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Downstream promoter sequence of an Indian isolate of Rice tungro bacilliform virus alters tissue-specific expression in host rice and acts differentially in heterologous system

机译:印度稻瘟病杆菌病毒的印度分离株的下游启动子序列改变宿主稻中的组织特异性表达,并在异源系统中起差异作用

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An Indian isolate of Rice tungro bacilliform virus from West Bengal (RTBV-WB) showed significant nucleotide differences in its putative promoter region when compared with a previously characterized isolate from Philippines. The transcription start site of RTBV-WB was mapped followed by assessing the activity and tissue-specificity of the full-length (FL) promoter (-231 to +645) and several of its upstream and downstream deletions by studying the expression of beta-Glucuronidase (GUS) reporter gene in transgenic rice (Oryza sativa L. subsp. indica) plants at various stages of development. In addition to the expected vascular-specific expression pattern, studied by histochemical staining, GUS enzymatic assay and northern and RT-PCR analysis, two novel patterns were revealed in some of the downstream deleted versions; a non-expressing type, representing no expression at any stage in any tissue and constitutive type, representing constitutive expression at all stages in most tissues. This indicated the presence of previously unreported positive and negative cis-regulatory elements in the downstream region. The negative element and a putative enhancer region in the upstream region specifically bound to rice nuclear proteins in vitro. The FL and its deletion derivatives were also active in heterologous systems like tobacco (Nicotiana tabacum) and wheat (Triticum durum). Expression patterns in tobacco were different from those observed in rice suggesting the importance of upstream elements in those systems and host-specific regulation of the promoter in diverse organisms. Thus, the RTBV-WB FL promoter and its derivatives contain an array of cis-elements, which control constitutive or tissue- and development-specific gene expression in a combinatorial fashion.
机译:与以前鉴定的菲律宾分离株相比,印度分离株来自西孟加拉邦的水稻通哥杆菌病毒(RTBV-WB)在其推定的启动子区域显示出明显的核苷酸差异。绘制RTBV-WB的转录起始位点,然后通过研究β-启动子的表达来评估全长(FL)启动子(-231至+645)及其上游和下游缺失的活性和组织特异性转基因水稻(Oryza sativa L. subsp。indica)植物处于不同发育阶段的葡萄糖醛酸酶(GUS)报告基因。除了通过组织化学染色,GUS酶法,Northern和RT-PCR分析研究的预期血管特异性表达模式外,在某些下游缺失版本中还发现了两种新颖的模式。非表达型,代表任何组织中任何阶段都不表达,组成型,代表大多数组织中所有阶段的组成性表达。这表明在下游区域中存在先前未报道的正和负顺式调节元件。上游区域中的负元件和推定的增强子区域在体外与水稻核蛋白特异性结合。 FL及其缺失衍生物在诸如烟草(Nicotiana tabacum)和小麦(Triticum durum)的异源系统中也有活性。烟草中的表达模式与水稻中的表达模式不同,这表明在这些系统中上游元件的重要性以及在多种生物中启动子的宿主特异性调节。因此,RTBV-WB FL启动子及其衍生物包含一系列顺式元素,以组合方式控制组成型或组织和发育特异性基因的表达。

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