An immunoglobulin mutator that targets G.C base pairs

• Published in: Proceedings of the National Academy of Sciences - PNAS Vol. 93; no. 2; pp. 851 - 855
• Main Authors: Bachl, J, Wabl, M
• Format: Journal Article
• Language: English
• Published: United States National Acad Sciences 23-01-1996
• Subjects: Animals; Antibodies - genetics; Antibody Affinity - genetics; Base Sequence; Cell Line; Cloning, Molecular; Enhancer Elements, Genetic; Genes, Immunoglobulin; Humans; Immunoglobulin kappa-Chains - genetics; Immunoglobulin mu-Chains - genetics; Mice; Molecular Sequence Data; Mutagenesis; Point Mutation; Sequence Analysis, DNA; Transfection
• ISSN: 0027-8424; 1091-6490
• DOI: 10.1073/pnas.93.2.851

Hypermutation can be defined as an enhancement of the spontaneous mutation rate which the organism uses in certain types of differentiated cells where a high mutation rate is advantageous. At the immunoglobulin loci this process increases the mutation rate > 10(5)-fold over the normal, spontaneous rate. Its proximate cause is called the immunoglobulin mutator system. The most important function of this system is to improve antibody affinity in an ongoing response; it is turned on and off during the differentiation of B lymphocytes. We have established an in vitro system to study hypermutation by transfecting a rearranged mu gene into a cell line in which an immunoglobulin mutator has been demonstrated. A construct containing the mu gene and the 3' kappa enhancer has all the cis-acting elements necessary for hypermutation of the endogenous gene segments encoding the variable region. The activity of the mutator does not seem to depend strongly on the position of the transfected gene in the genome. The mutator is not active in transformed cells of a later differentiation stage. It is also not active on a transfected lacZ gene. These results are consistent with the specificity of the mutator system being maintained and make it possible to delineate cis and trans mutator elements in vitro. Surprisingly, the mutator preferentially targets G-C base pairs. Two hypotheses are discussed: (i) the immunoglobulin mutator system in mammals consists of several mutators, of which the mutator described here is only one; or (ii) the primary specificity of the system is biased toward mutation of G-C base pairs, but this specificity is obscured by antigenic selection.