Sierecki Emma
EMBL Australia Node in Single Molecule Science, and School of Medical Sciences, Faculty of Medecine, The University of New South Wales, Sydney, Australia.
Semin Cell Dev Biol. 2020 Mar;99:20-30. doi: 10.1016/j.semcdb.2018.08.006. Epub 2018 Oct 16.
At the core of gene regulation, a complex network of dynamic interactions between proteins, DNA and RNA has to be integrated in order to generate a binary biological output. Large protein complexes, called adaptors, transfer information from the transcription factors to the transcription machinery [1,2]. Here we focus on Mediator, one of the largest adaptor proteins in humans [3]. Assembled from 30 different subunits, this system provides extraordinary illustrations for the various roles played by protein-protein interactions. Recruitment of new subunits during evolution is an adaptive mechanism to the growing complexity of the organism. Integration of information happens at multiple scales, with allosteric effects at the level of individual subunits resulting in large conformational changes. Mediator is also rich in disordered regions that increase the potential for interactions by presenting a malleable surface to its environment. Potentially, 3000 transcription factors can interact with Mediator and so understanding the molecular mechanisms that support the processing of this overload of information is one of the great challenges in molecular biology.
在基因调控的核心,蛋白质、DNA和RNA之间复杂的动态相互作用网络必须整合起来,以产生二元生物学输出。称为衔接子的大型蛋白质复合物将信息从转录因子传递到转录机制[1,2]。在这里,我们关注中介体,它是人类中最大的衔接子蛋白之一[3]。该系统由30个不同的亚基组装而成,为蛋白质-蛋白质相互作用所发挥的各种作用提供了非凡的例证。在进化过程中招募新的亚基是一种适应生物体日益复杂的机制。信息整合发生在多个尺度上,单个亚基水平的变构效应会导致大的构象变化。中介体还富含无序区域,通过向其周围环境呈现可塑表面增加了相互作用的潜力。潜在地,3000种转录因子可以与中介体相互作用,因此理解支持处理这种信息过载的分子机制是分子生物学中的重大挑战之一。