Biochemical Characterization of Yeast Xrn1

Abstract

Messenger RNA degradation is an important component of overall gene expression. During the final step of eukaryotic mRNA degradation, exoribonuclease 1 (Xrn1) carries out 5′ → 3′ processive, hydrolytic degradation of RNA molecules using divalent metal ion catalysis. To initiate studies of the 5′ → 3′ RNA decay machinery in our lab, we expressed a C-terminally truncated version of Saccharomyces cerevisiae Xrn1 and explored its enzymology using a second-generation, time-resolved fluorescence RNA degradation assay. Using this system, we quantitatively explored Xrn1’s preference for 5′-monophosphorylated RNA substrates, its pH dependence, and the importance of active site mutations in the molecule’s conserved catalytic core. Furthermore, we explore Xrn1’s preference for RNAs containing a 5′ single-stranded region both in an intermolecular hairpin structure and in an RNA–DNA hybrid duplex system. These results both expand and solidify our understanding of Xrn1, a centrally important enzyme whose biochemical properties have implications in numerous RNA degradation and processing pathways.