Kappes D J, Browne C P, Tonegawa S
Howard Hughes Medical Institute, Massachusetts Institute of Technology, Cambridge 02139.
Proc Natl Acad Sci U S A. 1991 Mar 15;88(6):2204-8. doi: 10.1073/pnas.88.6.2204.
The gamma delta and alpha beta 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 gamma 4-J gamma 1-C gamma 1 of the murine gamma-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 C gamma 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 gamma-chain gene enhancer is active in both gamma delta and alpha beta T cells, indicating that it is not primarily responsible for lineage-specificity of expression, but it is inactive in non-T-cells.
γδ和αβ T细胞抗原受体(TCR)异二聚体以谱系特异性、相互排斥的方式表达。表达的调控发生在转录水平。通过瞬时转染试验检测了包含小鼠γ链基因可变连接恒定区片段Vγ4-Jγ1-Cγ1的13千碱基(kb)DNA片段中是否存在转录增强元件。将该区域的DNA片段插入到一个测试质粒中,该质粒含有与人生长激素基因融合的异源启动子。发现在Cγ外显子III下游3 kb处的一个1800碱基对(bp)的片段在几种T细胞系中表现出增强活性。在某些细胞系中,最大增强活性可进一步定位到小至400 bp的片段。对这个400 bp片段的核苷酸序列分析揭示了与先前描述的核心增强元件以及其他TCR基因增强子的同源性。TCR γ链基因增强子在γδ和αβ T细胞中均有活性,这表明它不是表达谱系特异性的主要原因,但在非T细胞中无活性。