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α-N-methylation of CENP-B regulates its binding to the centromeric DNA

机译:CENP-B的α-N-甲基化调节其与焦化DNA的结合

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The eukaryotic centromere is an essential chromatin region required for accurate segregation of sister chromatids during cell division. Centromere protein B (CENP-B) is a highly conserved protein which can bind to the 17-bp CENP-B box on the centromeric DNA. In this study, we found that CENP-B could be α-N-methylated in human cells. We also showed that the level of the α-N-methylation was stimulated in cells in response to a variety of extracellular stimuli, including increased cell density, heat shock, and arsenite treatment, though the methylation level was not altered upon metaphase arrest. We identified NRMT as a major enzyme required for the CENP-B methylation. Additionally, we found that chromatin-bound CENP-B was primarily trimethylated and α-N-trimethylation could enhance CENP-B's binding to CENP-B box in cells. Our study also expands the function of protein α-N-methylation that has been known for decades and whose function remains largely unexplored.
机译:真核中心是一种必需的染色质区域,需要在细胞分裂期间精确地隔离姐妹染色体。 Centromere蛋白B(CENP-B)是一种高度保守的蛋白质,其可以与焦化DNA上的17-BP CENP-B盒结合。在这项研究中,我们发现CENP-B可以是人细胞中的α-N-甲基化。我们还表明,响应于各种细胞外刺激,包括增加细胞密度,热休克和砷酸盐处理,虽然甲基化水平未在中期骤离时不改变,但在细胞中刺激α-N-甲基化水平。我们将NRMT鉴定为CENP-B甲基化所需的主要酶。另外,我们发现染色质CENP-B主要是三甲基化,α-N-三甲基化可以增强CENP-B在细胞中与CENP-B盒的结合。我们的研究还扩大了几十年所知的蛋白质α-N-甲基化的功能,其功能仍然在很大程度上是未探索的。

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