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首页> 外文期刊>American Journal of Physiology >Hypertonicity-induced phosphorylation and nuclear localization of the transcription factor TonEBP.
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Hypertonicity-induced phosphorylation and nuclear localization of the transcription factor TonEBP.

机译:高渗诱导的转录因子TonEBP的磷酸化和核定位。

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摘要

The accumulation of compatible osmolytes during osmotic stress is observed in virtually all organisms. In mammals, the hypertonicity-induced expression of osmolyte transporters and synthetic enzymes is conferred by the presence of upstream tonicity-responsive enhancer (TonE) sequences. Recently, we described the cloning and initial characterization of TonE-binding protein (TonEBP), a transcription factor that translocates to the nucleus and associates with TonE sequences in a tonicity-dependent manner. We now report that hypertonicity induces an increase in TonEBP phosphorylation that temporally correlates with increased nuclear localization of the molecule. TonEBP phosphorylation is not affected by a number of kinase inhibitors, including the p38 inhibitor SB-203580. In addition, in vitro binding assays show that the association of TonEBP with TonE sequences is not affected by phosphorylation. Thus TonEBP phosphorylation is an early step in the response of cells to hypertonicity and may be required for nuclear import or retention.
机译:几乎在所有生物体中都观察到了渗透压期间相容性渗透质的积累。在哺乳动物中,高渗诱导的渗透压转运蛋白和合成酶的表达是由于上游的张力反应性增强子(TonE)序列的存在而引起的。最近,我们描述了TonE结合蛋白(TonEBP)的克隆和初步表征,TonEBP是一种转录因子,可转运至细胞核并以张度依赖性方式与TonE序列结合。现在我们报告高渗性诱导TonEBP磷酸化的增加,这与分子的核定位增加在时间上相关。 TonEBP的磷酸化不受许多激酶抑制剂的影响,包括p38抑制剂SB-203580。另外,体外结合试验表明,TonEBP与TonE序列的结合不受磷酸化的影响。因此,TonEBP磷酸化是细胞对高渗反应的早期步骤,可能是核输入或保留所必需的。

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