Oba Utako, Kohashi Kenichi, Sangatsuda Yuhei, Oda Yoshinao, Sonoda Koh-Hei, Ohga Shouichi, Yoshimoto Koji, Arai Yasuhito, Yachida Shinichi, Shibata Tatsuhiro, Ito Takashi, Miura Fumihito
Department of Biochemistry, Kyushu University Graduate School of Medical Sciences, 3-1-1 Maidashi, Higashi-Ku, Fukuoka 812-8582, Japan.
Department of Anatomic Pathology, Kyushu University Graduate School of Medical Sciences, 3-1-1 Maidashi, Higashi-Ku, Fukuoka 812-8582, Japan.
Biol Methods Protoc. 2022 Jul 26;7(1):bpac014. doi: 10.1093/biomethods/bpac014. eCollection 2022.
With the advent of new molecular diagnostic techniques, retrieving DNA from the formalin-fixed paraffin-embedded (FFPE) tissues has become an essential yet challenging step for efficient downstream processes. Owing to low quality and quantity of DNA retrieved from the FFPE sections, the process is often impractical and needs significant improvements. Here, we established an efficient method for the purification of DNA from FFPE specimens by optimizing incubation temperature, incubation time, and the concentration of a formalin scavenger tris(hydroxymethyl)aminomethane (Tris) for reverse-crosslinking. The optimized method, named "Highly concentrated Tris-mediated DNA extraction" (HiTE), yielded three times the DNA yield per tissue slice compared with a representative DNA extraction kit. Moreover, the use of HiTE-extracted DNA increased the yield of the sequencing library three times and accordingly yielded a log higher and more reproducible sequencing library compared with that obtained using the commonly used commercial kit. The sequencing library prepared from HiTE-extracted FFPE-DNA had longer inserts and produced reads that evenly covered the reference genome. Successful application of HiTE-extracted FFPE-DNA for whole-genome and targeted gene panel sequencing indicates its practical usability.
随着新的分子诊断技术的出现,从福尔马林固定石蜡包埋(FFPE)组织中提取DNA已成为高效下游流程中必不可少但具有挑战性的一步。由于从FFPE切片中提取的DNA质量和数量较低,该过程通常不切实际,需要重大改进。在此,我们通过优化孵育温度、孵育时间和用于反向交联的福尔马林清除剂三(羟甲基)氨基甲烷(Tris)的浓度,建立了一种从FFPE标本中纯化DNA的有效方法。这种优化后的方法名为“高浓度Tris介导的DNA提取”(HiTE),与代表性的DNA提取试剂盒相比,每个组织切片的DNA产量提高了两倍。此外,使用HiTE提取的DNA使测序文库的产量提高了两倍,因此与使用常用商业试剂盒获得的测序文库相比,产生的测序文库更高且更具重复性,读数更高。由HiTE提取的FFPE-DNA制备的测序文库具有更长的插入片段,并产生均匀覆盖参考基因组的读数。HiTE提取的FFPE-DNA成功应用于全基因组和靶向基因panel测序表明了其实际可用性。