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暴露于金属浓度增加环境下的拟南芥实时逆转录聚合酶链反应基因表达测量的标准化

Normalisation of real-time RT-PCR gene expression measurements in Arabidopsis thaliana exposed to increased metal concentrations.

作者信息

Remans Tony, Smeets Karen, Opdenakker Kelly, Mathijsen Dennis, Vangronsveld Jaco, Cuypers Ann

机构信息

Environmental Biology, Hasselt University, Agoralaan D, 3590, Diepenbeek, Belgium.

出版信息

Planta. 2008 May;227(6):1343-9. doi: 10.1007/s00425-008-0706-4. Epub 2008 Feb 14.

Abstract

Accurate quantification by real-time RT-PCR relies on normalisation of the measured gene expression data. Normalisation with multiple reference genes is becoming the standard, but the best reference genes for gene expression studies within one organism may depend on the applied treatments or the organs and tissues studied. Ideally, reference genes should be evaluated in all experimental systems. A number of candidate reference genes for Arabidopsis have been proposed, which can be used as a starting point to evaluate their expression stability in individual experimental systems by available computer algorithms like geNorm and NormFinder. Using this approach, we identified the best three reference genes from a set of ten candidates, which included three traditional "housekeeping" genes, for normalisation of gene expression when roots and leaves of Arabidopsis thaliana are exposed to cadmium (Cd) and copper (Cu). The expression stabilities of AT5G15710 (F-box protein), AT2G28390 (SAND family protein) and AT5G08290 (mitosis protein YLS8) were the highest when considering the effect to the roots and shoots of Cd and Cu treatments. Even though the effect of Cd and excess Cu on the plants is very different, the same best reference genes were identified when considering Cd or Cu treatments separately. This suggests that these three genes may also be suitable when studying the gene expression after exposure of Arabidopsis thaliana to increased concentrations of other metals.

摘要

实时逆转录聚合酶链反应(RT-PCR)的准确定量依赖于对测得的基因表达数据进行标准化。使用多个内参基因进行标准化正逐渐成为标准做法,但在一个生物体中进行基因表达研究时,最佳内参基因可能取决于所应用的处理方式或所研究的器官和组织。理想情况下,应在所有实验系统中对内参基因进行评估。已经提出了一些拟南芥的候选内参基因,可将其作为起点,通过诸如geNorm和NormFinder等可用的计算机算法来评估它们在各个实验系统中的表达稳定性。采用这种方法,我们从一组十个候选基因中确定了最佳的三个内参基因,其中包括三个传统的“管家”基因,用于在拟南芥的根和叶暴露于镉(Cd)和铜(Cu)时对基因表达进行标准化。考虑到镉和铜处理对根和芽的影响时,AT5G15710(F-box蛋白)、AT2G28390(SAND家族蛋白)和AT5G08290(有丝分裂蛋白YLS8)的表达稳定性最高。尽管镉和过量铜对植物的影响差异很大,但分别考虑镉或铜处理时,确定的最佳内参基因相同。这表明,在研究拟南芥暴露于其他金属浓度增加后的基因表达时,这三个基因可能也适用。

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