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A glycine residue exists at 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 , and what are they? How many will result if the wild-type codon is GGU?

Short Answer

Expert verified
Answer: For both GGA and GGU glycine codons, 6 out of 9 possible single-base substitutions result in an amino acid substitution at position 210.

Step by step solution

01

Identify possible single-base substitutions for GGA codon

In this step, we will list all possible single-base substitutions for the given glycine codon GGA. We have three positions to change and 3 possible nucleotides to change them to (excluding the original nucleotide), so we get the following 9 substitutions: - Position 1: GGA -> AGA, TGA, or CGA - Position 2: GGA -> GAA, GTA, or GCA - Position 3: GGA -> GGG, GGT, or GGC
02

Determine amino acids corresponding to the new codons

Now, we'll use an amino acid reference table to determine the amino acids corresponding to the new codons: - AGA: Arginine - TGA: Stop codon - CGA: Arginine - GAA: Glutamic acid - GTA: Valine - GCA: Alanine - GGG: Glycine - GGT: Glycine - GGC: Glycine
03

Count how many substitutions result in a different amino acid

In this step, we will count the number of substitutions that result in an amino acid different from glycine: - AGA: Arginine (Different) - TGA: Stop codon (Different) - CGA: Arginine (Different) - GAA: Glutamic acid (Different) - GTA: Valine (Different) - GCA: Alanine (Different) - GGG: Glycine (Same) - GGT: Glycine (Same) - GGC: Glycine (Same) For the GGA codon, a total of 6 out of 9 possible single-base substitutions result in an amino acid substitution at position 210. Now, let's perform the same steps for the GGU codon.
04

Identify possible single-base substitutions for GGU codon

In this step, we will list all possible single-base substitutions for the given glycine codon GGU: - Position 1: GGU -> AGU, TGU, or CGU - Position 2: GGU -> GAU, GTU, or GCU - Position 3: GGU -> GGG, GGT, or GGC
05

Determine amino acids corresponding to the new codons

Now, we'll use an amino acid reference table to determine the amino acids corresponding to the new codons: - AGU: Serine - TGU: Cysteine - CGU: Arginine - GAU: Aspartic acid - GTU: Valine - GCU: Alanine - GGG: Glycine - GGT: Glycine - GGC: Glycine
06

Count how many substitutions result in a different amino acid

In this step, we'll count the number of substitutions that result in an amino acid different from glycine: - AGU: Serine (Different) - TGU: Cysteine (Different) - CGU: Arginine (Different) - GAU: Aspartic acid (Different) - GTU: Valine (Different) - GCU: Alanine (Different) - GGG: Glycine (Same) - GGT: Glycine (Same) - GGC: Glycine (Same) For the GGU codon, a total of 6 out of 9 possible single-base substitutions result in an amino acid substitution at position 210 as well. In conclusion, for both GGA and GGU glycine codons, 6 out of 9 possible single-base substitutions result in an amino acid substitution at position 210.

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Most popular questions from this chapter

Alternative splicing is a common mechanism for eukaryotes to expand their repertoire of gene functions. At least one estimate indicates that approximately 50 percent of human genes use alternative splicing, and approximately 15 percent of diseasecausing 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. (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?

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Define the process of transcription. Where does this process fit into the central dogma of molecular genetics?

In studies of frameshift mutations, Crick, Barnett, Brenner, and Watts-Tobin found that either three nucleotide insertions or deletions restored the correct reading frame. (a) Assuming the code is a triplet, what effect would the addition or loss of six nucleotides have on the reading frame? (b) If the code were a sextuplet (consisting of six nucleotides), would the reading frame be restored by the addition or loss of three, six, or nine nucleotides?

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) How did we determine the compositions of codons encoding specific amino acids? (b) How were the specific sequences of triplet codes determined experimentally? (c) How were the experimentally derived triplet codon assignments verified in studies using bacteriophage MS2? (d) How do we know that mRNA exists and serves as an intermediate between information encoded in DNA and its concomitant gene product? (e) 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?

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