Tschowri Natalia, Schumacher Maria A, Schlimpert Susan, Chinnam Naga Babu, Findlay Kim C, Brennan Richard G, Buttner Mark J
Department of Molecular Microbiology, John Innes Centre, Norwich Research Park, Norwich NR4 7UH, UK.
Department of Biochemistry, Duke University School of Medicine, Durham, NC 27710, USA.
Cell. 2014 Aug 28;158(5):1136-1147. doi: 10.1016/j.cell.2014.07.022.
The cyclic dinucleotide c-di-GMP is a signaling molecule with diverse functions in cellular physiology. Here, we report that c-di-GMP can assemble into a tetramer that mediates the effective dimerization of a transcription factor, BldD, which controls the progression of multicellular differentiation in sporulating actinomycete bacteria. BldD represses expression of sporulation genes during vegetative growth in a manner that depends on c-di-GMP-mediated dimerization. Structural and biochemical analyses show that tetrameric c-di-GMP links two subunits of BldD through their C-terminal domains, which are otherwise separated by ~10 Å and thus cannot effect dimerization directly. Binding of the c-di-GMP tetramer by BldD is selective and requires a bipartite RXD-X8-RXXD signature. The findings indicate a unique mechanism of protein dimerization and the ability of nucleotide signaling molecules to assume alternative oligomeric states to effect different functions.
环二核苷酸c-di-GMP是一种在细胞生理学中具有多种功能的信号分子。在此,我们报道c-di-GMP可组装成四聚体,介导转录因子BldD的有效二聚化,BldD控制产孢放线菌中多细胞分化的进程。BldD在营养生长期间以依赖于c-di-GMP介导的二聚化的方式抑制孢子形成基因的表达。结构和生化分析表明,四聚体c-di-GMP通过其C端结构域连接BldD的两个亚基,否则这两个亚基相距约10 Å,因此不能直接实现二聚化。BldD对c-di-GMP四聚体的结合具有选择性,并且需要一个双重RXD-X8-RXXD基序。这些发现揭示了一种独特的蛋白质二聚化机制以及核苷酸信号分子呈现替代寡聚状态以实现不同功能的能力。