Inferring clocks when lacking rocks: the variable rates of molecular evolution in bacteria

BackgroundBecause bacteria do not have a robust fossil record, attempts to infer the timing of events in their evolutionary history requires comparisons of molecular sequences. This use of molecular clocks is based on the assumptions that substitution rates for homologous genes or sites are fairly constant through time and across taxa. Violation of these conditions can lead to erroneous inferences and result in estimates that are off by orders of magnitude. In this study, we examine the consistency of substitution rates among a set of conserved genes in diverse bacterial lineages, and address the questions regarding the validity of molecular dating.ResultsBy examining the evolution of 16S rRNA gene in obligate endosymbionts, which can be calibrated by the fossil record of their hosts, we found that the rates are consistent within a clade but varied widely across different bacterial lineages. Genome-wide estimates of nonsynonymous and synonymous substitutions suggest that these two measures are highly variable in their rates across bacterial taxa. Genetic drift plays a fundamental role in determining the accumulation of substitutions in 16S rRNA genes and at nonsynonymous sites. Moreover, divergence estimates based on a set of universally conserved protein-coding genes also exhibit low correspondence to those based on 16S rRNA genes.ConclusionOur results document a wide range of substitution rates across genes and bacterial taxa. This high level of variation cautions against the assumption of a universal molecular clock for inferring divergence times in bacteria. However, by applying relative-rate tests to homologous genes, it is possible to derive reliable local clocks that can be used to calibrate bacterial evolution.ReviewersThis article was reviewed by Adam Eyre-Walker, Simonetta Gribaldo and Tal Pupko (nominated by Dan Graur).

[1]  S. Hedges,et al.  A genomic timescale of prokaryote evolution: insights into the origin of methanogenesis, phototrophy, and the colonization of land , 2004, BMC Evolutionary Biology.

[2]  N. Moran,et al.  Sequence evolution in bacterial endosymbionts having extreme base compositions. , 1999, Molecular biology and evolution.

[3]  M. Bulmer,et al.  Reduced synonymous substitution rate at the start of enterobacterial genes. , 1993, Nucleic acids research.

[4]  Howard Ochman,et al.  Gene location and bacterial sequence divergence. , 2002, Molecular biology and evolution.

[5]  Serap Aksoy,et al.  Concordant Evolution of a Symbiont with Its Host Insect Species: Molecular Phylogeny of Genus Glossina and Its Bacteriome-Associated Endosymbiont, Wigglesworthia glossinidia , 1999, Journal of Molecular Evolution.

[6]  H. Ochman,et al.  Transcription increases multiple spontaneous point mutations in Salmonella enterica. , 2003, Nucleic acids research.

[7]  N. M. Brooke,et al.  A molecular timescale for vertebrate evolution , 1998, Nature.

[8]  S. Hedges,et al.  A major clade of prokaryotes with ancient adaptations to life on land. , 2009, Molecular biology and evolution.

[9]  J. Eisen,et al.  A simple, fast, and accurate method of phylogenomic inference , 2008, Genome Biology.

[10]  N. Moran,et al.  Co‐cladogenesis spanning three phyla: leafhoppers (Insecta: Hemiptera: Cicadellidae) and their dual bacterial symbionts , 2006, Molecular ecology.

[11]  K. Peterson,et al.  Dating the Time of Origin of Major Clades: Molecular Clocks and the Fossil Record , 2002 .

[12]  Mikhail S. Gelfand,et al.  Genome-Wide Molecular Clock and Horizontal Gene Transfer in Bacterial Evolution , 2004, Journal of bacteriology.

[13]  Howard Ochman,et al.  The consequences of genetic drift for bacterial genome complexity. , 2009, Genome research.

[14]  N. Moran,et al.  A molecular clock in endosymbiotic bacteria is calibrated using the insect hosts , 1993, Proceedings of the Royal Society of London. Series B: Biological Sciences.

[15]  D C Shields,et al.  Chromosomal location and evolutionary rate variation in enterobacterial genes. , 1989, Science.

[16]  J. M. Smith,et al.  Synonymous nucleotide divergence: what is "saturation"? , 1996, Genetics.

[17]  B. Snel,et al.  Toward Automatic Reconstruction of a Highly Resolved Tree of Life , 2006, Science.

[18]  N. Moran,et al.  Cospeciation of Psyllids and Their Primary Prokaryotic Endosymbionts , 2000, Applied and Environmental Microbiology.

[19]  Hidemi Watanabe,et al.  A genomic timescale for the origin of eukaryotes , 2001, BMC Evolutionary Biology.

[20]  N. Moran,et al.  Genomics and evolution of heritable bacterial symbionts. , 2008, Annual review of genetics.

[21]  R F Doolittle,et al.  Determining divergence times with a protein clock: update and reevaluation. , 1997, Proceedings of the National Academy of Sciences of the United States of America.

[22]  J. Miller,et al.  A set of lacZ mutations in Escherichia coli that allow rapid detection of each of the six base substitutions. , 1989, Proceedings of the National Academy of Sciences of the United States of America.

