MBE Advance Access originally published online on August 27, 2009
Molecular Biology and Evolution 2009 26(12):2795-2808; doi:10.1093/molbev/msp193
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Research Articles |
A Broadscale Phylogenetic Analysis of Group II Intron RNAs and Intron-Encoded Reverse Transcriptases
* Department of Biological Sciences, University of Calgary, Calgary, Alberta, Canada
Department of Biological Sciences, Idaho State University, Pocatello, ID
E-mail: zimmerly{at}ucalgary.ca.
Accepted for publication August 21, 2009.
Group II introns are self-splicing RNAs that are frequently assumed to be the ancestors of spliceosomal introns. They are widely distributed in bacteria and are also found in organelles of plants, fungi, and protists. In this study, we present a broadscale phylogenetic analysis of group II introns using sequence data from both the conserved RNA structure and the intron-encoded reverse transcriptase (RT). Two similar phylogenies are estimated for the RT open reading frame (ORF), based on either amino acid or nucleotide sequence, whereas one phylogeny is produced for the RNA. In making these estimates, we confronted nearly all the classic challenges to phylogenetic inference, including positional saturation, base composition heterogeneity, short internodes with low support, and sensitivity to taxon sampling. Although the major lineages are well-defined, robust resolution of topology is not possible between these lineages. The approximately unbiased (AU) and Shimodaira–Hasegawa topology tests indicated that the RT ORF and RNA ribozyme data sets are in significant conflict under a variety of models, revealing the possibility of imperfect coevolution between group II introns and their intron-encoded ORFs. The high level of sequence divergence, large timescale, and limited number of alignable characters in our study are representative of many RTs and group I introns, and our results suggest that phylogenetic analyses of any of these sequences could suffer from the same sources of error and instability identified in this study.
Key Words: group II intron • reverse transcriptase • retroelement • phylogeny • taxon sampling • base composition heterogeneity
1 Present address: Department of Biology, University of Nebraska at Kearney, Kearney, NE.
Barbara Holland, Associate Editor
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