{"title":"爪蟾胚胎正常原肾发育需要适当数量和活性的Wilms肿瘤抑制基因wt1。","authors":"Taisei Shiraki, Takuma Hayashi, Jotaro Ozue, Minoru Watanabe","doi":"10.3390/jdb10040046","DOIUrl":null,"url":null,"abstract":"<p><p>The Wilms' tumor suppressor gene, <i>wt1</i>, encodes a zinc finger-containing transcription factor that binds to a GC-rich motif and regulates the transcription of target genes. <i>wt1</i> was first identified as a tumor suppressor gene in Wilms' tumor, a pediatric kidney tumor, and has been implicated in normal kidney development. The WT1 protein has transcriptional activation and repression domains and acts as a transcriptional activator or repressor, depending on the target gene and context. In <i>Xenopus</i>, an ortholog of <i>wt1</i> has been isolated and shown to be expressed in the developing embryonic pronephros. To investigate the role of <i>wt1</i> in pronephros development in <i>Xenopus</i> embryos, we mutated <i>wt1</i> by CRISPR/Cas9 and found that the expression of pronephros marker genes was reduced. In reporter assays in which known WT1 binding sequences were placed upstream of the <i>luciferase</i> gene, WT1 activated transcription of the <i>luciferase</i> gene. The injection of wild-type or artificially altered transcriptional activity of <i>wt1</i> mRNA disrupted the expression of pronephros marker genes in the embryos. These results suggest that the appropriate amounts and activity of WT1 protein are required for normal pronephros development in <i>Xenopus</i> embryos.</p>","PeriodicalId":15563,"journal":{"name":"Journal of Developmental Biology","volume":"10 4","pages":""},"PeriodicalIF":2.2000,"publicationDate":"2022-10-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9680428/pdf/","citationCount":"1","resultStr":"{\"title\":\"Appropriate Amounts and Activity of the Wilms' Tumor Suppressor Gene, <i>wt1</i>, Are Required for Normal Pronephros Development of <i>Xenopus</i> Embryos.\",\"authors\":\"Taisei Shiraki, Takuma Hayashi, Jotaro Ozue, Minoru Watanabe\",\"doi\":\"10.3390/jdb10040046\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>The Wilms' tumor suppressor gene, <i>wt1</i>, encodes a zinc finger-containing transcription factor that binds to a GC-rich motif and regulates the transcription of target genes. <i>wt1</i> was first identified as a tumor suppressor gene in Wilms' tumor, a pediatric kidney tumor, and has been implicated in normal kidney development. The WT1 protein has transcriptional activation and repression domains and acts as a transcriptional activator or repressor, depending on the target gene and context. In <i>Xenopus</i>, an ortholog of <i>wt1</i> has been isolated and shown to be expressed in the developing embryonic pronephros. To investigate the role of <i>wt1</i> in pronephros development in <i>Xenopus</i> embryos, we mutated <i>wt1</i> by CRISPR/Cas9 and found that the expression of pronephros marker genes was reduced. In reporter assays in which known WT1 binding sequences were placed upstream of the <i>luciferase</i> gene, WT1 activated transcription of the <i>luciferase</i> gene. The injection of wild-type or artificially altered transcriptional activity of <i>wt1</i> mRNA disrupted the expression of pronephros marker genes in the embryos. These results suggest that the appropriate amounts and activity of WT1 protein are required for normal pronephros development in <i>Xenopus</i> embryos.</p>\",\"PeriodicalId\":15563,\"journal\":{\"name\":\"Journal of Developmental Biology\",\"volume\":\"10 4\",\"pages\":\"\"},\"PeriodicalIF\":2.2000,\"publicationDate\":\"2022-10-29\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9680428/pdf/\",\"citationCount\":\"1\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Developmental Biology\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.3390/jdb10040046\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"DEVELOPMENTAL BIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Developmental Biology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.3390/jdb10040046","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"DEVELOPMENTAL BIOLOGY","Score":null,"Total":0}
Appropriate Amounts and Activity of the Wilms' Tumor Suppressor Gene, wt1, Are Required for Normal Pronephros Development of Xenopus Embryos.
The Wilms' tumor suppressor gene, wt1, encodes a zinc finger-containing transcription factor that binds to a GC-rich motif and regulates the transcription of target genes. wt1 was first identified as a tumor suppressor gene in Wilms' tumor, a pediatric kidney tumor, and has been implicated in normal kidney development. The WT1 protein has transcriptional activation and repression domains and acts as a transcriptional activator or repressor, depending on the target gene and context. In Xenopus, an ortholog of wt1 has been isolated and shown to be expressed in the developing embryonic pronephros. To investigate the role of wt1 in pronephros development in Xenopus embryos, we mutated wt1 by CRISPR/Cas9 and found that the expression of pronephros marker genes was reduced. In reporter assays in which known WT1 binding sequences were placed upstream of the luciferase gene, WT1 activated transcription of the luciferase gene. The injection of wild-type or artificially altered transcriptional activity of wt1 mRNA disrupted the expression of pronephros marker genes in the embryos. These results suggest that the appropriate amounts and activity of WT1 protein are required for normal pronephros development in Xenopus embryos.
期刊介绍:
The Journal of Developmental Biology (ISSN 2221-3759) is an international, peer-reviewed, quick-refereeing, open access journal, which publishes reviews, research papers and communications on the development of multicellular organisms at the molecule, cell, tissue, organ and whole organism levels. Our aim is to encourage researchers to effortlessly publish their new findings or concepts rapidly in an open access medium, overseen by their peers. There is no restriction on the length of the papers; the full experimental details must be provided so that the results can be reproduced. Electronic files regarding the full details of the experimental procedure, if unable to be published in a normal way, can be deposited as supplementary material. Journal of Developmental Biology focuses on: -Development mechanisms and genetics -Cell differentiation -Embryonal development -Tissue/organism growth -Metamorphosis and regeneration of the organisms. It involves many biological fields, such as Molecular biology, Genetics, Physiology, Cell biology, Anatomy, Embryology, Cancer research, Neurobiology, Immunology, Ecology, Evolutionary biology.