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首页> 外文期刊>Chinese science bulletin >Reversible histone acetylation/deacetylation modification by p300 and HDAC3 is involved in the regulation of IL-18 promoter activity
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Reversible histone acetylation/deacetylation modification by p300 and HDAC3 is involved in the regulation of IL-18 promoter activity

机译:p300和HDAC3可逆的组蛋白乙酰化/去乙酰化修饰参与IL-18启动子活性的调节

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Interleukin-18 (IL-18) is a pleiotropic cytokine Involved in the development of T helper type 1 (Thl) cells, and it plays important roles in regulation of both the innate and acquired immune responses. The aim of this study was to elucidate whether the reversible histone acetylation/ deacetylation modification participates in the regulation of IL-18 transcription expression. The transcription coactivator p300 containing the histone acetyltransferase (HAT) activity, and the histone deacetylase 3 (HDAC3) were used in this study to analyze the effect of this modification in the regulation of mouse IL-18 gene. The results demonstrate that transfection of p300-expression plasmid promotes the endogenous IL-18 mRNA synthesis in J774 cells, and stimulates the activation of IL-18 promoter. It has been found that this stimulating effect of p300 was reversed by HDAC3, indicating the involvement of the reversible histone acetylation/deacetylation modification in IL-18 regulation. Furthermore, the data show that the HAT activity of p300 was essential to its function in activating IL-18 promoter. In addition, p300 was shown to be able to work synergistically with the transcription factor c-Fos on activation of IL-18 promoter and this effect could also be impaired by HDAC3. Results presented in this paper indicate that the reversible histone acetylation/deacetylation modification plays an important role in the transcriptional regulation of IL-18.
机译:白介素-18(IL-18)是一种多效性细胞因子,参与1型T辅助细胞(Th1)的发育,在调节先天和后天免疫应答中均起着重要作用。这项研究的目的是阐明可逆的组蛋白乙酰化/去乙酰化修饰是否参与IL-18转录表达的调节。在本研究中,使用了含有组蛋白乙酰转移酶(HAT)活性的转录共激活因子p300和组蛋白脱乙酰基酶3(HDAC3),来分析这种修饰在调节小鼠IL-18基因中的作用。结果表明,转染p300表达质粒可促进J774细胞内源性IL-18 mRNA的合成,并刺激IL-18启动子的激活。已经发现,HDAC3逆转了p300的这种刺激作用,表明可逆的组蛋白乙酰化/去乙酰化修饰参与IL-18调节。此外,数据表明,p300的HAT活性对其激活IL-18启动子的功能至关重要。另外,显示p300能够与转录因子c-Fos在IL-18启动子的激活上协同作用,并且这种作用也可能被HDAC3削弱。本文提出的结果表明,可逆的组蛋白乙酰化/去乙酰化修饰在IL-18的转录调控中起重要作用。

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