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从存档材料中分离病毒和宿主RNA序列并制备用于高通量DNA测序的cDNA文库。

Isolating Viral and Host RNA Sequences from Archival Material and Production of cDNA Libraries for High-Throughput DNA Sequencing.

作者信息

Xiao Yongli, Sheng Zong-Mei, Taubenberger Jeffery K

机构信息

Viral Pathogenesis and Evolution Section, Laboratory of Infectious Diseases, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland.

出版信息

Curr Protoc Microbiol. 2015 May 1;37:1E.8.1-16. doi: 10.1002/9780471729259.mc01e08s37.

Abstract

The vast majority of surgical biopsy and post-mortem tissue samples are formalin-fixed and paraffin-embedded (FFPE), but this process leads to RNA degradation that limits gene expression analysis. As an example, the viral RNA genome of the 1918 pandemic influenza A virus was previously determined in a 9-year effort by overlapping RT-PCR from post-mortem samples. Using the protocols described here, the full genome of the 1918 virus was determined at high coverage in one high-throughput sequencing run of a cDNA library derived from total RNA of a 1918 FFPE sample after duplex-specific nuclease treatments. This basic methodological approach should assist in the analysis of FFPE tissue samples isolated over the past century from a variety of infectious diseases.

摘要

绝大多数手术活检和尸检组织样本都是用福尔马林固定并石蜡包埋(FFPE)的,但这个过程会导致RNA降解,从而限制基因表达分析。例如,1918年甲型流感大流行病毒的病毒RNA基因组此前通过对尸检样本进行重叠逆转录聚合酶链反应(RT-PCR),历经9年努力才得以确定。使用本文所述的方法,在对一个1918年FFPE样本的总RNA进行双链特异性核酸酶处理后构建的cDNA文库进行一次高通量测序运行中,就以高覆盖率确定了1918年病毒的全基因组。这种基本的方法学途径应有助于分析过去一个世纪从各种传染病中分离出的FFPE组织样本。

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