Ratanavongsiri J, Igarashi S, Mangal S, Kilgannon P, Fu A, Fotedar A
Department of Immunology, University of Alberta, Edmonton, Canada.
J Immunol. 1990 Feb 1;144(3):1111-9.
The cis-acting sequences regulating transcription of the beta-chain of the TCR have been analyzed and multiple elements identified. The minimum 5' upstream sequence displaying promoter activity is a fragment extending 85 bp upstream of the transcriptional start site. Deletion of an additional 43 bp from the 5' end of this fragment abolished promoter activity. The presence of the conserved TCR beta-chain decanucleotide motif, an AP-1 consensus sequence and an inverted repeat in the deleted region, suggests their role as targets for transacting factors regulating transcription of the beta chain gene. Sequences between -343 and -85 increase transcription from the -85 fragment in T cells. The promoter is active in both T cells and fibroblasts. The enhancer was capable of enhancing TCR V beta 2 promoter activity in both T cells and fibroblasts. Sequences further upstream of the V beta 2 promoter down regulate V beta 2 promoter activity in the absence of the enhancer but its repressive influence is overcome in the presence of the TCR beta-chain enhancer.
已对调节TCRβ链转录的顺式作用序列进行了分析,并鉴定出多个元件。显示启动子活性的最小5'上游序列是一个在转录起始位点上游延伸85 bp的片段。从该片段的5'端再缺失43 bp会消除启动子活性。在缺失区域中存在保守的TCRβ链十核苷酸基序、一个AP-1共有序列和一个反向重复序列,表明它们作为调节β链基因转录的反式作用因子的靶标的作用。-343至-85之间的序列可增加T细胞中-85片段的转录。该启动子在T细胞和成纤维细胞中均有活性。该增强子能够增强T细胞和成纤维细胞中TCR Vβ2启动子的活性。在没有增强子的情况下,Vβ2启动子上游更远的序列会下调Vβ2启动子活性,但在存在TCRβ链增强子的情况下,其抑制作用会被克服。