ABO genotyping by PCR-RFLP and cloning and sequencing

A refined PCR-RFLP based method was established to genotype ABO blood groups. The main objective of this study was to make the techniques also suitable for working with degraded DNA. Specific primer design was carried out to choose fragments shorter than 200 bp as necessary in forensic and archaeological applications. Four fragments of exon 6 and 7 of the ABO gene were amplified and digested by in total 7 restriction endonucleases. Particular attention was paid to the base changes at nucleotide positions 261(delG), 297, 526, 703, 721, 771, 796 and 1060(delC) in order to distinguish the six common alleles A101, A201, B, O01, O02 and O03. Furthermore, this method also enables determination of seven of the less frequent alleles: A104, A204, Ax02, Ax03, O05, O06 and O07. The method was applied successfully to a series of blood samples with known phenotypes and genotypes as well as DNA extracted from a thirty year old blood stain and an ancient tooth sample. However, working with ancient DNA requires additional cloning and sequencing of the RFLP-typing results due to DNA post mortem damages such as deaminations, which could lead to false typing results.

ABO blood group system · Biology · Blood Stains · DNA · DNA extraction · Gene · Genotype · Genotyping · Polymerase chain reaction · Primer (cosmetics) · Restriction enzyme · Restriction fragment length polymorphism · Typing · Blood groups and transfusion · Chemistry · Erythrocyte Function and Pathophysiology · Forensic and Genetic Research · Genetics · Medicine · Molecular Biology

• Palaeoserology

  Open Access•R E M Hedges•Journal of Archaeological Science•1976

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