文献类型: 外文期刊
作者: Zhao, Lingcai 1 ; Li, Shengmin 1 ; Deng, Lulu 1 ; Zhang, Yijia 1 ; Jiang, Chenfeng 1 ; Wei, Yurong 2 ; Xia, Jun 3 ; Ping, Jihui 1 ;
作者机构: 1.Nanjing Agr Univ, Coll Vet Med, Joint Int Res Lab Anim Hlth & Food Safety, Engn Lab Anim Immun Jiangsu Prov,MOE, Nanjing 210095, Peoples R China
2.Xinjiang Acad Anim Sci, Inst Vet Med, Xinjiang Key Lab Anim Infect Dis, Urumqi 830013, Peoples R China
3.Minist Agr & Rural Affairs, Key Lab Herbivore Dis Prevent & Control Coconstruc, Beijing, Peoples R China
关键词: Polymerase activity (PB2627E); Lysosome-associated pathway; SRSF7
期刊名称:MICROBES AND INFECTION ( 影响因子:2.7; 五年影响因子:2.8 )
ISSN: 1286-4579
年卷期: 2024 年 26 卷 8 期
页码:
收录情况: SCI
摘要: Avian influenza viruses crossing the host barrier to infect humans have caused great panic in human society and seriously threatened public health. Herein, we revealed that knockdown of SRSF7 significantly down-regulated influenza virus titers and viral protein expression. We further observed for the first time that human SRSF7, but not avian SRSF7, significantly inhibited polymerase activity (PB2627E). Molecular mapping demonstrated that amino acids 206 to 228 of human SRSF7 play a decisive role in regulating the polymerase activity, which contains the amino acid motif absent in avian SRSF7. Importantly, our results illustrated that the PB2627K-encoding influenza virus induces SRSF7 protein degradation more strongly via the lysosome pathway and not via the proteasome pathway. Functional enrichment analysis of SRSF7-related KEGG pathways indicated that SRSF7 is closely related to cell growth and death. Lastly, our results showed that knocking down SRSF7 interferes with normal polymerase activity. Taken together, our results advance our understanding of interspecies transmission and our findings point out new targets for the development of drugs preventing or treating influenza virus infection. (c) 2024 The Author(s). Published by Elsevier Masson SAS on behalf of Institut Pasteur. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
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