scholarly journals Adaptive evolution is substantially impeded by Hill-Robertson interference in Drosophila

2015 ◽  
Author(s):  
David Castellano ◽  
Marta Coronado ◽  
Jose Campos ◽  
Antonio Barbadilla ◽  
Adam Eyre-Walker

It is known that rates of mutation and recombination vary across the genome in many species. Here we investigate whether these factors affect the rate at which genes undergo adaptive evolution both individually and in combination and quantify the degree to which Hill-Robertson interference (HRi) impedes the rate of adaptive evolution. To do this we compiled a dataset of 6,141 autosomal protein coding genes from Drosophila, for which we have polymorphism data from D. melanogaster and divergence out to D. yakuba. We estimated the rate of adaptive evolution using a derivative of the McDonald-Kreitman test that controls for the slightly deleterious mutations. We find that the rate of adaptive amino acid substitution is positively correlated to both the rates of recombination and mutation. We also find that these correlations are robust to controlling for each other, synonymous codon bias and gene functions related to immune response and testes. We estimate that HRi reduces the rate of adaptive evolution by ~27%. We also show that this fraction depends on a gene's mutation rate; genes with low mutation rates lose ~11% of their adaptive substitutions while genes with high mutation rates lose ~43%. In conclusion, we show that the mutation rate and the rate of recombination, are important modifiers of the rate of adaptive evolution in Drosophila.

2013 ◽  
Vol 10 (85) ◽  
pp. 20130329 ◽  
Author(s):  
Philip J. Gerrish ◽  
Alexandre Colato ◽  
Paul D. Sniegowski

When mutation rates are low, natural selection remains effective, and increasing the mutation rate can give rise to an increase in adaptation rate. When mutation rates are high to begin with, however, increasing the mutation rate may have a detrimental effect because of the overwhelming presence of deleterious mutations. Indeed, if mutation rates are high enough: (i) adaptive evolution may be neutralized, resulting in a zero (or negative) adaptation rate despite the continued availability of adaptive and/or compensatory mutations, or (ii) natural selection may be neutralized, because the fitness of lineages bearing adaptive and/or compensatory mutations—whether established or newly arising—is eroded by excessive mutation, causing such lineages to decline in frequency. We apply these two criteria to a standard model of asexual adaptive evolution and derive mathematical expressions—some new, some old in new guise—delineating the mutation rates under which either adaptive evolution or natural selection is neutralized. The expressions are simple and require no a priori knowledge of organism- and/or environment-specific parameters. Our discussion connects these results to each other and to previous theory, showing convergence or equivalence of the different results in most cases.


2021 ◽  
Author(s):  
Yoav Ram ◽  
Yitzhak Tzachi Pilpel ◽  
Gabriela Aleksandra Lobinska

The mutation rate is an important determinant of evolutionary dynamics. Because the mutation rate determines the rate of appearance of beneficial and deleterious mutations, it is subject to second-order selection. The mutation rate varies between and within species and populations, increases under stress, and is genetically controlled by mutator alleles. The mutation rate may also vary among genetically identical individuals: empirical evidence from bacteria suggests that the mutation rate may be affected by translation errors and expression noise in various proteins (1). Importantly, this non-genetic variation may be heritable via transgenerational epigenetic inheritance. Here we investigate how the inheritance mode of the mutation rate affects the rate of adaptive evolution on rugged fitness landscapes. We model an asexual population with two mutation rate phenotypes, non-mutator and mutator. An offspring may switch from its parental phenotype to the other phenotype. The rate of switching between the mutation rate phenotypes is allowed to span a range of values. Thus, the mutation rate can be interpreted as a genetically inherited trait when the switching rate is low, as an epigenetically inherited trait when the switching rate is intermediate, or as a randomly determined trait when the switching rate is high. We find that epigenetically inherited mutation rates result in the highest rates of adaptation on rugged fitness landscapes for most realistic parameter sets. This is because an intermediate switching rate can maintain the association between a mutator phenotype and pre-existing mutations, which facilitates the crossing of fitness valleys. Our results provide a rationale for the evolution of epigenetic inheritance of the mutation rate, suggesting that it could have been selected because it facilitates adaptive evolution.


