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Multiple Modification of Chromosomal Loci Using URA5.3 Selection Marker in the Unicellular Red Alga Cyanidioschyzon merolae

机译:URA5.3在U形红藻CyanidiosChyzon Merolae中使用URA5.3选择标记的多种修饰染色体基因座

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摘要

The unicellular red alga Cyanidioschyzon merolae has been used as a eukaryotic photosynthetic model for various basic and applied studies. Although the nuclear genome of C. merolae can be modified by homologous recombination with exogenously introduced DNA, it has been difficult to modify multiple chromosome loci within the same strain because of the limited number of available positive selection markers. Recently, we reported a modified URA5.3 gene cassette (URA5.3T), which can be used repeatedly for nuclear genome transformation using the pMKT plasmid vectors for epitope tagging (3x FLAG- or 3x Myc-) of nuclear-encoded proteins. In addition, these plasmid vectors can also be used to knock out multiple genes one by one. This report describes the construction of DNA fragments for transformation and the detailed transformation procedure.
机译:单细胞红藻藻藻藻苏氏菌被用作各种基本和应用研究的真核光合模型。尽管C. MuloLae的核基因组可以通过与外源引入的DNA同源重组来修饰,但由于有限数量的可用阳性选择标记,难以在相同的菌株内修饰多种染色体基因座。最近,我们报道了一种改进的URA5.3基因盒(URA5.3T),其可以使用用于核编码蛋白的表位标记(3x Flag或3x Myc-)的PMKT质粒载体反复用于核基因组转化。此外,这些质粒载体也可用于逐一敲出多种基因。本报告描述了转化和详细转化过程的DNA片段的构建。

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