T Cell-specific Expression of the MurineCD3δ Promoter

增强子 生物 发起人 分子生物学 抄写(语言学) 转录因子 响应元素 基因 调节顺序 基因表达 转录调控 YY1年 基因表达调控 遗传学 语言学 哲学
作者
Hongbin Ji,Anita Gupta,Susumu Okamoto,Michael D. Blum,Lujian Tan,Mary B. Goldring,Elizabeth Lacy,Ananda L. Roy,Cox Terhorst
出处
期刊:Journal of Biological Chemistry [Elsevier BV]
卷期号:277 (49): 47898-47906 被引量:25
标识
DOI:10.1074/jbc.m201025200
摘要

T cell-specific expression of human and mouse CD3delta is known to be governed by an enhancer element immediately downstream from the gene. Here we demonstrate by transgenic and in vitro studies that the murine CD3delta (mCD3delta) promoter prefers to be expressed in cells of the T lineage. Deletion analyses of a promoter segment (-401/+48 bp) followed by transient transfections indicate that upstream elements between -149 and -112 bp contribute to full expression of the gene. Furthermore, a core promoter region -37/+29 appears to contribute to a T cell specificity. Using substitution mutant scanning, four positive and one negative regulatory elements were found within the mCD3delta core promoter. The first two positive elements comprise two classical initiator-like sites, which recruit TFII-I, whereas a third contains a functional Ets binding site. Immediately adjacent to the observed transcription start site is a negative element that utilizes the transcription regulator YY1. The last positive regulatory element contains a potentially functional CREB binding site and the minor transcriptional start site. Because NERF-2, Elf-1, and Ets-1 are expressed preferentially in lymphocytes and because, in addition, YY1 represses the promoter activity strongly in non-T cells, we conclude that the combination of these transcription factors contributes to the T cell-specific expression pattern of mouse CD3delta.
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