Dynamic refolding of IFN-gamma mRNA enables it to function as PKR activator and translation template.

نویسندگان

  • Smadar Cohen-Chalamish
  • Anat Hasson
  • Dahlia Weinberg
  • Lise Sarah Namer
  • Yona Banai
  • Farhat Osman
  • Raymond Kaempfer
چکیده

Interferon-gamma mRNA activates the RNA-dependent protein kinase PKR, which in turn strongly attenuates translation of interferon-gamma mRNA. Unlike riboswitches restricted to noncoding regions, the interferon-gamma RNA domain that activates PKR comprises the 5' UTR and 26 translated codons. Extensive interferon-gamma coding sequence is thus dedicated to activating PKR and blocking interferon-gamma synthesis. This implies that the PKR activator is disrupted by ribosomes during translation initiation and must refold promptly to restore PKR activation. The activator structure harbors an essential kink-turn, probably to allow formation of a pseudoknot that is critical for PKR activation. Three indispensable short helices, bordered by orientation-sensitive base pairs, align with the pseudoknot stem, generating RNA helix of sufficient length to activate PKR. Through gain-of-function mutations, we show that the RNA activator can adopt alternative conformations that activate PKR. This flexibility promotes efficient refolding of interferon-gamma mRNA, which is necessary for its dual function as translation template and activator of PKR, and which thus prevents overexpression of this inflammatory cytokine.

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عنوان ژورنال:
  • Nature chemical biology

دوره 5 12  شماره 

صفحات  -

تاریخ انتشار 2009