Discrimination of haplotype in mitochondrial DNA mixtures using LNA-mediated PCR clamping

• Published in: Forensic science international : genetics Vol. 41; pp. 58 - 63
• Main Authors: Asari, Masaru, Isozaki, Shotaro, Hoshina, Chisato, Okuda, Katsuhiro, Tanaka, Hiroki, Horioka, Kie, Shiono, Hiroshi, Shimizu, Keiko
• Format: Journal Article
• Language: English
• Published: Netherlands Elsevier B.V 01-07-2019
• Subjects: Forensic science; Haplotype; Locked nucleic acid; Mitochondrial DNA; Mixed sample; PCR clamping; Mixed sample; Mitochondrial DNA; PCR clamping; Forensic science; Locked nucleic acid; Haplotype
• ISSN: 1872-4973; 1878-0326
• DOI: 10.1016/j.fsigen.2019.03.018

•We developed a discrimination method of mtDNA mixtures by PCR clamping using LNA.•The specificity of LNA-containing probes was evaluated by predicting Tm values.•Seven designed probes inhibited the amplification of exactly matched templates.•Our method distinguished each HV1 haplotype at the lower ratios from two-person mixture.•The haplotype existing at 10% were detected from three-person mixtures by adding two selected probes.
Locked nucleic acid (LNA) has been widely used for various genetic analyses, and has many benefits, in terms of the specificity or sensitivity of amplification, because LNA-containing primers/probes form more stable duplexes with template DNA than probes lacking LNA. Here, we developed a new method for discriminating HV1 haplotypes from mitochondrial DNA (mtDNA) mixtures by applying PCR clamping using LNA. PCR clamping is based on the selective inhibition of amplification using LNA-containing probes, which can discriminate single-nucleotide differences. Before designing probes, we selected 171 sequences with single-nucleotide variations from the HV1 region, and evaluated the specificity of LNA-containing probes for them by predicting Tm values. The differences of Tm between mismatched and exactly matched probe–template duplexes depended markedly on the type of LNA nucleotides for discriminating single-nucleotide differences, and the cytosine LNA nucleotide at the site of variations in the probes was most effective to discriminate these differences. For mixture analysis, each probe targeted one or two variations (16209C, 16217C, 16257A/16261T, 16297C/16298C, 16304C, 16362C, or 16362T) that are particularly common in the Japanese population, and seven designed probes completely inhibited the amplification of exactly matched templates. We prepared mixed samples by mixing DNA from two individuals at a ratio of 1:9, 1:4, 1:1, 4:1, or 9:1, and then performed Sanger sequencing analysis after PCR clamping with each probe. Our method distinguished each haplotype at lower ratios from two-person mixtures, and enabled sensitive detection at 12 pg of total DNA including 600 copies of mtDNA. Moreover, we analyzed three-person mixtures with representative sequences, and detected the minor haplotype of one individual present at a rate of 10% by adding two selected probes. The ability to discriminate haplotypes in mixed samples by using LNA-mediated PCR clamping indicates the potential value of mtDNA analysis in criminal investigations.