The interaction of flavivirus M protein with light chain Tctex-1 of human dynein plays a role in late stages of virus replication.

Jean-Baptiste Brault (1) , Mateusz Kudelko (2) , Pierre-Olivier Vidalain (3) , Frédéric Tangy (3) , Philippe Desprès (1) , Nathalie Pardigon (1)

1 Interactions Moléculaires Flavivirus-Hôtes
2 Centre de recherche Université de Hong-Kong-Pasteur
3 Génomique Virale et Vaccination

The role of the membrane protein (prM/M) in flavivirus life cycle remains unclear. Here, we identified a cellular interactor to the 40-residue-long ectodomain of prM/M (ectoM) using a yeast two-hybrid screen against a human cDNA library and GST pull-down assays. We showed that dynein light chain Tctex-1 interacts with the ectoM of dengue 1-4, West Nile, and Japanese encephalitis flaviviruses. No interaction was found with yellow fever and tick-borne flaviviruses. This interaction is highly specific since a single amino-acid change in the ectoM abrogates the interaction with Tctex-1. To understand the role of this interaction, silencing of Tctex-1 using siRNA was performed prior to infection. A significant decrease in progeny production was observed for dengue and West Nile viruses. Silencing Tctex-1 inhibited the production of recombinant dengue subviral particles (RSPs). Thus Tctex-1 may play a role in late stages of viral replication through its interaction with the membrane protein.

Domains: Life Sciences [q-bio]; Microbiology and Parasitology; Virology

Jean-Baptiste Brault, Mateusz Kudelko, Pierre-Olivier Vidalain, Frédéric Tangy, Philippe Desprès, et al.. The interaction of flavivirus M protein with light chain Tctex-1 of human dynein plays a role in late stages of virus replication.. Virology, 2011, 417 (2), pp.369-78. ⟨10.1016/j.virol.2011.06.022⟩. ⟨pasteur-00648668⟩