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Coding Joint Diversity in Mature and Immature B‐Cell Lines
Author(s) -
Yuan S. W.,
Agard E. A.,
Larijani M.,
Wu G. E.
Publication year - 2005
Publication title -
scandinavian journal of immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.934
H-Index - 88
eISSN - 1365-3083
pISSN - 0300-9475
DOI - 10.1111/j.1365-3083.2005.01619.x
Subject(s) - recombination signal sequences , v(d)j recombination , biology , gene , recombination , coding region , chromatin , genetics , recombination activating gene , nucleotide diversity , microbiology and biotechnology , haplotype , genotype
Antigen receptor gene rearrangement is regulated by many factors in B and T lymphocytes. The sequences of the gene segments themselves, their associated recombination signal sequences (RSS), expression of the RAG genes and the chromatin accessibility of the particular gene segments to be rearranged all influence the outcome of recombination and thus antigen receptor diversity. In the present study, we have evaluated the effect of variations in RAG activity level on the junctional diversity of coding joint sequences. Using the pre‐B‐like 204‐1‐8 and the mature B DR3 cell lines under different transfection conditions, we were able to investigate recombination activity levels that varied 100‐fold. We evaluated the sequences of the coding joints for junctional diversity resulting from nucleotide addition or deletion. Surprisingly, we found that the sequence of coding joints of these recombinants did not exhibit significant variation despite the large difference in recombination frequency. Our results indicate that the fidelity of the joining phase of V(D)J recombination is not jeopardized by varying RAG activity.