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Ch. 15 - Gene Mutation, DNA Repair, and Transposition

Chapter 15, Problem 14

A glycine residue is in position 210 of the tryptophan synthetase enzyme of wild-type E. coli. If the codon specifying glycine is GGA, how many single-base substitutions will result in an amino acid substitution at position 210? What are they? How many will result if the wild-type codon is GGU?

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Hello everyone here We have a question that says blank results in an amino acid substitution because the coding is changed and the new code on codes for a different amino acid. We have a single base deletion. A single base deletion is when a nucleotide is removed from a code on. This can lead to changes in the amino acid sequence of the protein. But it doesn't necessarily result in an amino acid substitution because the coding is not changed. So A. Is incorrect. Be single base insertion. As the name suggests, these are mutations in which an extra nucleotide is added to a code on. So B. Is incorrect. C single base substitution. This is right because single base substitution result in an amino acid substitution because the code on has changed and the new code on codes for a different amino acid. So our answer here is C. Single base substitution. Thank you for watching. Bye.
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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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DNA damage brought on by a variety of natural and artificial agents elicits a wide variety of cellular responses involving numerous signaling pathways. In addition to the activation of DNA repair mechanisms, there can be activation of pathways leading to apoptosis (programmed cell death) and cell-cycle arrest. Why would apoptosis and cell-cycle arrest often be part of a cellular response to DNA damage?
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Contrast the various types of DNA repair mechanisms known to counteract the effects of UV radiation. What is the role of visible light in repairing UV-induced mutations?
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Textbook Question

Refer to Figure 13.7 to respond to the following:

A base-substitution mutation that altered the sequence shown in part (a) eliminated the synthesis of all but one polypeptide. The altered sequence is shown here:

 5'-AUGCAUACCUAUGUGACCCUUGGA-3'

Determine why.

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The family of a sixth-grade boy in Palo Alto, California, was informed by school administrators that he would have to transfer out of his middle school because they believed his mutation of the CFTR gene, which does not produce any symptoms associated with cystic fibrosis, posed a risk to other students at the school who have cystic fibrosis. After missing 11 days of school, a settlement was reached to have the boy return to school. What ethical problems might you associate with this example?
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