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首页> 外文期刊>Nucleic Acids Research >The centrosomal kinase NEK2 is a novel splicing factor kinase involved in cell survival
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The centrosomal kinase NEK2 is a novel splicing factor kinase involved in cell survival

机译:中心体激酶NEK2是一种参与细胞存活的新型剪接因子激酶

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NEK2 is a serine/threonine kinase that promotes centrosome splitting and ensures correct chromosome segregation during the G2/M phase of the cell cycle, through phosphorylation of specific substrates. Aberrant expression and activity of NEK2 in cancer cells lead to dysregulation of the centrosome cycle and aneuploidy. Thus, a tight regulation of NEK2 function is needed during cell cycle progression. In this study, we found that NEK2 localizes in the nucleus of cancer cells derived from several tissues. In particular, NEK2 co-localizes in splicing speckles with SRSF1 and SRSF2. Moreover, NEK2 interacts with several splicing factors and phosphorylates some of them, including the oncogenic SRSF1 protein. Overexpression of NEK2 induces phosphorylation of endogenous SR proteins and affects the splicing activity of SRSF1 toward reporter minigenes and endogenous targets, independently of SRPK1. Conversely, knockdown of NEK2, like that of SRSF1, induces expression of pro-apoptotic variants from SRSF1-target genes and sensitizes cells to apoptosis. Our results identify NEK2 as a novel splicing factor kinase and suggest that part of its oncogenic activity may be ascribed to its ability to modulate alternative splicing, a key step in gene expression regulation that is frequently altered in cancer cells.
机译:NEK2是一种丝氨酸/苏氨酸激酶,可通过特定底物的磷酸化来促进中心体分裂,并在细胞周期的G2 / M阶段确保正确的染色体分离。 NEK2在癌细胞中的异常表达和活性导致中心体周期失调和非整倍性。因此,在细胞周期进程中需要严格调节NEK2功能。在这项研究中,我们发现NEK2定位在源自多个组织的癌细胞核中。特别是,NEK2与SRSF1和SRSF2共同位于拼接斑点中。此外,NEK2与几种剪接因子相互作用,并使其中一些磷酸化,包括致癌性SRSF1蛋白。 NEK2的过表达诱导内源性SR蛋白的磷酸化并影响SRSF1对报告基因小基因和内源性靶标的剪接活性,而与SRPK1独立。相反,像SRSF1一样,NEK2的敲低会诱导SRSF1靶基因表达促凋亡变体,并使细胞对凋亡敏感。我们的结果将NEK2鉴定为一种新型剪接因子激酶,并表明其部分致癌活性可能归因于其调节替代剪接的能力,这是在癌细胞中经常改变的基因表达调控的关键步骤。

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