Key result
Using microsatellite markers and sequence-based nucleotide polymorphisms, the breakpoint intervals of 30 murine recombinants were mapped to a 5-kb-long interval within the G7c gene adjacent to G7a.
The exact localization of crossovers in the G7c hot spot is important for mapping disease susceptibility genes and limits the number of candidate genes.
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Refines murine MHC susceptibility loci boundaries; leaves open translation to human disease gene mapping.
Recombination within the MHC does not occur at random, but crossovers are clustered in hot spots. We previously described a recombinational hotspot within the 50-kb Hsp70.3-G7 interval in the class III region of the mouse MHC. The parental haplotypes of recombinants with crossovers in this region represent the majority of the laboratory haplotypes (a, b, d, dx, k, m, p, px, q, s, and u). Using microsatellite markers and sequence-based nucleotide polymorphisms, the breakpoint intervals of 30 recombinants were mapped to a 5-kb-long interval within the G7c gene adjacent to G7a. Recombination within the G7c hot spot does not appear to be restricted to certain haplotypes. Sequence motifs that had been suggested to be associated with site-restricted meiotic recombination were absent in the vicinity of the G7c hot spot, and hence, these sequence motifs are no prerequisite for meiotic recombination. The G7c hot spot resides in a region to which a number of disease susceptibility loci have been mapped, including susceptibility to cleft palate, experimental autoimmune allergic orchitis, and chemically induced alveolar lung tumors. The exact localization of crossovers in recombinants that have been used in functional studies is important for mapping susceptibility genes and limits the number of candidate genes.
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Snoek et al. (1998) studied MHC recombination (n=30). Microsatellite markers and sequence-based nucleotide polymorphisms mapping was evaluated on Breakpoint intervals mapping. Using microsatellite markers and sequence-based nucleotide polymorphisms, the breakpoint intervals of 30 murine recombinants were mapped to a 5-kb-long interval within the G7c gene adjacent to G7a.
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