State Key Laboratory for Animal Disease Control and Prevention, National African Swine Fever Para-reference Laboratory, National High Containment Facilities for Animal Diseases Control and Prevention, Harbin Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Harbin, China.
National Laboratory of Biomacromolecules, Key Laboratory of Infection and Immunity, Institute of Biophysics, Chinese Academy of Sciences, Beijing, China.
Nat Commun. 2024 Nov 20;15(1):10058. doi: 10.1038/s41467-024-54461-1.
African swine fever virus (ASFV), which poses significant risks to the global economy, encodes a unique host-independent transcription system. This system comprises an eight-subunit RNA polymerase (vRNAP), temporally expressed transcription factors and transcript associated proteins, facilitating cross-species transmission via intermediate host. The protein composition of the virion and the presence of transcription factors in virus genome suggest existence of distinct transcription systems during viral infection. However, the precise mechanisms of transcription regulation remain elusive. Through analyses of dynamic transcriptome, vRNAP-associated components and cell-based assay, the critical role of M1249L in viral transcription regulation has been highlighted. Atomic-resolution structures of vRNAP-M1249L supercomplex, exhibiting a variety of conformations, have uncovered the dual functions of M1249L. During early transcription, M1249L could serve as multiple temporary transcription factors with C-terminal domain acting as a switcher for activation/inactivation, while during late transcription it aids in the packaging of the transcription machinery. The structural and functional characteristics of M1249L underscore its vital roles in ASFV transcription, packaging, and capsid assembly, presenting novel opportunities for therapeutic intervention.
非洲猪瘟病毒(ASFV)对全球经济构成重大风险,其编码了一个独特的宿主非依赖性转录系统。该系统由一个包含八个亚基的 RNA 聚合酶(vRNAP)、 temporally expressed transcription factors 和转录相关蛋白组成,通过中间宿主促进了种间传播。病毒粒子的蛋白组成和病毒基因组中转录因子的存在表明,在病毒感染过程中存在不同的转录系统。然而,转录调控的精确机制仍不清楚。通过对动态转录组、vRNAP 相关成分和基于细胞的测定的分析,突出了 M1249L 在病毒转录调控中的关键作用。vRNAP-M1249L 超复合物的原子分辨率结构,展示了多种构象,揭示了 M1249L 的双重功能。在早期转录中,M1249L 可以作为多个临时转录因子,其 C 端结构域充当激活/失活的开关,而在晚期转录中,它有助于转录机制的包装。M1249L 的结构和功能特征突出了其在 ASFV 转录、包装和衣壳组装中的重要作用,为治疗干预提供了新的机会。