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白细胞介素-2基因5'侧翼区域中组蛋白H3乙酰化的T细胞特异性增强。

T-cell specific enhancement of histone H3 acetylation in 5' flanking region of the IL-2 gene.

作者信息

Wang Lili, Kametani Yoshie, Katano Ikumi, Habu Sonoko

机构信息

Department of Immunology, Tokai University School of Medicine, Bohseidai, Isehara, Kanagawa 259-1193, Japan.

出版信息

Biochem Biophys Res Commun. 2005 Jun 3;331(2):589-94. doi: 10.1016/j.bbrc.2005.03.216.

Abstract

The IL-2 gene expression is highly T-cell specific in an activation-dependent manner. However, little is known about how T-cell specific expression is regulated, although related transcription factors have been identified. To address this issue, we examined the chromatin structure change of the IL-2 gene by analyzing histone acetylation status in the upstream of IL-2 gene transcription initiation site. Interestingly, the histone acetylation level was found to be higher in various sites on the widespread upstream region in resting T-cells than resting B-cells. After T-cell stimulation with PMA and ionomycin, the same regions were further acetylated on histone H3. Particularly, the distal enhancer region showed prompt enhancement of histone acetylation, followed by the IL-2 mRNA expression. These results suggest that the 5' flanking region including the distal enhancer region of the IL-2 gene is already accessible in T cells with constitutive acetylation of histone H3,which may serve for T-cell specific IL-2 expression.

摘要

IL-2基因表达以激活依赖的方式高度具有T细胞特异性。然而,尽管已经鉴定出相关转录因子,但对于T细胞特异性表达是如何调控的却知之甚少。为了解决这个问题,我们通过分析IL-2基因转录起始位点上游的组蛋白乙酰化状态,研究了IL-2基因的染色质结构变化。有趣的是,发现在静息T细胞中,广泛上游区域的各个位点的组蛋白乙酰化水平高于静息B细胞。用佛波酯(PMA)和离子霉素刺激T细胞后,相同区域的组蛋白H3进一步乙酰化。特别是,远端增强子区域显示组蛋白乙酰化迅速增强,随后是IL-2 mRNA表达。这些结果表明,包括IL-2基因远端增强子区域在内的5'侧翼区域在T细胞中已经可及,且组蛋白H3呈组成型乙酰化,这可能有助于T细胞特异性IL-2表达。

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