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人类细胞因子白细胞介素-4转录的T细胞特异性负调控。

T cell-specific negative regulation of transcription of the human cytokine IL-4.

作者信息

Li-Weber M, Eder A, Krafft-Czepa H, Krammer P H

机构信息

Institute for Immunology and Genetics, German Cancer Research Center, Heidelberg.

出版信息

J Immunol. 1992 Mar 15;148(6):1913-8.

PMID:1541828
Abstract

IL-4 secreted by activated T cells is a pleiotropic cytokine affecting growth and differentiation of diverse cell types such as T cells, B cells, and mast cells. We investigated the upstream regulatory elements of the human IL-4 promoter. A novel T cell-specific negative regulatory element (NRE) composed of two protein-binding sites were mapped in the 5' flanking region of the IL-4 gene: -311CTCCCTTCT-303 (NRE-I) and -288CTTTTTGCTT-TGC-300 (NRE-II). A T cell-specific protein Neg-1 and a ubiquitous protein Neg-2 binding to NRE-I and NRE-II, respectively, were identified. Furthermore, a positive regulatory element was found 45 bp downstream of the NRE. The enhancer activity of the PRE was completely suppressed when the NRE was present. These data suggest that IL-4 promoter activity is normally down-regulated by an NRE via repression of the enhancer positive regulatory element. These data may have implications for the stringent control of IL-4 expression in T cells.

摘要

活化T细胞分泌的白细胞介素-4(IL-4)是一种多效性细胞因子,可影响多种细胞类型(如T细胞、B细胞和肥大细胞)的生长和分化。我们研究了人类IL-4启动子的上游调控元件。在IL-4基因的5'侧翼区域定位了一个由两个蛋白质结合位点组成的新型T细胞特异性负调控元件(NRE):-311CTCCCTTCT-303(NRE-I)和-288CTTTTTGCTT-TGC-300(NRE-II)。分别鉴定出与NRE-I和NRE-II结合的T细胞特异性蛋白Neg-1和一种普遍存在的蛋白Neg-2。此外,在NRE下游45 bp处发现了一个正调控元件。当存在NRE时,PRE的增强子活性被完全抑制。这些数据表明,IL-4启动子活性通常通过NRE对增强子正调控元件的抑制而下调。这些数据可能对T细胞中IL-4表达的严格控制具有重要意义。

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