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Design rules for efficient transgene expression in plants

机译:植物高效转基因表达的设计规则

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摘要

Sustained expression of transgenes in specified developmental patterns is commonly needed in plant biotechnology, but obstructed by transgene silencing. Here, we present a set of gene design rules, tested on the silencing-susceptible beetle luc and bacterial ims genes, expressed in sugarcane. Designs tested independently or in combination included removal of rare codons, removal of RNA instability sequences, blocking of likely endogenous sRNA binding sites and randomization of non-rare codons. Stable transgene expression analyses, on multiple independent lines per construct, showed greatest improvement from the removal of RNA instability sequences, accompanied by greatly reduced transcript degradation evident in northern blot analysis. We provide a set of motifs that readily can be eliminated concurrently with rare codons and undesired structural features such as repeat sequences, using Gene Designer 2.0 software. These design rules yielded 935-and 5-fold increased expression in transgenic callus, relative to the native luc and ims sequences; and gave sustained expression under the control of sugarcane and heterologous promoters over several years in greenhouse and field trials. The rules can be applied easily with codon usage tables from any plant species, providing a simple and effective means to achieve sustained expression of otherwise silencing-prone transgenes in plants.
机译:在植物生物技术中通常需要在特定发育模式中进行转基因的持续表达,但是通过转基因沉默阻碍。在这里,我们提出了一组基因设计规则,在蔗糖中表达的沉默易感甲虫LUC和细菌IMS基因上测试。独立测试或组合测试的设计包括去除稀有密码子,去除RNA不稳定性序列,阻断可能的内源性SRNA结合位点和非稀有密码子的随机化。稳定的转基因表达分析在每个构建体的多个独立线上,从去除RNA不稳定性序列时显示出最大的改善,伴随着Northern印迹分析中的大大降低的转录物降解。我们提供了一组主题,可以随着稀有密码子和不期望的结构特征和不希望的结构特征,例如使用基因设计器2.0软件,易于消除一组图案。这些设计规则相对于天然LUC和IMS序列,在转基因愈伤组织中产生935和5倍的表达;在温室和田间试验中,在多年来甘蔗和异源启动子控制下给予持续的表达。这些规则可以用任何植物物种的密码子使用表来容易地应用,提供一种简单且有效的方法,以实现植物中其他沉默的转基因的持续表达。

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