Abstract
The γδ and αβ T-cell antigen receptor (TCR) heterodimers are expressed in a lineage-specific, mutually exclusive manner. Regulation of expression occurs at the transcriptional level. A 13-kilobase (kb) stretch of DNA encompassing variable-joining-constant segments V γ4-J γ1-Cγ1 of the murine y-chain gene was examined for the presence of transcriptional enhancing elements by a transient transfection assay. DNA fragments from this region were inserted into a test plasmid containing a heterologous promoter fused to the human growth hormone gene. An 1800-base-pair (bp) fragment located 3 kb 3′ to Cγ exon III was found to display enhancing activity in several T-cell lines. Maximum enhancing activity could be localized further to fragments as small as 400 bp in some cell lines. Nucleotide sequence analysis of this 400-bp segment revealed homologies to previously described core enhancer elements and to other TCR gene enhancers. The TCR γ-chain gene enhancer is active in both γδ and αβ T cells, indicating that it is not primarily responsible for lineagespecificity of expression, but it is inactive in non-T-cells.
| Original language | American English |
|---|---|
| Pages (from-to) | 2204-2208 |
| Number of pages | 5 |
| Journal | Proceedings of the National Academy of Sciences of the United States of America |
| Volume | 88 |
| Issue number | 6 |
| DOIs | |
| State | Published - Mar 1991 |
Keywords
- Animals
- Base Sequence
- Enhancer Elements, Genetic
- Macromolecular Substances
- Mice
- Molecular Sequence Data
- Plasmids
- Receptors, Antigen, T-Cell/genetics
- Repetitive Sequences, Nucleic Acid
- Restriction Mapping
- Sequence Homology, Nucleic Acid
- T-Lymphocytes/immunology
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