AI Article Synopsis

  • The adenovirus E4 11 k protein is crucial for viral infection as it helps accumulate late mRNAs and alters the structure of infected cell nuclei and cytoplasm.
  • E4 11 k relocalizes specific host proteins, particularly those in PML oncogenic domains, and may inactivate them, although the exact mechanism behind late mRNA accumulation remains unclear.
  • New findings show that 11 k also relocalizes proteins from cytoplasmic mRNA processing bodies (p-bodies) into aggresomes, suggesting a potential link between this modification and the increase in late mRNA levels during infection.

Article Abstract

The adenovirus E4 11 k protein, product of E4 ORF3, is required in infection for processes including normal accumulation of viral late mRNAs. 11 k restructures both the nucleus and cytoplasm of infected cells by relocalizing specific host cell target proteins, most strikingly components of nuclear PML oncogenic domains. It is likely that in many cases relocalization inactivates target proteins to produce 11 k's effects, although the mechanism and targets for stimulation of late mRNA accumulation is unknown. We have identified a new set of proteins relocalized by 11 k: at least five protein components of cytoplasmic mRNA processing bodies (p-bodies) are found in 11 k-induced cytoplasmic aggresomes, sites where proteins are inactivated or destroyed. One of these p-body proteins, RNA helicase Ddx6, binds 11 k, suggesting a mechanism for relocalization. Because p-bodies are sites for mRNA degradation, their modification by 11 k may provide an explanation for the role of 11 in viral late mRNA accumulation.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3152696PMC
http://dx.doi.org/10.1016/j.virol.2011.05.017DOI Listing

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