Activation of the mRNA Decay-Associated DEAD-Box ATPase Dhh1 Requires Deadenylation and Decapping Factors

Abstract

The DEAD-box ATPase Dhh1 (DDX6 in humans) is a general activator of 5-3 mRNA decay that acts between the deadenylation and decapping steps of the pathway, although the exact mechanism of its action remains unclear. Dhh1 has been shown to interact with the MIF4G domain of the central scaffold protein of the Ccr4-Not deadenylase complex, Not1, as well as the decapping activator Edc3. Although structures have been published of Dhh1 in complex with Not1MIF4G or an Edc3 peptide, the impact of these interactions on the catalytic cycle of Dhh1 are unknown. Here, we show Edc3 enhances ATP and RNA binding by Dhh1, whereas Not1MIF4G promotes the catalytic step of ATP hydrolysis. Additionally, the modulation of Dhh1 activity by Edc3 requires a more extensive set of interaction motifs and interfaces than was previously recognized. While the effect of either Not1MIF4G or Edc3 on the ATPase activity of Dhh1 is modest, together both proteins increase Dhh1 activity over 200-fold. The fact that Dhh1 biochemical activity is cooperatively tuned by deadenylation and decapping factors suggests that Dhh1 may coordinate deadenylation and decapping in the 5-3 mRNA decay pathway through changes in its ATP-coupled RNA binding affinity during its catalytic cycle. Graphical Abstract O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=75 SRC="FIGDIR/small/721454v2_ufig1.gif" ALT="Figure 1"> View larger version (18K): org.highwire.dtl.DTLVardef@12a38e2org.highwire.dtl.DTLVardef@fcb87forg.highwire.dtl.DTLVardef@1b4c77dorg.highwire.dtl.DTLVardef@194fc1d_HPS_FORMAT_FIGEXP M_FIG C_FIG