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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

01

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.
03

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.
04

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

Recent observations indicate that alternative splicing is a common way for eukaryotes to expand their repertoire of gene functions. Studies indicate that approximately 50 percent of human genes exhibit alternative splicing and approximately 15 percent of disease-causing mutations involve aberrant alternative splicing. Different tissues show remarkably different frequencies of alternative splicing, with the brain accounting for approximately 18 percent of such events (Xu et al., 2002 . Nuc. Acids Res. \(30: 3754-3766\) ). (a) Define alternative splicing and speculate on the evolutionary strategy alternative splicing offers to organisms. (b) Why might some tissues engage in more alternative splicing than others?

Predict the amino acid sequence produced during translation by the following short hypothetical mRNA sequences (note that the second sequence was formed from the first by a deletion of only one nucleotide): Sequence 1: 5'-AUGCCGGAUUAUAGUUGA-3' Sequence \(2: 5^{\prime}-\) AUGCCGGAUUAAGUUGA-3' What type of mutation gave rise to Sequence 2 ?

Present an overview of various forms of posttranscriptional processing in eukaryotes. For each, provide an example.

Write a paragraph describing the abbreviated chemical reactions that summarize RNA polymerase-directed transcription.

M. Klemke et al. (2001) discovered an interesting coding phenomenon in which an exon within a neurologic hormone receptor gene in mammals appears to produce two different protein entities (XL \(\alpha\) s, ALEX). Following is the DNA sequence of the exon's \(5^{\prime}\) end derived from a rat. The lowercase letters represent the initial coding portion for the XL \(\alpha\)s protein, and the uppercase letters indicate the portion where the ALEX entity is initiated. (For simplicity, and to correspond with the RNA coding dictionary, it is customary to represent the noncoding, nontemplate strand of the DNA segment.) \(5^{\prime}-\) gtcccaaccatgcccaccgatcttccgcctgcttctgaagATGCGGGCCCAG (a) Convert the noncoding DNA sequence to the coding RNA sequence. (b) Locate the initiator codon within the XL \(\alpha\) segment. (c) Locate the initiator codon within the ALEX segment. Are the two initiator codons in frame? (d) Provide the amino acid sequence for each coding sequence. In the region of overlap, are the two amino acid sequences the same? (e) Are there any evolutionary advantages to having the same DNA sequence code for two protein products? Are there any disadvantages?

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