The expressed immunoglobulin heavy chain genes of five γ2b-γ2a hybrid chain-producing variants of the mouse myeloma MPC-11 (γ2b, κ) have been characterized by genomic Southern blot analysis. Results show that a hybrid γ2b-γ2a gene was formed in each variant by recombination between the expressed γ2b gene of MPC-11 and a γ2a gene. The recombination sites are within regions of marked homology between γ2b and γ2a genes: at least three and probably four variants show γ2b-γ2a recombination within the heavy chain constant region 2 (C(H)2) domain, while the fifth has its recombination site between the penultimate nucleotide of C(H)1 and the eighth nucleotide of the hinge. An unexpected finding is that the hybrid heavy chain-producing variants fall into two subgroups based on their use of different γ2a gene forms in hybrid gene formation. This result leads to the speculation that either a tandem γ2a gene duplication was present in MPC-11 prior to variant generation or mitotic recombination between chromosomes occurred in the generation of one variant subgroup. The similarity of hybrid gene formation in MPC-11 variants to that apparently responsible for concerted evolution within multigene families and hybrid protein expression in various individuals is noted, and the possible relationship between hybrid gene formation and the heavy chain class switch is discussed.
|Original language||English (US)|
|Number of pages||5|
|Journal||Proceedings of the National Academy of Sciences of the United States of America|
|Issue number||22 I|
|Publication status||Published - Jan 1 1983|
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