Whole-genome prokaryotic phylogeny.

Stefan R Henz, Daniel H Huson, Alexander F Auch, Kay Nieselt-Struwe, Stephan C Schuster

Center for Bioinformatics Tübingen (ZBIT), Sand 14, Tübingen 72076, Germany.

Journal Article: Bioinformatics (impact factor: 4.93). 06/2005; 21(10):2329-35. DOI: 10.1093/bioinformatics/bth324

Abstract

Current understanding of the phylogeny of prokaryotes is based on the comparison of the highly conserved small ssu-rRNA subunit and similar regions. Although such molecules have proved to be very useful phylogenetic markers, mutational saturation is a problem, due to their restricted lengths. Now, a growing number of complete prokaryotic genomes are available. This paper addresses the problem of determining a prokaryotic phylogeny utilizing the comparison of complete genomes. We introduce a new strategy, GBDP, 'genome blast distance phylogeny', and show that different variants of this approach robustly produce phylogenies that are biologically sound, when applied to 91 prokaryotic genomes. In this approach, first Blast is used to compare genomes, then a distance matrix is computed, and finally a tree- or network-reconstruction method such as UPGMA, Neighbor-Joining, BioNJ or Neighbor-Net is applied.

Source: PubMed

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Keywords

'genome blast distance phylogeny'
 
91 prokaryotic genomes
 
approach robustly
 
biologically sound
 
complete genomes
 
complete prokaryotic genomes
 
conserved small ssu-rRNA subunit
 
Current understanding
 
first Blast
 
genomes
 
growing number
 
mutational saturation
 
Neighbor-Joining
 
Neighbor-Net
 
network-reconstruction method
 
new strategy
 
prokaryotic phylogeny utilizing
 
restricted lengths
 
UPGMA
 
useful phylogenetic markers