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在重金属胁迫下,柳枝稷 RT-qPCR 分析中参考基因的鉴定和验证。

Identification and Validation of Reference Genes for RT-qPCR Analysis in Switchgrass under Heavy Metal Stresses.

机构信息

Department of Grassland Science, Sichuan Agricultural University, Chengdu 611130, China.

Zonation Fringe Technology Co., Metro Vancouver, BC V5C 2A0, Canada.

出版信息

Genes (Basel). 2020 May 3;11(5):502. doi: 10.3390/genes11050502.

Abstract

Switchgrass ( L.) has been recognized as the new energy plant, which makes it ideal for the development of phytoremediation on heavy metal contamination in soils with great potential. This study aimed to screen the best internal reference genes for the real-time quantitative PCR (RT-qPCR) in leaves and roots of switchgrass for investigating its response to various heavy metals, such as cadmium (Cd), lead (Pb), mercury (Hg), chromium (Cr), and arsenic (As). The stability of fourteen candidate reference genes was evaluated by BestKeeper, GeNorm, NormFinder, and RefFinder software. Our results identified as the best reference gene in Cd, Hg, Cr, and As treated leaves as well as in Hg, Pb, As, and Cr stressed root tissues. In Pb treated leaf tissues, was demonstrated to be the best reference gene. was determined to be the optimal reference gene in Cd treated root tissues. The least stable reference gene was identified to be in all tested samples except for root tissues stressed by Pb. To further validate the initial screening results, we used the different sets of combinatory internal reference genes to analyze the expression of two metal transport associated genes ( and ) in young leaves and roots of switchgrass. Our results demonstrated that the relative expression of the target genes consistently changed during the treatment when , , or were combined as the internal reference genes. However, the time-dependent change pattern of the target genes was significantly altered when was used as the internal reference gene. Therefore, the selection of the internal reference genes appropriate for specific experimental conditions is critical to ensure the accuracy and reliability of RT-qPCR. Our findings established a solid foundation to further study the gene regulatory network of switchgrass in response to heavy metal stress.

摘要

柳枝稷( Panicum virgatum )被认为是一种新型能源植物,非常适合发展用于修复土壤中重金属污染的植物修复技术。本研究旨在筛选柳枝稷叶片和根系中实时定量 PCR(RT-qPCR)的最佳内参基因,以研究其对各种重金属(如镉(Cd)、铅(Pb)、汞(Hg)、铬(Cr)和砷(As))的响应。通过 BestKeeper、GeNorm、NormFinder 和 RefFinder 软件评估了 14 个候选内参基因的稳定性。我们的研究结果表明,在 Cd、Hg、Cr 和 As 处理的叶片以及 Hg、Pb、As 和 Cr 胁迫的根系组织中, 是最佳的内参基因。在 Pb 处理的叶片组织中, 被证明是最佳的内参基因。在 Cd 处理的根组织中, 是最佳的内参基因。除了 Pb 处理的根组织外,在所有测试样本中最不稳定的内参基因是 。为了进一步验证最初的筛选结果,我们使用不同的内参基因组合来分析柳枝稷幼叶和根系中两种金属转运相关基因( 和 )的表达。我们的研究结果表明,当 、 、 或 作为内参基因组合时,目标基因的相对表达在处理过程中始终发生变化。然而,当 作为内参基因时,目标基因的时间依赖性变化模式发生了显著改变。因此,选择适合特定实验条件的内参基因对于确保 RT-qPCR 的准确性和可靠性至关重要。我们的研究结果为进一步研究柳枝稷响应重金属胁迫的基因调控网络奠定了基础。

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