Literature DB >> 2060776

A study on a nearly neutral mutation model in finite populations.

H Tachida1.   

Abstract

As a nearly neutral mutation model, the house-of-cards model is studied in finite populations using computer simulations. The distribution of the mutant effect is assumed to be normal. The behavior is mainly determined by the product of the population size, N, and the standard deviation, sigma, of the distribution of the mutant effect. If 4N sigma is large compared to one, a few advantageous mutants are quickly fixed in early generations. Then most mutation becomes deleterious and very slow increase of the average selection coefficient follows. It takes very long for the population to reach the equilibrium state. Substitutions of alleles occur very infrequently in the later stage. If 4N sigma is the order of one or less, the behavior is qualitatively similar to that of the strict neutral case. Gradual increase of the average selection coefficient occurs and in generations of several times the inverse of the mutation rate the population almost reaches the equilibrium state. Both advantageous and neutral (including slightly deleterious) mutations are fixed. Except in the early stage, an increase of the standard deviation of the distribution of the mutant effect decreases the average heterozygosity. The substitution rate is reduced as 4N sigma is increased. Three tests of neutrality, one using the relationship between the average and the variance of heterozygosity, another using the relationship between the average heterozygosity and the average number of substitutions and Watterson's homozygosity test are applied to the consequences of the present model. It is found that deviation from the neutral expectation becomes apparent only when 4N sigma is more than two. Also a simple approximation for the model is developed which works well when the mutation rate is very small.

Mesh:

Year:  1991        PMID: 2060776      PMCID: PMC1204447     

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


  21 in total

1.  THE NUMBER OF ALLELES THAT CAN BE MAINTAINED IN A FINITE POPULATION.

Authors:  M KIMURA; J F CROW
Journal:  Genetics       Date:  1964-04       Impact factor: 4.562

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

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

3.  Model of effectively neutral mutations in which selective constraint is incorporated.

Authors:  M Kimura
Journal:  Proc Natl Acad Sci U S A       Date:  1979-07       Impact factor: 11.205

4.  The rosy region of Drosophila melanogaster and Drosophila simulans. I. Contrasting levels of naturally occurring DNA restriction map variation and divergence.

Authors:  C F Aquadro; K M Lado; W A Noon
Journal:  Genetics       Date:  1988-08       Impact factor: 4.562

5.  Statistical studies on protein polymorphism in natural populations. I. Distribution of single locus heterozygosity.

Authors:  P A Fuerst; R Chakraborty; M Nei
Journal:  Genetics       Date:  1977-06       Impact factor: 4.562

6.  Effects of mutation on selection limits in finite populations with multiple alleles.

Authors:  Z B Zeng; H Tachida; C C Cockerham
Journal:  Genetics       Date:  1989-08       Impact factor: 4.562

7.  Population size and rate of evolution.

Authors:  T Ohta
Journal:  J Mol Evol       Date:  1972       Impact factor: 2.395

8.  On the overdispersed molecular clock.

Authors:  N Takahata
Journal:  Genetics       Date:  1987-05       Impact factor: 4.562

9.  A Comprehensive Study of Genic Variation in Natural Populations of Drosophila melanogaster. III. Variations in Genetic Structure and Their Causes between Drosophila melanogaster and Its Sibling Species Drosophila simulans.

Authors:  M Choudhary; R S Singh
Journal:  Genetics       Date:  1987-12       Impact factor: 4.562

Review 10.  Molecular evolutionary clock and the neutral theory.

Authors:  M Kimura
Journal:  J Mol Evol       Date:  1987       Impact factor: 2.395

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  20 in total

Review 1.  Mechanisms of molecular evolution.

Authors:  T Ohta
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  2000-11-29       Impact factor: 6.237

2.  Understanding the overdispersed molecular clock.

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

3.  Estimation of effective population size of HIV-1 within a host: a pseudomaximum-likelihood approach.

Authors:  Tae-Kun Seo; Jeffrey L Thorne; Masami Hasegawa; Hirohisa Kishino
Journal:  Genetics       Date:  2002-04       Impact factor: 4.562

4.  Near-neutrality in evolution of genes and gene regulation.

Authors:  Tomoko Ohta
Journal:  Proc Natl Acad Sci U S A       Date:  2002-12-02       Impact factor: 11.205

5.  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

6.  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

7.  Theoretical study of near neutrality. II. Effect of subdivided population structure with local extinction and recolonization.

Authors:  T Ohta
Journal:  Genetics       Date:  1992-04       Impact factor: 4.562

8.  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

9.  Origin of the neutral and nearly neutral theories of evolution.

Authors:  Tomoko Ohta
Journal:  J Biosci       Date:  2003-06       Impact factor: 1.826

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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