Analysis of the biases in the estimation of deleterious mutation parameters from natural populations at mutation-selection balance.

Indirect estimates of the genomic rate of deleterious mutations (lambda), their average homozygous effect (s) and their degree of dominance (h) can be obtained from genetic parameters of natural populations, assuming that the frequencies of the loci controlling a given fitness trait are at mutation-selection equilibrium. In 1996, H.-W. Deng and M. Lynch developed a general methodology for obtaining these estimates from inbreeding/outbreeding experiments. The prediction of the sign and magnitude of the biases incurred by these estimators is essential for a correct interpretation of the empirical results. However, the assessment of these biases has been tested so far under a rather limited model of the distribution of dominance effects. In this paper, the application of this method to outbred populations is evaluated, focusing on the level of variation in h values (sigma(h)(2) and the magnitude of the negative correlation (rs,h) between s and h. It is shown that the method produces upwardly biased estimates of lambda and downwardly biased estimates of the average s in the reference situation where rs,h=0, particularly for large values of sigma(h)(2), and biases of different sign depending on the magnitude of the correlation. A modification of the method, substituting the estimates of the average h for alternative ones, allows estimates to be obtained with little or no bias for the case of rs,h=0, but is otherwise biased. Information on rs,h and sigma(h)(2), gathered from mutation-accumulation experiments, suggests that sigma(h)(2) may be rather large and rs,h is usually negative but not higher than about -0.2, although the data are scarce and noisy, and should be used with caution.

[1]  D. Halligan,et al.  Ubiquitous selective constraints in the Drosophila genome revealed by a genome-wide interspecies comparison. , 2006, Genome research.

[2]  Shu-Mei Chang,et al.  Gene Action of New Mutations in Arabidopsis thaliana , 2006, Genetics.

[3]  A. Caballero,et al.  Relaxation of Selection With Equalization of Parental Contributions in Conservation Programs: An Experimental Test With Drosophila melanogaster , 2006, Genetics.

[4]  A. Caballero,et al.  The Effect of Antagonistic Pleiotropy on the Estimation of the Average Coefficient of Dominance of Deleterious Mutations , 2005, Genetics.

[5]  D. Schoen DELETERIOUS MUTATION IN RELATED SPECIES OF THE PLANT GENUS AMSINCKIA WITH CONTRASTING MATING SYSTEMS , 2005, Evolution; international journal of organic evolution.

[6]  J. D. Fry,et al.  Widespread Correlations Between Dominance and Homozygous Effects of Mutations: Implications for Theories of Dominance , 2005, Genetics.

[7]  H. Deng,et al.  Estimation of the rate and effects of deleterious genomic mutations in finite populations with linkage disequilibrium , 2005, Heredity.

[8]  M. Lynch,et al.  Comparative evolutionary genetics of spontaneous mutations affecting fitness in rhabditid nematodes. , 2005, Proceedings of the National Academy of Sciences of the United States of America.

[9]  David W Hall,et al.  Spontaneous Mutations in Diploid Saccharomyces cerevisiae , 2004, Genetics.

[10]  A. Caballero,et al.  Analysis of the Estimators of the Average Coefficient of Dominance of Deleterious Mutations , 2004, Genetics.

[11]  Dee R. Denver,et al.  High mutation rate and predominance of insertions in the Caenorhabditis elegans nuclear genome , 2004, Nature.

[12]  B. Charlesworth,et al.  Estimates of the Genomic Mutation Rate for Detrimental Alleles in Drosophila melanogaster Dedicated to the memory of Terami Mukai, whose pioneering paper on mutation accumulation appeared in Genetics 40 years ago. , 2004, Genetics.

[13]  A. Caballero,et al.  Mutation‐selection balance accounting for genetic variation for viability in Drosophila melanogaster as deduced from an inbreeding and artificial selection experiment , 2004, Journal of evolutionary biology.

[14]  M. Lynch,et al.  Mutation Accumulation in Populations of Varying Size: The Distribution of Mutational Effects for Fitness Correlates in Caenorhabditis elegans , 2004, Genetics.

[15]  J. Crow,et al.  ON THE PERSISTENCE AND PERVASIVENESS OF A NEW MUTATION , 2003, Evolution; international journal of organic evolution.

[16]  A. D. Peters,et al.  Dominance and overdominance of mildly deleterious induced mutations for fitness traits in Caenorhabditis elegans. , 2003, Genetics.

[17]  R. Korona,et al.  Small fitness effects and weak genetic interactions between deleterious mutations in heterozygous loci of the yeast Saccharomyces cerevisiae. , 2003, Genetical research.

[18]  A. García-Dorado Tolerant versus sensitive genomes: The impact of deleterious mutation on fitness and conservation , 2003, Conservation Genetics.

[19]  C. Geyer,et al.  WHAT FRACTION OF MUTATIONS RED.UCES FITNESS? A REPLY TO KEIGHTLEY AND LYNCH , 2003 .

[20]  M. Lynch,et al.  TOWARD A REALISTIC MODEL OF MUTATIONS AFFECTING FITNESS , 2003, Evolution; international journal of organic evolution.

[21]  H. Deng,et al.  Estimation of deleterious genomic mutation parameters in natural populations by accounting for variable mutation effects across loci. , 2002, Genetics.

[22]  A. Caballero,et al.  ACCUMULATION OF DELETERIOUS MUTATIONS: ADDITIONAL DROSOPHILA MELANOGASTER ESTIMATES AND A SIMULATION OF THE EFFECTS OF SELECTION , 2002, Evolution; international journal of organic evolution.

