Reverse Transcription in the Saccharomyces cerevisiae Long-Terminal Repeat Retrotransposon Ty3

• Published in: Viruses Vol. 9; no. 3; p. 44
• Main Authors: Rausch, Jason, Miller, Jennifer, Le Grice, Stuart
• Format: Journal Article
• Language: English
• Published: Switzerland MDPI AG 15.03.2017; MDPI
• Subjects: Binding sites; DNA polymerase; Enzymes; Genomes; HIV; Human immunodeficiency virus; Insects; Laboratories; Leukemia; Medical research; Mutation; Nucleic acids; retroelement; Retroelements; retrotransposon; reverse transcriptase; Reverse Transcription; Review; ribonuclease H (RNase H); RNA-Directed DNA Polymerase - chemistry; RNA-Directed DNA Polymerase - genetics; RNA-Directed DNA Polymerase - metabolism; Saccharomyces cerevisiae - genetics; Saccharomyces cerevisiae Proteins - chemistry; Saccharomyces cerevisiae Proteins - genetics; Saccharomyces cerevisiae Proteins - metabolism; Terminal Repeat Sequences; Transfer RNA; Ty3; Viruses; retroelement; DNA polymerase; reverse transcriptase; retrotransposon; reverse transcription; Ty3; ribonuclease H (RNase H)
• ISSN: 1999-4915; 1999-4915
• DOI: 10.3390/v9030044

Converting the single-stranded retroviral RNA into integration-competent double-stranded DNA is achieved through a multi-step process mediated by the virus-coded reverse transcriptase (RT). With the exception that it is restricted to an intracellular life cycle, replication of the Saccharomyces cerevisiae long terminal repeat (LTR)-retrotransposon Ty3 genome is guided by equivalent events that, while generally similar, show many unique and subtle differences relative to the retroviral counterparts. Until only recently, our knowledge of RT structure and function was guided by a vast body of literature on the human immunodeficiency virus (HIV) enzyme. Although the recently-solved structure of Ty3 RT in the presence of an RNA/DNA hybrid adds little in terms of novelty to the mechanistic basis underlying DNA polymerase and ribonuclease H activity, it highlights quite remarkable topological differences between retroviral and LTR-retrotransposon RTs. The theme of overall similarity but distinct differences extends to the priming mechanisms used by Ty3 RT to initiate (−) and (+) strand DNA synthesis. The unique structural organization of the retrotransposon enzyme and interaction with its nucleic acid substrates, with emphasis on polypurine tract (PPT)-primed initiation of (+) strand synthesis, is the subject of this review.