Maira S M, Wurtz J M, Wasylyk B
Institut de Génétique et de Biologie Moléculaire et Cellulaire, CNRS, INSERM, ULP, Illkirch, France.
EMBO J. 1996 Nov 1;15(21):5849-65.
The three ternary complex factors (TCFs), Net (ERP/ SAP-2), ELK-1 and SAP-1, are highly related ets oncogene family members that participate in the response of the cell to Ras and growth signals. Understanding the different roles of these factors will provide insights into how the signals result in coordinate regulation of the cell. We show that Net inhibits transcription under basal conditions, in which SAP-1a is inactive and ELK-1 stimulates. Repression is mediated by the NID, the Net Inhibitory Domain of about 50 amino acids, which autoregulates the Net protein and also inhibits when it is isolated in a heterologous fusion protein. Net is particularly sensitive to Ras activation. Ras activates Net through the C-domain, which is conserved between the three TCFs, and the NID is an efficient inhibitor of Ras activation. The NID, as well as more C-terminal sequences, inhibit DNA binding. Net is more refractory to DNA binding than the other TCFs, possibly due to the presence of multiple inhibitory elements. The NID may adopt a helix-loop-helix (HLH) structure, as evidenced by homology to other HLH motifs, structure predictions, model building and mutagenesis of critical residues. The sequence resemblance with myogenic factors suggested that Net may form complexes with the same partners. Indeed, we found that Net can interact in vivo with the basic HLH factor, E47. We propose that Net is regulated at the level of its latent DNA-binding activity by protein interactions and/or phosphorylation. Net may form complexes with HLH proteins as well as SRF on specific promotor sequences. The identification of the novel inhibitory domain provides a new inroad into exploring the different roles of the ternary complex factors in growth control and transformation.
三种三元复合因子(TCFs),即Net(ERP/SAP-2)、ELK-1和SAP-1,是与ets癌基因家族高度相关的成员,它们参与细胞对Ras和生长信号的反应。了解这些因子的不同作用将有助于深入了解这些信号如何导致细胞的协调调节。我们发现,在基础条件下Net抑制转录,此时SAP-1a无活性而ELK-1起刺激作用。抑制作用由NID介导,即约50个氨基酸的Net抑制结构域,它能自动调节Net蛋白,并且当它在异源融合蛋白中分离时也具有抑制作用。Net对Ras激活特别敏感。Ras通过C结构域激活Net,该结构域在三种TCF中是保守的,而NID是Ras激活的有效抑制剂。NID以及更多的C末端序列抑制DNA结合。与其他TCF相比,Net对DNA结合更具抗性,这可能是由于存在多个抑制元件。NID可能采用螺旋-环-螺旋(HLH)结构,与其他HLH基序的同源性、结构预测、模型构建以及关键残基的诱变都证明了这一点。与肌源性因子的序列相似性表明Net可能与相同的伙伴形成复合物。事实上,我们发现Net在体内能与碱性HLH因子E47相互作用。我们提出,Net的潜在DNA结合活性在蛋白质相互作用和/或磷酸化水平上受到调节。Net可能在特定启动子序列上与HLH蛋白以及血清反应因子(SRF)形成复合物。新型抑制结构域的鉴定为探索三元复合因子在生长控制和转化中的不同作用提供了新的途径。