Evolution of Tom, 297, 17.6 and rover retrotransposons in Drosophilidae species

LTR retrotransposons are the most abundant transposable elements in Drosophila and are believed to have contributed significantly to genome evolution. Different reports have shown that many LTR retrotransposon families in Drosophila melanogaster emerged from recent evolutionary episodes of transposi...

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Veröffentlicht in:Molecular genetics and genomics : MGG 2009-10, Vol.282 (4), p.351-362
Hauptverfasser: Vidal, Newton Medeiros, Ludwig, Adriana, Loreto, Elgion Lucio Silva
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Sprache:eng
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Zusammenfassung:LTR retrotransposons are the most abundant transposable elements in Drosophila and are believed to have contributed significantly to genome evolution. Different reports have shown that many LTR retrotransposon families in Drosophila melanogaster emerged from recent evolutionary episodes of transpositional activity. To contribute to the knowledge of the evolutionary history of Drosophila LTR retrotransposons and the mechanisms that control their abundance, distribution and diversity, we conducted analyses of four related families of LTR retrotransposons, 297 , 17.6 , rover and Tom. Our results show that these elements seem to be restricted to species from the D. melanogaster group, except for 17.6 , which is also present in D. virilis and D. mojavensis . Genetic divergences and phylogenetic analyses of a 1-kb fragment region of the pol gene illustrate that the evolutionary dynamics of Tom , 297 , 17 . 6 and rover retrotransposons are similar in several aspects, such as low codon bias, the action of purifying selection and phylogenies that are incongruent with those of the host species. We found an extremely complex association among the retrotransposon sequences, indicating that different processes shaped the evolutionary history of these elements, and we detected a very high number of possible horizontal transfer events, corroborating the importance of lateral transmission in the evolution and maintenance of LTR retrotransposons.
ISSN:1617-4615
1617-4623
DOI:10.1007/s00438-009-0468-0