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Selection of Conserved Blocks from Multiple Alignments for Their Use in Phylogenetic Analysis

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Castresana, J.·2000·Molecular Biology and Evolution

Abstract

The use of some multiple-sequence alignments in phylogenetic analysis, particularly those that are not very well conserved, requires the elimination of poorly aligned positions and divergent regions, since they may not be homologous or may have been saturated by multiple substitutions. A computerized method that eliminates such positions and at the same time tries to minimize the loss of informative sites is presented here. The method is based on the selection of blocks of positions that fulfill a simple set of requirements with respect to the number of contiguous conserved positions, lack of gaps, and high conservation of flanking positions, making the final alignment more suitable for phylogenetic analysis. To illustrate the efficiency of this method, alignments of 10 mitochondrial proteins from several completely sequenced mitochondrial genomes belonging to diverse eukaryotes were used as examples. The percentages of removed positions were higher in the most divergent alignments. After removing divergent segments, the amino acid composition of the different sequences was more uniform, and pairwise distances became much smaller. Phylogenetic trees show that topologies can be different after removing conserved blocks, particularly when there are several poorly resolved nodes. Strong support was found for the grouping of animals and fungi but not for the position of more basal eukaryotes. The use of a computerized method such as the one presented here reduces to a certain extent the necessity of manually editing multiple alignments, makes the automation of phylogenetic analysis of large data sets feasible, and facilitates the reproduction of the final alignment by other researchers.

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Research works printed but not linked: 52

