Y‐STR mixture deconvolution by single‐cell analysis

口腔黏膜测试 基因分型 DNA DNA分析 打字 微卫星 Y型钢 分子生物学 生物 计算生物学 遗传学 化学 基因型 基因 等位基因
作者
Kaitlin Huffman,Erin Hanson,Jack Ballantyne
出处
期刊:Journal of Forensic Sciences [Wiley]
卷期号:68 (1): 275-288 被引量:7
标识
DOI:10.1111/1556-4029.15150
摘要

Abstract Since Y‐STR typing only amplifies male Y chromosomal DNA, it can simplify the interpretation of some DNA mixtures that contain female DNA. However, if there are multiple male contributors, mixed Y‐STR DNA profiles will often be obtained. Y‐STR mixture analysis cases are particularly challenging though as, currently, there are no validated probabilistic genotyping (PG) software solutions commercially available to aid in their interpretation. One approach to fully deconvoluting these challenging mixtures into their individual donors is to conduct single‐cell genotyping by isolating individual cells from a mixture prior to conducting DNA typing. In this work, a physical micromanipulation technique involving a tungsten needle and direct PCR with decreased reaction volume and increased cycle number was applied to equimolar 2‐ and 3‐person buccal cell male DNA mixtures and a mock touch DNA case scenario involving the consecutive firing of a handgun by two males. A consensus DNA profiling approach was then utilized to obtain YFiler™ Plus Y‐STR haplotypes. Buccal cells were used to optimize and test the direct single‐cell subsampling approach, and 2–3 person male buccal cell mixtures were fully deconvoluted into their individual donor Y‐STR haplotypes. Single‐cell (or agglomerated cell clump) subsampling from the gun's trigger recovered single‐source Y‐STR profiles from both individuals who fired the gun, the owner, and the other unrelated male. Only the non‐owner's DNA was found in the cells recovered from the handle. In summary, direct single‐cell subsampling as described represents a potential simple way to analyze and interpret Y‐STR mixtures.

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