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
. 1995 Jan 31;92(3):674-8.
doi: 10.1073/pnas.92.3.674.

Cloning and expression analysis of the murine lymphotoxin beta gene

Affiliations

Cloning and expression analysis of the murine lymphotoxin beta gene

D K Pokholok et al. Proc Natl Acad Sci U S A. .

Abstract

Tumor necrosis factor alpha (TNF-alpha) and soluble lymphotoxin (LT) (also called LT-alpha or TNF-beta) are cytokines with similar biological activities that are encoded by related and closely linked genes. TNF-alpha, a mediator of the inflammatory response, exists in soluble and transmembrane forms. LT-alpha can be secreted or retained at the cell surface by binding to a 33-kDa transmembrane subunit, LT-beta. The recently cloned human LT-beta gene encodes another TNF family member and is linked to the TNF/LT locus within the major histocompatibility complex locus. The cell surface LT is a heterotrimer consisting of LT-alpha and LT-beta, whose physiological function is not yet clearly defined. We now report the sequence analysis of the genomic region and cDNA of murine LT-beta gene, which is closely associated with the TNF-alpha and LT-alpha genes within the murine major histocompatibility complex locus. Unlike the TNF-alpha, LT-alpha, and human LT-beta genes, which contain four exons, the murine LT-beta contains three exons and encodes a 244-amino acid polypeptide with a 66-amino acid insert that is absent from the human homologue. In situ hybridization demonstrates constitutive expression of LT-beta in lymphoid and hematopoietic tissues. LT-beta transcription is maximal in the thymic medulla and in splenic white pulp. LT-beta mRNA is also detected in the skin and in specific regions of the brain. The LT-beta promoter region contains putative Ets-binding sites, suggesting that the expression of LT-beta may be regulated in part by Ets transcription factors whose pattern of lymphoid expression overlaps that of LT-beta.

PubMed Disclaimer

References

    1. Proc Natl Acad Sci U S A. 1986 Mar;83(6):1670-4 - PubMed
    1. J Immunol. 1991 Aug 15;147(4):1230-7 - PubMed
    1. Nucleic Acids Res. 1986 Oct 10;14(19):7713-25 - PubMed
    1. Proc Natl Acad Sci U S A. 1986 Nov;83(22):8699-702 - PubMed
    1. Nature. 1987 Jan 15-21;325(6101):265-7 - PubMed

Publication types

MeSH terms

Associated data