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Binding of 14-3-3 reader proteins to phosphorylated DNMT1 facilitates aberrant DNA methylation and gene expression

机译:14-3-3阅读器蛋白与磷酸化DNMT1的结合有助于异常DNA甲基化和基因表达

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摘要

Mammalian DNA (cytosine-5) methyltransferase 1 (DNMT1) is essential for maintenance methylation. Phosphorylation of Ser143 (pSer143) stabilizes DNMT1 during DNA replication. Here, we show 14-3-3 is a reader protein of DNMT1pSer143. In mammalian cells 14-3-3 colocalizes and binds DNMT1pSer143 post-DNA replication. The level of DNMT1pSer143 increased with overexpression of 14-3-3 and decreased by its depletion. Binding of 14-3-3 proteins with DNMT1pSer143 resulted in inhibition of DNA methylation activity in vitro. In addition, overexpression of 14-3-3 in NIH3T3 cells led to decrease in DNMT1 specific activity resulting in hypomethylation of the genome that was rescued by transfection of DNMT1. Genes representing cell migration, mobility, proliferation and focal adhesion pathway were hypomethylated and overexpressed. Furthermore, overexpression of 14-3-3 also resulted in enhanced cell invasion. Analysis of TCGA breast cancer patient data showed significant correlation for DNA hypomethylation and reduced patient survival with increased 14-3-3 expressions. Therefore, we suggest that 14-3-3 is a crucial reader of DNMT1pSer143 that regulates DNA methylation and altered gene expression that contributes to cell invasion.
机译:哺乳动物DNA(胞嘧啶5)甲基转移酶1(DNMT1)对于维持甲基化至关重要。 Ser143(pSer143)的磷酸化可在DNA复制过程中稳定DNMT1。在这里,我们显示14-3-3是DNMT1pSer143的阅读器蛋白。在哺乳动物细胞中,14-3-3与DNA复制后的DNMT1pSer143共定位并结合。 DNMT1pSer143的水平随着14-3-3的过表达而增加,而由于其耗竭而降低。 14-3-3蛋白与DNMT1pSer143的结合导致体外DNA甲基化活性的抑制。此外,NIH3T3细胞中14-3-3的过度表达导致DNMT1比活性降低,从而导致基因组的甲基化不足,该甲基化可通过转染DNMT1挽救。代表细胞迁移,迁移,增殖和粘着途径的基因被甲基化并过表达。此外,14-3-3的过表达也导致细胞侵袭增强。 TCGA乳腺癌患者数据的分析显示,DNA低甲基化与14-3-3表达增加之间存在显着相关性,并且降低了患者的生存率。因此,我们建议14-3-3是DNMT1pSer143的重要阅读者,它调节DNA甲基化和改变的基因表达,从而有助于细胞侵袭。

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