Literature DB >> 181584

The molecular evolution of cytochrome c in eukaryotes.

W M Fitch.   

Abstract

Using many more cytochrome sequences than previously available, we have confirmed: 1, the eukaryotic cytochrome c diverged from a common ancestor; 2, the ancestral eukaryotic cytochrome c was not greatly different in character from those present today; 3, fixations are non-randomly distributed among the codons, there being evidence for at least four classes of variability; 4, there are similar classes of variability when the data are considered according to the nucleotide position within the codon; 5, the number of covarions (concomitantly variable codons) in mammalian cytochrome c genes is about 12 and the same value has been obtained for dicotyledenous plants as well; 6, all of the hyper- and most highly variable codons are for external residues, nearly 60 per cent of the invariable codons are for internal residues and nearly half of the codons for internal residues are invariable; 7, the first nucleotide position of a codon is more likely and the second position less likely to fix mutations than would be expected on the basis of the number of ways that alternative amino acids can be reached; 8, the character of nucleotide replacements is enormously non-random, with G-A interchanges representing 42% of those observed in the first nucleotide position, but the observation does not stem from a bias in the DNA strand receiving the mutation, nor from the presence of a compositional equilibrium, nor from a bias in the frequency with which different nucleotides mutate, but rather from a bias in the acceptability of an alternative nucleotide as circumscribed by the functional acceptability of the new amino acid encoded; and 9, the unit evolutionary period is approximately 150 million years/observable (amino acid changing) nucleotide replacement/cytochrome c covarion in two diverging lines. Wherever non-randomness has been observed, it has always been consistent with the consideration that an alternative amino acid at any location is more likely to be acceptable the more closely it resembles the present amino acid in its physico-chemical properties. Finally, in no case did the a priori assumption of a biologically realistic phylogeny lead to any observations or conclusions that were in any way significantly different from those obtained when the phylogeny was based solely upon the sequences, proving that the earlier results were not a consequence of some internal circularity.

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Year:  1976        PMID: 181584     DOI: 10.1007/bf01738880

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


  69 in total

1.  The amino acid sequence of a cytochrome c from a protozoan Crithidia oncopelti.

Authors:  G W. Pettigrew
Journal:  FEBS Lett       Date:  1972-04-15       Impact factor: 4.124

2.  HUMAN HEART CYTOCHROME C. CHYMOTRYPTIC PEPTIDES, TRYPTIC PEPTIDES, AND THE COMPLETE AMINO ACID SEQUENCE.

Authors:  H MATSUBARA; E L SMITH
Journal:  J Biol Chem       Date:  1963-08       Impact factor: 5.157

Review 3.  Mutational pressure as the main cause of molecular evolution and polymorphism.

Authors:  T Ota
Journal:  Nature       Date:  1974-11-29       Impact factor: 49.962

4.  The amino acid sequence of cytochrome c from Debaryomyces kloeckeri.

Authors:  K Sugeno; K Narita; K Titani
Journal:  J Biochem       Date:  1971-10       Impact factor: 3.387

5.  Distinguishing homologous from analogous proteins.

Authors:  W M Fitch
Journal:  Syst Zool       Date:  1970-06

Review 6.  Construction of phylogenetic trees.

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

7.  Amino acid sequence of dog heart cytochrome c.

Authors:  M A McDowall; E L Smith
Journal:  J Biol Chem       Date:  1965-12       Impact factor: 5.157

8.  Properties and primary structure of the cytochrome c from the flight muscles of the moth, Samia cynthia.

Authors:  S K Chan; E Margoliash
Journal:  J Biol Chem       Date:  1966-01-25       Impact factor: 5.157

9.  Amino acid sequence of the cytochrome c from the dogfish, Squalus sucklii.

Authors:  A Goldstone; E L Smith
Journal:  J Biol Chem       Date:  1967-10-25       Impact factor: 5.157

10.  Primary structure of the cytochrome c from the snapping turtle, Chelydra serpentina.

Authors:  S K Chan; I Tulloss; E Margoliash
Journal:  Biochemistry       Date:  1966-08       Impact factor: 3.162

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  35 in total

Review 1.  Genomic biodiversity, phylogenetics and coevolution in proteins.

Authors:  David D Pollock
Journal:  Appl Bioinformatics       Date:  2002

2.  The covarion model for the evolution of proteins: parameter estimates and comparison with Holmquist, Cantor, and Jukes' stochastic model.

Authors:  J M Karon
Journal:  J Mol Evol       Date:  1979-03-15       Impact factor: 2.395

3.  Advances in Time Estimation Methods for Molecular Data.

Authors:  Sudhir Kumar; S Blair Hedges
Journal:  Mol Biol Evol       Date:  2016-02-16       Impact factor: 16.240

4.  Classification of methanogenic bacteria by 16S ribosomal RNA characterization.

Authors:  G E Fox; L J Magrum; W E Balch; R S Wolfe; C R Woese
Journal:  Proc Natl Acad Sci U S A       Date:  1977-10       Impact factor: 11.205

5.  A mixed branch length model of heterotachy improves phylogenetic accuracy.

Authors:  Bryan Kolaczkowski; Joseph W Thornton
Journal:  Mol Biol Evol       Date:  2008-03-03       Impact factor: 16.240

6.  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

7.  Estimation of DNA sequence divergence from comparison of restriction endonuclease digests.

Authors:  W B Upholt
Journal:  Nucleic Acids Res       Date:  1977       Impact factor: 16.971

8.  Use of Chou-Fasman amino acid conformational parameters to analyze the organization of the genetic code and to construct protein genealogies.

Authors:  M Goodman; G W Moore
Journal:  J Mol Evol       Date:  1977-09-20       Impact factor: 2.395

9.  The molecular evolution of pancreatic ribonuclease.

Authors:  J J Beintema; W Gaastra; J A Lenstra; G W Welling; W M Fitch
Journal:  J Mol Evol       Date:  1977-09-20       Impact factor: 2.395

10.  A view of early cellular evolution.

Authors:  R Mikelsaar
Journal:  J Mol Evol       Date:  1987       Impact factor: 2.395

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