Fox A H, Kowalski K, King G F, Mackay J P, Crossley M
Department of Biochemistry, University of Sydney, New South Wales, 2006 Australia.
J Biol Chem. 1998 Dec 11;273(50):33595-603. doi: 10.1074/jbc.273.50.33595.
Protein-protein interactions play significant roles in the control of gene expression. These interactions often occur between small, discrete domains within different transcription factors. In particular, zinc fingers, usually regarded as DNA-binding domains, are now also known to be involved in mediating contacts between proteins. We have investigated the interaction between the erythroid transcription factor GATA-1 and its partner, the 9 zinc finger protein, FOG (Friend Of GATA). We demonstrate that this interaction represents a genuine finger-finger contact, which is dependent on zinc-coordinating residues within each protein. We map the contact domains to the core of the N-terminal zinc finger of GATA-1 and the 6th zinc finger of FOG. Using a scanning substitution strategy we identify key residues within the GATA-1 N-finger which are required for FOG binding. These residues are conserved in the N-fingers of all GATA proteins known to bind FOG, but are not found in the respective C-fingers. This observation may, therefore, account for the particular specificity of FOG for N-fingers. Interestingly, the key N-finger residues are seen to form a contiguous surface, when mapped onto the structure of the N-finger of GATA-1.
蛋白质-蛋白质相互作用在基因表达调控中发挥着重要作用。这些相互作用通常发生在不同转录因子内的小的离散结构域之间。特别是,锌指结构通常被视为DNA结合结构域,现在也已知其参与介导蛋白质之间的相互作用。我们研究了红系转录因子GATA-1与其伙伴——9锌指蛋白FOG(GATA之友)之间的相互作用。我们证明这种相互作用代表了一种真正的指-指接触,它依赖于每种蛋白质内的锌配位残基。我们将接触结构域定位到GATA-1的N端锌指的核心和FOG的第6个锌指。使用扫描替代策略,我们确定了GATA-1 N指内FOG结合所需的关键残基。这些残基在所有已知能结合FOG的GATA蛋白的N指中保守,但在各自的C指中未发现。因此,这一观察结果可能解释了FOG对N指的特殊特异性。有趣的是,当映射到GATA-1的N指结构上时,关键的N指残基形成了一个连续的表面。