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Dephosphorylation of HuR protein during alphavirus infection is associated with HuR relocalization to the cytoplasm.

Abstract
We have demonstrated previously that the cellular HuR protein binds U-rich elements in the 3' untranslated region (UTR) of Sindbis virus RNA and relocalizes from the nucleus to the cytoplasm upon Sindbis virus infection in 293T cells. In this study, we show that two alphaviruses, Ross River virus and Chikungunya virus, lack the conserved high-affinity U-rich HuR binding element in their 3' UTRs but still maintain the ability to interact with HuR with nanomolar affinities through alternative binding elements. The relocalization of HuR protein occurs during Sindbis infection of multiple mammalian cell types as well as during infections with three other alphaviruses. Interestingly, the relocalization of HuR is not a general cellular reaction to viral infection, as HuR protein remained largely nuclear during infections with dengue and measles virus. Relocalization of HuR in a Sindbis infection required viral gene expression, was independent of the presence of a high-affinity U-rich HuR binding site in the 3' UTR of the virus, and was associated with an alteration in the phosphorylation state of HuR. Sindbis virus-induced HuR relocalization was mechanistically distinct from the movement of HuR observed during a cellular stress response, as there was no accumulation of caspase-mediated HuR cleavage products. Collectively, these data indicate that virus-induced HuR relocalization to the cytoplasm is specific to alphavirus infections and is associated with distinct posttranslational modifications of this RNA-binding protein.
AuthorsAlexa M Dickson, John R Anderson, Michael D Barnhart, Kevin J Sokoloski, Lauren Oko, Mateusz Opyrchal, Evanthia Galanis, Carol J Wilusz, Thomas E Morrison, Jeffrey Wilusz
JournalThe Journal of biological chemistry (J Biol Chem) Vol. 287 Issue 43 Pg. 36229-38 (Oct 19 2012) ISSN: 1083-351X [Electronic] United States
PMID22915590 (Publication Type: Journal Article, Research Support, N.I.H., Extramural)
Chemical References
  • 3' Untranslated Regions
  • ELAV Proteins
  • RNA, Viral
  • Caspases
Topics
  • 3' Untranslated Regions (physiology)
  • Alphavirus (genetics, metabolism)
  • Alphavirus Infections (genetics, metabolism)
  • Animals
  • Caspases (genetics, metabolism)
  • Chlorocebus aethiops
  • Cytoplasm (genetics, metabolism, virology)
  • ELAV Proteins (genetics, metabolism)
  • Gene Expression Regulation, Viral (physiology)
  • HEK293 Cells
  • Humans
  • Phosphorylation (genetics)
  • Protein Processing, Post-Translational
  • Protein Transport (genetics)
  • Proteolysis
  • RNA, Viral (genetics, metabolism)
  • Vero Cells

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