Chen Ye, Schnetz Michael P, Irarrazabal Carlos E, Shen Rong-Fong, Williams Chester K, Burg Maurice B, Ferraris Joan D
Laboratory of Kidney and Electrolyte Metabolism, National Heart, Lung, and Blood Institute, National Institutes of Health, Bethesda, Maryland 20892, USA.
Am J Physiol Renal Physiol. 2007 Mar;292(3):F981-92. doi: 10.1152/ajprenal.00493.2005. Epub 2006 Dec 5.
Hypertonicity (e.g., high NaCl) activates the transcription factor tonicity-responsive enhancer/osmotic response element-binding protein (TonEBP/OREBP), increasing transcription of protective genes. In the present studies, by stably expressing amino acids 1-547 of TonEBP/OREBP in HEK 293 cells and immunoprecipitating it plus associated proteins from the nuclei of cells exposed to high NaCl, we identify 14 proteins that are physically associated with TonEBP/OREBP. The associated proteins fall into several classes: 1) DNA-dependent protein kinase, both its catalytic subunit and regulatory subunit, Ku86; 2) RNA helicases, namely RNA helicase A, nucleolar RNA helicase II/Gu, and DEAD-box RNA helicase p72; 3) small or heterogeneous nuclear ribonucleoproteins (snRNPs or hnRNPs), namely U5 snRNP-specific 116 kDa protein, U5 snRNP-specific 200 kDa protein, hnRNP U, hnRNP M, hnRNP K, and hnRNP F; 4) heat shock proteins, namely Hsp90beta and Hsc70; and 5) poly(ADP-ribose) polymerase-1 (PARP-1). We confirm identification of most of the proteins by Western analysis and also demonstrate by electrophoretic mobility-shift assay that they are present in the large complex that binds specifically along with TonEBP/OREBP to its cognate DNA element. In addition, we find that PARP-1 and Hsp90 modulate TonEBP/OREBP activity. PARP-1 expression reduces TonEBP/OREBP transcriptional activity and the activity of its transactivating domain. Hsp90 enhances those activities and sustains the increased abundance of TonEBP/OREBP protein in cells exposed to high NaCl.
高渗性(如高浓度氯化钠)可激活转录因子张力反应增强子/渗透压反应元件结合蛋白(TonEBP/OREBP),增加保护性基因的转录。在本研究中,通过在HEK 293细胞中稳定表达TonEBP/OREBP的1 - 547位氨基酸,并从暴露于高浓度氯化钠的细胞细胞核中免疫沉淀该蛋白及其相关蛋白,我们鉴定出14种与TonEBP/OREBP存在物理关联的蛋白。这些相关蛋白分为几类:1)DNA依赖性蛋白激酶,包括其催化亚基和调节亚基Ku86;2)RNA解旋酶,即RNA解旋酶A、核仁RNA解旋酶II/Gu和DEAD框RNA解旋酶p72;3)小核核糖核蛋白或不均一核核糖核蛋白(snRNP或hnRNP),即U5 snRNP特异性116 kDa蛋白、U5 snRNP特异性200 kDa蛋白、hnRNP U、hnRNP M、hnRNP K和hnRNP F;4)热休克蛋白,即Hsp90β和Hsc70;5)聚(ADP - 核糖)聚合酶 - 1(PARP - 1)。我们通过蛋白质免疫印迹分析证实了大多数蛋白的鉴定结果,并通过电泳迁移率变动分析证明它们存在于与TonEBP/OREBP特异性结合其同源DNA元件的大复合物中。此外,我们发现PARP - 1和Hsp90调节TonEBP/OREBP的活性。PARP - 1的表达降低了TonEBP/OREBP的转录活性及其反式激活结构域的活性。Hsp90增强了这些活性,并维持了暴露于高浓度氯化钠的细胞中TonEBP/OREBP蛋白丰度的增加。