Avian and 1918 Spanish influenza a virus NS1 proteins bind to Crk/CrkL src homology 3 domains to activate host cell signaling

被引:83
作者
Heikkinen, Leena S. [1 ]
Kazlauskas, Arunas [1 ]
Melen, Krister [2 ]
Wagner, Ralf [3 ]
Ziegler, Thedi [2 ]
Julkunen, Ilkka [2 ]
Saksela, Kalle [1 ]
机构
[1] Univ Helsinki, Cent Hosp, Hoartman Inst, Dept Virol, FIN-00014 Helsinki, Finland
[2] Natl Inst Publ Hlth, Dept Viral Dis & Immunol, FIN-00300 Helsinki, Finland
[3] Univ Regensburg, Inst Med Microbiol & Hyg, D-93053 Regensburg, Germany
关键词
PRE-MESSENGER-RNAS; ADAPTER PROTEIN; SH3; DOMAINS; 3-KINASE/AKT PATHWAY; ANTIVIRAL RESPONSES; PANDEMIC INFLUENZA; PHAGE-DISPLAY; SPECIFICITY; INTERFERON; SEQUENCE;
D O I
10.1074/jbc.M707195200
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
NS1 (nonstructural protein 1) is an important virulence factor of the influenza A virus. We observed that NS1 proteins of the 1918 pandemic virus (A/ Brevig Mission/ 1/ 18) and many avian influenza A viruses contain a consensus Src homology 3 (SH3) domain-binding motif. Screening of a comprehensive human SH3 phage library revealed the N-terminal SH3 of Crk and CrkL as the preferred binding partners. Studies with recombinant proteins confirmed avid binding of NS1 proteins of the 1918 virus and a representative avian H7N3 strain to Crk/ CrkL SH3 but not to other SH3 domains tested, including p85 alpha and p85 beta. Endogenous CrkL readily co-precipitated NS1 from cells infected with the H7N3 virus. In transfected cells association with CrkL was observed for NS1 of the 1918 and H7N3 viruses but not A/ Udorn/ 72 or A/WSN/ 33 NS1 lacking this sequence motif. SH3 binding was dispensable for suppression of interferoninduced gene expression by NS1 but was associated with enhanced phosphatidylinositol 3-kinase signaling, as evidenced by increased Akt phosphorylation. Thus, the Spanish Flu virus resembles avian influenza A viruses in its ability to recruit Crk/CrkL to modulate host cell signaling.
引用
收藏
页码:5719 / 5727
页数:9
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