Literature DB >> 7851786

Substitution processes in molecular evolution. III. Deleterious alleles.

J H Gillespie1.   

Abstract

The substitution processes for various models of deleterious alleles are examined using computer simulations and mathematical analyses. Most of the work focuses on the house-of-cards model, which is a popular model of deleterious allele evolution. The rate of substitution is shown to be a concave function of the strength of selection as measured by alpha = 2N sigma, where N is the population size and sigma is the standard deviation of fitness. For alpha < 1, the house-of-cards model is essentially a neutral model; for alpha > 4, the model ceases to evolve. The stagnation for large alpha may be understood by appealing to the theory of records. The house-of-cards model evolves to a state where the vast majority of all mutations are deleterious, but precisely one-half of those mutations that fix are deleterious (the other half are advantageous). Thus, the model is not a model of exclusively deleterious evolution as is frequently claimed. It is argued that there are no biologically reasonable models of molecular evolution where the vast majority of all substitutions are deleterious. Other models examined include the exponential and gamma shift models, the Hartl-Dykhuizen-Dean (HDD) model, and the optimum model. Of all those examined, only the optimum and HDD models appear to be reasonable candidates for silent evolution. None of the models are viewed as good candidates for protein evolution, as none are both biologically reasonable and exhibit the variability in substitutions commonly observed in protein sequence data.

Mesh:

Year:  1994        PMID: 7851786      PMCID: PMC1206239     

Source DB:  PubMed          Journal:  Genetics        ISSN: 0016-6731            Impact factor:   4.562


  11 in total

1.  On the probability of fixation of mutant genes in a population.

Authors:  M KIMURA
Journal:  Genetics       Date:  1962-06       Impact factor: 4.562

2.  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

3.  Effect of temporal fluctuation of selection coefficient on gene frequency in a population.

Authors:  N Takahata; K Ishii; H Matsuda
Journal:  Proc Natl Acad Sci U S A       Date:  1975-11       Impact factor: 11.205

4.  Genetic variability maintained in a finite population under mutation and autocorrelated random fluctuation of selection intensity.

Authors:  N Takahata; M Kimura
Journal:  Proc Natl Acad Sci U S A       Date:  1979-11       Impact factor: 11.205

5.  More on the overdispersed molecular clock.

Authors:  J H Gillespie
Journal:  Genetics       Date:  1988-02       Impact factor: 4.562

6.  Molecular clock rates at loci under stabilizing selection.

Authors:  P Foley
Journal:  Proc Natl Acad Sci U S A       Date:  1987-11       Impact factor: 11.205

7.  Selection in finite populations with multiple alleles. II. Centripetal selection, mutation, and isoallelic variation.

Authors:  B D Latter
Journal:  Genetics       Date:  1970-09       Impact factor: 4.562

8.  Natural selection and the molecular clock.

Authors:  J H Gillespie
Journal:  Mol Biol Evol       Date:  1986-03       Impact factor: 16.240

9.  Substitution processes in molecular evolution. I. Uniform and clustered substitutions in a haploid model.

Authors:  J H Gillespie
Journal:  Genetics       Date:  1993-07       Impact factor: 4.562

10.  Possibility of extensive neutral evolution under stabilizing selection with special reference to nonrandom usage of synonymous codons.

Authors:  M Kimura
Journal:  Proc Natl Acad Sci U S A       Date:  1981-09       Impact factor: 11.205

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  22 in total

1.  Understanding the overdispersed molecular clock.

Authors:  D J Cutler
Journal:  Genetics       Date:  2000-03       Impact factor: 4.562

2.  The nearly neutral and selection theories of molecular evolution under the fisher geometrical framework: substitution rate, population size, and complexity.

Authors:  Pablo Razeto-Barry; Javier Díaz; Rodrigo A Vásquez
Journal:  Genetics       Date:  2012-03-16       Impact factor: 4.562

3.  Effective population size is positively correlated with levels of adaptive divergence among annual sunflowers.

Authors:  Jared L Strasburg; Nolan C Kane; Andrew R Raduski; Aurélie Bonin; Richard Michelmore; Loren H Rieseberg
Journal:  Mol Biol Evol       Date:  2010-10-15       Impact factor: 16.240

4.  Molecular evolution, mutation size and gene pleiotropy: a geometric reexamination.

Authors:  Pablo Razeto-Barry; Javier Díaz; Darko Cotoras; Rodrigo A Vásquez
Journal:  Genetics       Date:  2010-12-31       Impact factor: 4.562

5.  The other side of the nearly neutral theory, evidence of slightly advantageous back-mutations.

Authors:  Jane Charlesworth; Adam Eyre-Walker
Journal:  Proc Natl Acad Sci U S A       Date:  2007-10-16       Impact factor: 11.205

6.  Should we expect substitution rate to depend on population size?

Authors:  J L Cherry
Journal:  Genetics       Date:  1998-10       Impact factor: 4.562

7.  Bottleneck effect on evolutionary rate in the nearly neutral mutation model.

Authors:  H Araki; H Tachida
Journal:  Genetics       Date:  1997-10       Impact factor: 4.562

8.  Role of random genetic drift in the evolution of interactive systems.

Authors:  T Ohta
Journal:  J Mol Evol       Date:  1997       Impact factor: 2.395

Review 9.  Weak selection and protein evolution.

Authors:  Hiroshi Akashi; Naoki Osada; Tomoko Ohta
Journal:  Genetics       Date:  2012-09       Impact factor: 4.562

10.  Deleterious mutations at the mitochondrial ND3 gene in South American marsh rats (Holochilus).

Authors:  P Kennedy; M W Nachman
Journal:  Genetics       Date:  1998-09       Impact factor: 4.562

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