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Efficient silencing of reporter transgenes coupled to known functional promoters in sugarcane, a highly polyploid crop species

机译:高效转导的报告基因转基因与甘蔗(一种高度多倍体的农作物)中已知的功能启动子偶联

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Sugarcane is a crop of great interest for engineering of sustainable biomaterials and biofuel production. Isolated sugarcane promoters have generally not maintained the expected patterns of reporter transgene expression. This could arise from defective promoters on redundant alleles in the highly polyploid genome, or from efficient transgene silencing. To resolve this question we undertook detailed analysis of a sugarcane gene that combines a simple pattern in genomic Southern hybridization analysis with potentially useful, sink-specific, expression. Sequence analysis indicates that this gene encodes a member of the SHAQYF subfamily of MYB transcription factors. At least eight alleles were revealed by PCR analysis in sugarcane cultivar Q117 and a similar level of heterozygosity was seen in BAC clones from cultivar Q200. Eight distinct promoter sequences were isolated from Q117, of which at least three are associated with expressed alleles. All of the isolated promoter variants were tested for ability to drive reporter gene expression in sugarcane. Most were functional soon after transfer, but none drove reporter activity in mature stems of regenerated plants. These results show that the ineffectiveness of previously tested sugarcane promoters is not simply due to the isolation of non-functional promoter copies from the polyploid genome. If the unpredictable onset of silencing observed in most other plant species is associated with developmental polyploidy, approaches that avoid efficient transgene silencing in polyploid sugarcane are likely to have much wider utility in molecular improvement. Keywords Allelic variation - Promoter function - Saccharum - Transgene silencing
机译:甘蔗对于可持续生物材料和生物燃料生产的工程设计具有重大意义。分离的甘蔗启动子通常不能维持报道基因转基因表达的预期模式。这可能是由于高度多倍体基因组中多余等位基因上的启动子缺陷或有效的转基因沉默引起的。为了解决这个问题,我们对甘蔗基因进行了详细分析,该基因结合了基因组Southern杂交分析中的简单模式和潜在有用的,特定于汇的表达。序列分析表明该基因编码MYB转录因子的SHAQYF亚家族的成员。通过PCR分析在甘蔗品种Q117中揭示了至少八个等位基因,并且在来自品种Q200的BAC克隆中观察到相似的杂合水平。从Q117分离出八个不同的启动子序列,其中至少三个与表达的等位基因相关。测试了所有分离的启动子变体在甘蔗中驱动报告基因表达的能力。大部分在转移后不久即可发挥功能,但没有一个能促进再生植物成熟茎中的报道基因活性。这些结果表明,先前测试的甘蔗启动子的无效不仅仅是由于从多倍体基因组中分离了非功能性启动子拷贝。如果在大多数其他植物物种中观察到的无法预测的沉默发生与发育多倍体有关,那么避免多倍体甘蔗中有效转基因沉默的方法可能在分子改良中具有更广泛的用途。关键词等位变异-启动子功能-糖-转基因沉默

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