B. Stacks et Mm. Witte, SEX DETERMINATION OF DRIED BLOOD STAINS USING THE POLYMERASE CHAIN-REACTION (PCR) WITH HOMOLOGOUS X-Y PRIMERS OF THE ZINC-FINGER PROTEIN GENE, Journal of forensic sciences, 41(2), 1996, pp. 287-290
The ability to ''sex'' unknown dried bloodstains is frequently of evid
entiary value in forensic casework. Chelex-extracted DNA from 115 spec
imens (105 dried blood standards and 10 casework samples) was amplifie
d for specific ZFX and ZFY regions of the X and Y chromosomes and subs
equent restriction enzyme digestion. The polymerase chain reaction (PC
R) yielded a 209 base pair (bp) product containing a polymorphic posit
ion with a Y chromosome portion including an additional Hae III restri
ction site while the X chromosome portion contains only one. The diges
ted PCR product was separated by polyacrylamide gel electrophoresis (P
AGE) and detected by silver staining. Female samples exhibit bands of
172 bp and 37 bp only while male samples (XY) exhibit 2 additional ban
ds appearing as an 88/84 bp doublet. Initially the 105 known bloodstai
ns were typed according to the procedure discussed here and correct ge
nder determination was achieved for all samples therefore establishing
the reliability of this method. The 10 casework samples yielded the e
xpected results as well. This assay demonstrates potential in both pre
sumptive and confirmatory capacities.