Laboratory of Kidney and Electrolyte Metabolism, National Heart, Lung and Blood Institute, Bethesda, Maryland, United States of America.
PLoS One. 2010 Aug 11;5(8):e12108. doi: 10.1371/journal.pone.0012108.
Hypertonicity, such as induced by high NaCl, increases the activity of the transcription factor TonEBP/OREBP whose target genes increase osmoprotective organic osmolytes and heat shock proteins.
We used mass spectrometry to analyze proteins that coimmunoprecipitate with TonEBP/OREBP in order to identify ones that might contribute to its high NaCl-induced activation.
We identified 20 unique peptides from Mediator of DNA Damage Checkpoint 1 (MDC1) with high probability. The identification was confirmed by Western analysis. We used small interfering RNA knockdown of MDC1 to characterize its osmotic function. Knocking down MDC1 reduces high NaCl-induced increases in TonEBP/OREBP transcriptional and transactivating activity, but has no significant effect on its nuclear localization. We confirm six previously known phosphorylation sites in MDC1, but do not find evidence that high NaCl increases phosphorylation of MDC1. It is suggestive that MDC1 acts as a DNA damage response protein since hypertonicity reversibly increases DNA breaks, and other DNA damage response proteins, like ATM, also associate with TonEBP/OREBP and contribute to its activation by hypertonicity.
CONCLUSIONS/SIGNIFICANCE: MDC1 associates with TonEBP/OREBP and contributes to high NaCl-induced increase of that factor's transcriptional activity.
高渗环境(如高浓度 NaCl 诱导)会增加转录因子 TonEBP/OREBP 的活性,后者的靶基因增加了渗透压保护的有机渗透物和热休克蛋白。
我们使用质谱分析法分析与 TonEBP/OREBP 共免疫沉淀的蛋白质,以鉴定可能有助于其高盐诱导激活的蛋白质。
我们从 DNA 损伤检查点 1 的 Mediator(MDC1)中鉴定出 20 个具有高可能性的独特肽段。Western 分析证实了这一鉴定。我们使用小干扰 RNA 敲低 MDC1 来表征其渗透功能。敲低 MDC1 会降低高盐诱导的 TonEBP/OREBP 转录和转录激活活性,但对其核定位没有显著影响。我们确认了 MDC1 中的六个先前已知的磷酸化位点,但没有发现高盐增加 MDC1 磷酸化的证据。这表明 MDC1 作为一种 DNA 损伤反应蛋白发挥作用,因为高渗环境可逆地增加 DNA 断裂,而其他 DNA 损伤反应蛋白,如 ATM,也与 TonEBP/OREBP 相关联,并有助于其被高渗激活。
结论/意义:MDC1 与 TonEBP/OREBP 结合,并有助于高盐诱导的该因子转录活性的增加。