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首页> 外文期刊>BMC Genomics >Transcriptome-wide identification of optimal reference genes for expression analysis of Pyropia yezoensis responses to abiotic stress
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Transcriptome-wide identification of optimal reference genes for expression analysis of Pyropia yezoensis responses to abiotic stress

机译:转录组范围内的最佳参考基因鉴定,用于对拟南芥对非生物胁迫的响应进行表达分析

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Pyropia yezoensis, a marine red alga, is an ideal research model for studying the mechanisms of abiotic stress tolerance in intertidal seaweed. Real-time quantitative polymerase chain reaction (RT-qPCR) is the most commonly used method to analyze gene expression levels. To accurately quantify gene expression, selection and validation of stable reference genes is required. We used transcriptome profiling data from different abiotic stress treatments to identify six genes with relatively stable expression levels: MAP, ATPase, CGS1, PPK, DPE2, and FHP. These six genes and three conventional reference genes, UBC, EF1-α, and eif4A, were chosen as candidates for optimal reference gene selection. Five common statistical approaches (geNorm, ΔCt method, NormFinder, BestKeeper, and ReFinder) were used to identify the stability of each reference gene. Our results show that: MAP, UBC, and FHP are stably expressed in all analyzed conditions; CGS1 and UBC are stably expressed under conditions of dehydration stress; and MAP, UBC, and CGS1 are stably expressed under conditions of temperature stress. We have identified appropriate reference genes for RT-qPCR in P. yezoensis under different abiotic stress conditions which will facilitate studies of gene expression under these conditions.
机译:海洋红藻斑叶紫菜(Pyropia yezoensis)是研究潮间带海藻非生物胁迫耐受性机制的理想研究模型。实时定量聚合酶链反应(RT-qPCR)是分析基因表达水平的最常用方法。为了准确定量基因表达,需要选择和验证稳定的参考基因。我们使用了来自不同非生物胁迫处理的转录组分析数据,以鉴定具有相对稳定表达水平的六个基因:MAP,ATPase,CGS1,PPK,DPE2和FHP。选择这六个基因和三个常规参考基因UBC,EF1-α和eif4A作为最佳参考基因选择的候选对象。五种常见的统计方法(geNorm,ΔCt方法,NormFinder,BestKeeper和ReFinder)用于识别每个参考基因的稳定性。我们的结果表明:MAP,UBC和FHP在所有分析条件下均稳定表达; CGS1和UBC在脱水胁迫条件下稳定表达; MAP,UBC和CGS1在温度应力条件下稳定表达。我们已经确定了合适的参考基因,用于在不同的非生物胁迫条件下在假山拟南芥中进行RT-qPCR,这将有助于研究在这些条件下的基因表达。

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