By the use of restriction fragment length polymorphism analysis 10 Taq
I fragments could be identified for the MhcMamu-DQA1 region. A strong
correlation exists between the occurrence of Mamu-DQA1/Taq I fragment
s and Mamu-DAQ1 allelic sequence variation. Most restriction fragments
correspond with a unique Mamu-DQA1 allele, with one exception being t
he Taq I 4.5 kb fragment that is associated with two Mamu-DQA1 alleles
. The RFLP technique allowed the identification of 15 Mamu-DQB1/Taq I
restriction fragments, whereas sequence analysis has permitted the cha
racterization of at least 20 different Mamu-DQB1 alleles. In this comm
unication two unpublished Mamu-DQB1 sequences are described. For Mamu-
DQB1, on only four occasions was it possible to demonstrate a correlat
ion between a certain fragment and an allelic sequence. These analyses
, performed on material from truly homozygous animals, allowed us to d
efine which combinations of Mamu-DQA1 and - DQB1 molecules form hetero
dimers at the cell surface. In addition, these studies are helpful in
typing non-human primate species that are used in biomedical research.