Yadav Rajiv K, Bragalini Claudia, Fraissinet-Tachet Laurence, Marmeisse Roland, Luis Patricia
Ecologie Microbienne, UMR CNRS 5557, USC INRA 1364, Université Lyon 1, Université de Lyon, 43 Boulevard du 11 Novembre 1918, 69622, Villeurbanne Cedex, France.
Department of Life Sciences and Systems Biology, University of Turin, viale Mattioli 25, 10125, Turin, Italy.
Methods Mol Biol. 2016;1399:273-87. doi: 10.1007/978-1-4939-3369-3_16.
Functions expressed by eukaryotic organisms in soil can be specifically studied by analyzing the pool of eukaryotic-specific polyadenylated mRNA directly extracted from environmental samples. In this chapter, we describe two alternative protocols for the extraction of high-quality RNA from soil samples. Total soil RNA or mRNA can be converted to cDNA for direct high-throughput sequencing. Polyadenylated mRNA-derived full-length cDNAs can also be cloned in expression plasmid vectors to constitute soil cDNA libraries, which can be subsequently screened for functional gene categories. Alternatively, the diversity of specific gene families can also be explored following cDNA sequence capture using exploratory oligonucleotide probes.
通过分析直接从环境样品中提取的真核生物特异性多聚腺苷酸化mRNA库,可以专门研究土壤中真核生物表达的功能。在本章中,我们描述了从土壤样品中提取高质量RNA的两种替代方案。土壤总RNA或mRNA可以转化为cDNA用于直接高通量测序。多聚腺苷酸化mRNA衍生的全长cDNA也可以克隆到表达质粒载体中以构建土壤cDNA文库,随后可以对其进行功能基因类别的筛选。或者,在使用探索性寡核苷酸探针进行cDNA序列捕获后,也可以探索特定基因家族的多样性。