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Polyubiquitin-regulated DsRed marker for transgenic insects

机译:聚泛素调节的DsRed标记用于转基因昆虫

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摘要

Genetic transformation of most insect systems requires dominant-acting markers that do not depend on reverting a mutant phenotype in a host strain, and for this purpose GFP has proven to be useful in several insect orders. However, detection of multiple transgenes and reporters for gene expression requires the development of new visible markers that can be unambiguously detected when co-expressed with GFP. The DsRed fluorescent protein has spectral characteristics that are most distinct from GFP and GFP variants, and we have explored the use of DsRed as a selectable marker for piggy-Bac transformation in Drosophila melanogaster and its use as a reporter when co-expressed with GFP. Transformants marked with polyubiquitin-regulated DsRed1 were detected throughout development at a relatively high frequency, and they exhibited brighter fluorescence than transformants marked with EGFP. The use of a Texas Red (R) filter set eliminated detection of EGFP fluorescence and autofluorescence, and DsRed expressed from a reporter construct could be unambiguously detected when co-expressed with EGFP. DsRed should prove to be a highly efficient marker system for the selection of transformant insects and as a reporter in gene expression studies.
机译:大多数昆虫系统的遗传转化需要不依赖于恢复宿主菌株突变表型的显性作用标记,并且为此目的,GFP已被证明可用于多种昆虫。然而,检测多个转基因和报告基因的表达需要开发新的可见标记,当与GFP共表达时可以明确检测到。 DsRed荧光蛋白具有与GFP和GFP变体最不同的光谱特征,我们已经探索了将DsRed用作黑腹果蝇(Drosophila melanogaster)piggy-Bac转化的选择标记,以及与GFP共表达时用作报告子的用途。在整个发育过程中,以相对较高的频率检测到标记有多聚泛素调节的DsRed1的转化子,它们显示的荧光比标记为EGFP的转化子亮。使用Texas Red(R)滤光片组消除了对EGFP荧光和自发荧光的检测,当与EGFP共表达时,可以清楚地检测到由报告基因构建体表达的DsRed。 DsRed应该被证明是用于选择转化昆虫的高效标记系统,并在基因表达研究中作为报告基因。

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