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液相杂交与固相检测:一种用于动植物中微小RNA检测的高灵敏且准确的策略。

Liquid Hybridization and Solid Phase Detection: A Highly Sensitive and Accurate Strategy for MicroRNA Detection in Plants and Animals.

作者信息

Li Fosheng, Mei Lanju, Zhan Cheng, Mao Qiang, Yao Min, Wang Shenghua, Tang Lin, Chen Fang

机构信息

Key Laboratory of Bio-resources and Eco-environment, Ministry of Education, College of Life Science, Sichuan University, Chengdu 610000, Sichuan, China.

Chengdu Botanical Garden, Chengdu 610083, Sichuan, China.

出版信息

Int J Mol Sci. 2016 Sep 1;17(9):1457. doi: 10.3390/ijms17091457.

Abstract

MicroRNAs (miRNAs) play important roles in nearly every aspect of biology, including physiological, biochemical, developmental and pathological processes. Therefore, a highly sensitive and accurate method of detection of miRNAs has great potential in research on theory and application, such as the clinical approach to medicine, animal and plant production, as well as stress response. Here, we report a strategic method to detect miRNAs from multicellular organisms, which mainly includes liquid hybridization and solid phase detection (LHSPD); it has been verified in various species and is much more sensitive than traditional biotin-labeled Northern blots. By using this strategy and chemiluminescent detection with digoxigenin (DIG)-labeled or biotin-labeled oligonucleotide probes, as low as 0.01-0.25 fmol [for DIG-CDP Star (disodium2-chloro-5-(4-methoxyspiro{1,2-dioxetane-3,2'-(5'-chloro)tricyclo[3.3.1.13,7]decan}-4-yl)phenyl phosphate) system], 0.005-0.1 fmol (for biotin-CDP Star system), or 0.05-0.5 fmol (for biotin-luminol system) of miRNA can be detected and one-base difference can be distinguished between miRNA sequences. Moreover, LHSPD performed very well in the quantitative analysis of miRNAs, and the whole process can be completed within about 9 h. The strategy of LHSPD provides an effective solution for rapid, accurate, and sensitive detection and quantitative analysis of miRNAs in plants and animals.

摘要

微小RNA(miRNA)在生物学的几乎各个方面都发挥着重要作用,包括生理、生化、发育和病理过程。因此,一种高灵敏度和准确性的miRNA检测方法在理论研究和应用方面具有巨大潜力,如临床医学、动植物生产以及应激反应等领域。在此,我们报道了一种从多细胞生物中检测miRNA的策略方法,主要包括液相杂交和固相检测(LHSPD);该方法已在多种物种中得到验证,并且比传统的生物素标记Northern印迹法更为灵敏。通过使用该策略以及用洋地黄毒苷(DIG)标记或生物素标记的寡核苷酸探针进行化学发光检测,低至0.01 - 0.25 fmol [对于DIG - CDP Star(2 - 氯 - 5 - (4 - 甲氧基螺{1,2 - 二氧杂环丁烷 - 3,2' - (5' - 氯)三环[3.3.1.13,7]癸烷}-4 - 基)苯基磷酸二钠)系统]、0.005 - 0.1 fmol(对于生物素 - CDP Star系统)或0.05 - 0.5 fmol(对于生物素 - 鲁米诺系统)的miRNA均可被检测到,并且可以区分miRNA序列之间的单碱基差异。此外,LHSPD在miRNA的定量分析中表现出色,整个过程大约可在9小时内完成。LHSPD策略为快速、准确和灵敏地检测及定量分析动植物中的miRNA提供了一种有效的解决方案。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a0d/5037736/2df3109d6d69/ijms-17-01457-g001.jpg

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