Is a mutator analogous to the Ig hypermutator of the sheep ileal Peyer's patch active on MHC class I genes in the germ line?

Citation
La. Guethlein et Jc. Howard, Is a mutator analogous to the Ig hypermutator of the sheep ileal Peyer's patch active on MHC class I genes in the germ line?, IMMUNOGENET, 51(6), 2000, pp. 462-472
Citations number
32
Categorie Soggetti
Immunology
Journal title
IMMUNOGENETICS
ISSN journal
00937711 → ACNP
Volume
51
Issue
6
Year of publication
2000
Pages
462 - 472
Database
ISI
SICI code
0093-7711(200005)51:6<462:IAMATT>2.0.ZU;2-W
Abstract
Polymorphic sequence variation in the peptide-binding domains of MHC class I molecules appears to have been driven largely by the constructive action of natural selection on the specificity of the peptide-binding groove. Simi lar features are displayed by the variable domains of immunoglobulins gener ated in the sheep ileal Peyer's patch, but in this case there is evidence t hat the action of a targeted hypermutator acting on a selected substrate ra ther than antigen-driven selection is responsible for the pattern of variat ion in the system. Such a hypermutator acting in the germ line would not on ly mimic the action of natural selection but also, by convergent mutation, generate similar patterns of variation in unrelated alleles that could be i nterpreted as evidence for short-tract gene conversion. We analyzed human c lass I MHC alleles in the light of these data, but failed to find evidence of the action of a similar hypermutator. A search for other mutationally dr iven patterns of variation also failed, even in hypervariable residues from parsimonious phylogenies. Single-nucleotide variation at these residues is also frequent in recent allelic variants, but the data are as consistent w ith short-tract gene conversion as with base mutation. We conclude that the patterns of allelic variation in MHC molecules are not driven by mutationa l pressure, but rather by conventional mutational processes, accompanied by short-tract gene conversion and intense natural selection.