Iwamoto Sadahiko, Kumada Maki, Kamesaki Toyomi, Okuda Hiroshi, Kajii Eiji, Inagaki Takeshi, Saikawa Daisuke, Takeuchi Kouichi, Ohkawara Sigeo, Takahashi Riichi, Ueda Shoji, Inoue Seiichiro, Tahara Kazunori, Hakamata Yoji, Kobayashi Eiji
Department of Legal Medicine and Human Genetics, Jichi Medical School, Tochigi, Japan.
J Biol Chem. 2002 Nov 29;277(48):46463-9. doi: 10.1074/jbc.M206439200. Epub 2002 Sep 16.
We cloned a rat ABO homologue and established human A- and B-transferase transgenic rats. A DNA fragment corresponding to exon 7 of the human ABO gene was amplified from Wistar rat genomic DNA and sequenced. Using the amplified fragments as a probe for Southern blotting, multiple hybridized bands appeared on both EcoRI- and BamHI-digested genomes of seven rat strains, which showed variations in the band numbers among the strains. Four cDNAs were cloned from a Wistar rat, three of which showed A-transferase activity and one of which showed B-transferase activity. These activities were dependent on the equivalent residues at 266 and 268 of human ABO transferase. Wild Wistar rats expressed A-antigen in salivary gland, intestine, and urinary bladder tissue, but B-antigen was not stained in any organs studied, whereas a transcript from the ABO homologue with B-transferase activity was ubiquitous. Human A-transferase and B-transferase were transferred into Wistar rats. A-transgenic rats expressed A-antigen in ectopic tissue of the brain plexus, type II lung epithelium, pancreas, and epidermis. B-antigen in the B-transgenic rat was expressed in the same organs as A-transgenic rats. These results may shed light on the function and evolution of the ABO gene in primates.