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Germ line variable regions that match hypermutated sequences in genes encoding murine anti-hapten antibodies.

TitleGerm line variable regions that match hypermutated sequences in genes encoding murine anti-hapten antibodies.
Publication TypeJournal Article
Year of Publication1992
AuthorsDavid V, Folk NL, Maizels N
JournalGenetics
Volume132
Issue3
Pagination799-811
Date Published1992 Nov
ISSN0016-6731
KeywordsAnimals, Base Sequence, DNA Probes, Gene Conversion, Gene Rearrangement, B-Lymphocyte, Genes, Immunoglobulin, Genetic Variation, Immunoglobulin Variable Region, Mice, Mice, Inbred BALB C, Mice, Inbred C57BL, Molecular Sequence Data, Mutation, Oxazolone, Sequence Alignment
Abstract

We asked whether there are germ line immunoglobulin variable (V) segments that match sites of hypermutation in V regions encoding murine antibodies. Murine germ line DNA was probed with a panel of short deoxyoligonucleotides identical in sequence to segments of hypermutated V regions from hybridomas generated in the BALB/c response to the hapten 2-phenyloxazolone (Ox). Germ line sequences that match mutations in both heavy and kappa light chain V regions were identified, and clones of some of these germ line V segments were obtained. Comparison of these clones with hypermutated V regions revealed regions of identity ranging in size from 7 to over 50 nucleotides. In an effort to separate the effects of antigen selection from the mutagenic process, we also searched for matches to a panel of silent mutations in VH regions from germinal center B cells. Fourteen silent mutations occur among a collection of 36 hypermutated VH regions from two separate germinal centers of C57BL/6 mice stimulated with the hapten 4-hydroxy-3-nitrophenyl. Matches to nine of these silent mutations can be found among published sequences of C57BL/6 VH regions of the J558 family. Taken together, these data are consistent with the possibility that a template-dependent mutational process, like gene conversion, may contribute to somatic hypermutation.

Alternate JournalGenetics
PubMed ID1468632


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