Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 1986;24(2):103-14.
doi: 10.1007/BF00373117.

Biochemical genetics of TL antigens

Biochemical genetics of TL antigens

J Michaelson et al. Immunogenetics. 1986.

Abstract

TL antigens are class I glycoproteins which are expressed on thymocytes and which are coded by the Tla region of the major histocompatibility complex of the mouse. Biochemical analysis of TL molecules from different strains of mice revealed structural variation determined by the Tla region which is detectable by peptide mapping, isoelectric focusing, sodium dodecyl sulfate-polyacrylamide gel electrophoresis, two-dimensional gels, and by differential reactivity of allelic forms of TL molecules with a panel of anti-TL reagents. The quantity of TL expressed on thymocytes is also influenced by the Tla region; three quantitative phenotypes were identified: high (Tlaa, Tlad, Tlae), intermediate (Tlac, Tlaf), and low (Tlab). (Relative amounts: 1000: 100: 1.) Some thymic leukemias arising in (Tlab, Tlac) mice with genetically determined reduced levels of thymic TL were found to express TL molecules which were structurally indistinguishable from TL isolated from thymocytes but were present in larger amounts. This suggests that TL structural genes are intrinsically capable of full expression in all mice but that the Tla region of mice expressing an intermediate or low quantity of TL is marked by some feature which causes the thymocyte to express less than the full amount of TL possible.

PubMed Disclaimer

References

    1. Transplant Proc. 1983 Dec;15(4):2033-8 - PubMed
    1. Nature. 1970 Aug 15;227(5259):680-5 - PubMed
    1. J Exp Med. 1979 Oct 1;150(4):777-91 - PubMed
    1. Eur J Immunol. 1982 Apr;12(4):257-61 - PubMed
    1. Immunogenetics. 1983;17(3):219-60 - PubMed

Publication types

LinkOut - more resources