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Inferring the Pattern of Spontaneous Mutation from the Pattern of Substitution in Unitary Pseudogenes of Mycobacterium leprae and a Comparison of Mutation Patterns Among Distantly Related Organisms

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Abstract

The pattern of spontaneous mutation can be inferred from the pattern of substitution in pseudogenes, which are known to be under very weak or no selective constraint. We modified an existing method (Gojobori T, et al., J Mol Evol 18:360, 1982) to infer the pattern of mutation in bacteria by using 569 pseudogenes from Mycobacterium leprae. In Gojobori et al.’s method, the pattern is inferred by using comparisons involving a pseudogene, a conspecific functional paralog, and an outgroup functional ortholog. Because pseudogenes in M. leprae are unitary, we replaced the missing paralogs by functional orthologs from M. tuberculosis. Functional orthologs from Streptomyces coelicolor served as outgroups. We compiled a database consisting of 69,378 inferred mutations. Transitional mutations were found to constitute more than 56% of all mutations. The transitional bias was mainly due to C→T and G→A, which were also the most frequent mutations on the leading strand and the only ones that were significantly more frequent than the random expectation. The least frequent mutations on the leading strand were A→T and T→A, each with a relative frequency of less than 3%. The mutation pattern was found to differ between the leading and the lagging strands. This asymmetry is thought to be the cause for the typical chirochoric structure of bacterial genomes. The physical distance of the pseudogene from the origin of replication (ori) was found to have almost no effect on the pattern of mutation. A surprising similarity was found between the mutation pattern in M. leprae and previously inferred patterns for such distant taxa as human and Drosophila. The mutation pattern on the leading strand of M. leprae was also found to share some common features with the pattern inferred for the heavy strand of the human mitochondrial genome. These findings indicate that taxon-specific factors may only play secondary roles in determining patterns of mutation.

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References

  • Altschul SF, Gish W, Miller W, Myers EW, Lipman DJ (1990) Basic local alignment search tool. J Mol Biol 215:403–410

    Article  PubMed  CAS  Google Scholar 

  • Andersson JO, Andersson SGE, (1999) Genome degradation is an ongoing process in Rickettsia. Mol Biol Evol 16:1178–1191

    PubMed  CAS  Google Scholar 

  • Brown JR, Douady CJ, Italia MJ, Marshall WE, Stanhope MJ (2001) Universal trees based on large combined protein sequence data sets. Nature Genet 28:281–285

    Article  PubMed  CAS  Google Scholar 

  • Bulmer M. (1991) Strand symmetry of mutation rates in the b-globin region. J Mol Evol 33:305–310

    Article  PubMed  CAS  Google Scholar 

  • Clayton DA (1982) Replication of animal mitochondrial DNA. Cell 28:693–705

    Article  PubMed  CAS  Google Scholar 

  • Cole ST, Brosch R, Parkhill J, et al. (1998) Deciphering the biology of Mycobacterium tuberculosis from the complete genome sequence. Nature 393:537–544

    PubMed  CAS  Google Scholar 

  • de Miranda AB, Alvarex-Valin F, Jabbari K, Degrave WM, Bernardi G (2000) Gene expression, amino acid conservation, and hydrophobicity are the main factors shaping codon preferences in Mycobacterium tuberculosis and Mycobacterium leprae. J Mol Evol 50:45–55

    PubMed  Google Scholar 

  • EyreWalker A (1997) Problems with parsimony in sequences of biased base composition. J Mol Evol 47:686–690

    Google Scholar 

  • Forsdyke DR (1995) Relative roles of primary sequence and (G+C)% in determining the hierarchy of frequencies of complementary trinucleotide pairs in DNAs of different species. J Mol Evol 41:573–581

    PubMed  CAS  Google Scholar 

  • Francino MP, Chao L, Riley MA, Ochman H (1996) Asymmetries generated by transcription-coupled repair in enterobacterial genes. Science 272:107–109

    PubMed  CAS  Google Scholar 

  • Cole ST, Eiglmeier K, Parkhill J, et al. (2001) Massive gene decay in the leprosy bacillus. Nature 409:1007–1011

    Article  PubMed  CAS  Google Scholar 

  • Frank AC, Lobry JR (2000) ORILOC: Prediction of replication boundaries in unannotated bacterial chromosomes. Bioinformatics 16:560–561

    Article  PubMed  CAS  Google Scholar 

  • Galtier N, Lobry JR (1997) Relationships between genomic G+C content, RNA secondary structures, and optimal growth temperature in prokaryotes. J Mol Evol 44:632–636

    PubMed  CAS  Google Scholar 

  • Galtier N, Piganeau G, Mouchiroud D, Duret L, (2001) GC-content evolution in mammalian genomes: The biased gene conversion hypothesis. Genetics 159:907–911

    PubMed  CAS  Google Scholar 

  • Gojobori T, Li WH, Graur D (1982) Patterns of nucleotide substitution in pseudogenes and functional genes. J Mol Evol 18:360–369

    PubMed  CAS  Google Scholar 

  • Graur D, Li WH (2000) Fundamentals of molecular evolution. Sinauer Associates, Sunderland, MA

