Abstract
The lck gene, which encodes the lymphoid cell-specific tyrosine protein kinase p56lck, is expressed from two widely separated promoters. The proximal promoter gives rise to a type I lck transcript, and the distal promoter gives rise to a type II transcript. We found that the ratio of the two transcripts changed during T-cell maturation. Type I lck mRNA was twofold more abundant than the type II transcript in early fetal thymocytes. In the adult, the type I and type II lck mRNAs were present in approximately equal amounts in immature thymocytes expressing the heat-stable antigen. In contrast, there was five- to ninefold more type II lck than type I lck mRNA in more mature thymocytes that did not express the heat-stable antigen and in splenic T cells. This change in relative transcript abundance probably reflects activation of the distal promoter and inactivation of the proximal promoter during T-cell maturation in the thymus. It is possible that the two promoters are regulated by different trans-acting factors whose expression is regulated during T-cell maturation.
MeSH Terms
Animals
Antigens, Differentiation, T-Lymphocyte/analysis
CD4 Antigens/analysis
CD8 Antigens
Cell Differentiation
Fetus
Genes
Mice
Mice, Inbred AKR
Protein-Tyrosine Kinases/genetics
RNA, Messenger/genetics
Spleen/enzymology,immunology
T-Lymphocytes/cytology,enzymology,immunology
Thymus Gland/enzymology
Transcription, Genetic
Chemicals
Antigens, Differentiation, T-Lymphocyte
CD4 Antigens
CD8 Antigens
RNA, Messenger
Protein-Tyrosine Kinases
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Reynolds P J
Salk Institute, San Diego, California 92138-9216.
Lesley J
Trotter J
Schulte R
Hyman R
Sefton B M
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