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Functional characteristics of histone H3 kinases MSK1 and MSK2 in oncogene-transformed cells

机译:组蛋白H3激酶MSK1和MSK2在致癌基因转化细胞中的功能特征

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摘要

Stimulation of the Ras-MAPK signal transduction pathway by growth factors (EGF) or phorbol esters (TPA) in parental (IOTV2) and oncogene (H-ras)-transformed (Ciras-3) mouse fibroblasts induces rapid phosphorylation of histone H3. Phosphorylation of H3 occurs on SerlO and Ser28 in the NH_2-terminal tail. This phosphorylation event is implicated in the transcriptional regulation of immediate early genes, such as c-fos and c-jun.
机译:亲本(IOTV2)和致癌基因(H-ras)转化(Ciras-3)小鼠成纤维细胞中生长因子(EGF)或佛波酯(TPA)刺激Ras-MAPK信号转导途径诱导组蛋白H3的快速磷酸化。 H3的磷酸化发生在NH_2末端尾部的Ser10和Ser28上。该磷酸化事件与立即早期基因例如c-fos和c-jun的转录调控有关。

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