Gene clusters in the blood group system B of cattle

In this report the linear order of genetic determinants for the blood group system B of cattle has been worked out in more detail. Two groups of antigenic specificities — inclusion groups — showing serologic relationship are described. Recombination frequencies do suggest that these specificities are controlled by two clusters of genetic determinants. The structures of these inclusion groups and clusters are compared with those of antigenic complexes in other species, especially in mice. Several similarities and also dissimilarities between the blood group system B of cattle and the H-2 system in mice are described.     

Gene clusters in the blood group system B of cattle.

In this report the linear order of genetic determinants for the blood group system B of cattle has been worked out in more detail. Two groups of antigenic specificities--inclusion groups--showing serologic relationship are described. Recombination frequencies do suggest that these specificities are controlled by two clusters of genetic determinants. The structures of these inclusion groups and clusters are compared with those of antigenic complexes in other species, especially in mice. Several similarities and also dissimilarities between the blood group system B of cattle and the H-2 system in mice are described.     

The genetic map of the B system of cattle blood groups as observed in French breeds

40 cases of irregular inheritance of phenogroups in the B system of cattle blood groups, that were presumed to have arisen from single crossing-over, have been used to establish a partial genetic map of this system. In addition, the relative positions in the map of several antigenic factors were inferred from relationships observed between particular phenogroups occurring in French breeds. The tentative map thus obtained shows an overall similarity to that established by Ruiterkamp et al. (1977) in Dutch Friesian cattle. This result, in addition to other arguments, supports the hypothesis that the genetic structure of the B system of cattle blood groups is basically the same in all taurine breeds. Evidence is given, for the first time, for the occurrence in the B system of genetic events other than single crossing-over (double crossing-over or gene conversion, and possibly deletion). The rate of recombination between the genetic determinants of the terminal factors of the system, Q and I', was calculated in the progeny of some Normande bulls heterozygous for these two determinants (447 gametes); a value of 1.34 centimorgan was obtained. However complementary data indicate that 0.7 centimorgan would be a better estimate.     

The genetic map of the B system of cattle blood groups as observed in French breeds

40 cases of irregular inheritance of phenogroups in the B system of cattle blood groups, that were presumed to have arisen from single crossing-over, have been used to establish a partial genetic map of this system. In addition, the relative positions in the map of several antigenic factors were inferred from relationships observed between particular phenogroups occurring in French breeds.
The tentative map thus obtained shows an overall similarity to that established by Ruiterkamp et al. (1977) in Dutch Friesian cattle. This result, in addition to other arguments, supports the hypothesis that the genetic structure of the B system of cattle blood groups is basically the same in all taurine breeds.
Evidence is given, for the first time, for the occurrence in the B system of genetic events other than single crossing-over (double crossing-over or gene conversion, and possibly deletion).
The rate of recombination between the genetic determinants of the terminal factors of the system, Q and I', was calculated in the progeny of some Normande bulls heterozygous for these two determinants (447 gametes); a value of 1.34 centimor-gan¹ was obtained. However complementary data indicate that 0.7 centimorgan would be a better estimate.     

Prezygotic selection in the B blood group locus in cattle

Genotypes of B-locus of blood groups in cattle have been studied for peculiarities of their formation. Studies of different populations have shown that some parental alleles have an advantage during formation of the descendant genotype for the above mentioned locus.     

The C system of cattle blood groups. 1. Additional factors in the system

Four additional cattle blood group antigenic factors, provisionally termed Fl, F6, F10 and F15, were shown to belong to the C system. Factor Fl appears to be a linear subtype of C(initially designated F2, or P1B1). It is suggested that future international nomenclature should adopt C, and C₂ in place of Fl and C . No phenogroup was found to include C together with C₂ or C₁, but a few phenogroups lack the three factors. Thus C₁, C₂ and Cdo not form a closed system within the C system as concluded by Duniec et al. (1973). The effectiveness of the additional factors to uncover the genetic variability of the C system, and to translate phenotypes into genotypes is exemplified in the Charolais breed.     

The C system of cattle blood groups. 1. Additional factors in the system

Four additional cattle blood group antigenic factors, provisionally termed F1, F6, F10 and F15, were shown to belong to the C system. Factor F1 appears to be a linear subtype of C" (initially designated F2, or P1B1). It is suggested that future international nomenclature should adopt C"1 and C"2 in place of F1 and C". No phenogroup was found to include C" together with C2 or C1, but a few phenogroups lack the three factors. Thus C1, C2 and C" do not form a closed system within the C system as concluded by Duniec et al. (1973). The effectiveness of the additional factors to uncover the genetic variability of the C system, and to translate phenotypes into genotypes is exemplified in the Charolais breed.     

The C system of cattle blood groups. 2. Partial genetic map of the system

20 cases of irregular inheritance of phenogroups in the C system of cattle blood groups were used to deduce a partial genetic map of this system, taking into consideration the 11 internationally recognized antigenic factors and the 4 additional factors recently described by Grosclaude et al. (1980). This partial map bears resemblance to that established by Bouw et al. (1974) in Dutch cattle.
The operational length of the DNA sequence coding for the C system was estimated to be 0.3 centimorgan, a value which is approximately half of that obtained for the B system by Grosclaude et al. (1979). It is concluded that the phenogroups of the C system, like those of the B system, are controlled by a cluster of loci.     

The C system of cattle blood groups. 2. Partial genetic map of the system

20 cases of irregular inheritance of phenogroups in the C system of cattle blood groups were used to deduce a partial genetic map of this system, taking into consideration the 11 internationally recognized antigenic factors and the 4 additional factors recently described by Grosclaude et al. (1980). This partial map bears resemblance to that established by Bouw et al. (1974) in Dutch cattle. The operational length of the DNA sequence coding for the C system was estimated to be 0.3 centimorgan, a value which is approximately half of that obtained for the B system by Grosclaude et al. (1979). It is concluded that the phenogroups of the C system. like those of the B system, are controlled by a cluster of loci.     

Caprine blood groups. 1. The B system

Twelve of 24 monospecific caprine reagents produced by absorption of alloimmune antisera identified a complex blood group system of goats which was designated B, based on the results of a small comparison test with ovine reagents. The frequencies of the 12 B factors differed significantly among the Australian Angora, Texan Angora, Cashmere, and Dairy goat breeds. Three of the antigens detected by the reagents were shown to be related as linear subtypes, designated Ba₁, Ba₂, and Ba₃, and inherited as alleles. The segregations of B factors in 80 sire groups involving 1086 offspring demonstrated that groups of B factors (phenogroups) segregated as products of allelic genes. This work was supported by a grant from the Australian Stud Book, Alison Road, Randwick, New South Wales 2031, Australia.     

The relationship between the S system of blood groups and potassium levels in red blood cells of cattle

Red cell potassium concentrations were determined in 5 breeds of cattle. Most cattle had red cells with less than 50 mmol K/litre and although a few Hereford and Friesian cows had levels approaching 70 mmol K/litre, it was only in the Jersey breed that values above this were found. Attempts were made to correlate potassium levels with serological specificity using cattle S system and sheep M system blood typing reagents. Red cells negative for cattle factors S, H', and S were never positive for sheep L; cells positive for H' were usually positive for M, and those positive for S were always positive for L. No obvious relationship was found between potassium levels and serological type, although some consistent trends were noted in Friesians and Herefords. Limited family data indicated that a major difference in potassium levels of red cells in cattle may be controlled by two codomi-nant alleles.