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A novel keratin18 promoter that drives reporter gene expression in the intrahepatic and extrahepatic biliary system allows isolation of cell-type specific transcripts from zebrafish liver

机译:一个新型的keratin18启动子可在肝内和肝外胆道系统中驱动报告基因的表达从而可从斑马鱼肝脏中分离出细胞类型的特定转录本

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摘要

Heritable and acquired biliary disorders are an important cause of acute and chronic human liver disease. Biliary development and physiology have been studied extensively in rodent models and more recently, zebrafish have been used to uncover pathogenic mechanisms and potential therapies for these conditions. Here we report development of novel transgenic lines labeling the intrahepatic and extrahepatic biliary system of zebrafish larvae that can be used for lineage tracing and isolation of biliary-specific RNAs from mixed populations of liver cells. We show that GFP expression driven by a 4.4 kilobase promoter fragment from the zebrafish keratin18 (krt18) gene allows visualization of all components of the developing biliary system as early as 3 days post-fertilization. In addition, expression of a ribosomal fusion protein (EGFP-Rpl10a) in krt18:TRAP transgenic fish allows for enrichment of translated biliary cell mRNAs via translating ribosome affinity purification (TRAP). Future studies utilizing these reagents will enhance our understanding of the morphologic and molecular processes involved in biliary development and disease.
机译:遗传性和获得性胆道疾病是急性和慢性人类肝脏疾病的重要原因。在啮齿动物模型中对胆汁的发育和生理学进行了广泛的研究,最近,斑马鱼已被用于揭示这些疾病的致病机制和潜在疗法。在这里,我们报告标记斑马鱼幼虫的肝内和肝外胆道系统的新型转基因品系的发展,该系统可用于谱系追踪和从混合肝细胞群体中分离胆汁特异性RNA。我们显示由斑马鱼角蛋白18(krt18)基因的4.4千碱基启动子片段驱动的GFP表达允许在受精后3天内可视化发育​​中的胆道系统的所有组件。此外,在krt18:TRAP转基因鱼中表达核糖体融合蛋白(EGFP-Rpl10a)可以通过翻译核糖体亲和纯化(TRAP)富集翻译的胆管细胞mRNA。未来使用这些试剂的研究将增进我们对胆汁发育和疾病所涉及的形态学和分子过程的理解。

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