Literature DB >> 10430917

Genome signature comparisons among prokaryote, plasmid, and mitochondrial DNA.

A Campbell1, J Mrázek, S Karlin.   

Abstract

Our basic observation is that each genome has a characteristic "signature" defined as the ratios between the observed dinucleotide frequencies and the frequencies expected if neighbors were chosen at random (dinucleotide relative abundances). The remarkable fact is that the signature is relatively constant throughout the genome; i.e. , the patterns and levels of dinucleotide relative abundances of every 50-kb segment of the genome are about the same. Comparison of the signatures of different genomes provides a measure of similarity which has the advantage that it looks at all the DNA of an organism and does not depend on the ability to align homologous sequences of specific genes. Genome signature comparisons show that plasmids, both specialized and broad-range, and their hosts have substantially compatible (similar) genome signatures. Mammalian mitochondrial (Mt) genomes are very similar, and animal and fungal Mt are generally moderately similar, but they diverge significantly from plant and protist Mt sets. Moreover, Mt genome signature differences between species parallel the corresponding nuclear genome signature differences, despite large differences between Mt and host nuclear signatures. In signature terms, we find that the archaea are not a coherent clade. For example, Sulfolobus and Halobacterium are extremely divergent. There is no consistent pattern of signature differences among thermophiles. More generally, grouping prokaryotes by environmental criteria (e.g., habitat propensities, osmolarity tolerance, chemical conditions) reveals no correlations in genome signature.

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Year:  1999        PMID: 10430917      PMCID: PMC17754          DOI: 10.1073/pnas.96.16.9184

Source DB:  PubMed          Journal:  Proc Natl Acad Sci U S A        ISSN: 0027-8424            Impact factor:   11.205


  23 in total

1.  A chimeric prokaryotic ancestry of mitochondria and primitive eukaryotes.

Authors:  S Karlin; L Brocchieri; J Mrázek; A M Campbell; A M Spormann
Journal:  Proc Natl Acad Sci U S A       Date:  1999-08-03       Impact factor: 11.205

Review 2.  Global dinucleotide signatures and analysis of genomic heterogeneity.

Authors:  S Karlin
Journal:  Curr Opin Microbiol       Date:  1998-10       Impact factor: 7.934

3.  Enzymatic synthesis of deoxyribonucleic acid. VIII. Frequencies of nearest neighbor base sequences in deoxyribonucleic acid.

Authors:  J JOSSE; A D KAISER; A KORNBERG
Journal:  J Biol Chem       Date:  1961-03       Impact factor: 5.157

4.  New insights into the phylogeny of eukaryotes based on ciliate Hsp70 sequences.

Authors:  K Budin; H Philippe
Journal:  Mol Biol Evol       Date:  1998-08       Impact factor: 16.240

Review 5.  Protein phylogenies and signature sequences: A reappraisal of evolutionary relationships among archaebacteria, eubacteria, and eukaryotes.

Authors:  R S Gupta
Journal:  Microbiol Mol Biol Rev       Date:  1998-12       Impact factor: 11.056

Review 6.  Comparative DNA analysis across diverse genomes.

Authors:  S Karlin; A M Campbell; J Mrázek
Journal:  Annu Rev Genet       Date:  1998       Impact factor: 16.830

Review 7.  Archaea and the prokaryote-to-eukaryote transition.

Authors:  J R Brown; W F Doolittle
Journal:  Microbiol Mol Biol Rev       Date:  1997-12       Impact factor: 11.056

8.  Compositional differences within and between eukaryotic genomes.

Authors:  S Karlin; J Mrázek
Journal:  Proc Natl Acad Sci U S A       Date:  1997-09-16       Impact factor: 11.205

9.  Host range and properties of the Pseudomonas aeruginosa R factor R1822.

Authors:  R H Olsen; P Shipley
Journal:  J Bacteriol       Date:  1973-02       Impact factor: 3.490

10.  Codon usages in different gene classes of the Escherichia coli genome.

Authors:  S Karlin; J Mrázek; A M Campbell
Journal:  Mol Microbiol       Date:  1998-09       Impact factor: 3.501

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  81 in total

1.  Genome-scale compositional comparisons in eukaryotes.

Authors:  A J Gentles; S Karlin
Journal:  Genome Res       Date:  2001-04       Impact factor: 9.043

2.  A chimeric prokaryotic ancestry of mitochondria and primitive eukaryotes.

Authors:  S Karlin; L Brocchieri; J Mrázek; A M Campbell; A M Spormann
Journal:  Proc Natl Acad Sci U S A       Date:  1999-08-03       Impact factor: 11.205

3.  Whole-genome trees based on the occurrence of folds and orthologs: implications for comparing genomes on different levels.

Authors:  J Lin; M Gerstein
Journal:  Genome Res       Date:  2000-06       Impact factor: 9.043

4.  Global analysis of predicted proteomes: functional adaptation of physical properties.

Authors:  Christopher G Knight; Rees Kassen; Holger Hebestreit; Paul B Rainey
Journal:  Proc Natl Acad Sci U S A       Date:  2004-05-18       Impact factor: 11.205

5.  Environmental signatures in proteome properties.

Authors:  Luciano Brocchieri
Journal:  Proc Natl Acad Sci U S A       Date:  2004-05-24       Impact factor: 11.205

6.  Sephardic signature in haplogroup T mitochondrial DNA.

Authors:  Felice L Bedford
Journal:  Eur J Hum Genet       Date:  2011-11-23       Impact factor: 4.246

7.  Tracing common origins of Genomic Islands in prokaryotes based on genome signature analyses.

Authors:  Mark Wj van Passel
Journal:  Mob Genet Elements       Date:  2011-09-01

8.  Normal and compound poisson approximations for pattern occurrences in NGS reads.

Authors:  Zhiyuan Zhai; Gesine Reinert; Kai Song; Michael S Waterman; Yihui Luan; Fengzhu Sun
Journal:  J Comput Biol       Date:  2012-06       Impact factor: 1.479

9.  Predicting plasmid promiscuity based on genomic signature.

Authors:  Haruo Suzuki; Hirokazu Yano; Celeste J Brown; Eva M Top
Journal:  J Bacteriol       Date:  2010-09-17       Impact factor: 3.490

10.  Bacterial DNA uptake sequences can accumulate by molecular drive alone.

Authors:  H Maughan; L A Wilson; R J Redfield
Journal:  Genetics       Date:  2010-07-13       Impact factor: 4.562

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