{"title":"干扰素调节因子-7是斑马鱼胚胎发育过程中毛细胞发育所必需的","authors":"Song-Qun Hu, Hui-Min Xu, Fu-Ping Qian, Chang-Sheng Chen, Xin Wang, Dong Liu, Lei Cheng","doi":"10.1002/dneu.22860","DOIUrl":null,"url":null,"abstract":"<p>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 <i>irf7</i> 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 <i>irf7</i> 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 <i>irf7</i>. Compared to the wild-type siblings, knockdown of <i>irf7</i> 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 <i>irf7</i> mRNA could partially rescued the defects of the morphants. <i>atp1b2b</i> mRNA injection can also partially rescue the phenotype induced by <i>irf7</i> gene deficiency. Loss of hair cells in <i>irf7</i>-morphants does not result from cell apoptosis. Gene expression profiles show that, compared to wild-type, knockdown of <i>irf7</i> 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 <i>irf7</i> plays an essential role in hair cell development in zebrafish, indicating that <i>irf7</i> may be a member of deafness gene family.</p>","PeriodicalId":11300,"journal":{"name":"Developmental Neurobiology","volume":"82 1","pages":"88-97"},"PeriodicalIF":2.7000,"publicationDate":"2021-11-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/49/fd/DNEU-82-88.PMC9305156.pdf","citationCount":"1","resultStr":"{\"title\":\"Interferon regulatory factor-7 is required for hair cell development during zebrafish embryogenesis\",\"authors\":\"Song-Qun Hu, Hui-Min Xu, Fu-Ping Qian, Chang-Sheng Chen, Xin Wang, Dong Liu, Lei Cheng\",\"doi\":\"10.1002/dneu.22860\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>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 <i>irf7</i> 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 <i>irf7</i> 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 <i>irf7</i>. Compared to the wild-type siblings, knockdown of <i>irf7</i> 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 <i>irf7</i> mRNA could partially rescued the defects of the morphants. <i>atp1b2b</i> mRNA injection can also partially rescue the phenotype induced by <i>irf7</i> gene deficiency. Loss of hair cells in <i>irf7</i>-morphants does not result from cell apoptosis. Gene expression profiles show that, compared to wild-type, knockdown of <i>irf7</i> 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 <i>irf7</i> plays an essential role in hair cell development in zebrafish, indicating that <i>irf7</i> may be a member of deafness gene family.</p>\",\"PeriodicalId\":11300,\"journal\":{\"name\":\"Developmental Neurobiology\",\"volume\":\"82 1\",\"pages\":\"88-97\"},\"PeriodicalIF\":2.7000,\"publicationDate\":\"2021-11-14\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/49/fd/DNEU-82-88.PMC9305156.pdf\",\"citationCount\":\"1\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Developmental Neurobiology\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://onlinelibrary.wiley.com/doi/10.1002/dneu.22860\",\"RegionNum\":4,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"DEVELOPMENTAL BIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Developmental Neurobiology","FirstCategoryId":"3","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/dneu.22860","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"DEVELOPMENTAL BIOLOGY","Score":null,"Total":0}
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 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.
期刊介绍:
Developmental Neurobiology (previously the Journal of Neurobiology ) publishes original research articles on development, regeneration, repair and plasticity of the nervous system and on the ontogeny of behavior. High quality contributions in these areas are solicited, with an emphasis on experimental as opposed to purely descriptive work. The Journal also will consider manuscripts reporting novel approaches and techniques for the study of the development of the nervous system as well as occasional special issues on topics of significant current interest. We welcome suggestions on possible topics from our readers.