[23]  C. Geyer,et al.  A COMPREHENSIVE MODEL OF MUTATIONS AFFECTING FITNESS AND INFERENCES FOR ARABIDOPSIS THALIANA , 2002, Evolution; international journal of organic evolution.

[24]  A. Kondrashov Sex and U. , 2001, Trends in genetics : TIG.

[25]  P. Keightley,et al.  Deleterious mutations and the evolution of sex. , 2000, Science.

[26]  A. D. Peters,et al.  Properties of ethylmethane sulfonate-induced mutations affecting life-history traits in Caenorhabditis elegans and inferences about bivariate distributions of mutation effects. , 2000, Genetics.

[27]  A. Caballero,et al.  On the average coefficient of dominance of deleterious spontaneous mutations. , 2000, Genetics.

[28]  H. Deng,et al.  Estimation of parameters of deleterious mutations in partial selfing or partial outcrossing populations and in nonequilibrium populations. , 2000, Genetics.

[29]  A. Caballero,et al.  Properties of spontaneous mutations affecting quantitative traits. , 1999, Genetical research.

[30]  Jun Yu Li,et al.  On the experimental design and data analysis of mutation accumulation experiments. , 1999, Genetical research.

[31]  J. Cheverud Genetics and analysis of quantitative traits , 1999 .

[32]  H. Deng,et al.  The effect of overdominance on characterizing deleterious mutations in large natural populations. , 1999, Genetics.

[33]  H. Deng Characterization of deleterious mutations in outcrossing populations. , 1998, Genetics.

[34]  H. Deng Estimating within-locus nonadditive coefficient and discriminating dominance versus overdominance as the genetic cause of heterosis. , 1998, Genetics.

[35]  M. Turelli,et al.  Average dominance for polygenes: drawbacks of regression estimates. , 1997, Genetics.

[36]  M. Lynch,et al.  Inbreeding depression and inferred deleterious-mutation parameters in Daphnia. , 1997, Genetics.

[37]  A. García-Dorado THE RATE AND EFFECTS DISTRIBUTION OF VIABILITY MUTATION IN DROSOPHILA: MINIMUM DISTANCE ESTIMATION , 1997, Evolution; international journal of organic evolution.

[38]  C. López-Fanjul,et al.  Spontaneous mutational variances and covariances for fitness-related traits in Drosophila melanogaster. , 1996, Genetics.

[39]  P. Keightley A metabolic basis for dominance and recessivity. , 1996, Genetics.

[40]  T. Mackay,et al.  Effects of single P-element insertions on bristle number and viability in Drosophila melanogaster. , 1996, Genetics.

[41]  M. Johnston,et al.  Mutation Rates and Dominance Levels of Genes Affecting Total Fitness in Two Angiosperm Species , 1995, Science.

[42]  D. Charlesworth,et al.  Inbreeding depression in two highly inbreeding populations of Leavenworthia , 1994, Proceedings of the Royal Society of London. Series B: Biological Sciences.

[43]  P. Keightley The distribution of mutation effects on viability in Drosophila melanogaster. , 1994, Genetics.

[44]  P. Keightley,et al.  A pleiotropic nonadditive model of variation in quantitative traits. , 1994, Genetics.

[45]  T. Mackay,et al.  Effects of P element insertions on quantitative traits in Drosophila melanogaster. , 1992, Genetics.

[46]  B. Charlesworth,et al.  Genetic loads and estimates of mutation rates in highly inbred plant populations , 1990, Nature.

[47]  T. Mukai,et al.  The Genetic Structure of Natural Populations of DROSOPHILA MELANOGASTER. Xvii. a Population Carrying Genetic Variability Explicable by the Classical Hypothesis. , 1984, Genetics.

[48]  H. Kacser,et al.  The molecular basis of dominance. , 1981, Genetics.

[49]  T. Mukai,et al.  The genetic structure of natural populations of Drosophila melanogaster. XI. Genetic variability in a local population. , 1974, Genetics.

[50]  J. Crow,et al.  Mutation rate and dominance of genes affecting viability in Drosophila melanogaster. , 1972, Genetics.

[51]  T MUKAI,et al.  THE GENETIC STRUCTURE OF NATURAL POPULATIONS OF DROSOPHILA MELANOGASTER. I. SPONTANEOUS MUTATION RATE OF POLYGENES CONTROLLING VIABILITY. , 1964, Genetics.

[52]  N. Morton,et al.  AN ESTIMATE OF THE MUTATIONAL DAMAGE IN MAN FROM DATA ON CONSANGUINEOUS MARRIAGES. , 1956, Proceedings of the National Academy of Sciences of the United States of America.

[53]  S. Wright,et al.  THE DISTRIBUTION OF GENE FREQUENCIES IN POPULATIONS. , 1937, Science.

[54]  S. Wright,et al.  The Distribution of Gene Frequencies in Populations. , 1937, Proceedings of the National Academy of Sciences of the United States of America.

[55]  C. Geyer,et al.  WHAT FRACTION OF MUTATIONS REDUCES FITNESS? A REPLY TO KEIGHTLEY AND LYNCH , 2003 .

[56]  T. Mukai THE GENETIC STRUCTURE OF NATURAL POPULATIONS OF DRQSOPHZLA MELANOGASTER. VIII. NATURAL SELECTION ON THE DEGREE OF DOMINANCE OF VIABILITY POLYGENES , 2003 .

[57]  M. Lynch,et al.  Genetics and Analysis of Quantitative Traits , 1996 .

[58]  J. Crow,et al.  Mutations affecting fitness in Drosophila populations. , 1977, Annual review of genetics.

[59]  F. THE MUTATION LOAD IN SMALL POPULATIONS , 2022 .