Viral-induced alternative splicing of host genes promotes influenza replication

被引:43
|
作者
Thompson, Matthew G. [1 ,2 ]
Dittmar, Mark [3 ]
Mallory, Michael J. [2 ]
Bhat, Prasanna [4 ]
Ferretti, Max B. [2 ,3 ]
Fontoura, Beatriz M. A. [4 ]
Cherry, Sara [1 ,2 ,3 ]
Lynch, Kristen W. [1 ,2 ]
机构
[1] Univ Penn, Biochem & Mol Biophys Grad Grp, Philadelphia, PA 19104 USA
[2] Univ Penn, Dept Biochem & Biophys, Philadelphia, PA 19104 USA
[3] Univ Penn, Dept Pathol, Perelman Sch Med, Philadelphia, PA 19104 USA
[4] UT Southwestern Med Ctr, Dept Cell Biol, Dallas, TX USA
来源
ELIFE | 2020年 / 9卷
基金
美国国家卫生研究院;
关键词
TRACT BINDING-PROTEIN; A VIRUS; MULTIPLE; CLK1; INFECTION; RESPONSES; REGION; CELLS;
D O I
10.7554/eLife.55500
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Viral infection induces the expression of numerous host genes that impact the outcome of infection. Here, we show that infection of human lung epithelial cells with influenza A virus (IAV) also induces a broad program of alternative splicing of host genes. Although these splicing-regulated genes are not enriched for canonical regulators of viral infection, we find that many of these genes do impact replication of IAV. Moreover, in several cases, specific inhibition of the IAV-induced splicing pattern also attenuates viral infection. We further show that approximately a quarter of the IAV-induced splicing events are regulated by hnRNP K, a host protein required for efficient splicing of the IAV M transcript in nuclear speckles. Finally, we find an increase in hnRNP K in nuclear speckles upon IAV infection, which may alter accessibility of hnRNP K for host transcripts thereby leading to a program of host splicing changes that promote IAV replication.
引用
收藏
页数:20
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