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Interferon regulatory factor‐7 is required for hair cell development during zebrafish embryogenesis
Interferon regulatory factor‐7 (IRF7) is an essential regulator of both innate and adaptive immunity. It is also expressed in the otic vesicle of zebrafish embryos. However, any role for irf7 in hair cell development was uncharacterized. Does it work as a potential deaf gene to regulate hair cell de...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9305156/ https://www.ncbi.nlm.nih.gov/pubmed/34779143 http://dx.doi.org/10.1002/dneu.22860 |
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author | Hu, Song‐Qun Xu, Hui‐Min Qian, Fu‐Ping Chen, Chang‐Sheng Wang, Xin Liu, Dong Cheng, Lei |
author_facet | Hu, Song‐Qun Xu, Hui‐Min Qian, Fu‐Ping Chen, Chang‐Sheng Wang, Xin Liu, Dong Cheng, Lei |
author_sort | Hu, Song‐Qun |
collection | PubMed |
description | Interferon regulatory factor‐7 (IRF7) is an essential regulator of both innate and adaptive immunity. It is also expressed in the otic vesicle of zebrafish embryos. However, any role for irf7 in hair cell development was uncharacterized. Does it work as a potential deaf gene to regulate hair cell development? We used whole‐mount in situ hybridization (WISH) assay and morpholino‐mediated gene knockdown method to investigate the role of irf7 in the development of otic vesicle hair cells during zebrafish embryogenesis. We performed RNA sequencing to gain a detailed insight into the molecules/genes which are altered upon downregulation of irf7. Compared to the wild‐type siblings, knockdown of irf7 resulted in severe developmental retardation in zebrafish embryos as well as loss of neuromasts and damage to hair cells at an early stage (within 3 days post fertilization). Coinjection of zebrafish irf7 mRNA could partially rescued the defects of the morphants. atp1b2b mRNA injection can also partially rescue the phenotype induced by irf7 gene deficiency. Loss of hair cells in irf7‐morphants does not result from cell apoptosis. Gene expression profiles show that, compared to wild‐type, knockdown of irf7 can lead to 2053 and 2678 genes being upregulated and downregulated, respectively. Among them, 18 genes were annotated to hair cell (HC) development or posterior lateral line (PLL) development. All results suggest that irf7 plays an essential role in hair cell development in zebrafish, indicating that irf7 may be a member of deafness gene family. |
format | Online Article Text |
id | pubmed-9305156 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-93051562022-07-28 Interferon regulatory factor‐7 is required for hair cell development during zebrafish embryogenesis Hu, Song‐Qun Xu, Hui‐Min Qian, Fu‐Ping Chen, Chang‐Sheng Wang, Xin Liu, Dong Cheng, Lei Dev Neurobiol Research Articles Interferon regulatory factor‐7 (IRF7) is an essential regulator of both innate and adaptive immunity. It is also expressed in the otic vesicle of zebrafish embryos. However, any role for irf7 in hair cell development was uncharacterized. Does it work as a potential deaf gene to regulate hair cell development? We used whole‐mount in situ hybridization (WISH) assay and morpholino‐mediated gene knockdown method to investigate the role of irf7 in the development of otic vesicle hair cells during zebrafish embryogenesis. We performed RNA sequencing to gain a detailed insight into the molecules/genes which are altered upon downregulation of irf7. Compared to the wild‐type siblings, knockdown of irf7 resulted in severe developmental retardation in zebrafish embryos as well as loss of neuromasts and damage to hair cells at an early stage (within 3 days post fertilization). Coinjection of zebrafish irf7 mRNA could partially rescued the defects of the morphants. atp1b2b mRNA injection can also partially rescue the phenotype induced by irf7 gene deficiency. Loss of hair cells in irf7‐morphants does not result from cell apoptosis. Gene expression profiles show that, compared to wild‐type, knockdown of irf7 can lead to 2053 and 2678 genes being upregulated and downregulated, respectively. Among them, 18 genes were annotated to hair cell (HC) development or posterior lateral line (PLL) development. All results suggest that irf7 plays an essential role in hair cell development in zebrafish, indicating that irf7 may be a member of deafness gene family. John Wiley and Sons Inc. 2021-12-22 2022 /pmc/articles/PMC9305156/ /pubmed/34779143 http://dx.doi.org/10.1002/dneu.22860 Text en © 2021 The Authors. Developmental Neurobiology published by Wiley Periodicals LLC. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Research Articles Hu, Song‐Qun Xu, Hui‐Min Qian, Fu‐Ping Chen, Chang‐Sheng Wang, Xin Liu, Dong Cheng, Lei Interferon regulatory factor‐7 is required for hair cell development during zebrafish embryogenesis |
title | Interferon regulatory factor‐7 is required for hair cell development during zebrafish embryogenesis |
title_full | Interferon regulatory factor‐7 is required for hair cell development during zebrafish embryogenesis |
title_fullStr | Interferon regulatory factor‐7 is required for hair cell development during zebrafish embryogenesis |
title_full_unstemmed | Interferon regulatory factor‐7 is required for hair cell development during zebrafish embryogenesis |
title_short | Interferon regulatory factor‐7 is required for hair cell development during zebrafish embryogenesis |
title_sort | interferon regulatory factor‐7 is required for hair cell development during zebrafish embryogenesis |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9305156/ https://www.ncbi.nlm.nih.gov/pubmed/34779143 http://dx.doi.org/10.1002/dneu.22860 |
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