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沙漠植物柳枝稷中 RT-qPCR 定量基因表达的参考基因选择。

Selection of the reference genes for quantitative gene expression by RT-qPCR in the desert plant Stipagrostis pennata.

机构信息

Key Laboratory of Oasis Town and Mountain-Basin System Ecology of Xinjiang Production and Construction Corps, College of Life Sciences, Shihezi University, Shihezi, Xinjiang, China.

Key Laboratory of Xinjiang Phytomedicine Resource and Utilization of Ministry of Education, Shihezi University, Shihezi, Xinjiang, China.

出版信息

Sci Rep. 2021 Nov 5;11(1):21711. doi: 10.1038/s41598-021-00833-2.

DOI:10.1038/s41598-021-00833-2
PMID:34741052
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8571334/
Abstract

The desert pioneer plant Stipagrostis pennata plays an important role in sand fixation, wind prevention, and desert ecosystem recovery. An absence of reference genes greatly limits investigations into the regulatory mechanism by which S. pennata adapts to adverse desert environments at the molecular and genetic levels. In this study, eight candidate reference genes were identified from rhizosheath development transcriptome data from S. pennata, and their expression stability in the rhizosheaths at different development stages, in a variety of plant tissues, and under drought stress was evaluated using four procedures, including geNorm, NormFinder, BestKeeper, and RefFinder. The results showed that GAPDH and elF were the most stable reference genes under drought stress and in rhizosheath development, and ARP6 and ALDH were relatively stable in all plant tissues. In addition, elF was the most suitable reference gene for all treatments. Analysis of the consistency between the reverse transcription-quantitative PCR (RT-qPCR) and RNA sequencing data showed that the identified elF and GAPDH reference genes were stable during rhizosheath development. These results provide reliable reference genes for assuring the accuracy of RT-qPCR and offer a foundation for further investigations into the genetic responses of S. pennata to abiotic stress.

摘要

荒漠先锋植物短柄拂子茅在固定沙、防风固沙和荒漠生态系统恢复中发挥着重要作用。缺乏参考基因极大地限制了对短柄拂子茅适应不良沙漠环境的分子和遗传水平调控机制的研究。在本研究中,从短柄拂子茅根鞘发育转录组数据中鉴定了 8 个候选参考基因,并使用 geNorm、NormFinder、BestKeeper 和 RefFinder 四种程序评估了它们在不同发育阶段的根鞘、各种植物组织以及干旱胁迫下的表达稳定性。结果表明,在干旱胁迫和根鞘发育过程中,GAPDH 和 eIF 是最稳定的参考基因,而在所有植物组织中,ARP6 和 ALDH 相对稳定。此外,eIF 是所有处理中最适合的参考基因。对逆转录定量 PCR(RT-qPCR)和 RNA 测序数据一致性的分析表明,在根鞘发育过程中鉴定出的 eIF 和 GAPDH 参考基因是稳定的。这些结果为确保 RT-qPCR 的准确性提供了可靠的参考基因,并为进一步研究短柄拂子茅对非生物胁迫的遗传响应提供了基础。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/977b/8571334/8d5ea5fd5a8c/41598_2021_833_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/977b/8571334/d10d2b9bb78b/41598_2021_833_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/977b/8571334/e1b4da9e0b70/41598_2021_833_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/977b/8571334/b02d9ed6f387/41598_2021_833_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/977b/8571334/5483edd5fd70/41598_2021_833_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/977b/8571334/8d5ea5fd5a8c/41598_2021_833_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/977b/8571334/d10d2b9bb78b/41598_2021_833_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/977b/8571334/e1b4da9e0b70/41598_2021_833_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/977b/8571334/b02d9ed6f387/41598_2021_833_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/977b/8571334/5483edd5fd70/41598_2021_833_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/977b/8571334/8d5ea5fd5a8c/41598_2021_833_Fig5_HTML.jpg

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2
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3
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6
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7
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8
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Molecules. 2022 Jun 21;27(13):3980. doi: 10.3390/molecules27133980.
野生和栽培大麻中用于RT-qPCR分析的内参基因评估
Biosci Biotechnol Biochem. 2018 Nov;82(11):1902-1910. doi: 10.1080/09168451.2018.1506253. Epub 2018 Aug 21.
4
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Front Genet. 2018 Jul 23;9:269. doi: 10.3389/fgene.2018.00269. eCollection 2018.
5
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