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The original source of new alleles, upon which selection operates, is mutation, a random event that occurs without regard to selectional value in the organism. Although many model organisms have been used to study mutational events in populations, some investigators have developed abiotic molecular models. Soll et al. (2006. Genetics 175:267-275) examined one such model to study the relationship between both deleterious and advantageous mutations and population size in a ligase molecule composed of RNA (a ribozyme). Soll found that the smaller the population of molecules, the more likely it was that not only deleterious mutations but also advantageous mutations would disappear. Why would population size influence the survival of both types of mutations (deleterious and advantageous) in populations?

Short Answer

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Answer: Population size influences the survival of both deleterious and advantageous mutations in populations due to the effects of genetic drift. Genetic drift is a random change in the frequency of alleles in a population because of chance events. In smaller populations, genetic drift is more significant, which can lead to an increased prominence of deleterious mutations and the loss of advantageous mutations. This can impact the ability of the population to adapt to changing environments and evolve.

Step by step solution

01

Understanding mutations in populations

Mutations are random changes in an organism's DNA and are the original source of new alleles, which selection acts upon. They can be classified into deleterious mutations, which have negative effects on the fitness of an organism, and advantageous mutations, which have positive effects on its fitness.
02

Genetic drift and its effect on populations

Genetic drift is a random change in the frequency of alleles in a population due to chance events. It plays a significant role in smaller populations, as random events have a larger impact on the frequency of alleles. The effects of genetic drift in a population are the loss of genetic variability, fixation of alleles, and the potential of the population to adapt to changing environments.
03

Population size and the survival of deleterious mutations

In smaller populations, genetic drift has a more significant effect which can lead to a higher chance of deleterious mutations becoming fixed in the population. This can occur as a result of the random chance events outweighing the selection pressure acting against these deleterious mutations. Moreover, smaller populations have limited genetic variation, increasing the likelihood of deleterious mutations becoming prominent in successive generations.
04

Population size and the survival of advantageous mutations

Similarly, in smaller populations, the survival of advantageous mutations is also affected. Even if an advantageous mutation occurs, genetic drift can cause the mutation to be lost from the population due to random chance events. This prevents advantageous mutations from becoming fixed in the population, reducing the potential for adaptive evolution.
05

Conclusion

In conclusion, population size greatly influences the survival of both deleterious and advantageous mutations in populations. Smaller populations are more susceptible to the effects of genetic drift, which can lead to the increased prominence of deleterious mutations and the loss of advantageous mutations. This can, in turn, impact the ability of the population to adapt to changing environments and evolve.

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Most popular questions from this chapter

Describe how populations with substantial genetic differences can form. What is the role of natural selection?

HOW DO WE KNOW? Population geneticists study changes in the nature and amount of genetic variation in populations, the distribution of different genotypes, and how forces such as selection and drift act on genetic variation to bring about evolutionary change in populations and the formation of new species. From the explanation given in the chapter, what answers would you propose to the following fundamental questions? (a) How do we know how much genetic variation is in a population? (b) How do geneticists detect the presence of genetic variation as different alleles in a population? (c) How do we know whether the genetic structure of a population is static or dynamic? (d) How do we know when populations have diverged to the point that they form two different species? (e) How do we know the age of the last common ancestor shared by two species?

Recent reconstructions of evolutionary history are often dependent on assigning divergence in terms of changes in amino acid or nucleotide sequences. For example, a comparison of cytochrome c shows 10 amino acid differences between humans and dogs, 24 differences between humans and moths, and 38 differences between humans and yeast. Such data provide no information as to the absolute times of divergence for humans, dogs, moths, and yeast. How might one calibrate the molecular clock to an absolute time clock? What problems might one encounter in such a calibration?

A recent study examining the mutation rates of 5669 mammalian genes \((17,208\) sequences) indicates that, contrary to popular belief, mutation rates among lineages with vastly different generation lengths and physiological attributes are remarkably constant [Kumar, S., and Subramanian, S. \((2002) .\) Proc. Natl. Acad. Sci.USA99:803-808|.Theaveragerateisestimatedat12.2 \(\times 10^{-9}\) perbp per year. What is the significance of this finding in terms of mammalian evolution?

One of the first Mendelian traits identified in humans was a dominant condition known as brachydactyly. This gene causes an abnormal shortening of the fingers or toes (or both). At the time, some researchers thought that the dominant trait would spread until 75 percent of the population would be affected (because the phenotypic ratio of dominant to recessive is 3: 1 ). Show that the reasoning was incorrect.

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