Yan Yong-Wei, Zhu Ting, Zou Bin, Quan Zhe-Xue
Ministry of Education Key Laboratory for Biodiversity Science and Ecological Engineering, Institute of Biodiversity Science, School of Life Sciences, Fudan University, Shanghai, China.
Bio Protoc. 2018 May 5;8(9):e2828. doi: 10.21769/BioProtoc.2828.
We propose a modified RNA-Seq method for small subunit ribosomal RNA (SSU rRNA)-based microbial community analysis that depends on the direct ligation of a 5' adaptor to RNA before reverse-transcription. The method requires only a low-input quantity of RNA (10-100 ng) and does not require a DNA removal step. Using this method, we could obtain more 16S rRNA sequences of the same regions (variable regions V1-V2) without the interference of DNA in order to analyze OTU (operational taxonomic unit)-based microbial communities and diversity. The generated SSU rRNA sequences are also suitable for the coverage evaluation for bacterial universal primer 8F ( position 8 to 27), which is commonly used for bacterial 16S rRNA gene amplification. The modified RNA-Seq method will be useful to determine potentially active microbial community structures and diversity for various environmental samples, and will also be useful for identifying novel microbial taxa.
我们提出了一种改进的RNA测序方法,用于基于小亚基核糖体RNA(SSU rRNA)的微生物群落分析,该方法依赖于在逆转录之前将5'接头直接连接到RNA上。该方法仅需要少量的RNA输入(10-100 ng),并且不需要DNA去除步骤。使用这种方法,我们可以在没有DNA干扰的情况下获得更多相同区域(可变区V1-V2)的16S rRNA序列,以便分析基于操作分类单元(OTU)的微生物群落和多样性。生成的SSU rRNA序列也适用于对常用于细菌16S rRNA基因扩增的细菌通用引物8F(第8至27位)的覆盖范围评估。改进的RNA测序方法将有助于确定各种环境样品中潜在活跃的微生物群落结构和多样性,也将有助于鉴定新的微生物分类群。