Abstract
A series of genes on the 17th chromosome of the mouse, called the major histocompatibility complex, has critical roles in the immune response. The classical transplantation antigens (or H-2 antigens) are encoded by genes located in several loci of this complex - H-2K, H-2D and H-2L (refs 1, 2; Fig. 1). The antigens are cell-surface glycoproteins consisting of a single polypeptide chain of about 350 amino acids, non-covalently associated to a shorter polypeptide chain, β2-microglobulin, which is not encoded by the 17th chromosome. Within a given H-2 haplotype, H-2K, -D or -L antigens differ by discrete antigenic sites, probably due to changes in their amino acid sequences3. As many as 50 alleles have been found for each K and D locus in the laboratory mouse; thus H-2 loci are very polymorphic2. We report here a preliminary study of the structure of H-2 genes, in which the number of H-2-related sequences in the mouse genome has been estimated from the number of DNA fragments able to hybridize specifically with a cDNA carrying an H-2 sequence.
| Original language | English |
|---|---|
| Pages (from-to) | 673-675 |
| Number of pages | 3 |
| Journal | Nature |
| Volume | 291 |
| Issue number | 5817 |
| DOIs | |
| State | Published - 1981 |
| Externally published | Yes |