首页> 外文期刊>Polar biology >Identification and validation of new reference genes for accurate quantitative reverse transcriptase-PCR normalization in the Antarctic plant Colobanthus quitensis under abiotic stress conditions
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Identification and validation of new reference genes for accurate quantitative reverse transcriptase-PCR normalization in the Antarctic plant Colobanthus quitensis under abiotic stress conditions

机译:非生物胁迫条件下南极植物Colobanthus quity的新参考基因的鉴定与验证。

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摘要

The Antarctic ecotype of Colobanthus quitensis is a vascular plant highly adapted to the harsh environmental conditions of Maritime Antarctica which is now facing with the rapid local warming experienced in the Antarctic Peninsula during the last decades. Thus, the identification of the molecular mechanisms leading to the adaptation to this warming trend is a new target for modern cell physiology. The selection of suitable reference genes for quantification of key stress-responsive genes through quantitative Reverse Transcriptase-Polymerase Chain Reaction (qRT-PCR) is important to ensure accurate and reliable results. In this study, we evaluated the expression stability of eleven candidate genes in C. quitensis under different abiotic stress conditions using geNorm and RefFinder tools. The statistical analysis showed that the appropriate reference genes varied depending on the experimental conditions, even if EF1 alpha and PP2Acs ranked as the most stable reference genes when all stress conditions were considered. To further validate the stability of the selected reference genes, the expression patterns of C. quitensis catalase gene (CqCAT) was analyzed. The reference genes validated in this study will be useful for improving the accuracy of qRT-PCR analysis for gene expression studies of the Antarctic ecotype of C. quitensis and could be extended to other ecotypes adapted to low temperatures.
机译:Colobanthus Quitensis的南极生态型是一个血管厂,高度适应海事南极的恶劣环境条件,目前在过去几十年中南极半岛经历的快速局部变暖。因此,鉴定导致对这种变暖趋势的适应的分子机制是现代细胞生理学的新目标。通过定量逆转录酶 - 聚合酶链反应(QRT-PCR)来选择适当的参考基因,用于定量关键应力响应基因的定量(QRT-PCR)对于确保准确可靠的结果是重要的。在该研究中,我们在不同的非生物胁迫条件下评估了在C. quitensis中11候选基因的表达稳定性使用Genorm和Reffides工具。统计分析表明,即使EF1α和PP2Acs在考虑所有压力条件时,也根据实验条件,根据实验条件等于最稳定的参考基因而变化的适当参考基因。为了进一步验证所选参考基因的稳定性,分析了C. Quitensis过氧化氢酶基因(CQCAT)的表达模式。本研究验证的参考基因对于提高C. quitensis南极生态型的基因表达研究的QRT-PCR分析的准确性是有用的,并且可以扩展到适应低温的其他生态型。

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  • 来源
    《Polar biology》 |2021年第2期|389-405|共17页
  • 作者单位

    Univ Tuscia Dept Ecol & Biol Sci Viterbo Italy;

    Univ Tuscia Dept Ecol & Biol Sci Viterbo Italy;

    Univ Tuscia Dept Ecol & Biol Sci Viterbo Italy;

    Univ Tuscia Dept Ecol & Biol Sci Viterbo Italy;

    Univ La Frontera Dept Ciencias Agron & Recursos Nat Lab Fisiol & Biol Mol Vegetal Fac Ciencias Agr & Forest Inst Agroind Temuco Chile|Univ La Frontera Ctr Plant Soil Interact & Nat Resources Biotechno Sci & Technol Bioresource Nucleus Temuco Chile;

    Univ Autonoma Chile Inst Ciencias Biomed Fac Ciencias Salud Temuco Chile;

    Univ Tuscia Dept Ecol & Biol Sci Viterbo Italy;

  • 收录信息
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    Colobanthus quitensis; Gene expression validation; qRT-PCR; Reference genes;

    机译:Colobanthus quitensis;基因表达验证;QRT-PCR;参考基因;
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