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Reference Gene Selection for Quantitative Real-time PCR Normalization in Caragana intermedia under Different Abiotic Stress Conditions

机译:不同非生物胁迫条件下中间锦鸡儿定量实时PCR标准化的参考基因选择

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摘要

Quantitative real-time reverse transcription polymerase chain reaction (qPCR), a sensitive technique for gene expression analysis, depends on the stability of the reference genes used for data normalization. Caragana intermedia, a native desert shrub with strong drought-resistance, sand-fixing capacity and high forage value that is widespread in the desert land of west and northwest China, has not been investigated regarding the identification of reference genes suitable for the normalization of qPCR data. In this study, 10 candidate reference genes were analyzed in C. intermedia subjected to different abiotic (osmotic, salt, cold and heat) stresses, in two distinct plant organs (roots and leaves). The expression stability of these genes was assessed using geNorm, NormFinder and BestKeeper algorithms. The best-ranked reference genes differed across the different sets of samples, but UNK2, PP2A and SAND were the most stable across all tested samples. UNK2 and SAND would be appropriate for normalizing gene expression data for salt-treated roots, whereas the combination of UNK2, SAND and EF-1α would be appropriate for salt-treated leaves. UNK1, UNK2 and PP2A would be appropriate for PEG-treated (osmotic) roots, whereas the combination of TIP41 and PP2A was the most suitable for PEG-treated leaves. SAND, PP2A and TIP41 exhibited the most stable expression in heat-treated leaves. In cold-treated leaves, SAND and EF-1α were the most stably expressed. To further validate the suitability of the reference genes identified in this study, the expression levels of DREB1 and DREB2 (homologs of AtDREB1 and AtDREB2) were studied in parallel. This study is the first systematic analysis for the selection of superior reference genes for qPCR in C. intermedia under different abiotic stress conditions, and will benefit future studies on gene expression in C. intermedia and other species of the leguminous genus Caragana.
机译:实时定量逆转录聚合酶链反应(qPCR)是一种用于基因表达分析的灵敏技术,取决于用于数据标准化的参考基因的稳定性。中间锦鸡儿(Caragana intermedia)是一种具有较强的抗旱性,固沙能力和较高草料价值的原生沙漠灌木,广泛分布于中国西部和西北部的荒漠地区,尚未进行关于鉴定适合qPCR标准化的参考基因的研究。数据。在这项研究中,在两个不同的植物器官(根和叶)中经受不同非生物(渗透,盐,冷和热)胁迫的中间棒状线虫中分析了10个候选参考基因。使用geNorm,NormFinder和BestKeeper算法评估了这些基因的表达稳定性。排名最高的参考基因在不同的样品组中有所不同,但UNK2,PP2A和SAND在所有测试样品中最稳定。 UNK2和SAND适用于标准化盐处理过的根的基因表达数据,而UNK2,SAND和EF-1α的组合适用于盐处理过的叶子。 UNK1,UNK2和PP2A适用于PEG处理的(渗透性)根,而TIP41和PP2A的组合最适合PEG处理的叶子。 SAND, PP2A TIP41 在热处理后的叶片中表达最稳定。在冷处理的叶片中, SAND EF-1α的表达最稳定。为了进一步验证本研究中鉴定的参考基因的适用性, DREB1 DREB2 的表达水平( AtDREB1 的同源物并行研究了AtDREB2 )。这项研究是为 C中的qPCR选择优良参考基因的第一个系统分析。 intermedia 在不同的非生物胁迫条件下,将有助于将来在 C中表达基因的研究。中间种和豆科植物锦鸡儿(Caragana)的其他种类。

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