  1. Adachi, J., and M. Hasegawa. 1996a. Model of amino acid substitution in proteins encoded by mitochondrial DNA. J. Mol. Evol. 42:459–468. · DOI · Paper page
  2. Arnason, U., X. Xu, and A. Gullberg. 1996. Comparison between the complete mitochondrial DNA sequences of Homo and the common chimpanzee based on nonchimeric sequences. J. Mol. Evol. 42:145–152. · DOI
  3. Asakawa, S., H. Himeno, K. Miura, and K. Watanabe. 1995. Nucleotide sequence and gene organization of the starfish Asterina pectinifera mitochondrial genome. Genetics 140:1047–1060. · DOI
  4. Bairoch, A., and R. Apweiler. 1998. The SWISS-PROT protein sequence data bank and its supplement TrEMBL in 1998. Nucleic Acids Res. 26:38–42. · DOI · Paper page
  5. Baldauf, S. L., and J. D. Palmer. 1993. Animals and fungi are each other's closest relatives: congruent evidence from multiple proteins. Proc. Natl. Acad. Sci. USA 90:11558–11562. · DOI · Paper page
  6. Beagley, C. T., R. Okimoto, and D. R. Wolstenholme. 1998. The mitochondrial genome of the sea anemone Metridium senile (Cnidaria): introns, a paucity of tRNA genes, and a near-standard genetic code. Genetics 148:1091–1108. · DOI
  7. Boore, J. L., and W. M. Brown. 1994. Complete DNA sequence of the mitochondrial genome of the black chiton, Katharina tunicata. Genetics 138:423–443. · DOI
  8. ———. 1995. Complete sequence of the mitochondrial DNA of the annelid worm Lumbricus terrestris. Genetics 141:305–319. · DOI
  9. Borchiellini, C., N. Boury-Esnault, J. Vacelet, and Y. Le Parco. 1998. Phylogenetic analysis of the Hsp70 sequences reveals the monophyly of Metazoa and specific phylogenetic relationships between animals and fungi. Mol. Biol. Evol. 15:647–655. · DOI
  10. Burger, G., I. Plante, K. M. Lonergan, and M. W. Gray. 1995. The mitochondrial DNA of the amoeboid protozoon, Acanthamoeba castellanii: complete sequence, gene content and genome organization. J. Mol. Biol. 245:522–537. · DOI
  11. Burger, G., D. Saint-Louis, M. W. Gray, and B. F. Lang. 1999. Complete sequence of the mitochondrial DNA of the red alga Porphyra purpurea: cyanobacterial introns and shared ancestry of red and green algae. Plant Cell 11:1675–1694. · DOI
  12. Castresana, J., G. Feldmaier-Fuchs, and S. Pääbo. 1998. Codon reassignment and amino acid composition in hemichordate mitochondria. Proc. Natl. Acad. Sci. USA 95:3703–3707. · DOI
  13. Castresana, J., G. Feldmaier-Fuchs, S. Yokobori, N. Satoh, and S. Pääbo. 1998. The mitochondrial genome of the hemichordate Balanoglossus carnosus and the evolution of deuterostome mitochondria. Genetics 150:1115–1123. · DOI
  14. Cavalier-Smith, T. 1993. Kingdom protozoa and its 18 phyla. Microbiol. Rev. 57:953–994. · DOI
  15. Cummings, D. J., K. L. McNally, J. M. Domenico, and E. T. Matsuura. 1990. The complete DNA sequence of the mitochondrial genome of Podospora anserina. Curr. Genet. 17:375–402. · DOI
  16. Dayhoff, M. O., R. M. Schwartz, and B. C. Orcutt. 1978. A model of evolutionary change in proteins. Pp. 345–352 in M. O. Dayhoff, ed. Atlas of protein sequence structure. National Biomedical Research Foundation, Washington, D.C.
  17. Denovan-Wright, E. M., A. M. Nedelcu, and R. W. Lee. 1998. Complete sequence of the mitochondrial DNA of Chlamydomonas eugametos. Plant Mol. Biol. 36:285–295. · DOI
  18. Fernandes, A. P., K. Nelson, and S. M. Beverley. 1993. Evolution of nuclear ribosomal RNAs in kinetoplastid protozoa: perspectives on the age and origins of parasitism. Proc. Natl. Acad. Sci. USA 90:11608–11612. · DOI
  19. Foster, P. G., L. S. Jermiin, and D. A. Hickey. 1997. Nucleotide composition bias affects amino acid content in proteins coded by animal mitochondria. J. Mol. Evol. 44:282–288. · DOI
  20. Gatesy, J., R. DeSalle, and W. Wheeler. 1993. Alignment-ambiguous nucleotide sites and the exclusion of systematic data. Mol. Phylogenet. Evol. 2:152–157. · DOI · Paper page
  21. Goldman, N. 1998. Phylogenetic information and experimental design in molecular systematics. Proc. R. Soc. Lond. B Biol. Sci. 265:1779–1786. · DOI
  22. Gray, M. W., G. Burger, and B. F. Lang. 1999. Mitochondrial evolution. Science 283:1476–1481. · DOI
  23. Greenacre, M. J. 1984. Theory and applications of correspondence analysis. Academic Press, London.
  24. Herrmann, G., A. Schon, R. Brack-Werner, and T. Werner. 1996. CONRAD: a method for identification of variable and conserved regions within proteins by scale-space filtering. Comput. Appl. Biosci. 12:197–203. · DOI
  25. Kishino, H., and M. Hasegawa. 1989. Evaluation of the maximum likelihood estimate of the evolutionary tree topologies from DNA sequence data, and the branching order in hominoidea. J. Mol. Evol. 29:170–179. · DOI · Paper page
  26. Kishino, H., T. Miyata, and M. Hasegawa. 1990. Maximum likelihood inference of protein phylogeny and the origin of chloroplasts. J. Mol. Evol. 31:151–160. · DOI
  27. Kumar, S., and A. Rzhetsky. 1996. Evolutionary relationships of eukaryotic kingdoms. J. Mol. Evol. 42:183–193. · DOI
  28. Leblanc, C., C. Boyen, O. Richard, G. Bonnard, J. M. Grienenberger, and B. Kloareg. 1995. Complete sequence of the mitochondrial DNA of the rhodophyte Chondrus crispus (Gigartinales): gene content and genome organization. J. Mol. Biol. 250:484–495. · DOI
  29. Lewis, D. L., C. L. Farr, and L. S. Kaguni. 1995. Drosophila melanogaster mitochondrial DNA: completion of the nucleotide sequence and evolutionary comparisons. Insect Mol. Biol. 4:263–278. · DOI
  30. Morrison, D. A., and J. T. Ellis. 1997. Effects of nucleotide sequence alignment on phylogeny estimation: a case study of 18S rDNAs of apicomplexa. Mol. Biol. Evol. 14:428–441. · DOI · Paper page
  31. Oda, K., K. Yamato, E. Ohta et al. (11 co-authors). 1992. Gene organization deduced from the complete sequence of liverwort Marchantia polymorpha mitochondrial DNA: a primitive form of plant mitochondrial genome. J. Mol. Biol. 223:1–7. · DOI · Paper page
  32. Ohta, N., N. Sato, and T. Kuroiwa. 1998. Structure and organization of the mitochondrial genome of the unicellular red alga Cyanidioschyzon merolae deduced from the complete nucleotide sequence. Nucleic Acids Res. 26:5190–5298. · DOI
  33. Olsen, G. J., and C. R. Woese. 1993. Ribosomal RNA: a key to phylogeny. FASEB J. 7:113–123. · DOI
  34. Paquin, B., and B. F. Lang. 1996. The mitochondrial DNA of Allomyces macrogynus: the complete genomic sequence from an ancestral fungus. J. Mol. Biol. 255:688–701. · DOI
  35. Pesole, G., M. Attimonelli, G. Preparata, and C. Saccone. 1992. A statistical method for detecting regions with different evolutionary dynamics in multialigned sequences. Mol. Phylogenet. Evol. 1:91–96. · DOI
  36. Philippe, H., and A. Adoutte. 1998. The molecular phylogeny of protozoa: solid facts and uncertainties. Pp. 25–56 in G. H. Coombs, K. Vickerman, M. A. Sleigh, and A. Warren, eds. Evolutionary relationships among protozoa. Kluwer Academic Publishers, Dordrecht, the Netherlands.
  37. Rodrigo, A. G., P. R. Bergquist, and P. L. Bergquist. 1994. Inadequate support for an evolutionary link between the Metazoa and the Fungi. Syst. Biol. 43:578–584. · DOI
  38. Sekito, T., K. Okamoto, H. Kitano, and K. Yoshida. 1995. The complete mitochondrial DNA sequence of Hansenula wingei reveals new characteristics of yeast mitochondria. Curr. Genet. 28:39–53. · DOI
  39. Stoesser, G., M. A. Moseley, J. Sleep, M. McGowran, M. Garcia-Pastor, and P. Sterk. 1998. The EMBL nucleotide sequence database. Nucleic Acids Res. 26:8–15. · DOI
  40. Swofford, D. L., G. J. Olsen, P. J. Waddell, and D. M. Hillis. 1996. Phylogenetic inference. Pp. 407–514 in D. M. Hillis, C. Moritz, and B. K. Mable, eds. Molecular systematics. Sinauer, Sunderland, Mass.
  41. Thioulouse, J., D. Chessel, S. Doledec, and J. M. Olivier. 1997. ADE-4: a multivariate analysis and graphical display software. Stat. Comput. 7:75–83. · DOI · Paper page
  42. Thompson, J. D., T. J. Gibson, F. Plewniak, F. Jeanmougin, and D. G. Higgins. 1997. The CLUSTAL_X windows interface: flexible strategies for multiple sequence alignment aided by quality analysis tools. Nucleic Acids Res. 25:4876–4882. · DOI · Paper page
  43. Thompson, J. D., D. G. Higgins, and T. J. Gibson. 1994. CLUSTAL W: improving the sensitivity of progressive multiple sequence alignment through sequence weighting, position-specific gap penalties and weight matrix choice. Nucleic Acids Res. 22:4673–4680. · DOI · Paper page
  44. Turmel, M., C. Lemieux, G. Burger, B. F. Lang, C. Otis, I. Plante, and M. W. Gray. 1999. The complete mitochondrial DNA sequences of Nephroselmis olivacea and Pedinomonas minor: two radically different evolutionary patterns within green algae. Plant Cell 11:1717–1730. · DOI
  45. Unseld, M., J. R. Marienfeld, P. Brandt, and A. Brennicke. 1997. The mitochondrial genome of Arabidopsis thaliana contains 57 genes in 366,924 nucleotides. Nat. Genet. 15:57–61. · DOI · Paper page
  46. Veuthey, A. L., and G. Bittar. 1998. Phylogenetic relationships of Fungi, Plantae, and Animalia inferred from homologous comparison of ribosomal proteins. J. Mol. Evol. 47:81–92. · DOI
  47. Wainright, P. O., G. Hinkle, M. L. Sogin, and S. K. Stickel. 1993. Monophyletic origins of the metazoa: an evolutionary link with fungi. Science 260:340–342. · DOI · Paper page
  48. Wheeler, W. C., J. Gatesy, and R. DeSalle. 1995. Elision: a method for accommodating multiple molecular sequence alignments with alignment-ambiguous sites. Mol. Phylogenet. Evol. 4:1–9. · DOI
  49. Wolff, G., I. Plante, B. F. Lang, U. Kuck, and G. Burger. 1994. Complete sequence of the mitochondrial DNA of the chlorophyte alga Prototheca wickerhamii: gene content and genome organization. J. Mol. Biol. 237:75–86. · DOI
  50. Yagi, T. 1993. The bacterial energy-transducing NADH-quinone oxidoreductases. Biochim. Biophys. Acta 1141:1–17. · DOI
  51. Yang, D., Y. Oyaizu, H. Oyaizu, G. J. Olsen, and C. R. Woese. 1985. Mitochondrial origins. Proc. Natl. Acad. Sci. USA 82:4443–4447. · DOI
  52. Yang, Z. 1998. On the best evolutionary rate for phylogenetic analysis. Syst. Biol. 47:125–133. · DOI · Paper page

Cited by

Metadata

Authors
Castresana, J.
Venue
Molecular Biology and Evolution
Published
2000-04-01
Volume
17
Issue
4
Pages
540-552
ISSN
  • 0737-4038 (ISSN-L)
  • 1537-1719
OpenAlex
W1963957860
Cited by
10,508
References
2
FWCI
6.65
Type
journal article
Language
en
Open access
bronze

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