SETD6对转录因子E2F1的甲基化通过正反馈机制调节SETD6的表达。

The Journal of Biological Chemistry Pub Date : 2023-10-01 Epub Date: 2023-09-09 DOI:10.1016/j.jbc.2023.105236
Margarita Kublanovsky, Gizem T Ulu, Sara Weirich, Nurit Levy, Michal Feldman, Albert Jeltsch, Dan Levy
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引用次数: 0

摘要

含有蛋白质赖氨酸甲基转移酶SET结构域的蛋白质6(SETD6)已被证明影响不同的细胞活性,并严重参与不同发育和病理过程的调节。然而,调节SETD6 mRNA表达的上游信号尚不清楚。生物信息学分析显示SETD6启动子具有转录因子E2F1的结合位点。使用各种实验方法,我们发现E2F1与SETD6启动子结合并调节SETD6 mRNA的表达。我们进一步观察到这种现象是SETD6依赖性的,这表明SETD6和E2F1是有联系的。接下来,我们在体外和细胞中证明SETD6在K117特异性地单甲基化E2F1。最后,我们发现K117的E2F1甲基化正向调节SETD6 mRNA的表达水平。SETD6的缺失或不能被SETD6甲基化的E2F1K117R突变体的过表达逆转了这种作用。总之,我们的数据为正反馈机制提供了证据,该机制以SETD6甲基化依赖的方式调节E2F1对SETD6的表达,并强调了蛋白质赖氨酸甲基转移酶和赖氨酸甲酯化信号在基因转录调节中的重要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Methylation of the transcription factor E2F1 by SETD6 regulates SETD6 expression via a positive feedback mechanism.

Methylation of the transcription factor E2F1 by SETD6 regulates SETD6 expression via a positive feedback mechanism.

Methylation of the transcription factor E2F1 by SETD6 regulates SETD6 expression via a positive feedback mechanism.

Methylation of the transcription factor E2F1 by SETD6 regulates SETD6 expression via a positive feedback mechanism.

The protein lysine methyltransferase SET domain-containing protein 6 (SETD6) has been shown to influence different cellular activities and to be critically involved in the regulation of diverse developmental and pathological processes. However, the upstream signals that regulate the mRNA expression of SETD6 are not known. Bioinformatic analysis revealed that the SETD6 promoter has a binding site for the transcription factor E2F1. Using various experimental approaches, we show that E2F1 binds to the SETD6 promoter and regulates SETD6 mRNA expression. Our further observation that this phenomenon is SETD6 dependent suggested that SETD6 and E2F1 are linked. We next demonstrate that SETD6 monomethylates E2F1 specifically at K117 in vitro and in cells. Finally, we show that E2F1 methylation at K117 positively regulates the expression level of SETD6 mRNA. Depletion of SETD6 or overexpression of E2F1 K117R mutant, which cannot be methylated by SETD6, reverses the effect. Taken together, our data provide evidence for a positive feedback mechanism, which regulates the expression of SETD6 by E2F1 in a SETD6 methylation-dependent manner, and highlight the importance of protein lysine methyltransferases and lysine methylation signaling in the regulation of gene transcription.

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