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

Chapter 15, Problem 15

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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Video transcript

Hello everyone and welcome to today's video in an RNA sequence to be translated which we have here. A mutation occur where the mutated sequence led to the termination of protein synthesis after the formation of tyrosine. The mutated sequence we have here. This is the reason for the mutated sequence. And we're given two main choices. We can either do transition or trans version mutations. So if we look at the two sequences we can see that the mutation occurred here in the fourth position. We have a wanting being swamped by a Euro. So now wanting is appearing and your sl is perimeter. When such a mutation occurs we call it trans version. So we're going to eliminate the first answer choice as it cannot be true. Now we have that this trans version or her and the mutated sequence lead to the termination of protein synthesis. So protein synthesis stopped. So I stopped coding was reached which is said to be you. A. Which is the second code on that we have here. So this one is being stopped by your cell created as stop coding. When I stopped coding is created. We call this a nonsense mutation. So this is a trans version mutation that led to a nonsense mutation. So the correct answer choice here is going to be answer choice C. So I mean a trans version led to a nonsense mutation occurring forming the stop code on you. A I really hope this video helped you and I hope to see you on the next one
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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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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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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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A significant number of mutations in the HBB gene that cause human β-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.

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Textbook Question

Dominant mutations can be categorized according to whether they increase or decrease the overall activity of a gene or gene product. Although a loss-of-function mutation (a mutation that inactivates the gene product) is usually recessive, for some genes, one dose of the normal gene product, encoded by the normal allele, is not sufficient to produce a normal phenotype. In this case, a loss-of-function mutation in the gene will be dominant, and the gene is said to be haploinsufficient. A second category of dominant mutation is the gain-of-function mutation, which results in a new activity or increased activity or expression of a gene or gene product. The gene therapy technique currently being used in clinical trials involves the 'addition' to somatic cells of a normal copy of a gene. In other words, a normal copy of the gene is inserted into the genome of the mutant somatic cell, but the mutated copy of the gene is not removed or replaced. Will this strategy work for either of the two aforementioned types of dominant mutations?

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