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?
Table of contents
- 1. Introduction to Genetics51m
- 2. Mendel's Laws of Inheritance3h 37m
- 3. Extensions to Mendelian Inheritance2h 41m
- 4. Genetic Mapping and Linkage2h 28m
- 5. Genetics of Bacteria and Viruses1h 21m
- 6. Chromosomal Variation1h 48m
- 7. DNA and Chromosome Structure56m
- 8. DNA Replication1h 10m
- 9. Mitosis and Meiosis1h 34m
- 10. Transcription1h 0m
- 11. Translation58m
- 12. Gene Regulation in Prokaryotes1h 19m
- 13. Gene Regulation in Eukaryotes44m
- 14. Genetic Control of Development44m
- 15. Genomes and Genomics1h 50m
- 16. Transposable Elements47m
- 17. Mutation, Repair, and Recombination1h 6m
- 18. Molecular Genetic Tools19m
- 19. Cancer Genetics29m
- 20. Quantitative Genetics1h 26m
- 21. Population Genetics50m
- 22. Evolutionary Genetics29m
17. Mutation, Repair, and Recombination
Types of Mutations
Problem 19b
Textbook Question
Using the adenine–thymine base pair in this DNA sequence
...GCTC...
...CGAG...
Give the sequence after a transversion mutation.

1
Identify the original DNA sequence provided in the problem. In this case, the sequence is shown as two complementary strands: 'CCTTAGGATTCC' and 'GGAATCCTTAAGG'.
Understand the concept of a transversion mutation. A transversion mutation occurs when a purine (adenine or guanine) is replaced by a pyrimidine (cytosine or thymine), or vice versa.
Locate the site of the mutation in the sequence. From the image, the mutation occurs in the second strand where 'G' is replaced by 'C'. This change also affects the complementary strand, where 'C' is replaced by 'G'.
Update the sequence to reflect the transversion mutation. Replace the affected base pair in both strands: 'CCTTAGGATTCC' becomes 'CCTTAGGAGTCC', and 'GGAATCCTTAAGG' becomes 'GGAATCCTCAGG'.
Verify that the new sequence maintains proper base pairing rules (adenine pairs with thymine, and guanine pairs with cytosine) after the mutation. Ensure the complementary strand reflects the change accurately.

This video solution was recommended by our tutors as helpful for the problem above
Video duration:
1mPlay a video:
Was this helpful?
Key Concepts
Here are the essential concepts you must grasp in order to answer the question correctly.
Transversion Mutation
A transversion mutation is a type of point mutation where a purine base (adenine or guanine) is replaced by a pyrimidine base (cytosine or thymine), or vice versa. This contrasts with transitions, where a purine is replaced by another purine or a pyrimidine by another pyrimidine. Transversions can lead to significant changes in the protein sequence, potentially altering the function of the resulting protein.
Recommended video:
Guided course
Point Mutations
DNA Base Pairing
DNA base pairing refers to the specific pairing of nitrogenous bases in the DNA double helix, where adenine pairs with thymine (A-T) and guanine pairs with cytosine (G-C). This complementary base pairing is crucial for DNA replication and transcription, ensuring that genetic information is accurately copied and expressed. Understanding base pairing is essential for predicting the effects of mutations on DNA sequences.
Recommended video:
Guided course
DNA Structure
Effects of Mutations on Protein Synthesis
Mutations can have various effects on protein synthesis, ranging from silent mutations that do not change the amino acid sequence to missense mutations that result in a different amino acid being incorporated. In some cases, mutations can lead to nonsense mutations, creating premature stop codons that truncate the protein. The specific impact of a mutation depends on its nature and location within the gene, influencing the overall function of the protein produced.
Recommended video:
Guided course
Proteins
Related Videos
Related Practice
Textbook Question
491
views