Literature DB >> 8876205

Molecular clock or erratic evolution? A tale of two genes.

F J Ayala1, E Barrio, J Kwiatowski.   

Abstract

We have investigated the evolution of glycerol-3-phosphate dehydrogenase (Gpdh). The rate of amino acid replacements is 1 x 10(-10)/site/year when Drosophila species are compared. The rate is 2.7 times greater when Drosophila and Chymomyza species are compared; and about 5 times greater when any of those species are compared with the medfly Ceratitis capitata. This rate of 5 x 10(-10)/site/year is also the rate observed in comparisons between mammals, or between different animal phyla, or between the three multicellular kingdoms. We have also studied the evolution of Cu,Zn superoxide dismutase (Sod). The rate of amino acid replacements is about 17 x 10(-10)/site/year when comparisons are made between dipterans or between mammals, but only 5 x 10(-10) when animal phyla are compared, and only 3 x 10(-10) when the multicellular kingdoms are compared. The apparent decrease by about a factor of 5 in the rate of SOD evolution as the divergence between species increases can be consistent with the molecular clock hypothesis by assuming the covarion hypothesis (namely, that the number of amino acids that can change is constant, but the set of such amino acids changes from time to time and from lineage to lineage). However, we know of no model consistent with the molecular clock hypothesis that would account for the increase in the rate of GPDH evolution as the divergence between species increases.

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Year:  1996        PMID: 8876205      PMCID: PMC38126          DOI: 10.1073/pnas.93.21.11729

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


  14 in total

1.  Role of very slightly deleterious mutations in molecular evolution and polymorphism.

Authors:  T Ohta
Journal:  Theor Popul Biol       Date:  1976-12       Impact factor: 1.570

2.  Rates of nucleotide substitution in primates and rodents and the generation-time effect hypothesis.

Authors:  W H Li; D L Ellsworth; J Krushkal; B H Chang; D Hewett-Emmett
Journal:  Mol Phylogenet Evol       Date:  1996-02       Impact factor: 4.286

3.  On the virtues and pitfalls of the molecular evolutionary clock.

Authors:  F J Ayala
Journal:  J Hered       Date:  1986 Jul-Aug       Impact factor: 2.645

4.  Evolutionary rate at the molecular level.

Authors:  M Kimura
Journal:  Nature       Date:  1968-02-17       Impact factor: 49.962

5.  A simple method for estimating evolutionary rates of base substitutions through comparative studies of nucleotide sequences.

Authors:  M Kimura
Journal:  J Mol Evol       Date:  1980-12       Impact factor: 2.395

Review 6.  Biochemical evolution.

Authors:  A C Wilson; S S Carlson; T J White
Journal:  Annu Rev Biochem       Date:  1977       Impact factor: 23.643

7.  Structural characterization of the alpha-glycerol-3-phosphate dehydrogenase-encoding gene of Drosophila melanogaster.

Authors:  L von Kalm; J Weaver; J DeMarco; R J MacIntyre; D T Sullivan
Journal:  Proc Natl Acad Sci U S A       Date:  1989-07       Impact factor: 11.205

8.  Phylogeny of Drosophila and related genera inferred from the nucleotide sequence of the Cu,Zn Sod gene.

Authors:  J Kwiatowski; D Skarecky; K Bailey; F J Ayala
Journal:  J Mol Evol       Date:  1994-05       Impact factor: 2.395

9.  The superoxide dismutase molecular clock revisited.

Authors:  W M Fitch; F J Ayala
Journal:  Proc Natl Acad Sci U S A       Date:  1994-07-19       Impact factor: 11.205

10.  Drosophila sn-glycerol-3-phosphate dehydrogenase isozymes are generated by alternate pathways of RNA processing resulting in different carboxyl-terminal amino acid sequences.

Authors:  J L Cook; G C Bewley; J B Shaffer
Journal:  J Biol Chem       Date:  1988-08-05       Impact factor: 5.157

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  8 in total

1.  Vagaries of the molecular clock.

Authors:  F J Ayala
Journal:  Proc Natl Acad Sci U S A       Date:  1997-07-22       Impact factor: 11.205

2.  IS6110 transposition and evolutionary scenario of the direct repeat locus in a group of closely related Mycobacterium tuberculosis strains.

Authors:  Z Fang; N Morrison; B Watt; C Doig; K J Forbes
Journal:  J Bacteriol       Date:  1998-04       Impact factor: 3.490

3.  Origin of the metazoan phyla: molecular clocks confirm paleontological estimates.

Authors:  F J Ayala; A Rzhetsky; F J Ayala
Journal:  Proc Natl Acad Sci U S A       Date:  1998-01-20       Impact factor: 11.205

4.  Erratic overdispersion of three molecular clocks: GPDH, SOD, and XDH.

Authors:  F Rodríguez-Trelles; R Tarrío; F J Ayala
Journal:  Proc Natl Acad Sci U S A       Date:  2001-09-11       Impact factor: 11.205

5.  A highly conserved sequence in the 3'-untranslated region of the drosophila Adh gene plays a functional role in Adh expression.

Authors:  J Parsch; W Stephan; S Tanda
Journal:  Genetics       Date:  1999-02       Impact factor: 4.562

6.  Sniffing out chemosensory genes from the Mediterranean fruit fly, Ceratitis capitata.

Authors:  Paolo Siciliano; Francesca Scolari; Ludvik M Gomulski; Marco Falchetto; Mosè Manni; Paolo Gabrieli; Linda M Field; Jing-Jiang Zhou; Giuliano Gasperi; Anna R Malacrida
Journal:  PLoS One       Date:  2014-01-08       Impact factor: 3.240

7.  Copper/Zinc Superoxide Dismutase from the Crocodile Icefish Chionodraco hamatus: Antioxidant Defense at Constant Sub-Zero Temperature.

Authors:  Evangelia Chatzidimitriou; Paola Bisaccia; Francesca Corrà; Marco Bonato; Paola Irato; Laura Manuto; Stefano Toppo; Rigers Bakiu; Gianfranco Santovito
Journal:  Antioxidants (Basel)       Date:  2020-04-17

8.  Maximum gene-support tree.

Authors:  Yunfeng Shan; Xiu-Qing Li
Journal:  Evol Bioinform Online       Date:  2008-05-15       Impact factor: 1.625

  8 in total

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