Answers are grounded in this paper and cite their sources.
The number of antigenic components detectable in system s such as H-2 in mice depends in part upon technical developments. It is also limited by the number of genetically different individuals available for study and a formula for deducing the number of antigenic components detectable for N unrelated systems is given in the text. If parental types and descendants derived from them by crossing over are included the possibilities are decreased. A new antigenic factor(s) has been brought to light by technical improvements and two more have been revealed by crossing over. Three cross-over combinations H-2g, H-2h and H-2i are now available as homozygotes. A preliminary map gives the order DCVK for genes within the H-2 system. The relative positions of E and K are not yet known but their genes are closely linked. The frequency of recombination between D and K was 1⋅03% for both sexes and 1⋅4% for females. Values obtained by other workers are given in the text. It is concluded that crossing over must make a material contribution to the polymorphism of the H-2 system. No convincing example of mutation within the system has been published as yet. One new cross-over system H-2i appears to have certain selective disadvantages whilst statistical evidence strongly indicates that H-2b, H-2d and H-2k are favoured by selection under laboratory conditions.
No takes yet. Share an insight, caveat, or question.
Gorer et al. (1959) studied this question.
Synapse has enriched 10 related papers. Consider them for comparative context: