Literature DB >> 1177324

Phylogenies from amino acid sequences aligned with gaps: the problem of gap weighting.

W M Fitch, K T Yasunobu.   

Abstract

The common but generally overlooked problem of how best to construct phylogenies from orthologous amino acid sequences, when their alignment requires the placement therein of gaps denoting insertions/deletions in the evolutionary history of their genes since their common ancestor, has been studied. Three diverse methods were examined: 1. each missing residue in a gap is weighted as equivalent to the average number of minimum nucleotide replacements in known conjugate amino acid pairs of those same two sequences, which weight necessarily differs for each pair of sequences; 2. each missing residue in a gap is weighted as equivalent to a fixed number of nucleotide replacements; and 3. each gap, regardless of length, is weighted as equivalent to a fixed number of nucleotide replacements. For the flavodoxins, each method yielded a different best tree and suggests that the choice of method may be crucial. For the plant ferredoxins, all methods give results inconsistent with botanical classification and suggests the sequences may not all be orthologous. For the bacterial ferredoxins, the method was less germane than the actual weight used, five different best trees being obtained depending upon the weight. The best tree for all ferredoxins (prokaryotic plus eukaryotic) combined proved to be greatly dependent upon the gap locations with several reasonable aligments yielding different best trees. They also suggest that functional equivalence may well prove to be a poor guide to which residues have a common ancestral codon. The rubredoxin sequences show that a partial internal gene duplication occurred in the Pseudomonas line, probably very soon after its divergence from the other genera. Together, the results clearly indicate that the phylogenetic answer one gets may greatly depend upon how one treats the gaps but they fail to indicate what treatment may be best.

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Year:  1975        PMID: 1177324     DOI: 10.1007/bf01732010

Source DB:  PubMed          Journal:  J Mol Evol        ISSN: 0022-2844            Impact factor:   2.395


  38 in total

1.  Evolution of the structure of ferredoxin based on living relics of primitive amino Acid sequences.

Authors:  R V Eck; M O Dayhoff
Journal:  Science       Date:  1966-04-15       Impact factor: 47.728

2.  Amino acid sequence determination of the Clostridium M-E ferredoxin and a comment on the role of the aromatic residues in the clostridial ferredoxins.

Authors:  M Tanaka; M Haniu; K T Yasunobu; J B Jones; T C Stadtman
Journal:  Biochemistry       Date:  1974-12-17       Impact factor: 3.162

3.  A method for constructing maximum parsimony ancestral amino acid sequences on a given network.

Authors:  G W Moore; J Barnabas; M Goodman
Journal:  J Theor Biol       Date:  1973-03       Impact factor: 2.691

4.  Structural and evolutionary relationships of ferredoxins.

Authors:  H Matsubara; T H Jukes; C R Cantor
Journal:  Brookhaven Symp Biol       Date:  1968-06

Review 5.  Construction of phylogenetic trees.

Authors:  W M Fitch; E Margoliash
Journal:  Science       Date:  1967-01-20       Impact factor: 47.728

6.  Evolutionary and phylogenetic relationships of rubredoxin-containing microbes.

Authors:  A Benson; K Tomoda; J Chang; G Matsueda; E T Lode; M J Coon; K T Yasunobu
Journal:  Biochem Biophys Res Commun       Date:  1971-02-19       Impact factor: 3.575

7.  The amino acid sequence of ferredoxin from Clostridium acidi-urici.

Authors:  S C Rall; R E Bolinger; R D Cole
Journal:  Biochemistry       Date:  1969-06       Impact factor: 3.162

8.  Horsetail ferredoxin: isolation and some chemical studies.

Authors:  S J Aggarwal; K K Rao; H Matsubara
Journal:  J Biochem       Date:  1971-03       Impact factor: 3.387

9.  Multiple genes for lysozyme in birds.

Authors:  N Arnheim; R Steller
Journal:  Arch Biochem Biophys       Date:  1970-12       Impact factor: 4.013

10.  The amino acid sequence of ferredoxin from the sulfate reducing bacterium, Desulfovibrio gigas.

Authors:  J Travis; D J Newman; J LeGall; H D Peck
Journal:  Biochem Biophys Res Commun       Date:  1971-10-15       Impact factor: 3.575

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  7 in total

1.  Evolutionary change in invertebrate cytochrome C.

Authors:  A Lyddiatt; D Peacock; D Boulter
Journal:  J Mol Evol       Date:  1978-05-12       Impact factor: 2.395

2.  Comparative studies on two ferredoxins from the cyanobacterium Nostoc strain MAC.

Authors:  K G Hutson; L J Rogers; B G Haslett; D Boulter; R Cammack
Journal:  Biochem J       Date:  1978-06-15       Impact factor: 3.857

3.  On the evolution of beta-galactosidase.

Authors:  J M Hood; A V Fowler; I Zabin
Journal:  Proc Natl Acad Sci U S A       Date:  1978-01       Impact factor: 11.205

4.  The alignment of sets of sequences and the construction of phyletic trees: an integrated method.

Authors:  P Hogeweg; B Hesper
Journal:  J Mol Evol       Date:  1984       Impact factor: 2.395

5.  Comparative biosequence metrics.

Authors:  T F Smith; M S Waterman; W M Fitch
Journal:  J Mol Evol       Date:  1981       Impact factor: 2.395

6.  The possible evolutionary significance of repeat elements near and within an early chorion gene in the late chorion locus of Bombyx mori.

Authors:  G C Rodakis; R Lecanidou
Journal:  J Mol Evol       Date:  1992-04       Impact factor: 2.395

7.  Ferredoxin and formyltetrahydrofolate synthetase: comparative studies with Clostridium acidiurici, Clostridium cylindrosporum, and newly isolated anaerobic uric acid-fermenting strains.

Authors:  A B Champion; J C Rabinowitz
Journal:  J Bacteriol       Date:  1977-12       Impact factor: 3.490

  7 in total

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