Chapter 14: Problem 6
Why is a random mutation more likely to be deleterious than beneficial?
Chapter 14: Problem 6
Why is a random mutation more likely to be deleterious than beneficial?
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Get started for freeIt has been noted that most transposons in humans and other organisms are lacated in noncoding regions of the genome regions such as introns, pseudogenes, and stretches of particular types of repetitive DNA. There are several ways to interpret this observation. Describe two possible interpretations. Which interpretation do you favor? Why?
In maize, a \(D s\) or \(A c\) transposon can alter the function of genes at or near the site of transposon insertion. It is possible for these elements to transpose away from their original insertion site, causing a reversion of the mutant phenotype. In some cases, however, even more severe phenotypes appear, due to events at or near the mutant allele. What might be happening to the transposon or the nearby gene to create more severe mutations?
Why are frameshift mutations likely to be more detrimental than point mutations, in which a single pyrimidine or purine has been substituted?
Why are X rays more potent mutagens than UV radiation?
What is the difference between a silent mutation and a neutral mutation?
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