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Reference gene selection for quantitative reverse transcription-polymerase chain reaction normalization during in vitro adventitious rooting in Eucalyptus globulus Labill

机译:桉树球形不定根体外不定根期间定量逆转录-聚合酶链反应正常化的参考基因选择

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摘要

BackgroundEucalyptus globulus and its hybrids are very important for the cellulose and paper industry mainly due to their low lignin content and frost resistance. However, rooting of cuttings of this species is recalcitrant and exogenous auxin application is often necessary for good root development. To date one of the most accurate methods available for gene expression analysis is quantitative reverse transcription-polymerase chain reaction (qPCR); however, reliable use of this technique requires reference genes for normalization. There is no single reference gene that can be regarded as universal for all experiments and biological materials. Thus, the identification of reliable reference genes must be done for every species and experimental approach. The present study aimed at identifying suitable control genes for normalization of gene expression associated with adventitious rooting in E. globulus microcuttings.
机译:背景技术桉树及其杂种对纤维素和造纸工业非常重要,这主要是由于其木质素含量低和抗冻性。然而,该物种的插条生根是顽强的,外源生长素的施用通常是良好的根发育所必需的。迄今为止,用于基因表达分析的最准确的方法之一是定量逆转录-聚合酶链反应(qPCR)。但是,可靠使用此技术需要参考基因进行标准化。没有一个参考基因可以被视为所有实验和生物材料的通用基因。因此,必须针对每种物种和实验方法进行可靠参考基因的鉴定。本研究旨在确定合适的控制基因,以使与不定根在小球藻微切口中相关的基因表达正常化。

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