DNA genotyping of unbuffered formalin fixed paraffin embedded tissues

被引:44
作者
Legrand, B
de Mazancourt, P
Durigon, M
Khalifat, V
Crainic, K
机构
[1] Univ Paris 05, Dept Univ Med Legale & Droit Med, F-75270 Paris 06, France
[2] Hop Ray Poincare, Lab Biochim & Genet Mol, F-92380 Garches, France
[3] Hop Ray Poincare, Serv Anat Pathol & Med Legale, F-92380 Garches, France
关键词
DNA fingerprinting; formalin fixed tissues; STR; archival DNA genotyping;
D O I
10.1016/S0379-0738(01)00641-7
中图分类号
DF [法律]; D9 [法律]; R [医药、卫生];
学科分类号
0301 ; 10 ;
摘要
Formal in-induced DNA degradation was studied at different fixation times (3, 7, 16 and 32 days) each on 10 formalin fixed paraffin embedded tissues (FFPET) stored for 15 years at room temperature. The four different extraction protocols used in this study showed that Chelex((R))100 extracts performed the best at 3 and 7 days of formalin fixation (DFF) (with regard to the quantity and the quality of the DNA). However, Qiamp extracts showed better results for long sized alleles, as well for single polymerase chain reaction (PCR) amplifications after 16 and 32 DFF, as for multiplex PCR at shorter fixation times. DNA degradation is expressed by the size of the amplified alleles, only 100 by templates surviving after 32 DFF (AMG locus). Single locus amplifications (CD4 and FES/FPS alleles) performed better than multiplex PCR (ProfilerPlus), with nearly 100% positive results at 7 DFF. In both types of amplifications, the success rate decreased proportionally with the time of formalin fixation and, consequently, with the size of the required DNA template. (C) 2002 Elsevier Science Ireland Ltd. All rights reserved.
引用
收藏
页码:205 / 211
页数:7
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