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A promoter from sugarcane bacilliform badnavirus drives transgene expression in banana and other monocot and dicot plants

机译:甘蔗杆状病毒的启动子驱动香蕉和其他单子叶植物和双子叶植物中的转基因表达

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摘要

A 1369 bp DNA fragment (Sc) was isolated from a full-length clone of sugarcane bacilliform badnavirus (ScBV) and was shown to have promoter activity in transient expression assays using monocot (banana, maize, millet and sorghum) and dicot plant species (tobacco, sunflower, canola and Nicotiana benthamiana). This promoter was also tested for stable expression in transgenic banana and tobacco plants. These experiments showed that this promoter could drive high-level expression of the beta -glucuronidase (GUS) reporter gene in most plant cells. The expression level was comparable to the maize ubiquitin promoter in standardised transient assays in maize. In transgenic banana plants the expression levels were variable for different transgenic lines but was generally comparable with the activities of both the maize ubiquitin promoter and the enhanced cauliflower mosaic virus (CaMV) 35S promoter. The Sc promoter appears to express in a near-constitutive manner in transgenic banana and tobacco plants. The promoter from sugarcane bacilliform virus represents a useful tool for the high-level expression of foreign genes in both monocot and dicot transgenic plants that could be used similarly to the CaMV 35S or maize polyubiquitin promoter.
机译:从甘蔗杆状病毒(ScBV)的全长克隆中分离到一个1369 bp的DNA片段(Sc),并在使用单子叶植物(香蕉,玉米,粟和高粱)和双子叶植物物种的瞬时表达测定中显示具有启动子活性。烟草,向日葵,低芥酸菜子和烟草本塔米纳)。还测试了该启动子在转基因香蕉和烟草植物中的稳定表达。这些实验表明,该启动子可以驱动大多数植物细胞中β-葡萄糖醛酸酶(GUS)报告基因的高水平表达。在玉米的标准化瞬时测定中,表达水平与玉米泛素启动子相当。在转基因香蕉植物中,表达水平对于不同的转基因品系是可变的,但是通常与玉米泛素启动子和增强的花椰菜花叶病毒(CaMV)35S启动子的活性相当。 Sc启动子似乎在转基因香蕉和烟草植物中以近组成方式表达。甘蔗杆状病毒的启动子是在单子叶植物和双子叶植物转基因植物中高表达外源基因的有用工具,可以与CaMV 35S或玉米多泛素启动子类似地使用。

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