- THIS ARTICLE
- Full Text (PDF)
- Alert me when this article is cited
- Alert me if a correction is posted
- SERVICES
- Similar articles in this journal
- Similar articles in PubMed
- Alert me to new issues of the journal
- Download to citation manager
- Reprints & Permissions
- CITING ARTICLES
- Citing Articles via HighWire
- Citing Articles via Google Scholar
- GOOGLE SCHOLAR
- Articles by Kondrashov, A. S.
- Search for Related Content
- PUBMED
- PubMed Citation
- Articles by Kondrashov, A. S.
DELETERIOUS MUTATIONS AS AN EVOLUTIONARY FACTOR. II. FACULTATIVE APOMIXIS AND SELFING
Alexey S. Kondrashov 1
1 Research Computer Centre of the Academy of Sciences of the
USSR, 142292 Pushchino, Moscow Region, USSR
A population with u deleterious mutations per genome
per generation is considered in which only those individuals that carry less
than a critical number k of mutations are viable. Besides a large
number of loci subject to mutation and selection, the genome contains one
or two special loci responsible for the mode of reproduction. Amphimixis
vs. selfing are considered separately. In the first case, the genome
degradation rate v (=u/
k) is found to play the decisive
role, as in the case of recombination. When v > 1.25, obligate
amphimixis is established. If v decreases below this value, the alleles
with first low and then larger penetrance are fixed, until alleles conferring
obligate asexual reproduction become advantageous. The proportion of resources
allocated to produce seeds also increases with decrease of v. These
results are unlikely to depend on the genetic basis of the mode of reproduction.
The result of competition between outcrossing and selfing depends on both
u and k, as well as on whether the mutations are recessive.
The alleles for selfing with low penetrance are selected against if the mutations
are at all recessive. The fitness of alleles with high penetrance depends
primarily on u, decreasing when u increases. There may exist
conditions when only the alleles providing intermediate selfing rates can
be fixed in a population. In other cases a population may exist with either
obligate outcrossing or selfing at a high rate. Thus, truncation selection
against deleterious mutations may be a factor supporting obligate or facultative
sex despite the twofold advantage of apomixis or selfing.
Accepted on May 29, 1985
This article has been cited by other articles:
![]() |
J. K. Kelly Epistasis in Monkeyflowers Genetics, December 1, 2005; 171(4): 1917 - 1931. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. M. Cuevas, S. F. Elena, and A. Moya Molecular Basis of Adaptive Convergence in Experimental Populations of RNA Viruses Genetics, October 1, 2002; 162(2): 533 - 542. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. D. Peters and P. D. Keightley A Test for Epistasis Among Induced Mutations in Caenorhabditis elegans Genetics, December 1, 2000; 156(4): 1635 - 1647. [Abstract] [Full Text] |
||||
![]() |
J. Li and H.-W. Deng Estimation of Parameters of Deleterious Mutations in Partial Selfing or Partial Outcrossing Populations and in Nonequilibrium Populations Genetics, April 1, 2000; 154(4): 1893 - 1906. [Abstract] [Full Text] |
||||
![]() |
J.-L. Li, J. Li, and H.-W. Deng The Effect of Overdominance on Characterizing Deleterious Mutations in Large Natural Populations Genetics, February 1, 1999; 151(2): 895 - 913. [Abstract] [Full Text] |
||||
![]() |
H.-W. Deng Characterization of Deleterious Mutations in Outcrossing Populations Genetics, October 1, 1998; 150(2): 945 - 956. [Abstract] [Full Text] |
||||
![]() |
D. J. Schoen, J. L. David, and T. M. Bataillon Deleterious mutation accumulation and the regeneration of genetic resources PNAS, January 6, 1998; 95(1): 394 - 399. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. O. Johnston and D. J. Schoen Mutation Rates and Dominance Levels of Genes Affecting Total Fitness in Two Angiosperm Species Science, January 13, 1995; 267(5195): 226 - 229. [Abstract] [PDF] |
||||


