Chapter 22: Problem 22
Are there nucleotide substitutions that will not be detected by electrophoretic studies of a gene's protein product?
Chapter 22: Problem 22
Are there nucleotide substitutions that will not be detected by electrophoretic studies of a gene's protein product?
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Get started for freePopulation 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?
The use of nucleotide sequence data to measure genetic variability is complicated by the fact that the genes of higher eukaryotes are complex in organization and contain \(5^{\prime}\) and \(3^{\prime}\) flanking regions as well as introns. Researchers have compared the nucleotide sequence of two cloned alleles of the \(\gamma\) -globin gene from a single individual and found a variation of 1 percent. Those differences include 13 substitutions of one nucleotide for another and 3 short DNA segments that have been inserted in one allele or deleted in the other. None of the changes takes place in the gene's exons (coding regions). Why do you think this is so, and should it change our concept of genetic variation?
In a recent study of cichlid fish inhabiting Lake Victoria in Africa, Nagl et al. (1998. Proc. Natl. Acad. Sci. IUSA/ 95: \(14,238-14,243\) ) examined suspected neutral sequence polymorphisms in noncoding genomic loci in 12 species and their putative river-living ancestors. At all loci, the same polymorphism was found in nearly all of the tested species from Lake Victoria, both lacustrine and riverine. Different polymorphisms at these loci were found in cichlids at other African lakes. (a) Why would you suspect neutral sequences to be located in noncoding genomic regions? (b) What conclusions can be drawn from these polymorphism data in terms of cichlid ancestry in these lakes?
In a population of cattle, the following color distribution was noted: \(36 \%\) red \((R R), 48 \%\) roan \((R r),\) and \(16 \%\) white \((r r) .\) Is this population in a Hardy-Weinberg equilibrium? What will be the distribution of genotypes in the next generation if the HardyWeinberg assumptions are met?
What is the original source of genetic variation in a population? Which natural factors affect changes in this original variation?
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