Each ancestral or extended HLA haplotype contains a unique combination of a
lleles among which some may be entirely specific for that haplotype (haplos
pecific alleles). In the course of evolution many recombination events occu
rred which disrupted the original haplotypic combination. We analysed the s
ites of historical recombinations in four extended HLA haplotypes (B8-DR3;
B18-DR3; B50-DR7 and B57-DR7) in 60 random Italian individuals selected thr
ough the presence of haplospecific alleles. In general the distribution of
recombinations in each interval was similar for the four extended haplotype
s and no haplospecific recombination "hot spot" could be detected. However
some differences between the four haplotypes can be pointed out: a) only 48
% fragmented B8-DR3 were found in contrast to 83% B18-DR3, 89% B50-DR7 and
88% B57-DR7; b) in the B8-DR3 haplotype recombinations fall preferentially
in the B/TNF interval. In fact among 22 historical recombination events, 50
% were mapped in this region; c) conversely, no recombination event was det
ected in the B/TNF interval among the 19 disrupted B18-DR3 haplotypes thus
evidencing the presence of a putative recombination "cold spot".