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An NS-segment exonic splicing enhancer regulates influenza A virus replication in mammalian cells.


ABSTRACT: 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.

SUBMITTER: Huang X 

PROVIDER: S-EPMC5364394 | biostudies-literature | 2017 Mar

REPOSITORIES: biostudies-literature

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An NS-segment exonic splicing enhancer regulates influenza A virus replication in mammalian cells.

Huang Xiaofeng X   Zheng Min M   Wang Pui P   Mok Bobo Wing-Yee BW   Liu Siwen S   Lau Siu-Ying SY   Chen Pin P   Liu Yen-Chin YC   Liu Honglian H   Chen Yixin Y   Song Wenjun W   Yuen Kwok-Yung KY   Chen Honglin H  

Nature communications 20170321


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 regul  ...[more]

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