Abstract

BackgroundIn addition to vertical transmission, organisms can also acquire genes from other distantly related species or from their extra-chromosomal elements (plasmids and viruses) via horizontal gene transfer (HGT). It has been suggested that phages represent substantial forces in prokaryotic evolution. In eukaryotes, retroviruses, which can integrate into host genome as an obligate step in their replication strategy, comprise approximately 8% of the human genome. Unlike retroviruses, few members of other virus families are known to transfer genes to host genomes.ResultsHere we performed a systematic search for sequences related to circular single-stranded DNA (ssDNA) viruses in publicly available eukaryotic genome databases followed by comprehensive phylogenetic analysis. We conclude that the replication initiation protein (Rep)-related sequences of geminiviruses, nanoviruses and circoviruses have been frequently transferred to a broad range of eukaryotic species, including plants, fungi, animals and protists. Some of the transferred viral genes were conserved and expressed, suggesting that these genes have been coopted to assume cellular functions in the host genomes. We also identified geminivirus-like and parvovirus-like transposable elements in genomes of fungi and lower animals, respectively, and thereby provide direct evidence that eukaryotic transposons could derive from ssDNA viruses.ConclusionsOur discovery extends the host range of circular ssDNA viruses and sheds light on the origin and evolution of these viruses. It also suggests that ssDNA viruses act as an unforeseen source of genetic innovation in their hosts.

Highlights

  • In addition to vertical transmission, organisms can acquire genes from other distantly related species or from their extra-chromosomal elements via horizontal gene transfer (HGT)

  • Animal retroviruses, which can integrate into host genome as an obligate step in their replication strategy, comprise approximately 8% of the human

  • We found that two sequences of human gut viral metagenome from Genomic Survey Sequence (GSS) database share sequence similarities with the replication initiation protein (Rep)-like genes of G. intestinalis and with their neighboring genes (Figure 1B)

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Summary

Introduction

In addition to vertical transmission, organisms can acquire genes from other distantly related species or from their extra-chromosomal elements (plasmids and viruses) via horizontal gene transfer (HGT). Retroviruses, which can integrate into host genome as an obligate step in their replication strategy, comprise approximately 8% of the human genome. Few members of other virus families are known to transfer genes to host genomes. In addition to vertical transmission and gene acquisition from other distantly related species via horizontal gene transfer (HGT), organisms can capture genetic material from extra-chromosomal elements (plasmids and viruses) during evolution. Animal retroviruses, which can integrate into host genome as an obligate step in their replication strategy, comprise approximately 8% of the human. Recent viral metagenomic studies have shown that small circular ssDNA viruses are more prevalent and diverse in the environment than previously recognized [18,19,20,21,22]

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