2018 ◽  
Vol 115 (13) ◽  
pp. 3422-3427 ◽  
Author(s):  
Yevgeniy Raynes ◽  
C. Scott Wylie ◽  
Paul D. Sniegowski ◽  
Daniel M. Weinreich

The influence of population size (N) on natural selection acting on alleles that affect fitness has been understood for almost a century. AsNdeclines, genetic drift overwhelms selection and alleles with direct fitness effects are rendered neutral. Often, however, alleles experience so-called indirect selection, meaning they affect not the fitness of an individual but the fitness distribution of its offspring. Some of the best-studied examples of indirect selection include alleles that modify aspects of the genetic system such as recombination and mutation rates. Here, we use analytics, simulations, and experimental populations ofSaccharomyces cerevisiaeto examine the influence ofNon indirect selection acting on alleles that increase the genomic mutation rate (mutators). Mutators experience indirect selection via genomic associations with beneficial and deleterious mutations they generate. We show that, asNdeclines, indirect selection driven by linked beneficial mutations is overpowered by drift before drift can neutralize the cost of the deleterious load. As a result, mutators transition from being favored by indirect selection in large populations to being disfavored asNdeclines. This surprising phenomenon of sign inversion in selective effect demonstrates that indirect selection on mutators exhibits a profound and qualitatively distinct dependence onN.


2017 ◽  
Author(s):  
Sarah Northey ◽  
Courtney Hove ◽  
Justine Kao ◽  
Jon Ide ◽  
Janel McKinney ◽  
...  

Algal blooms have been the subject of considerable research as they occur over various spatial and temporal scales and can produce toxins that disrupt their ecosystem. Algal blooms are often governed by nutrient availability however other limitations exist. Algae are primary producers and therefore subject to predation which can keep populations below levels supported by nutrient availability. If algae as prey mutate to gain the ability to produce toxins deterring predators, they may increase their survival rates and form blooms unless other factors counter their effective increase in growth rate. Where might such mutations come from? Clearly, large populations of algae will repeatedly experience mutations knocking-out DNA repair genes, increasing mutation rates, and with them the chance of acquiring de-novo mutations producing a toxin against predators. We investigate this hypothetical scenario by simulation in the Evolvix modeling language. We modeled a sequence of steps that in principle can allow a typical asexual algal population to escape predation pressure and form a bloom with the help of mutators. We then turn our attention to the unavoidable side effect of generally increased mutation rates, many slightly deleterious mutations. If these accumulate at sufficient speed, their combined impact on fitness might place upper limits on the duration of algal blooms. These steps are required: (1) Random mutations result in the loss of DNA repair mechanisms. (2) Increased mutation rates make it more likely to acquire the ability to produce toxins by altering metabolism. (3) Toxins deter predators providing algae with growth advantages that can mask linked slightly deleterious mutational effects. (4) Reduced predation pressure enables blooms if algae have sufficient nutrients. (5) Lack of recombination results in the accumulation of slightly deleterious mutations as predicted by Muller’s ratchet. (6) If fast enough, deleterious mutation accumulation eventually leads to mutational meltdown of toxic blooming algae. (7) Non-mutator algal populations are not affected due to ongoing predation pressure. Our simulation models integrate ecological continuous-time dynamics of predator-prey systems with the population genetics of a simplified Muller’s ratchet model using Evolvix. Evolvix maps these models to Continuous-Time Markov Chain models that can be simulated deterministically or stochastically depending on the question. The current model is incomplete; we plan to investigate many parameter combinations to produce a more robust model ensemble with stable links to reasonable parameter estimates. However, our model already has several intriguing features that may allow for the eventual development of observation methods for monitoring ecosystem health. Our work also highlights a growing need to simulate integrated models combining ecological processes, multi-level population dynamics, and evolutionary genetics in a single computational run.


2017 ◽  
Author(s):  
Sarah Northey ◽  
Courtney Hove ◽  
Justine Kao ◽  
Jon Ide ◽  
Janel McKinney ◽  
...  