    Google Scholar 

  • Hoppe FM (ed) (1993) Multiple comparisons, selections and applications in biometry. Marcel Dekker, New York

    Google Scholar 

  • Kreutzer DA, Essigmann JM (1998) Oxidized, deaminated cytosines are a source of C transitions in vivo. Proc Natl Acad Sci USA 95:3578–3582

    Article  PubMed  CAS  Google Scholar 

  • Lawrence JG, Hendrix RW, Casjens S (2001) Where are the pseudogenes in bacterial genomes? Trends Microbiol 9:535–540

    Article  PubMed  CAS  Google Scholar 

  • Li WH, Wu CI, Luo CC (1984) Nonrandomness of point mutation as reflected in nucleotide substitutions in pseudogenes and its evolutionary implications. J Mol Evol 21:58–71

    Article  PubMed  CAS  Google Scholar 

  • Lindahl T (1993) Instability and decay of the primary structure of DNA. Nature 362:709–715

    Article  PubMed  CAS  Google Scholar 

  • Liu Y, Harrison PM, Kunin V, GersteinM (2004) Comprehensive analysis of pseudogenes in prokaryotes: Widespread gene decay and failure of putative horizontally transferred genes. Genome Biol 5:R64

    Article  PubMed  Google Scholar 

  • Lobry JR (1996) Asymmetric substitution patterns in the two DNA strands of bacteria. Mol Biol Evol 13:660–665

    PubMed  CAS  Google Scholar 

  • Mira A, Ochman H (2002) Gene location and bacterial sequence divergence. Mol Evol 19:1350–1358

    CAS  Google Scholar 

  • Morton BR, Clegg MT (1993) A chloroplast DNA mutational hotspot and gene conversion in a noncoding region near rbcL in the grass family (Poaceae). Curr Genet 24:357–365

    Article  PubMed  CAS  Google Scholar 

  • Ochman H (2003) Neutral substitutions in bacterial genomes. Mol Biol Evol 20:2091–2096

    PubMed  CAS  Google Scholar 

  • Parkhill JM, Sebaihia A, Preston LD, et al. (2003) Comparative analysis of the genome sequences of Bordetella pertussis, Bordetella parapertussis and Bordetella bronchiseptica. Nature Genet 35:32–40

    Article  PubMed  Google Scholar 

  • Petrov DA, Hartl DL (1999) Patterns of nucleotide substitution in Drosophila and mammalian genomes. Proc Natl Acad Sci USA 96:1475–1479

    Article  PubMed  CAS  Google Scholar 

  • Razin A, Riggs AD (1980) DNA methylation and gene-function. Science 210:604–610

    PubMed  CAS  Google Scholar 

  • Rocha EPC, Danchin A (2001) Ongoing evolution of strand composition in bacterial genomes. Mol Biol Evol 18:1789–1799

    PubMed  CAS  Google Scholar 

  • Rocha EPC, Danchin A Viari A (1999) Universal replication biases in bacteria. Mol Microbiol 32:11–16

    Article  PubMed  CAS  Google Scholar 

  • Salazar L, Fsihi H, deRossi E, Riccardi G, Rios C, Cole ST, Takiff HE (1996) Organization of the origins of replication of the chromosomes of Mycobacterium smegmatis, Mycobactenum leprae and Mycobacterium tuberculosis and isolation of a functional origin from M. smeginatis. Mol Microbiol 20:283–293

    PubMed  CAS  Google Scholar 

  • Sharp PM, Shields DC, Wolfe KH, Li WH (1989) chromosomal location and evolutionary rate variation in enterobacterial Genes. Science 246:808–810

    PubMed  CAS  Google Scholar 

  • Sueoka N (2003) Intrastrand parity rules of DNA base composition and usage biases of synonymous codons. J Mol Evol 40:318–325

    Google Scholar 

  • Tajima F, Nei M (1982) Biases of the estimation of DNA divergence obtained by the restriction enzyme technique. Mol Biol Evol 18:115–120

    CAS  Google Scholar 

  • Tamura F, Nei M (1993) Estimation of the number of nucleotide substitutions in the control region of mitochondrial-DNA in humans and chimpanzees. Mol Biol Evol 10:512–526

    PubMed  CAS  Google Scholar 

  • Tanaka M, Ozawa T (1994) Strand asymmetry in human mitochondrial-DNA mutations. Genomics 22:327–335

    Article  PubMed  CAS  Google Scholar 

  • Thompson JD, Higgins DG, Gibson TJ (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

    PubMed  CAS  Google Scholar 

  • Zar JH (1999) Biostatisticial analysis. Prentice–Hall, Upper Saddle River, NJ

    Google Scholar 

Download references

Acknowledgments

This study was supported in part by a grant from the Israel Science Foundation.

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Correspondence to Dan Graur.

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[Reviewing Editor:Dr. Dmitri Petrov]

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Mitchell, A., Graur, D. Inferring the Pattern of Spontaneous Mutation from the Pattern of Substitution in Unitary Pseudogenes of Mycobacterium leprae and a Comparison of Mutation Patterns Among Distantly Related Organisms. J Mol Evol 61, 795–803 (2005). https://doi.org/10.1007/s00239-004-0235-0

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