Abstract
Orthologous gene-specific PCR primers have been designed to amplify the putative transmembrane domain (TM) 4 of the Nramp1 gene in mammals. Sequencing of the dog PCR fragment showed to be Nramp1 gene and it was used as a probe for Southern blot analysis, confirming the specific amplification of this gene also in other species. In order to analyse the relationship between Nramp and Leishmaniosis in dogs, a PCR-RFLP protocol has been optimised to look for TM4 polymorphism. Results showed a conserved Gly169residue in all animals tested and only two intronic polymorphisms.
Original language | English |
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Pages (from-to) | 126-129 |
Journal | Archives Animal Breeding |
Volume | 42 |
Publication status | Published - 1 Dec 1999 |