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Demonstration of Protein-Based Human Identification Using the Hair Shaft Proteome
Author(s) -
Glendon J. Parker,
Mark Leppert,
Deon S. Anex,
Jonathan K. Hilmer,
Nori Matsunami,
Lisa Baird,
Jeffery Stevens,
Krishna Parsawar,
Blythe DurbinJohnson,
David M. Rocke,
Chad Nelson,
Daniel J. Fairbanks,
A. S. Wilson,
Robert H. Rice,
Scott R. Woodward,
Brian Bothner,
Bradley R. Hart
Publication year - 2016
Publication title -
plos one
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.99
H-Index - 332
ISSN - 1932-6203
DOI - 10.1371/journal.pone.0160653
Subject(s) - biology , genetics , forensic identification , sanger sequencing , single nucleotide polymorphism , population , allele , allele frequency , shotgun , dna sequencing , gene , genotype , demography , sociology
Human identification from biological material is largely dependent on the ability to characterize genetic polymorphisms in DNA. Unfortunately, DNA can degrade in the environment, sometimes below the level at which it can be amplified by PCR. Protein however is chemically more robust than DNA and can persist for longer periods. Protein also contains genetic variation in the form of single amino acid polymorphisms. These can be used to infer the status of non-synonymous single nucleotide polymorphism alleles. To demonstrate this, we used mass spectrometry-based shotgun proteomics to characterize hair shaft proteins in 66 European-American subjects. A total of 596 single nucleotide polymorphism alleles were correctly imputed in 32 loci from 22 genes of subjects’ DNA and directly validated using Sanger sequencing. Estimates of the probability of resulting individual non-synonymous single nucleotide polymorphism allelic profiles in the European population, using the product rule, resulted in a maximum power of discrimination of 1 in 12,500. Imputed non-synonymous single nucleotide polymorphism profiles from European–American subjects were considerably less frequent in the African population (maximum likelihood ratio = 11,000). The converse was true for hair shafts collected from an additional 10 subjects with African ancestry, where some profiles were more frequent in the African population. Genetically variant peptides were also identified in hair shaft datasets from six archaeological skeletal remains (up to 260 years old). This study demonstrates that quantifiable measures of identity discrimination and biogeographic background can be obtained from detecting genetically variant peptides in hair shaft protein, including hair from bioarchaeological contexts.

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