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Translation of the radioresistance kinase TLK1B is induced by γ-irradiation through activation of mTOR and phosphorylation of 4E-BP1

机译:γ射线通过激活mTOR和4E-BP1磷酸化来诱导抗辐射激酶TLK1B的翻译

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摘要

BackgroundThe mammalian protein kinase TLK1 is a homologue of Tousled, a gene involved in flower development in Arabidopsis thaliana. The function of TLK1 is not well known, although knockout of the gene in Drosophila, or expression of a dominant negative mutant in mouse cells causes loss of nuclear divisions and chromosome missegregation probably due to alterations in chromatin remodeling capacity. Overexpression of TLK1B, a spliced variant of the TLK1 mRNA, in a model mouse cell line increases their resistance to ionizing radiation, also likely through changes in chromatin remodeling. The TLK1B mRNA is translationally repressed by its 5'UTR and is regulated by the availability of eIF4E. We now report that radiation or doxorubicin result in an increase in the translation of TLK1B, and we have uncovered the likely mechanism for this effect.
机译:背景哺乳动物蛋白激酶TLK1是拟南芥Tousled的一个同源基因,该基因与拟南芥的花发育有关。尽管果蝇中的基因敲除或小鼠细胞中显性负突变体的表达导致核分裂的丧失和染色体错聚,可能是由于染色质重塑能力的改变,但TLK1的功能尚不清楚。 TLK1B(TLK1 mRNA的剪接变体)在模型小鼠细胞系中的过表达增加了它们对电离辐射的抗性,也可能是通过染色质重塑的改变来实现的。 TLK1B mRNA被其5'UTR翻译抑制,并受eIF4E的可用性调节。现在,我们报告辐射或阿霉素导致TLK1B的翻译增加,并且我们已经发现了这种作用的可能机制。

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