Abstract

Chlorella virus PBCV-1 topoisomerase II is the only functional type II enzyme known to be encoded by a virus that infects eukaryotic cells. However, it has not been established whether the protein is expressed following viral infection or whether the enzyme has any catalytic features that distinguish it from cellular type II topoisomerases. Therefore, the present study characterized the physiological expression of PBCV-1 topoisomerase II and individual reaction steps catalyzed by the enzyme. Results indicate that the topoisomerase II gene is widely distributed among Chlorella viruses and that the protein is expressed 60-90 min after viral infection of algal cells. Furthermore, the enzyme has an extremely high DNA cleavage activity that sets it apart from all known eukaryotic type II topoisomerases. Levels of DNA scission generated by the viral enzyme are approximately 30 times greater than those observed with human topoisomerase IIalpha. The high levels of cleavage are not due to inordinately tight enzyme-DNA binding or to impaired DNA religation. Thus, they most likely reflect an elevated forward rate of scission. The robust DNA cleavage activity of PBCV-1 topoisomerase II provides a unique tool for studying the catalytic functions of type II topoisomerases.

Highlights

  • Topoisomerases play key roles in virtually every cellular DNA process, including replication, transcription, recombination, and chromosome segregation [1,2,3,4,5,6]

  • Open reading frames predicted to encode type II topoisomerases recently have been reported in three eukaryotic viral genomes: the asfarvirus African swine fever virus [21, 22], the phycodnavirus Paramecium bursaria Chlorella virus (PBCV-1)1 [23], and the iridovirus Chilo iridescent virus [24]

  • Results indicate that PBCV-1 topoisomerase II is synthesized in vivo post-infection

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Summary

Introduction

Topoisomerases play key roles in virtually every cellular DNA process, including replication, transcription, recombination, and chromosome segregation [1,2,3,4,5,6]. Levels of DNA scission generated by the viral enzyme are ϳ30 times greater than those observed with human topoisomerase II␣. Because the high DNA cleavage activity of PBCV-1 topoisomerase II is atypical of eukaryotic type II enzymes, the requirement for a divalent cation in this process was examined (Fig. 8).

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