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Transgenic alternative-splicing reporters reveal tissue-specific expression profiles and regulation mechanisms in vivo

机译:转基因替代拼接记者揭示体内组织特异性表达谱和调控机制

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Alternative splicing of pre-mRNAs allows multicellar organisms to create a huge diversity of proteomes from a finite number of genes. But extensive studies in vitro or in cultured cells have not fully explained the regulation mechanisms of tissue-specific or developmentally regulated alternative splicing in living organisms. Here we report a transgenic reporter system that allows visualization of expression profiles of mutually exclusive exons in Caenorhabditis elegans. Reporters for egl-15 exons 5A and 5B showed tissue-specific profiles, and we isolated mutants defective in the tissue specificity. We identified alternative-splicing defective-1 (asd-1), encoding a new RNA-binding protein of the evolutionarily conserved Fox-1 family, as a regulator of the egl-15 reporter. Furthermore, an asd-1; fox-1 double mutant was defective in the expression of endogenous egl-15 (5A) and phenocopied egl-15 (5A) mutant. This transgenic reporter system can be a powerful experimental tool for the comprehensive study of expression profiles and regulation mechanisms of alternative splicing in metazoans.
机译:前mRNA的选择性剪接使多细胞生物可以从有限数量的基因中产生大量的蛋白质组。但是体外或培养细胞的广泛研究尚未完全解释活生物体中组织特异性或发育调控的选择性剪接的调控机制。在这里,我们报告了一个转基因报告系统,可以可视化秀丽隐杆线虫相互排斥的外显子的表达谱。 egl-15外显子5A和5B的报告者显示了组织特异性的概况,我们分离了组织特异性有缺陷的突变体。我们确定替代拼接缺陷-1(asd-1),编码进化上保守的Fox-1家族的新RNA结合蛋白,作为egl-15报告基因的调节剂。此外,一个asd-1; fox-1双突变体在内源性egl-15(5A)和表型egl-15(5A)突变体的表达中存在缺陷。该转基因报道基因系统可以是一个强大的实验工具,可用于全面研究后生动物中可变剪接的表达谱和调控机制。

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