Evaluating the Efficiency of Primer Extension Capture as a Method to Enrich DNA Extractions

被引:1
|
作者
Winters, Misa [1 ,2 ]
Monroe, Cara [3 ,4 ]
Barta, Jodi Lynn [5 ]
Kemp, Brian M. [3 ,4 ]
机构
[1] Washington State Univ, Dept Anthropol, Pullman, WA 99164 USA
[2] Washington State Univ, Sch Biol Sci, Pullman, WA 99164 USA
[3] Labs Mol Anthropol & Microbiome Res, Norman, OK 73019 USA
[4] Univ Oklahoma, Dept Anthropol, Norman, OK 73019 USA
[5] Madonna Univ, Dept Forens Sci, Livonia, MI 48150 USA
关键词
forensic science; forensic DNA; quantitative PCR (qPCR); primer extension capture (PEC); CODIS; DNA capture; ancient DNA (aDNA); ANCIENT DNA; GENOME SEQUENCE; PCR;
D O I
10.1111/1556-4029.13973
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
In this study, we sought to document the efficiency of primer extension capture (PEC) as a method to enrich DNA eluates of targeted DNA molecules and remove nontarget molecules from pools containing both. Efficiency of the method was estimated by comparing number of "copies in" to "copies out" by quantitative polymerase chain reaction. PEC retention of DNA targets ranging 109-288 base pairs (bps) in length was 15.88-2.14% (i.e., loss of 84.12-97.86% of target molecules). Experimental modifications of the PEC method resulted in no significant improvements. However, the benefit of PEC was revealed in its ability to remove most nontarget DNA molecules (99.99%). We also discovered that many (56.69%) of the target molecules are "lost" prior to their immobilization on the streptavidin-coated beads. These estimates of methodological efficiency are directly comparable to previous ones observed following "fishing" for DNA, an alternative method for DNA enrichment.
引用
收藏
页码:1145 / 1151
页数:7
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