Chapter 15: Problem 3
What is a spontaneous mutation, and why are spontaneous mutations rare?
Chapter 15: Problem 3
What is a spontaneous mutation, and why are spontaneous mutations rare?
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Get started for freeIt has been noted that most transposons in humans and other organisms are located 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?
A yeast strain that has a regulated overexpression of HindIII endonuclease has been generated. What would be the consequence of this overexpression? Which repair pathway may be functional in this yeast cell and why?
Presented here are hypothetical findings from studies of heterokaryons formed from seven human xeroderma pigmentosum cell strains: $$\begin{array}{lccccccc} & X P 1 & X P 2 & X P 3 & X P 4 & X P 5 & X P 6 & X P 7 \\ X P 1 & \- & & & & & & \\ X P 2 & \- & \- & & & & & \\ X P 3 & \- & \- & \- & & & & \\ X P 4 & \+ & \+ & \+ & \- & & & \\ X P S & \+ & \+ & \+ & \+ & \- & & \\ X P 6 & \+ & \+ & \+ & \+ & \- & \- & \\ X P 7 & \+ & \+ & \+ & \+ & \- & \- & - \end{array}$$ These data are measurements of the occurrence or nonoccur- rence of unscheduled DNA synthesis in the fused heterokaryon. None of the strains alone shows any unscheduled DNA synthesis. Which strains fall into the same complementation groups? How many different groups are revealed based on these data? What can we conclude about the genetic basis of XP from these data?
Most mutations are thought to be deleterious. Why, then, is it reasonable to state that mutations are essential to the evolutionary process?
In which phases of the cell cycle would you expect doublestrand break repair and nonhomologous end joining to occur and why?
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