Genetics, Vol 138, 943-952, Copyright © 1994


INVESTIGATIONS

Substitution Processes in Molecular Evolution. III. Deleterious Alleles

J. H. Gillespie
Section of Evolution and Ecology, University of California, Davis, California 95616

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.


This article has been cited by other articles:


Home page
Proc. Natl. Acad. Sci. USAHome page
J. Charlesworth and A. Eyre-Walker
The other side of the nearly neutral theory, evidence of slightly advantageous back-mutations
PNAS, October 23, 2007; 104(43): 16992 - 16997.
[Abstract] [Full Text] [PDF]


Home page
GeneticsHome page
A. D. Kern, C. D. Jones, and D. J. Begun
Molecular Population Genetics of Male Accessory Gland Proteins in the Drosophila simulans Complex
Genetics, June 1, 2004; 167(2): 725 - 735.
[Abstract] [Full Text] [PDF]


Home page
Mol Biol EvolHome page
M. Woolfit and L. Bromham
Increased Rates of Sequence Evolution in Endosymbiotic Bacteria and Fungi with Small Effective Population Sizes
Mol. Biol. Evol., September 1, 2003; 20(9): 1545 - 1555.
[Abstract] [Full Text] [PDF]


Home page
GeneticsHome page
B. C. Verrelli and W. F. Eanes
Clinal Variation for Amino Acid Polymorphisms at the Pgm Locus in Drosophila melanogaster
Genetics, April 1, 2001; 157(4): 1649 - 1663.
[Abstract] [Full Text]


Home page
GeneticsHome page
B. C. Verrelli and W. F. Eanes
Extensive Amino Acid Polymorphism at the Pgm Locus Is Consistent With Adaptive Protein Evolution in Drosophila melanogaster
Genetics, December 1, 2000; 156(4): 1737 - 1752.
[Abstract] [Full Text]


Home page
GeneticsHome page
R. G. Shaw, D. L. Byers, and E. Darmo
Spontaneous Mutational Effects on Reproductive Traits of Arabidopsis thaliana
Genetics, May 1, 2000; 155(1): 369 - 378.
[Abstract] [Full Text]


Home page
GeneticsHome page
D. J. Cutler
Understanding the Overdispersed Molecular Clock
Genetics, March 1, 2000; 154(3): 1403 - 1417.
[Abstract] [Full Text]


Home page
GeneticsHome page
T. Takano-Shimizu
Local Recombination and Mutation Effects on Molecular Evolution in Drosophila
Genetics, November 1, 1999; 153(3): 1285 - 1296.
[Abstract] [Full Text]


Home page
GeneticsHome page
J. L. Cherry
Should We Expect Substitution Rate to Depend on Population Size?
Genetics, October 1, 1998; 150(2): 911 - 919.
[Abstract] [Full Text]


Home page
GeneticsHome page
P. Kennedy and M. W. Nachman
Deleterious Mutations at the Mitochondrial ND3 Gene in South American Marsh Rats (Holochilus)
Genetics, September 1, 1998; 150(1): 359 - 368.
[Abstract] [Full Text] [PDF]