| Literature DB >> 25391811 |
Nicole Nascimento Da Fré1,2, Rodrigo Rodenbusch1,2, André Zoratto Gastaldo1,2, Erin Hanson3,4,5, Jack Ballantyne3,4,5, Clarice Sampaio Alho6.
Abstract
We evaluated haplotype and allele frequencies, as well as statistical forensic parameters, for 23 Y-chromosome short tandem repeats (STRs) loci of the PowerPlex®Y23 system (DYS19, DYS385a/b, DYS389I/II, DYS390, DYS391, DYS392, DYS393, DYS437, DYS438, DYS439, DYS448, DYS456, DYS458, DYS635, Y-GATA-H4, DYS481, DYS533, DYS549, DYS570, DYS576, DYS643) in a sample of 150 apparently healthy males, resident in South Brazil. A total of 150 different haplotypes were identified. The highest gene diversity (GD) was observed for the single locus marker DYS570 (GD = 0.7888) and for a two-locus system DYS385 (GD = 0.9009). We also examined 150 father-son pairs by the same system, and a total of 13 mutations were identified in the 3450 father-son allelic transfers, with an overall mutation rate across the 23 loci of 3.768 × 10(-3) (95% CI: 3.542 × 10(-3) to 3.944 × 10(-3)). In all cases there was only one locus mutated with gain/loss of repeats in the son (5 one-repeat gains, and 7 one-repeat and 1 two-repeat losses); we observed no instances of mutations involving a non-integral number of repeats.Entities:
Keywords: DNA; Genetic marker; Mutation rate; Paternity; Y-STR
Mesh:
Year: 2014 PMID: 25391811 DOI: 10.1007/s00414-014-1101-2
Source DB: PubMed Journal: Int J Legal Med ISSN: 0937-9827 Impact factor: 2.686