Abstract

Human cytomegalovirus (HCMV) UL84 is required for lytic DNA replication and is proposed to be the key factor in initiation of viral DNA synthesis. We now show that UL84 has a high degree of homology to the DExD/H (where x can be any amino acid) box family of helicases, displays UTPase activity, and is phosphorylated at serine residues. Affinity column-purified UL84-FLAG fusion protein was used in an in vitro nucleoside triphosphatase (NTPase) assay to show that UL84 has NTPase activity, preferring UTP. This UTPase activity was linear with respect to enzyme concentration and slightly enhanced by the addition of nucleic acid substrates. UL84 UTPase was the highest at low salt concentrations, a pH of 7.5, and a temperature of 45 degrees C. The enzyme preferred Mg2+ as the divalent cation but was also able to catalyze the UTPase reaction in the presence of Mn2+, Ca2+, and Zn2+ albeit at lower levels. The evidence presented here suggests that the UL84 UTPase activity may be part of an energy-generating system for helicase activity associated with the initiation of HCMV DNA replication.

Highlights

  • Human cytomegalovirus (HCMV)1 lytic DNA replication involves the core replication proteins: UL54, UL44, UL57, UL70, UL102, and UL105

  • UL84 Is Phosphorylated at Serine Residues—All known herpesvirus origin-binding proteins (OBP) are phosphorylated by cellular kinases

  • To determine whether UL84 was phosphorylated by cellular kinases and assess the similarities between UL84 and other OBPs, we obtained purifed UL84 from Vero cells infected with a recombinant adenovirus expressing UL84-FLAG fusion protein

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Summary

Introduction

Human cytomegalovirus (HCMV)1 lytic DNA replication involves the core replication proteins: UL54 (polymerase), UL44 (polymerase accessory protein), UL57 (single-stranded DNA binding protein), UL70 (primase), UL102 (primase-associated factor), and UL105 (helicase). We show that UL84 has a high degree of homology to the DExD/H (where x can be any amino acid) box family of helicases, displays UTPase activity, and is phosphorylated at serine residues. This UTPase activity was linear with respect to enzyme concentration and slightly enhanced by the addition of nucleic acid substrates.

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