Department of Pharmacy and Biotechnology (FaBiT), University of Bologna, 40126 Bologna, Italy.
Istituto di Tecnologie Biomediche-Consiglio Nazionale delle Ricerche (ITB-CNR), 20054 Segrate, Italy.
Int J Mol Sci. 2021 Jul 22;22(15):7848. doi: 10.3390/ijms22157848.
HP1043 is an essential orphan response regulator of orchestrating multiple crucial cellular processes. Classified as a member of the OmpR/PhoB family of two-component systems, HP1043 exhibits a highly degenerate receiver domain and evolved to function independently of phosphorylation. Here, we investigated the HP1043 binding mode to a target sequence in the promoter (). Scanning mutagenesis of HP1043 DNA-binding domain and consensus sequence led to the identification of residues relevant for the interaction of the protein with a target DNA. These determinants were used as restraints to guide a data-driven protein-DNA docking. Results suggested that, differently from most other response regulators of the same family, HP1043 binds in a head-to-head conformation to the target promoter. HP1043 interacts with DNA largely through charged residues and contacts with both major and minor grooves of the DNA are required for a stable binding. Computational alanine scanning on molecular dynamics trajectory was performed to corroborate our findings. Additionally, in vitro transcription assays confirmed that HP1043 positively stimulates the activity of RNA polymerase.
HP1043 是一种必需的孤儿反应调节剂,能够协调多个关键的细胞过程。它被归类为双组分系统 OmpR/PhoB 家族的成员,具有高度退化的受体结构域,并进化为独立于磷酸化而发挥作用。在这里,我们研究了 HP1043 与 启动子()中靶序列的结合模式。HP1043 DNA 结合结构域和保守序列的扫描突变导致鉴定出与蛋白质与靶 DNA 相互作用相关的残基。这些决定因素被用作约束条件来指导数据驱动的蛋白-DNA 对接。结果表明,与同一家族的大多数其他反应调节剂不同,HP1043 以头对头的构象结合到 靶启动子。HP1043 与 DNA 的相互作用主要通过带电残基进行,并且需要与 DNA 的大沟和小沟都接触,才能实现稳定结合。在分子动力学轨迹上进行的计算丙氨酸扫描实验证实了我们的发现。此外,体外转录实验证实 HP1043 可正向刺激 RNA 聚合酶的活性。