Li Minke, Wu Yixi, Li Huanhuan, Song Wenjun, Chen Zhenxing, Peng Yuzhou, Yang Boyao, Xu Chang, Zhang Jihua, Xing Lei, Weng Zhuangfeng, Liu Yingfang, Liang Huanhuan
Shenzhen Key Laboratory of Systems Medicine for Inflammatory Diseases, School of Pharmaceutical Sciences (Shenzhen), Shenzhen Campus of Sun Yat-sen University, No.66, Gongchang Road, Guangming District, Shenzhen, 518107, Guangdong, China.
Shenzhen Key Laboratory of Systems Medicine for Inflammatory Diseases, School of Medicine, Shenzhen Campus of Sun Yat-sen University, No.66, Gongchang Road, Guangming District, Shenzhen, 518107, Guangdong, China.
Nucleic Acids Res. 2025 Jan 24;53(3). doi: 10.1093/nar/gkae1225.
Influenza polymerase (FluPol) carries out both viral transcription and replication using the same viral genome segment as a template to yield distinct end products. However, it remains largely unclear how FluPol synthesizes transcripts containing poly (A) tails during transcription termination, while producing fully complementary products during replication termination. In this study, through structural analysis combined with cell-based and biochemical assays, we identified that the PB1 Leu675/Asn676 and PB2 Arg38 residues of FluPol are critical for transcription termination and polyadenylation. During transcription termination, these three residues adopt the PB1 Leu675/Asn676down and PB2 Arg38out conformations, with their side chains positioned against the G12 and G14 residues of the RNA template at the 5' end. These steric hindrances block template translocation and facilitate FluPol 'stuttering' at U17, which is required for viral messenger RNA polyadenylation. Importantly, both structural analysis and mutational studies suggest that this specific conformation of these residues is unique to the transcription termination state. Overall, our findings provide novel insights into the mechanisms by which FluPol generates distinct 3' end products during transcription and replication termination.
流感病毒聚合酶(FluPol)利用同一病毒基因组片段作为模板进行病毒转录和复制,以产生不同的终产物。然而,在转录终止过程中FluPol如何合成含聚腺苷酸(poly (A))尾的转录本,同时在复制终止过程中产生完全互补的产物,目前仍不清楚。在本研究中,通过结构分析结合基于细胞和生化的实验,我们确定FluPol的PB1 675位亮氨酸/676位天冬酰胺以及PB2 38位精氨酸残基对转录终止和聚腺苷酸化至关重要。在转录终止过程中,这三个残基呈现PB1 675位亮氨酸/676位天冬酰胺向下以及PB2 38位精氨酸向外的构象,其侧链位于RNA模板5'端的G12和G14残基处。这些空间位阻阻碍模板移位,并促进FluPol在U17处“口吃”,这是病毒信使RNA聚腺苷酸化所必需的。重要的是,结构分析和突变研究均表明,这些残基的这种特定构象是转录终止状态所特有的。总体而言,我们的研究结果为FluPol在转录和复制终止过程中产生不同3'端产物的机制提供了新的见解。