prmt1依赖性精氨酸甲基化在细胞对基因毒性应激反应中的双重作用。

Molecular & cellular oncology Pub Date : 2020-04-07 eCollection Date: 2020-01-01 DOI:10.1080/23723556.2020.1743808
Roberto Giambruno, Tiziana Bonaldi
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引用次数: 2

摘要

我们最近表明,精氨酸蛋白n -甲基转移酶1 (PRMT1)的精氨酸甲基化控制卵巢癌细胞对顺铂的反应。除了染色质蛋白甲基化增加有利于衰老相关分泌表型(SASP)激活外,我们的研究还揭示了rna结合蛋白的整体低甲基化,我们推测这可能促进了它们的相分离和应激颗粒的形成。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Dual role of PRMT1-dependent arginine methylation in cellular responses to genotoxic stress.

Dual role of PRMT1-dependent arginine methylation in cellular responses to genotoxic stress.

Dual role of PRMT1-dependent arginine methylation in cellular responses to genotoxic stress.

We have recently shown that arginine methylation by protein arginine N-methyltransferase 1 (PRMT1) controls the response to cisplatin in ovarian cancer cells. In addition to increased methylation of chromatin proteins that favors senescence-associated secretory phenotype (SASP) activation, our study unraveled global hypo-methylation of RNA-binding proteins, which - we speculate - may promote their phase separation and stress granules formation.

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