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首页> 外文期刊>Physiology and Molecular Biology of Plants >Selection of reference genes for quantitative real-time PCR analysis of photosynthesis-related genes expression in Lilium regale
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Selection of reference genes for quantitative real-time PCR analysis of photosynthesis-related genes expression in Lilium regale

机译:荔枝植物中光合作用基因表达的定量实时PCR分析的参考基因的选择

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Photosynthesis is closely related to the growth of plants. A stable reference gene is fundamental for studies of the molecular mechanism of photosynthesis in Lilium regale. Therefore, it is very important to select a suitable reference gene for qRT-PCR analysis on genes of photosynthetic system, chlorophyll biosynthetic pathway and chloroplast development in Lilium regale. Three kinds of tissues, leaves and bulbs (abnormal leaves) of tissue culture plantlets and cotyledons of seedlings of the wild-type and mutant Lilium regale were selected as materials for qRT-PCR. Six housekeeping genes were selected as candidate genes from transcriptome sequencing data of the wild-type and yellow seedling lethal mutant of Lilium regale. Finally, the expression stability of six candidate reference genes was analyzed using geNorm, NormFinder, and BestKeeper software, the comparative ACt method, and the RefFinder program. The results showed that LrActin2 was the best reference gene for qRT-PCR analysis of photosynthesis-related genes expression in leaves of tissue culture plantlets and seedlings of Lilium regale. This study provided useful data for further research on molecular mechanism of photosynthesis in the Lilium.
机译:光合作用与植物的生长密切相关。稳定的参考基因是研究百合升级光合作用的分子机制的基础。因此,选择合适的参考基因对光合体系的基因,叶绿素生物合成途径和叶绿体升值中的叶绿素中源性发育。选择野生型和突变体植物植物幼苗的组织培养植物和子叶的三种组织,叶和鳞片(异常叶子)作为QRT-PCR的材料。选择六个家庭内政基因作为来自百合胞质的转录组测序数据的候选基因,黄色幼苗致疱疹的植物静脉突变体。最后,使用Genorm,Normfinder和Bestkeyper软件,比较法方法和Reffinder计划分析六个候选参考基因的表达稳定性。结果表明,LRACTIN2是QRT-PCR分析的最佳参考基因,用于组织培养植物叶片中的光合作用相关基因和植物幼苗幼苗的幼苗。本研究提供了有用的数据,以进一步研究百合光合作用的分子机制。

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