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螨类RNA提取方法的改进及其质量检测

Improvement on the extraction method of RNA in mites and its quality test.

作者信息

Zhao YaE, Hu Li, Yang Yuan Jun, Niu Dong Ling, Wang Rui Ling, Li Wen Hao, Ma Si Jia, Cheng Juan

机构信息

Department of Pathogen Biology and Immunology, School of Basic Medical Sciences, Xi'an Jiaotong University, No. 76 Yanta West Road, Xi'an, 710061, China.

出版信息

Parasitol Res. 2016 Feb;115(2):851-8. doi: 10.1007/s00436-015-4815-2. Epub 2015 Nov 7.

Abstract

To solve the long-existing difficult problems in extracting RNA and constructing a complementary DNA (cDNA) library for trace mites, we conducted a further comparative experiment among three RNA extraction methods (TRIzol method, Omega method, and Azanno method) based on our previous attempts at the construction of cDNA library of mites, with Psoroptes cuniculi still used as the experimental subject. By subsequently decreasing the number of mites, the least number of mites needed for RNA extraction of each method were found by criteria of completeness, concentration, and purity of the extracted RNA. Specific primers were designed according to the allergen Pso c1, Pso c2, and Actin gene sequences of Psoroptes to test the reliability of cDNA library. The results showed that Azanno method needed only 10 mites with sensitivity 204 times higher than previously used TRIzol method and 20 times higher than Omega method; clear RNA band was detected by agarose gel electrophoresis; and ultraviolet spectrophotometer determination showed that RNA concentration, 260/280, and 260/230 were in the range of 102 to 166 ng/μl, 1.83 to 1.99, and 1.49 to 1.72, respectively. Finally, specific primers detection showed that the amplified sequences had 98.33, 98.19, and 99.52% identities with those of P. cuniculi or Psoroptes ovis in GenBank, respectively, indicating that the cDNA library constructed using 10 mites was successful and it could meet the requirements for molecular biology research. Therefore, we concluded that Azanno method was more effective than TRIzol method and Omega method in RNA extraction and cDNA library construction of trace mites.

摘要

为解决长期存在的微量螨类RNA提取及互补DNA(cDNA)文库构建难题,基于我们之前构建螨类cDNA文库的尝试,仍以兔痒螨为实验对象,对三种RNA提取方法(TRIzol法、Omega法和Azanno法)进行了进一步比较实验。随后通过减少螨类数量,依据提取RNA的完整性、浓度和纯度标准,找出了每种方法进行RNA提取所需的最少螨类数量。根据兔痒螨的变应原Pso c1、Pso c2和肌动蛋白基因序列设计特异性引物,以检测cDNA文库的可靠性。结果表明,Azanno法仅需10只螨,灵敏度比之前使用的TRIzol法高204倍,比Omega法高20倍;琼脂糖凝胶电泳检测到清晰的RNA条带;紫外分光光度计测定显示,RNA浓度、260/280及260/230分别在102至166 ng/μl、1.83至1.99及1.49至1.72范围内。最后,特异性引物检测表明,扩增序列与GenBank中兔痒螨或绵羊痒螨的序列分别具有98.33%、98.19%和99.52%的同一性,表明使用10只螨构建的cDNA文库成功,可满足分子生物学研究需求。因此,我们得出结论,在微量螨类的RNA提取和cDNA文库构建方面,Azanno法比TRIzol法和Omega法更有效。

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