Abstract
DNA structural analysis of the Qa region in two BALB/c mouse substrains with different Qa-2 phenotypes reveals that a deletion of DNA has occurred in BALB/cBy (Qa-2-) mice relative to BALB/c (Qa-2+) mice. We propose that this deletion arises from unequal crossing-over and recombination between adjacent BALB/c class I genes and results in the generation of a hybrid class I gene in BALB/cBy mice. Furthermore, we suggest that this is a direct cause of the change in Qa-2 phenotype. Further support for this model was obtained from transfection experiments in which cloned genes from the equivalent part of the Qa region in C57BL/10 mice were introduced into L cells. Four C57BL/10 genes, arranged in two almost identical pairs, encode polypeptides that are precipitated from lysates of transfectants with anti-Qa-2/3 antiserum. Although loss of one pair of these genes in BALB/c mice has no qualitative effect on Qa-2 phenotype, the loss of both pairs of genes via gene fusion leads to the loss of the Qa-2+ phenotype in BALB/cBy mice.
MeSH Terms
Animals
Antigens, Surface/genetics
Chromosome Deletion
Cloning, Molecular
Gene Expression Regulation
Genes
Histocompatibility Antigens Class I
L Cells
Major Histocompatibility Complex
Membrane Proteins/genetics
Mice
Mice, Inbred BALB C/genetics
Plasmids
Transfection
Chemicals
Antigens, Surface
Histocompatibility Antigens Class I
Membrane Proteins
Q surface antigens
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Mellor A L
Antoniou J
Robinson P J
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13 references, click to expand
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