Shown below are two homologous lengths of the alpha and beta chains of human hemoglobin. Consult a genetic code dictionary (Figure 13.7 ) and determine how many amino acid substitutions may have occurred as a result of a single nucleotide substitution. For any that cannot occur as a result of a single change, determine the minimal mutational distance.

Short Answer

Expert verified
Answer: In the given Alpha and Beta chain sequences, one amino acid substitution (Proline to Serine) can occur as a result of a single nucleotide substitution.

Step by step solution

01

Divide the sequences into codons

We'll divide the given sequences into codons - groups of 3 nucleotides each that correspond to an amino acid. Alpha chain: ATG CCA GTG Beta chain: ATG TCA GTG
02

Identify amino acids for each codon using a genetic code dictionary

Using a genetic code dictionary (Figure 13.7), we will identify the corresponding amino acids for each codon. Alpha chain: Met Pro Val Beta chain: Met Ser Val
03

Determine single nucleotide substitutions that lead to amino acid changes

Now we need to analyze the differences in amino acid sequences caused by single nucleotide substitutions. For the second amino acid, we have Proline (Pro) in the Alpha chain and Serine (Ser) in the Beta chain. Let's consult the genetic code dictionary to see if there is a single nucleotide substitution that can cause this change. Proline (Pro) codons: CCU, CCC, CCA, CCG Serine (Ser) codons: UCU, UCC, UCA, UCG, AGU, AGC It's easy to notice that by changing the second nucleotide of the Proline codon CCA (Alpha chain) to a T, we get the Serine codon TCA (Beta chain). So, it's a single nucleotide substitution which results in an amino acid change.
04

Calculate minimal mutational distance for cases where single nucleotide substitution does not result in an amino acid change

In this particular example, all observed amino acid changes can occur as a result of single nucleotide substitutions. However, let's consider a hypothetical case where an amino acid change does not occur with a single change: Alpha chain: Met Pro Val Beta chain: Met Phe Val Phenylalanine (Phe) codons: UUU, UUC In this case, there is no single nucleotide substitution that can convert a Proline codon to a Phenylalanine codon. To find the minimal mutational distance, we need to find the shortest number of nucleotide changes required for the conversion: - CCA (Pro) -> UCA (Ser) -> UUA (Leu) -> UUA (Phe) (3 changes) So, the minimal mutational distance in this hypothetical case is 3. In conclusion, for the given Alpha and Beta chain sequences, there is one amino acid substitution (Pro->Ser) that can occur as a result of a single nucleotide substitution. For other cases where single substitution does not lead to amino acid change, it may be necessary to calculate the minimal mutational distance as shown in the example.

Unlock Step-by-Step Solutions & Ace Your Exams!

  • Full Textbook Solutions

    Get detailed explanations and key concepts

  • Unlimited Al creation

    Al flashcards, explanations, exams and more...

  • Ads-free access

    To over 500 millions flashcards

  • Money-back guarantee

    We refund you if you fail your exam.

Over 30 million students worldwide already upgrade their learning with Vaia!

One App. One Place for Learning.

All the tools & learning materials you need for study success - in one app.

Get started for free

Most popular questions from this chapter

Read the Chapter Concepts list on page \(681 .\) All these pertain to the principles of population genetics and the evolution of species. Write a short essay describing the roles of mutation, migration, and selection in bringing about speciation.

In a population of 10,000 individuals, where 3600 are \(M M\) 1600 are \(N N,\) and 4800 are \(M N,\) what are the frequencies of the \(M\) alleles and the \(N\) alleles?

Consider a population in which the frequency of allele \(A\) is \(p=0.7\) and the frequency of allele \(a\) is \(q=0.3,\) and where the alleles are codominant. What will be the allele frequencies after one generation if the following occurs? (a) \(w_{A A}=1, w_{A a}=0.9, w_{a a}=0.8\) (b) \(w_{A A}=1, w_{A a}=0.95, w_{a a}=0.9\) (c) \(w_{A A}=1, w_{A a}=0.99, w_{a a}=0.98\) (d) \(w_{A A}=0.8, w_{A a}=1, w_{a a}=0.8\)

A certain form of albinism in humans is recessive and autosomal. Assume that \(1 \%\) of the individuals in a given population are albino. Assuming that the population is in HardyWeinberg equilibrium, what percentage of the individuals in this population is expected to be heterozygous?

Price et al. (1999. J. Bacteriol. 181: 2358-2362) conducted a genetic study of the toxin transport protein (PA) of Bacillus anthracis, the bacterium that causes anthrax in humans. Within the 2294 -nucleotide gene in 26 strains they identified five point mutations-two missense and three synonyms-among different isolates. Necropsy samples from an anthrax outbreak in 1979 revealed a novel missense mutation and five unique nucleotide changes among ten victims. The authors concluded that these data indicate little or no horizontal transfer between different \(B\). anthracis strains. (a) Which types of nucleotide changes (missense or synonyms) cause amino acid changes? (b) What is meant by horizontal transfer? (c) On what basis did the authors conclude that evidence of horizontal transfer is absent from their data?

See all solutions

Recommended explanations on Biology Textbooks

View all explanations

What do you think about this solution?

We value your feedback to improve our textbook solutions.

Study anywhere. Anytime. Across all devices.

Sign-up for free