughly 21 million children worldwide. Microphthalmia and anophthalmia are relatively common congenital defects, with approximately 20% of human cases caused by mutations in SOX2. Recently, we identified the RNA-binding motif protein 24a (Rbm24a) which binds to and regulates sox2 in zebrafish and mice. Here we show that morpholino knockdown of rbm24a leads to microphthalmia and visual impairment. By utilizing sequential injections, we demonstrate that addition of exogenous sox2 RNA to rbm24a-deplete embryos is sufficient to suppress morphological and visual defects. This research demonstrates a critical role for understanding the post-transcriptional regulation of genes needed for development. |
format | Online Article Text |
id | pubmed-7909789 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-79097892021-02-27 Functional Role of the RNA-Binding Protein Rbm24a and Its Target sox2 in Microphthalmia Brastrom, Lindy K. Scott, C. Anthony Wang, Kai Slusarski, Diane C. Biomedicines Article Congenital eye defects represent a large class of disorders affecting roughly 21 million children worldwide. Microphthalmia and anophthalmia are relatively common congenital defects, with approximately 20% of human cases caused by mutations in SOX2. Recently, we identified the RNA-binding motif protein 24a (Rbm24a) which binds to and regulates sox2 in zebrafish and mice. Here we show that morpholino knockdown of rbm24a leads to microphthalmia and visual impairment. By utilizing sequential injections, we demonstrate that addition of exogenous sox2 RNA to rbm24a-deplete embryos is sufficient to suppress morphological and visual defects. This research demonstrates a critical role for understanding the post-transcriptional regulation of genes needed for development. MDPI 2021-01-21 /pmc/articles/PMC7909789/ /pubmed/33494192 http://dx.doi.org/10.3390/biomedicines9020100 Text en © 2021 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Brastrom, Lindy K. Scott, C. Anthony Wang, Kai Slusarski, Diane C. Functional Role of the RNA-Binding Protein Rbm24a and Its Target sox2 in Microphthalmia |
title | Functional Role of the RNA-Binding Protein Rbm24a and Its Target sox2 in Microphthalmia |
title_full | Functional Role of the RNA-Binding Protein Rbm24a and Its Target sox2 in Microphthalmia |
title_fullStr | Functional Role of the RNA-Binding Protein Rbm24a and Its Target sox2 in Microphthalmia |
title_full_unstemmed | Functional Role of the RNA-Binding Protein Rbm24a and Its Target sox2 in Microphthalmia |
title_short | Functional Role of the RNA-Binding Protein Rbm24a and Its Target sox2 in Microphthalmia |
title_sort | functional role of the rna-binding protein rbm24a and its target sox2 in microphthalmia |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7909789/ https://www.ncbi.nlm.nih.gov/pubmed/33494192 http://dx.doi.org/10.3390/biomedicines9020100 |
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