An efficient procedure for the recovery of DNA from formalin-fixed paraffin-embedded tissue sections

Author:

Oba Utako12,Kohashi Kenichi3,Sangatsuda Yuhei4,Oda Yoshinao3,Sonoda Koh-Hei5,Ohga Shouichi2,Yoshimoto Koji4,Arai Yasuhito6,Yachida Shinichi78,Shibata Tatsuhiro69,Ito Takashi1,Miura Fumihito1ORCID

Affiliation:

1. Department of Biochemistry, Kyushu University Graduate School of Medical Sciences , 3-1-1 Maidashi, Higashi-Ku , Fukuoka 812-8582, Japan

2. Department of Pediatrics, Kyushu University Graduate School of Medical Sciences , 3-1-1 Maidashi, Higashi-Ku , Fukuoka 812-8582, Japan

3. Department of Anatomic Pathology, Kyushu University Graduate School of Medical Sciences , 3-1-1 Maidashi, Higashi-Ku , Fukuoka 812-8582, Japan

4. Department of Neurosurgery, Kyushu University Graduate School of Medical Sciences , 3-1-1 Maidashi, Higashi-Ku , Fukuoka 812-8582, Japan

5. Department of Ophthalmology, Kyushu University Graduate School of Medical Sciences , 3-1-1 Maidashi, Higashi-Ku , Fukuoka 812-8582, Japan

6. Division of Cancer Genomics, National Cancer Center Research Institute , 5-1-1 Tsukiji , Chuo-ku, Tokyo 104-0045, Japan

7. Department of Cancer Genome Informatics, Graduate School of Medicine, Osaka University , 2-2 Yamadaoka , Suita, Osaka 565-0871, Japan

8. Division of Genomic Medicine, National Cancer Center Research Institute , 5-1-1 Tsukiji , Chuo-ku, Tokyo 104-0045, Japan

9. Laboratory of Molecular Medicine, Human Genome Center, The Institute of Medical Science, The University of Tokyo , 4-6-1, Shirokanedai , Minato-ku, Tokyo 108-0071, Japan

Abstract

Abstract 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.

Funder

Platform Project for Supporting Drug Discovery and Life Science Research

Japan Agency for Medical Research and Development

Publisher

Oxford University Press (OUP)

Subject

General Agricultural and Biological Sciences,General Biochemistry, Genetics and Molecular Biology

Reference32 articles.

1. Use of FFPE-derived DNA in next generation sequencing: DNA extraction methods;McDonough;PLoS ONE,2019

2. Evaluation of commercial DNA and RNA extraction methods for high-throughput sequencing of FFPE samples;Kresse;PLoS ONE,2018

3. Performance comparison of three DNA extraction kits on human whole-exome data from formalin-fixed paraffin-embedded normal and tumor samples;Bonnet;PLoS ONE,2018

4. Clinical whole-genome sequencing from routine formalin-fixed, paraffin-embedded specimens: pilot study for the 100,000 Genomes Project;Robbe;Genet Med,2018

5. Assessment of the quality of DNA from various formalin-fixed paraffin-embedded (FFPE) tissues and the use of this DNA for next-generation sequencing (NGS) with no artifactual mutation;Einaga;PLoS ONE,2017

Cited by 11 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3