Abstract

Recombination is a major source of genetic heterogeneity in the human immunodeficiency virus type 1 (HIV-1) population. The main mechanism responsible for the generation of recombinant viruses is a process of copy choice between the two copies of genomic RNA during reverse transcription. We previously identified, after a single cycle of infection of cells in culture, a recombination hot spot within the gp120 gene, corresponding to the top portion of a RNA hairpin. Here, we determine that the hot region is circumscribed to 18 nucleotides located in the descending strand of the stem, following the sense of reverse transcription. Three factors appeared to be important, albeit at different extents, for the high rate of recombination observed in this region. The position of the hot sequence in the context of the RNA structure appears crucial, because changing its location within this structure triggered differences in recombination up to 20-fold. Another pivotal factor is the presence of a perfectly identical sequence between donor and acceptor RNA in the region of transfer, because single or double nucleotide differences in the hot spot were sufficient to almost completely abolish recombination in the region. Last, the primary structure of the hot region also influenced recombination, although with effects only in the 2-3-fold range. Altogether, these results provide the first molecular dissection of a hot spot in infected cells and indicate that several factors contribute to the generation of a site of preferential copy choice.

Highlights

  • Occurrence of coinfection of a cell by genetically divergent viruses [5,6,7,8] favor the generation of viral particles carrying two non-identical copies of genomic RNA

  • The two genomic plasmids will, instead, direct the synthesis of two defective genomic RNAs that will be encapsidated in the viral particles, and that share a region of homology on which recombination is studied

  • In the present work we characterize a recombination hot spot we previously identified in the top portion of a RNA hairpin, in a region of the human immunodeficiency virus type 1 (HIV-1) env gene coding for the C2 portion of the gp120 protein

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Summary

Introduction

Occurrence of coinfection of a cell by genetically divergent viruses [5,6,7,8] favor the generation of viral particles carrying two non-identical copies of genomic RNA.

Results
Conclusion
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