We studied genes of the rabbit immune system by techniques of molecular biology and immunology. We used anti-RAG-1 and 2 antibodies in studies of developing rabbit appendix tissues. The surface markers CD43 and IgM distinguished appendix cell populations from 6 to 9-week-old rabbits that contained RAG-1 and RAG-2 proteins. The appearance of CD43 during different stages of B-cell maturation may be related to the function of the appendix as a site of both B-cell development and diversification. In the ali mutant rabbit, a small deletion at the 3' end of the V/H gene cluster led to loss of V/H1 and one V/H pseudogene. Although homozygous mutant ali/ali rabbits lack the V/H1a2 gene, B cells with a2-like surface Ig develop and expand in numbers. We sequenced immunoglobulin heavy chain variable regions (V/H) from expressed mRNA of sorted a2-positive and negative appendix B cell populations from young ali rabbits. The a2 positive cells appear to have rearranged V/H4, the first functional gene in the mutants' V/H cluster. Sequence alterations in FR1 and FR3 can be accounted for by gene-conversion-like changes that utilized candidate donor sequences upstream V/H4. Our studies of the appearance of cells bearing a2-like epitopes in the appendix of mutant rabbits suggested that there was positive selection and expansion based on framework region structures (V/Ha allotypes). We suggested that the preferential expansion and survival of B cells based on FR1 and FR3 expression may involve """"""""superantigen""""""""-like interactions with endogenous and exogenous ligands. One endogenous ligand appears to be CD5. In man and mouse, the 3'-most D/H gene, DQ52, is preferentially rearranged early in B-cell development. To test whether this preference for rearranging a D/H gene segment based on 3' end proximity exists in rabbit, we cloned and sequenced the rabbit DQ52 gene. The coding region sequence is identical to a mouse DQ52 but the 3' recombination signal sequence has an atypical nonamer. The DQ52 gene was utilized very infrequently; one VDJ sequence from 28 day fetal liver had 8 bp that matched the germline DQ52 sequence. In contrast to man and mouse, instead of rearranging DQ52 early in B cell ontogeny, rabbits preferentially express another D/H gene (Df) located in the middle of the D/H region about 32 kb upstream of the JH genes. This may correlate with more frequent initial rearrangement of V/H to D/H in rabbit B cells.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Intramural Research (Z01)
Project #
1Z01AI000226-16
Application #
6160565
Study Section
Special Emphasis Panel (LI)
Project Start
Project End
Budget Start
Budget End
Support Year
16
Fiscal Year
1997
Total Cost
Indirect Cost
City
State
Country
United States
Zip Code
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