MBE Advance Access originally published online on October 19, 2005
Molecular Biology and Evolution 2006 23(2):268-278; doi:10.1093/molbev/msj041
| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Research Article |
Dense Taxonomic EST Sampling and Its Applications for Molecular Systematics of the Coleoptera (Beetles)
,1,2
,2




* Department of Entomology, The Natural History Museum, London, United Kingdom;
Department of Biological Sciences, Imperial College London, Silwood Park Campus, Ascot, United Kingdom; and
Department of Zoology, The Natural History Museum, London, United Kingdom
E-mail: j.hughes{at}bio.gla.ac.uk.
Expressed sequence tag (EST) sequences can provide a wealth of data for phylogenetic and genomic studies, but the utility of these resources is restricted by poor taxonomic sampling. Here, we use small EST libraries (<1,000 clones) to generate phylogenetic markers across a broad sample of insects, focusing on the species-rich Coleoptera (beetles). We sequenced over 23,000 ESTs from 34 taxa, which produced 8,728 unique sequences after clustering nonredundant sequences. Between taxa, the sequences could be grouped into 731 gene clusters, with the largest corresponding to mitochondrial DNA transcripts and gene families chymotrypsin, actin, troponin, and tubulin. While levels of paralogy were high in most gene clusters, several midsized clusters including many ribosomal protein (RP) genes appeared to be free of expressed paralogs. To evaluate the utility of EST data for molecular systematics, we curated available transcripts for 66 RP genes from representatives of the major groups of Coleoptera. Using supertree and supermatrix approaches for phylogenetic analysis, the results were consistent with the emerging phylogenetic conclusions about basal relationships in Coleoptera. Numerous small EST libraries from a taxonomically densely sampled lineage can provide a core set of genes that together act as a scaffold in phylogenetic reconstruction, comparative genomics, and studies of gene evolution.
Key Words: phylogenomics gene ontology shallow genomics expressed sequence tag
![]()
CiteULike
Connotea
Del.icio.us What's this?
This article has been cited by other articles:
![]() |
W. J. Baker, V. Savolainen, C. B. Asmussen-Lange, M. W. Chase, J. Dransfield, F. Forest, M. M. Harley, N. W. Uhl, and M. Wilkinson Complete Generic-Level Phylogenetic Analyses of Palms (Arecaceae) with Comparisons of Supertree and Supermatrix Approaches Syst Biol, May 30, 2009; (2009) syp021v1. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. J. Sanderson Phylogenetic Signal in the Eukaryotic Tree of Life Science, July 4, 2008; 321(5885): 121 - 123. [Abstract] [Full Text] [PDF] |
||||
![]() |
B. Hausdorf, M. Helmkampf, A. Meyer, A. Witek, H. Herlyn, I. Bruchhaus, T. Hankeln, T. H. Struck, and B. Lieb Spiralian Phylogenomics Supports the Resurrection of Bryozoa Comprising Ectoprocta and Entoprocta Mol. Biol. Evol., December 1, 2007; 24(12): 2723 - 2729. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. Savard, D. Tautz, S. Richards, G. M. Weinstock, R. A. Gibbs, J. H. Werren, H. Tettelin, and M. J. Lercher Phylogenomic analysis reveals bees and wasps (Hymenoptera) at the base of the radiation of Holometabolous insects Genome Res., November 1, 2006; 16(11): 1334 - 1338. [Abstract] [Full Text] [PDF] |
||||



