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Sydney Brenner argued that the code was nonoverlapping because he considered that coding restrictions would occur if it were overlapping. A second major argument against an overlapping code involved the effect of a single nucleotide change. In an overlapping code, how many adjacent amino acids would be affected by a point mutation? In a nonoverlapping code, how many amino acid(s) would be affected?

Short Answer

Expert verified
Answer: In an overlapping code, a point mutation would affect 2 adjacent amino acids, whereas in a nonoverlapping code, it would affect only 1 amino acid.

Step by step solution

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1. Understanding overlapping and nonoverlapping codes

An overlapping code is when a single nucleotide is part of more than one codon (a sequence of 3 nucleotides that code for a specific amino acid). In contrast, a nonoverlapping code is when a single nucleotide is part of only one codon.
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2. Considering point mutations in overlapping codes

In an overlapping code, a point mutation (change in one nucleotide) would affect the amino acid coded by the codon it is a part of, as well as the amino acid(s) encoded by the adjacent codon(s) sharing the mutated nucleotide. This is because the mutated nucleotide is part of more than one codon.
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3. Calculating the number of affected amino acids in overlapping codes

Let's consider a point mutation occurs at the second nucleotide of a codon, in an overlapping code: Original: A-T-A | T-G-C Mutation: A-G-A | G-G-C The mutated nucleotide affects two codons and their encoded amino acids because the second nucleotide (T) is part of both the first and second codons (bolded): ATA - Original amino acid 1 *AGA - New amino acid 1 due to mutation* TGC - Original amino acid 2 *GGC - New amino acid 2 due to mutation* So, in an overlapping code, a point mutation would affect 2 adjacent amino acids.
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4. Considering point mutations in nonoverlapping codes

In a nonoverlapping code, a point mutation would affect only the amino acid coded by the mutated codon, since that nucleotide is not part of any other codon.
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5. Calculating the number of affected amino acids in nonoverlapping codes

Let's consider a point mutation occurs at the second nucleotide of a codon, in a nonoverlapping code: Original: A-T-A | G-C-A Mutation: A-G-A | G-C-A The mutated nucleotide affects only one codon and its encoded amino acid: ATA - Original amino acid 1 *AGA - New amino acid 1 due to mutation* GCA - Unaffected amino acid 2 So, in a nonoverlapping code, a point mutation would affect only 1 amino acid. In summary, in an overlapping code, a point mutation will affect 2 adjacent amino acids, while in a nonoverlapping code, it will affect only 1 amino acid.

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Most popular questions from this chapter

The concept of consensus sequences of DNA was defined in this chapter as sequences that are similar (homologous) in different genes of the same organism or in genes of different organisms. Examples were the Pribnow box and the -35 region in prokaryotes and the TATA-box region in eukaryotes. One study found that among 73 isolates from the virus HIV-Type \(1 \mathrm{C}\) (a major contributor to the AIDS epidemic), a GGGNNNNNCC consensus sequence exists (where \(\mathrm{N}\) equals any nitrogenous base) in the promoter-enhancer region of the \(\mathrm{NF}-\kappa \mathrm{B}\) transcription factor, a cis- acting element that is critical for initiating HIV transcription in human macrophages (Novitsky et al., 2002 ). The authors contend that finding this and other conserved sequences may be of value in designing an AIDS vaccine. What advantages would knowing these consensus sequences confer? Are there disadvantages as a vaccine is designed?

Review the Chapter Concepts list on \(\mathrm{p} .342 .\) These all center around how genetic information is stored in DNA and transferred to RNA prior to translation into proteins. Write a short essay that summarizes the key properties of the genetic code and the process by which \(\mathrm{RNA}\) is transcribed on a DNA template.

In this chapter, we focused on the genetic code and the transcription of genetic information stored in DNA into complementary RNA molecules. Along the way, we found many opportunities to consider the methods and reasoning by which much of this information was acquired. From the explanations given in the chapter, what answers would you propose to the following fundamental questions: (a) Why did geneticists believe, even before direct experimental evidence was obtained, that the genetic code would turn out to be composed of triplet sequences and be nonoverlapping? Experimentally, how were these suppositions shown to be correct? (b) What experimental evidence provided the initial insights into the compositions of codons encoding specific amino acids? (c) How were the specific sequences of triplet codes determined experimentally? (d) How were the experimentally derived triplet codon assignments verified in studies using bacteriophage MS2? (e) What evidence do we have that the expression of the information encoded in DNA involves an RNA intermediate? (f) How do we know that the initial transcript of a eukaryotic gene contains noncoding sequences that must be removed before accurate translation into proteins can occur?

When the amino acid sequences of insulin isolated from different organisms were determined, differences were noted. For example, alanine was substituted for threonine, serine for glycine, and valine for isoleucine at corresponding positions in the protein. List the single-base changes that could occur in codons of the genetic code to produce these amino acid changes.

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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