TY - JOUR
T1 - An efficient procedure for the recovery of DNA from formalin-fixed paraffin-embedded tissue sections
AU - Oba, Utako
AU - Kouhashi, Kenichi
AU - Sangatsuda, Yuhei
AU - Oda, Yoshinao
AU - Sonoda, Koh Hei
AU - Ohga, Shouichi
AU - Yoshimoto, Koji
AU - Arai, Yasuhito
AU - Yachida, Shinichi
AU - Shibata, Tatsuhiro
AU - Ito, Takashi
AU - Miura, Fumihito
N1 - Publisher Copyright:
© 2022 The Author(s). Published by Oxford University Press.
PY - 2022
Y1 - 2022
N2 - 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.
AB - 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.
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U2 - 10.1093/biomethods/bpac014
DO - 10.1093/biomethods/bpac014
M3 - Article
AN - SCOPUS:85136715125
SN - 2396-8923
VL - 7
JO - Biology Methods and Protocols
JF - Biology Methods and Protocols
IS - 1
M1 - bpac014
ER -