Algal blooms have been the subject of considerable research as they occur over various spatial and temporal scales and can produce toxins that disrupt their ecosystem. Algal blooms are often governed by nutrient availability however other limitations exist. Algae are primary producers and therefore subject to predation which can keep populations below levels supported by nutrient availability. If algae as prey mutate to gain the ability to produce toxins deterring predators, they may increase their survival rates and form blooms unless other factors counter their effective increase in growth rate. Where might such mutations come from? Clearly, large populations of algae will repeatedly experience mutations knocking-out DNA repair genes, increasing mutation rates, and with them the chance of acquiring de-novo mutations producing a toxin against predators. We investigate this hypothetical scenario by simulation in the Evolvix modeling language. We modeled a sequence of steps that in principle can allow a typical asexual algal population to escape predation pressure and form a bloom with the help of mutators. We then turn our attention to the unavoidable side effect of generally increased mutation rates, many slightly deleterious mutations. If these accumulate at sufficient speed, their combined impact on fitness might place upper limits on the duration of algal blooms. These steps are required: (1) Random mutations result in the loss of DNA repair mechanisms. (2) Increased mutation rates make it more likely to acquire the ability to produce toxins by altering metabolism. (3) Toxins deter predators providing algae with growth advantages that can mask linked slightly deleterious mutational effects. (4) Reduced predation pressure enables blooms if algae have sufficient nutrients. (5) Lack of recombination results in the accumulation of slightly deleterious mutations as predicted by Muller’s ratchet. (6) If fast enough, deleterious mutation accumulation eventually leads to mutational meltdown of toxic blooming algae. (7) Non-mutator algal populations are not affected due to ongoing predation pressure. Our simulation models integrate ecological continuous-time dynamics of predator-prey systems with the population genetics of a simplified Muller’s ratchet model using Evolvix. Evolvix maps these models to Continuous-Time Markov Chain models that can be simulated deterministically or stochastically depending on the question. The current model is incomplete; we plan to investigate many parameter combinations to produce a more robust model ensemble with stable links to reasonable parameter estimates. However, our model already has several intriguing features that may allow for the eventual development of observation methods for monitoring ecosystem health. Our work also highlights a growing need to simulate integrated models combining ecological processes, multi-level population dynamics, and evolutionary genetics in a single computational run.


Genetics ◽  
1999 ◽  
Vol 151 (4) ◽  
pp. 1621-1631 ◽  
Author(s):  
Toby Johnson

Abstract Natural selection acts in three ways on heritable variation for mutation rates. A modifier allele that increases the mutation rate is (i) disfavored due to association with deleterious mutations, but is also favored due to (ii) association with beneficial mutations and (iii) the reduced costs of lower fidelity replication. When a unique beneficial mutation arises and sweeps to fixation, genetic hitchhiking may cause a substantial change in the frequency of a modifier of mutation rate. In previous studies of the evolution of mutation rates in sexual populations, this effect has been underestimated. This article models the long-term effect of a series of such hitchhiking events and determines the resulting strength of indirect selection on the modifier. This is compared to the indirect selection due to deleterious mutations, when both types of mutations are randomly scattered over a given genetic map. Relative to an asexual population, increased levels of recombination reduce the effects of beneficial mutations more rapidly than those of deleterious mutations. However, the role of beneficial mutations in determining the evolutionarily stable mutation rate may still be significant if the function describing the cost of high-fidelity replication has a shallow gradient.


2017 ◽  
Vol 13 (3) ◽  
pp. 20160849 ◽  
Author(s):  
Tanya Singh ◽  
Meredith Hyun ◽  
Paul Sniegowski

Mutation is the ultimate source of the genetic variation—including variation for mutation rate itself—that fuels evolution. Natural selection can raise or lower the genomic mutation rate of a population by changing the frequencies of mutation rate modifier alleles associated with beneficial and deleterious mutations. Existing theory and observations suggest that where selection is minimized, rapid systematic evolution of mutation rate either up or down is unlikely. Here, we report systematic evolution of higher and lower mutation rates in replicate hypermutable Escherichia coli populations experimentally propagated at very small effective size—a circumstance under which selection is greatly reduced. Several populations went extinct during this experiment, and these populations tended to evolve elevated mutation rates. In contrast, populations that survived to the end of the experiment tended to evolve decreased mutation rates. We discuss the relevance of our results to current ideas about the evolution, maintenance and consequences of high mutation rates.


2016 ◽  
Author(s):  
Benjamin H. Good ◽  
Michael M. Desai

Mutator and antimutator alleles often arise and spread in both natural microbial populations and laboratory evolution experiments. The evolutionary dynamics of these mutation rate modifiers are determined by indirect selection on linked beneficial and deleterious mutations. These indirect selection pressures have been the focus of much earlier theoretical and empirical work, but we still have a limited analytical understanding of how the interplay between hitchhiking and deleterious load influences the fates of modifier alleles. Our understanding is particularly limited when clonal interference is common, which is the regime of primary interest in laboratory microbial evolution experiments. Here, we calculate the fixation probability of a mutator or antimutator allele in a rapidly adapting asexual population, and we show how this quantity depends on the population size, the beneficial and deleterious mutation rates, and the strength of a typical driver mutation. In the absence of deleterious mutations, we find that clonal interference enhances the fixation probability of mutators, even as they provide a diminishing benefit to the overall rate of adaptation. When deleterious mutations are included, natural selection pushes the population towards a stable mutation rate that can be suboptimal for the adaptation of the population as a whole. The approach to this stable mutation rate is not necessarily monotonic, and selection can favor mutator and antimutator alleles that overshoot the stable mutation rate by substantial amounts.


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