RNase L regulates the antiviral proteome by accelerating mRNA1decay, inhibiting nuclear mRNA export, and repressing RNAPII-2mediated transcription

Abstract

Ribonuclease L (RNase L) is an antiviral endoribonuclease that triggers widespread degradation of cellular mRNAs. Here, we show that the degradation of cellular mRNA by RNase L is a conserved response to flaviviruses, including Zika virus (ZIKV), dengue virus serotype 2 (DENV-2), and West Nile virus (WNV). Quantitative mass spectrometry in response to dsRNA or ZIKV infection shows that RNase L broadly downregulates the cellular proteome, reducing proteins with short half-lives involved in cell cycle progression, cellular metabolism, and protein synthesis. The mRNAs encoded by interferon-stimulated genes (ISGs) evade mRNA decay by RNase L, allowing for protein synthesis of ISG-encoding mRNAs. However, RNase L dampens ISG protein synthesis by triggering a block in nuclear mRNA export and repressing RNAPII-mediated transcription at later times during the antiviral response. These findings implicate reprograming of the cellular proteome as primary means by which RNase L combats viral infection, tumorigenesis, and immune dysregulation. HIGHLIGHTSO_LIRNase L initiates widespread decay of cellular mRNA in response to flaviviruses C_LIO_LIRNase L-mediated mRNA decay broadly downregulates the homoeostatic proteome C_LIO_LIAntiviral mRNAs are translated due to their ability to evade RNase L-mediated decay C_LIO_LIRNase L reduces antiviral proteins by inhibiting mRNA export and RNAPII-mediated transcription C_LI O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=194 SRC="FIGDIR/small/665572v1_ufig1.gif" ALT="Figure 1"> View larger version (43K): org.highwire.dtl.DTLVardef@13c4940org.highwire.dtl.DTLVardef@ed1bd9org.highwire.dtl.DTLVardef@bf5057org.highwire.dtl.DTLVardef@33bca9_HPS_FORMAT_FIGEXP M_FIG C_FIG