Chapter 15: Problem 11
Acridine dyes induce frameshift mutations. Why are frameshift mutations likely to be more detrimental than point mutations, in which a single pyrimidine or purine has been substituted?
Chapter 15: Problem 11
Acridine dyes induce frameshift mutations. Why are frameshift mutations likely to be more detrimental than point mutations, in which a single pyrimidine or purine has been substituted?
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Get started for freeMost mutations are thought to be deleterious. Why, then, is it reasonable to state that mutations are essential to the evolutionary process?
In this chapter, we focused on how gene mutations arise and how cells repair DNA damage. At the same time, we found opportunities to consider the methods and reasoning by which much of this information was acquired. From the explanations given in the chapter, (a) How do we know that mutations occur spontaneously? (b) How do we know that certain chemicals and wavelengths of radiation induce mutations in DNA? (c) How do we know that DNA repair mechanisms detect and correct the majority of spontaneous and induced mutations?
A significant number of mutations in the \(H B B\) gene that cause human \(\beta\) -thalassemia occur within introns or in upstream noncoding sequences. Explain why mutations in these regions often lead to severe disease, although they may not directly alter the coding regions of the gene.
Why would a mutation in a somatic cell of a multicellular organism escape detection?
Why would a mutation in a mismatch repair gene lead to a mutator phenotype in a cell?
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