State Key Laboratory for Emerging Infectious Diseases, Department of Microbiology, The University of Hong Kong, Hong Kong SAR, China.
Collaborative Innovation Center for Diagnosis and Treatment of Infectious Diseases, The University of Hong Kong, Hong Kong SAR, China.
Nat Commun. 2017 Mar 21;8:14751. doi: 10.1038/ncomms14751.
Influenza virus utilizes host splicing machinery to process viral mRNAs expressed from both M and NS segments. Through genetic analysis and functional characterization, we here show that the NS segment of H7N9 virus contains a unique G540A substitution, located within a previously undefined exonic splicing enhancer (ESE) motif present in the NEP mRNA of influenza A viruses. G540A supports virus replication in mammalian cells while retaining replication ability in avian cells. Host splicing regulator, SF2, interacts with this ESE to regulate splicing of NEP/NS1 mRNA and G540A substitution affects SF2-ESE interaction. The NS1 protein directly interacts with SF2 in the nucleus and modulates splicing of NS mRNAs during virus replication. We demonstrate that splicing of NEP/NS1 mRNA is regulated through a cis NEP-ESE motif and suggest a unique NEP-ESE may contribute to provide H7N9 virus with the ability to both circulate efficiently in avian hosts and replicate in mammalian cells.
流感病毒利用宿主剪接机制来加工来自 M 和 NS 片段的病毒 mRNA。通过遗传分析和功能特征分析,我们在这里表明,H7N9 病毒的 NS 片段包含一个独特的 G540A 取代,位于流感 A 病毒的 NEP mRNA 中一个先前未定义的外显子剪接增强子(ESE)基序内。G540A 支持病毒在哺乳动物细胞中的复制,同时保留在禽类细胞中的复制能力。宿主剪接调节剂 SF2 与该 ESE 相互作用,调节 NEP/NS1 mRNA 的剪接,而 G540A 取代会影响 SF2-ESE 相互作用。NS1 蛋白在核内直接与 SF2 相互作用,并在病毒复制过程中调节 NS mRNAs 的剪接。我们证明,NEP/NS1 mRNA 的剪接是通过顺式 NEP-ESE 基序来调节的,并提出独特的 NEP-ESE 可能有助于使 H7N9 病毒能够在禽类宿主中有效传播并在哺乳动物细胞中复制。