[23]  Z. Yang,et al.  Estimating synonymous and nonsynonymous substitution rates under realistic evolutionary models. , 2000, Molecular biology and evolution.

[24]  Paul Baumann,et al.  Faster evolutionary rates in endosymbiotic bacteria than in cospeciating insect hosts , 2004, Journal of Molecular Evolution.

[25]  N. Moran,et al.  Calibrating bacterial evolution. , 1999, Proceedings of the National Academy of Sciences of the United States of America.

[26]  Richard E. Lenski,et al.  Rates of DNA Sequence Evolution in Experimental Populations of Escherichia coli During 20,000 Generations , 2003, Journal of Molecular Evolution.

[27]  Ziheng Yang PAML 4: phylogenetic analysis by maximum likelihood. , 2007, Molecular biology and evolution.

[28]  David L. Wheeler,et al.  GenBank , 2015, Nucleic Acids Res..

[29]  M. Sanderson,et al.  ABSOLUTE DIVERSIFICATION RATES IN ANGIOSPERM CLADES , 2001, Evolution; international journal of organic evolution.

[30]  Erko Stackebrandt,et al.  Taxonomic Note: A Place for DNA-DNA Reassociation and 16S rRNA Sequence Analysis in the Present Species Definition in Bacteriology , 1994 .

[31]  C. Stoeckert,et al.  OrthoMCL: identification of ortholog groups for eukaryotic genomes. , 2003, Genome research.

[32]  Inna Dubchak,et al.  Trends in Prokaryotic Evolution Revealed by Comparison of Closely Related Bacterial and Archaeal Genomes , 2008, Journal of bacteriology.

[33]  A. Wilson,et al.  Generation time and genomic evolution in primates. , 1973, Science.

[34]  N. Gerardo,et al.  Symbiosis and Insect Diversification: an Ancient Symbiont of Sap-Feeding Insects from the Bacterial Phylum Bacteroidetes , 2005, Applied and Environmental Microbiology.

[35]  David Tollervey,et al.  Coding-Sequence Determinants of Gene Expression in Escherichia coli , 2009, Science.

[36]  Wen-Hsiung Li,et al.  The rate of synonymous substitution in enterobacterial genes is inversely related to codon usage bias. , 1987, Molecular biology and evolution.

[37]  Peer Bork,et al.  PAL2NAL: robust conversion of protein sequence alignments into the corresponding codon alignments , 2006, Nucleic Acids Res..

[38]  Valeria Souza,et al.  Stress-Induced Mutagenesis in Bacteria , 2003, Science.

[39]  Michael D. Hendy,et al.  The Power of Relative Rates Tests Depends on the Data , 2000, Journal of Molecular Evolution.

[40]  Chad D. Brock,et al.  Host-symbiont stability and fast evolutionary rates in an ant-bacterium association: cospeciation of camponotus species and their endosymbionts, candidatus blochmannia. , 2004, Systematic biology.

[41]  N. Moran,et al.  Intracellular symbionts of sharpshooters (Insecta: Hemiptera: Cicadellinae) form a distinct clade with a small genome. , 2003, Environmental microbiology.

[42]  James R. Cole,et al.  The Ribosomal Database Project (RDP-II): previewing a new autoaligner that allows regular updates and the new prokaryotic taxonomy , 2003, Nucleic Acids Res..

[43]  C. Bandi,et al.  Evidence for cocladogenesis between diverse dictyopteran lineages and their intracellular endosymbionts. , 2003, Molecular biology and evolution.

[44]  Robert C. Edgar,et al.  MUSCLE: multiple sequence alignment with high accuracy and high throughput. , 2004, Nucleic acids research.

[45]  E. Myers,et al.  Basic local alignment search tool. , 1990, Journal of molecular biology.

[46]  Anu Raghunathan,et al.  Comparative genome sequencing of Escherichia coli allows observation of bacterial evolution on a laboratory timescale , 2006, Nature Genetics.

[47]  Geoffrey E. Morse,et al.  Phylogenetic congruence of armored scale insects (Hemiptera: Diaspididae) and their primary endosymbionts from the phylum Bacteroidetes. , 2007, Molecular phylogenetics and evolution.

[48]  N. Moran,et al.  The eubacterial endosymbionts of whiteflies (homoptera: Aleyrodoidea) constitute a lineage distinct from the endosymbionts of aphids and mealybugs , 1992, Current Microbiology.

[49]  H. Ochman,et al.  Evolution in bacteria: Evidence for a universal substitution rate in cellular genomes , 1987, Journal of Molecular Evolution.

[50]  Matthew R. Pocock,et al.  The Bioperl toolkit: Perl modules for the life sciences. , 2002, Genome research.

[51]  W. Li,et al.  Evidence for higher rates of nucleotide substitution in rodents than in man. , 1985, Proceedings of the National Academy of Sciences of the United States of America.

[52]  O. Berg Synonymous Nucleotide Divergence and Saturation: Effects of Site-Specific Variations in Codon Bias and Mutation Rates , 1999, Journal of Molecular Evolution.

[53]  Howard Ochman,et al.  Neutral mutations and neutral substitutions in bacterial genomes. , 2003, Molecular biology and evolution.