Singer Avinoam, Ramos Alejandra, Keating Amy E
MIT Department of Biology, Cambridge, Massachusetts, USA.
MIT Department of Biological Engineering, Cambridge, Massachusetts, USA.
bioRxiv. 2024 Apr 11:2024.01.23.576863. doi: 10.1101/2024.01.23.576863.
Short sequences that mediate interactions with modular binding domains are ubiquitous throughout eukaryotic proteomes. Networks of Short Linear Motifs (SLiMs) and their corresponding binding domains orchestrate many cellular processes, and the low mutational barrier to evolving novel interactions provides a way for biological systems to rapidly sample selectable phenotypes. Mapping SLiM binding specificity and the rules that govern SLiM evolution is fundamental to uncovering the pathways regulated by these networks and developing the tools to manipulate them. We used high-throughput screening of the human proteome to identify sequences that bind to the Enabled/VASP homology 1 (EVH1) domain of the postsynaptic density scaffolding protein Homer1. In doing so, we expanded current understanding of the determinants of Homer EVH1 binding preferences and defined a new motif that can facilitate the discovery of additional Homer-mediated interactions. Interestingly, the Homer1 EVH1 domain preferentially binds to sequences containing an N-terminally overlapping motif that is bound by the paralogous family of Ena/VASP actin polymerases, and many of these sequences can bind to EVH1 domains from both protein families. We provide evidence from orthologous EVH1 domains in pre-metazoan organisms that the overlap in human Ena/VASP and Homer binding preferences corresponds to an incomplete divergence from a common Ena/VASP ancestor. Given this overlap in binding profiles, promiscuous sequences that can be recognized by both families either achieve specificity through extrinsic regulatory strategies or may provide functional benefits via multi-specificity. This may explain why these paralogs incompletely diverged despite the accessibility of further diverged isoforms.
介导与模块化结合域相互作用的短序列在整个真核生物蛋白质组中普遍存在。短线性基序(SLiMs)及其相应结合域的网络协调着许多细胞过程,并且进化出新相互作用的低突变障碍为生物系统快速筛选可选择表型提供了一种方式。绘制SLiM结合特异性以及控制SLiM进化的规则对于揭示这些网络调控的途径和开发操纵它们的工具至关重要。我们通过对人类蛋白质组进行高通量筛选,以鉴定与突触后致密支架蛋白Homer1的Enabled/VASP同源1(EVH1)结构域结合的序列。在此过程中,我们扩展了当前对Homer EVH1结合偏好决定因素的理解,并定义了一个新的基序,该基序有助于发现其他由Homer介导的相互作用。有趣地是,Homer1 EVH1结构域优先结合包含N端重叠基序的序列,该基序由Ena/VASP肌动蛋白聚合酶的旁系同源家族结合,并且这些序列中的许多都可以与这两个蛋白质家族的EVH1结构域结合。我们提供了来自后生动物前体生物中直系同源EVH1结构域的证据,表明人类Ena/VASP和Homer结合偏好的重叠对应于与共同的Ena/VASP祖先的不完全分化。鉴于这种结合谱的重叠,两个家族都能识别的混杂序列要么通过外在调控策略实现特异性,要么可能通过多特异性提供功能益处。这可能解释了为什么尽管有进一步分化的异构体可供选择,这些旁系同源物仍未完全分化。