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Comparative Study
. 1988;28(1):13-21.
doi: 10.1007/BF00372524.

Characterization of a new subfamily of class I genes in the H-2 complex of the mouse

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Comparative Study

Characterization of a new subfamily of class I genes in the H-2 complex of the mouse

D S Singer et al. Immunogenetics. 1988.

Abstract

A previously undescribed subfamily of mouse class I MHC genes, consisting of two to three members, has been identified. The structure and organization of one of these, Mb1, has been determined. Mb1 consists of five exons with open reading frames and potentially encodes a class I-like transmembrane protein. In the genome, Mb1 is linked to the H-2 complex, mapping telomeric to Qa. However, this gene has low (ca. 60%) nucleotide identity with other class I sequences and is no more related to mouse class I genes than to class I genes from other species. Mb1 transcripts have not been found in a variety of adult tissues or cell lines, suggesting that, if Mb1 is expressed, its expression is highly regulated. From DNA sequence identity and intron-exon organization, Mb1 appears to be a primordial gene which antedates mouse speciation and which has evolved independently of the rest of the class I gene family. Examination of various species of wild mice demonstrates the presence of a discrete Mb1 subfamily over long evolutionary periods of time.

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References

    1. Science. 1982 Feb 5;215(4533):679-82 - PubMed
    1. Proc Natl Acad Sci U S A. 1980 Oct;77(10):6081-5 - PubMed
    1. Cell. 1977 Nov;12(3):721-32 - PubMed
    1. Proc Natl Acad Sci U S A. 1983 Jan;80(1):242-6 - PubMed
    1. Immunol Today. 1986 Jan;7(1):19-24 - PubMed

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