TY - JOUR
T1 - Thogoto virus ML protein suppresses IRF3 function
AU - Jennings, Stephanie
AU - Martínez-Sobrido, Luis
AU - García-Sastre, Adolfo
AU - Weber, Friedemann
AU - Kochs, Georg
N1 - Funding Information:
This work was supported by grants from the Wissenschaftliche Gesellschaft in Freiburg and the Deutsche Forschungsgemeinschaft (Ko 1579/3-5 and Ko 1579/4-1) to G.K. and from the NIH (AI46954) to A.G.-S. We would like to thank Otto Haller and Peter Palese for constant support and suggestions; Richard Cadagan, Simone Gruber, and Valentina Wagner for excellent technical assistance; and Kathrin Hagmaier, Martin Spiegel, and Peter Staeheli for discussions and critical comments on the manuscript. We are grateful to Richard Eckner, Takashi Fujita, Peter Howley, and Tom Maniatis for expression constructs, reporter plasmids, and antibodies.
PY - 2005/1/5
Y1 - 2005/1/5
N2 - The Thogoto virus (THOV) is a member of the family Orthomyxoviridae. It prevents induction of alpha/beta interferons (IFN) in cell culture and in vivo via the action of the viral ML protein. Phenotypically, the effect of THOV ML resembles that of the NS1 protein of influenza A virus (FLUAV) in that it blocks the expression of IFN genes. IFN expression depends on IFN regulatory factor 3 (IRF3). Upon activation, IRF3 forms homodimers and accumulates in the nucleus where it binds the transcriptional coactivator CREB-binding protein (CBP). Here, we show that expression of ML blocked the transcriptional activity of IRF3 after stimulation by virus infection. Further biochemical analysis revealed that ML acts by blocking IRF3 dimerization and association with CBP. Surprisingly, however, ML did not interfere with the nuclear transport of IRF3. Thus, the action of ML differs strikingly from that of FLUAV NS1 that prevents IFN induction by retaining IRF3 in the cytoplasm.
AB - The Thogoto virus (THOV) is a member of the family Orthomyxoviridae. It prevents induction of alpha/beta interferons (IFN) in cell culture and in vivo via the action of the viral ML protein. Phenotypically, the effect of THOV ML resembles that of the NS1 protein of influenza A virus (FLUAV) in that it blocks the expression of IFN genes. IFN expression depends on IFN regulatory factor 3 (IRF3). Upon activation, IRF3 forms homodimers and accumulates in the nucleus where it binds the transcriptional coactivator CREB-binding protein (CBP). Here, we show that expression of ML blocked the transcriptional activity of IRF3 after stimulation by virus infection. Further biochemical analysis revealed that ML acts by blocking IRF3 dimerization and association with CBP. Surprisingly, however, ML did not interfere with the nuclear transport of IRF3. Thus, the action of ML differs strikingly from that of FLUAV NS1 that prevents IFN induction by retaining IRF3 in the cytoplasm.
KW - IRF3
KW - Influenza virus
KW - Interferon antagonist
KW - Interferon-regulatory factor 3
KW - ML protein
KW - NS1 protein
KW - Orthomyxoviruses
KW - Thogoto virus
UR - http://www.scopus.com/inward/record.url?scp=9944221945&partnerID=8YFLogxK
U2 - 10.1016/j.virol.2004.10.015
DO - 10.1016/j.virol.2004.10.015
M3 - Article
C2 - 15582653
AN - SCOPUS:9944221945
SN - 0042-6822
VL - 331
SP - 63
EP - 72
JO - Virology
JF - Virology
IS - 1
ER -