The mouse T lymphocyte a!ioantigens Tpre (1), Tthy (2), Tind (3), and Tsu (4) have been characterized by the development of specific monoclonal antibodies. These four aiioantigens are encoded by genes on chromosome 12 near the immunoglobulin heavy chain (lgh) genes and are expressed on T lymphocytes at discrete stages of development (4, 1). The developmental pathway suggested by the sequential expression of these antigens does not directly parallel that marked by the Lyt-1, Lyt-2, and Lyt-3 alloantigens (5, 6). Their genetic location near the Igh complex and other data have raised the possibility that these four alloantigens may form part of the T cell receptor for antigen (1-8).The expression of these four alloantigens in 26 lgh recombinant (IghR) and recombinant inbred (RI) mouse strains and 15 inbred strains is detailed in this paper. This study was undertaken to identify recombination between the genes coding for these antigens, to order these genes and more precisely map them on chromosome 12. In doing so, these experiments also address the question of whether these four alloantigens are products of distinct genes or instead are alternative products of a single gene. Indeed, we have found several monoclonal antibodies that bind two or more of the four antigens in various combinations (F. Owen, unpublished observations). This could indicate a structural relatedness deriving by gene duplication from a common evolutionary origin, or it could reflect a common structure modified in different cell types to create the four alloantigens. These alternatives can be distinguished by genetic test; recombination resulting in expression of only a partial set of the antigens most probably indicates individual genes for the separated antigens.The results indicate that the expression of the four antigens is controlled by two to four genes in a tightly linked cluster distal to Igh-1 and proximal to Pre-1, the locus for serum prealbumin. The map position is consistent with data obtained for Tsu (7) using alloantiserum and in vivo functional assays (8).
MethodsStrains of Mice. NX8 recombinant inbred (RI) strains and various Igh recombinant (IghR) strains (8, 9; Riblet, unpublished results) listed in Table II were bred and