Abstract

Non-long terminal repeat retrotransposons, widespread among eukaryotic genomes, transpose by reverse transcription of an RNA intermediate. Some of them, like L1 in the human, terminate at the 3'-end with a poly(dA) stretch whereas others, like the I factor in Drosophila melanogaster, have instead a short sequence repeated in tandem. This suggests different requirements for the initiation of reverse transcription. Here, we have used an RNA circularization/reverse transcription-PCR technique to analyze the 5'- and 3'-ends of the full-length transcripts produced by the I factor at the time of active retrotransposition. These transcripts are capped and polyadenylated similar to conventional messenger RNAs. We have analyzed the 3'-ends of transcripts and transposed copies produced by I elements mutated at the 3'-ends. Transcripts devoid of tandem UAA repeats, although capable of building the components of the retrotransposition machinery, are inefficiently used as retrotransposition intermediates. Such transcripts produce rare new integrated copies issued from the inaccurate initiation of reverse transcription near the 3'-end of the element. The tandem UAA repeats at the 3'-end of the transcripts of I are required for the efficient and precise initiation of reverse transcription. This strong specificity of the I factor reverse transcriptase for its own transcript has implications for the impact of I factor retrotransposition on the host genome.

Highlights

  • Very little is known about the mechanism of retrotransposition of non-LTR1 elements that are widespread among eukaryotic genomes

  • Most current knowledge comes from in vitro studies of the site-specific R2 elements from Bombyx mori. These studies indicate that reverse transcription of a full-length RNA intermediate of transposition occurs at the site of integration, using a 3Ј-hydroxyl group generated by endonucleolytic cleavage of the genomic DNA to prime synthesis of the first cDNA strand [1]

  • We have used a technique that relies on RNA circularization followed by RT-PCR to characterize in detail the structures of the 5Ј- and 3Ј-ends of full-length transcripts produced by actively transposing I factors

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Summary

Mechanism of Retrotransposition of the I Factor

Ucts of the two open reading frames and as the retrotransposition intermediate [22, 23]. We have used a technique that relies on RNA circularization followed by RT-PCR to characterize in detail the structures of the 5Ј- and 3Ј-ends of full-length transcripts produced by actively transposing I factors. These transcripts follow the classical messenger RNA maturation pathway. The study of transcripts and transposed copies produced by elements modified at the 3Ј-ends indicate that the tandem TAA repeats at the 3Ј-end of the I factor are essential for efficient and precise retrotransposition

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