4.3 Article

Effect of divergence time and recombination rate on molecular evolution of Drosophila INE-1 transposable elements and other candidates for neutrally evolving sites

期刊

JOURNAL OF MOLECULAR EVOLUTION
卷 65, 期 6, 页码 627-639

出版社

SPRINGER
DOI: 10.1007/s00239-007-9028-6

关键词

INE-1; Drosophila; neutral evolution; substitution rate; crossing-over

资金

  1. Biotechnology and Biological Sciences Research Council [BB/D015480/1] Funding Source: Medline
  2. Wellcome Trust Funding Source: Medline
  3. Biotechnology and Biological Sciences Research Council [BB/D015480/1] Funding Source: researchfish
  4. BBSRC [BB/D015480/1] Funding Source: UKRI

向作者/读者索取更多资源

Interspecies divergence of orthologous transposable element remnants is often assumed to be simply due to genetic drift of neutral mutations that occurred after the divergence of the species. However, divergence may also be affected by other factors, such as variation in the mutation rate, ancestral polymorphisms, or selection. Here we attempt to determine the impact of these forces on divergence of three classes of sites that are often assumed to be selectively unconstrained (INE-1 TE remnants, sites within short introns, and fourfold degenerate sites) in two different pairwise comparisons of Drosophila (D. melanogaster vs. D. simulans and D. simulans vs. D. sechellia). We find that divergence of these three classes of sites is strongly influenced by the recombination environment in which they are located, and this is especially true for the closer D. simulans vs. D. sechellia comparison. We suggest that this is mainly a result of the contribution of ancestral polymorphisms in different recombination regions. We also find that intergenic INE-1 elements are significantly more diverged than intronic INE-1 in both pairwise comparisons, implying the presence of either negative selection or lower mutation rates in introns. Furthermore, we show that substitution rates in INE-1 elements are not associated with the length of the noncoding sequence in which they are located, suggesting that reduced divergence in long noncoding sequences is not due to reduced mutation rates in these regions. Finally, we show that GC content for each site within INE-1 sequences has evolved toward an equilibrium value (similar to 33%) since insertion.

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