Huang X L, Tamaki K, Yamamoto T, Yoshimoto T, Mizutani M, Leong Y K, Tanaka M, Nozawa H, Uchihi R, Katsumata Y
Department of Forensic Medicine, Tokai University School of Medicine, Isehara, 259-1193, Japan.
Leg Med (Tokyo). 1999 Sep;1(1):37-43. doi: 10.1016/s1344-6223(99)80009-1.
Minisatellite variant repeat (MVR) mapping using polymerase chain reaction (PCR) was applied to a practical case of paternity testing to evaluate the paternity probability. In order to obtain single allele mapping by allele-specific MVR-PCR, three flanking polymorphic sites for each of the MS31A and MS32 loci were investigated and all three individuals were typed as heterozygous for at least one flanking polymorphic site at each locus. Allele-specific MVR-PCR was then performed using genomic DNA. It was confirmed that one allele in the child was identical to that from the mother and the other one in the child was identical to that from the alleged father. Mapped allele codes were also compared with those in the database by dot-matrix analysis, and no identical allele was found although some motifs were shared with Japanese alleles. The paternity index and the probability of paternity exclusion in the case at these two MVR loci were calculated using the presumed values of the allele frequencies. These studies seem to illustrate the practical value of MVR mapping of MS31A and MS32 loci in paternity testing.
