Related Experiment Video
Updated: Jul 11, 2026

11:36
A Protocol for Functional Assessment of Whole-Protein Saturation Mutagenesis Libraries Utilizing High-Throughput Sequencing
Published on: July 3, 2016
Population evolution on a multiplicative single-peak fitness landscape
1Department of Physics, University of Sheffield, U.K.
Journal of Theoretical Biology
|March 7, 1996
Summary
Finite populations evolve differently than infinite ones. This study models sequence evolution, showing populations balance mutation and selection, leading to stable evolution rates independent of selection strength.
Area of Science:
- Evolutionary biology
- Population genetics
- Molecular evolution
Background:
- Evolutionary models often assume infinite populations, neglecting finite size effects.
- Adaptive walk models simplify populations to single sequences, which is unrealistic.
- Finite populations with related sequences exhibit unique evolutionary dynamics.
Purpose of the Study:
- To develop and analyze a model for population evolution in a fitness landscape with a single peak, considering finite population size.
- To investigate the balance between mutation and selection in finite populations.
- To understand how sequence evolution rate depends on population size, sequence length, selection strength, and mutation rate.
Main Methods:
- Developed a model representing each individual by a sequence of L genes with fitness Wk = (1-s)k.
- Analyzed the model in the limit of infinite sequence length (L-->infinity), relating it to Muller's Ratchet.
- Used numerical simulations and approximate theory to study finite length sequences and their evolution.
- Investigated the mean overlap between gene sequences over time (Q(t)) and analyzed a simplified solvable model.
Main Results:
- Finite populations evolve away from the fitness peak until a mutation-selection balance is reached.
- Populations wander in sequence space at a constant mean Hamming distance from the optimum.
- Evolutionary rate within this 'spherical shell' is independent of selection strength, depending only on mutation rate (u).
- Selection is less effective in smaller populations (N), increasing the mean Hamming distance (
). - In a model with favorable/unfavorable mutations, an optimal non-zero mutation rate (U) maximizes fitness increase.
Conclusions:
- Finite population size significantly impacts evolutionary trajectories compared to infinite population models.
- A balance between mutation and selection leads to a stable, albeit evolving, population state in sequence space.
- The rate of molecular evolution can be independent of selection strength, primarily driven by mutation.
- Natural selection may favor non-zero mutation rates under certain conditions, optimizing evolutionary potential.
Related Concept Videos
Population Growth
Population size is dynamic, increasing with birth rates and immigration, and decreasing with death rates and emigration. In ideal conditions with unlimited resources, populations can increase exponentially, which plots as a J-shaped growth rate curve of population size against time. This type of curve is characteristic of newly-introduced invasive species, or populations that have suffered catastrophic declines and are rebounding.However, realistic environmental conditions limit the number of...
Hardy-Weinberg Principle
Diploid organisms have two alleles of each gene, one from each parent, in their somatic cells. Therefore, each individual contributes two alleles to the gene pool of the population. The gene pool of a population is the sum of every allele of all genes within that population and has some degree of variation. Genetic variation is typically expressed as a relative frequency, which is the percentage of the total population that has a given allele, genotype or phenotype.In the early 20th century,...
Genetics of Speciation
Speciation is the evolutionary process resulting in the formation of new, distinct species—groups of reproductively isolated populations.The genetics of speciation involves the different traits or isolating mechanisms preventing gene exchange, leading to reproductive isolation. Reproductive isolation can be due to reproductive barriers that have effects either before or after the formation of a zygote. Pre-zygotic mechanisms prevent fertilization from occurring, and post-zygotic mechanisms...
Genetic Drift
Natural selection—probably the most well-known evolutionary mechanism—increases the prevalence of traits that enhance survival and reproduction. However, evolution does not merely propagate favorable traits, nor does it always benefit populations.Life is not fair. A deer grazing contentedly in a field can have her meal cut tragically short by a bolt of lightning. If the doomed doe is one of only three in the population, 1/3 of the population’s gene pool is lost. Random events like this can...
Exponential Equations for Modeling Growth
Exponential models are essential for describing rapid, multiplicative changes in natural systems, such as population growth. When a population doubles at regular intervals, the process can be modeled using a suitable base. For instance, a bacterial culture that doubles every three hours follows the model n(t)=n0⋅2t/3, where n(t) is the population at the time t.A more general model uses the natural base e, especially for continuous growth. This takes the form n(t)=n0⋅ert, where r is the relative...
Modeling with Differential Equations
Population dynamics can be described mathematically by considering the population size P(t) as a function of time. The rate of change of the population is then represented by the derivative of P(t). A simple assumption is that the rate of growth is proportional to the size of the population itself. This leads to an exponential growth model, where the population increases rapidly without bound. While this is a useful first approximation, it does not reflect realistic long-term...

