Abstract

Retroviruses are among the best studied viruses in last decades due to their pivotal involvement in cellular processes and, most importantly, in causing human diseases, most notably—acquired immunodeficiency syndrome (AIDS) that is triggered by human immunodeficiency viruses types 1 and 2 (HIV-1 and HIV-2, respectively). Numerous studied were conducted to understand the involvement of the three cardinal retroviral enzymes, reverse transcriptase, integrase and protease, in the life cycle of the viruses. These studies have led to the development of many inhibitors of these enzymes as anti-retroviral specific drugs that are used for routine treatments of HIV/AIDS patients. Interestingly, a fourth virus-encoded enzyme, the deoxyuridine 5′-triphosphate nucleotidohydrolase (dUTPase) is also found in several major retroviral groups. The presence and the importance of this enzyme to the life cycle of retroviruses were usually overlooked by most retrovirologists, although the occurrence of dUTPases, particularly in beta-retroviruses and in non-primate retroviruses, is known for more than 20 years. Only more recently, retroviral dUTPases were brought into the limelight and were shown in several cases to be essential for viral replication. Therefore, it is likely that future studies on this enzyme will advance our knowledge to a level that will allow designing novel, specific and potent anti-dUTPase drugs that are effective in combating retroviral diseases. The aim of this review is to give concise background information on dUTPases in general and to summarize the most relevant data on retroviral dUTPases and their involvement in the replication processes and pathogenicity of the viruses, as well as in possibly-associated human diseases.

Highlights

  • The hallmark of all retroviruses is their replication strategy that relies on two critical steps

  • The data summarized in this review describe the importance of deoxyuridine 5′-triphosphate nucleotidohydrolase (dUTPase) to the retroviral life cycle in conjunction with cellular dUTPases, dUTP levels and mutagenesis

  • Only several groups of retroviruses have evolved to express their own dUTPase, while others either take advantage of the cellular dUTPase or recruit a cellular uracil DNA glucosidases (UNG) that initiates the correction of dUTP misincorporation

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Summary

Introduction

The hallmark of all retroviruses is their replication strategy that relies on two critical steps. The first is the reverse transcription of the viral plus strand RNA into linear double-stranded DNA that is catalyzed by the viral reverse transcriptase (RT). The second step occurs when the synthesized DNA is subsequently integrated by the viral integrase (IN) enzyme into the cell genomic DNA [1,2,3,4]. The proviral DNA becomes a part of the cellular genomic DNA. The genome of all retroviruses is organized in three major distinct genes: gag, pol and env. The pol gene encodes for all three basic retroviral enzymes, the protease (PR), RT

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