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上游刺激因子调节主要组织相容性复合体I类基因表达:U2DeltaE4剪接变体消除E盒活性。

Upstream stimulatory factor regulates major histocompatibility complex class I gene expression: the U2DeltaE4 splice variant abrogates E-box activity.

作者信息

Howcroft T K, Murphy C, Weissman J D, Huber S J, Sawadogo M, Singer D S

机构信息

Experimental Immunology Branch, National Cancer Institute, National Institutes of Health, Bethesda, Maryland 20892-1360, USA.

出版信息

Mol Cell Biol. 1999 Jul;19(7):4788-97. doi: 10.1128/MCB.19.7.4788.

DOI:10.1128/MCB.19.7.4788
PMID:10373528
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC84277/
Abstract

The tissue-specific expression of major histocompatibility complex class I genes is determined by a series of upstream regulatory elements, many of which remain ill defined. We now report that a distal E-box element, located between bp -309 and -314 upstream of transcription initiation, acts as a cell type-specific enhancer of class I promoter activity. The class I E box is very active in a neuroblastoma cell line, CHP-126, but is relatively inactive in the HeLa epithelial cell line. The basic helix-loop-helix leucine zipper proteins upstream stimulatory factor 1 (USF1) and USF2 were shown to specifically recognize the class I E box, resulting in the activation of the downstream promoter. Fine mapping of USF1 and USF2 amino-terminal functional domains revealed differences in their abilities to activate the class I E box. Whereas USF1 contained only an extended activation domain, USF2 contained both an activation domain and a negative regulatory region. Surprisingly, the naturally occurring splice variant of USF2 lacking the exon 4 domain, U2DeltaE4, acted as a dominant-negative regulator of USF-mediated activation of the class I promoter. This latter activity is in sharp contrast to the known ability of U2DeltaE4 to activate the adenovirus major late promoter. Class I E-box function is correlated with the relative amount of U2DeltaE4 in a cell, leading to the proposal that U2DeltaE4 modulates class I E-box activity and may represent one mechanism to fine-tune class I expression in various tissues.

摘要

主要组织相容性复合体I类基因的组织特异性表达由一系列上游调控元件决定,其中许多元件仍未明确。我们现在报告,位于转录起始点上游-309至-314碱基对之间的一个远端E盒元件,作为I类启动子活性的细胞类型特异性增强子发挥作用。I类E盒在神经母细胞瘤细胞系CHP-126中非常活跃,但在HeLa上皮细胞系中相对不活跃。已证明碱性螺旋-环-螺旋亮氨酸拉链蛋白上游刺激因子1(USF1)和USF2能特异性识别I类E盒,从而激活下游启动子。对USF1和USF2氨基末端功能域的精细定位揭示了它们激活I类E盒能力的差异。USF1仅包含一个扩展的激活域,而USF2既包含一个激活域又包含一个负调控区域。令人惊讶的是,缺乏外显子4结构域的USF2天然剪接变体U2DeltaE4,作为USF介导的I类启动子激活的显性负调控因子发挥作用。后一种活性与U2DeltaE4激活腺病毒主要晚期启动子的已知能力形成鲜明对比。I类E盒功能与细胞中U2DeltaE4的相对含量相关,这导致有人提出U2DeltaE4调节I类E盒活性,并且可能代表一种在各种组织中微调I类表达的机制。

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