Parua Pabitra K, Young Elton T
Department of Biochemistry, University of Washington, Seattle, Washington, USA.
Eukaryot Cell. 2014 Jan;13(1):21-30. doi: 10.1128/EC.00240-13. Epub 2013 Oct 18.
Evolutionarily conserved 14-3-3 proteins have important functions as dimers in numerous cellular signaling processes, including regulation of transcription. Yeast 14-3-3 proteins, known as Bmh, inhibit a post-DNA binding step in transcription activation by Adr1, a glucose-regulated transcription factor, by binding to its regulatory domain, residues 226 to 240. The domain was originally defined by regulatory mutations, ADR1(c) alleles that alter activator-dependent gene expression. Here, we report that ADR1(c) alleles and other mutations in the regulatory domain impair Bmh binding and abolish Bmh-dependent regulation both directly and indirectly. The indirect effect is caused by mutations that inhibit phosphorylation of Ser230 and thus inhibit Bmh binding, which requires phosphorylated Ser230. However, several mutations inhibit Bmh binding without inhibiting phosphorylation and thus define residues that provide important interaction sites between Adr1 and Bmh. Our proposed model of the Adr1 regulatory domain bound to Bmh suggests that residues Ser238 and Tyr239 could provide cross-dimer contacts to stabilize the complex and that this might explain the failure of a dimerization-deficient Bmh mutant to bind Adr1 and to inhibit its activity. A bioinformatics analysis of Bmh-interacting proteins suggests that residues outside the canonical 14-3-3 motif might be a general property of Bmh target proteins and might help explain the ability of 14-3-3 to distinguish target and nontarget proteins. Bmh binding to the Adr1 regulatory domain, and its failure to bind when mutations are present, explains at a molecular level the transcriptional phenotype of ADR1(c) mutants.
进化上保守的14-3-3蛋白作为二聚体在众多细胞信号传导过程中发挥重要作用,包括转录调控。酵母14-3-3蛋白,即Bmh,通过与葡萄糖调节转录因子Adr1的调控结构域(第226至240位残基)结合,抑制转录激活中DNA结合后的步骤。该结构域最初由调控突变定义,即改变激活剂依赖性基因表达的ADR1(c)等位基因。在这里,我们报告ADR1(c)等位基因和调控结构域中的其他突变直接和间接损害Bmh结合并消除Bmh依赖性调控。间接效应是由抑制Ser230磷酸化从而抑制Bmh结合的突变引起的,而Bmh结合需要磷酸化的Ser230。然而,一些突变在不抑制磷酸化的情况下抑制Bmh结合,从而确定了在Adr1和Bmh之间提供重要相互作用位点的残基。我们提出的Adr1调控结构域与Bmh结合的模型表明,Ser238和Tyr239残基可以提供跨二聚体接触以稳定复合物,这可能解释了二聚化缺陷的Bmh突变体无法结合Adr1并抑制其活性的原因。对与Bmh相互作用蛋白的生物信息学分析表明,经典14-3-3基序之外的残基可能是Bmh靶蛋白的普遍特性,这可能有助于解释14-3-3区分靶蛋白和非靶蛋白的能力。Bmh与Adr1调控结构域的结合以及存在突变时其无法结合,在分子水平上解释了ADR1(c)突变体的转录表型。