Question 1
A student has the DNA sequence: ATG · CAT · GGA · TCA. A single base 'A' is inserted after the third base, giving: ATG · ACA · TGG · ATC · A... What type of mutation has occurred, and what is its likely effect?No clue? Show me the answer
Correct answer
Correct!
IncorrectStep-by-step walkthrough
Choose a solution method
Method #1Direct ApproachStep 1: Identify the type of change in the sequence
Comparing the original and new sequence, an extra base 'A' has been added into the sequence. This is an insertion mutation — one or more extra bases are added.
Step 2: Determine whether a frameshift occurs
The genetic code is read in groups of three (codons). Adding one base shifts the reading frame for every codon after the insertion point. This is called a frameshift mutation.
Step 3: Assess the extent of the effect
Because all codons downstream of the insertion are changed, a completely different set of amino acids is produced from that point onwards. The resulting protein is almost certainly non-functional.
Step 4: Select the correct answer
The correct description is an insertion mutation causing a frameshift that alters all codons after the insertion point.
Method #2Process of EliminationStep 1: Identify what the question is asking
We need to identify the type of mutation and its effect on the genetic code.
Step 2: Eliminate 'Substitution mutation'
A substitution swaps one base for another — no extra base is added. The question clearly states a base is inserted, so the option 'Substitution mutation causing a single amino acid change' is incorrect.
Step 3: Eliminate 'Deletion mutation'
A deletion removes a base. Here a base is added, not removed. Also, frameshifts alter codons after the mutation point, not before. This option is doubly incorrect.
Step 4: Eliminate 'no effect because of degeneracy'
Degeneracy (multiple codons coding for the same amino acid) can make a substitution silent, but it cannot rescue a frameshift — the entire reading frame is disrupted, affecting many codons simultaneously.
Step 5: Select the correct answer
The remaining option — insertion mutation causing a frameshift with all downstream codons altered — correctly describes what happens when an extra base is added to a DNA sequence.
Question 2
A smoker develops lung cancer due to mutations caused by chemicals in tobacco smoke. Which of the following correctly explains why their children will NOT inherit this lung cancer?No clue? Show me the answer
Correct answer
Correct!
IncorrectStep-by-step walkthrough
Choose a solution method
Method #1Direct ApproachStep 1: Identify the key distinction in mutation inheritance
Only germline mutations (in sex cells — eggs and sperm) can be passed to offspring. Somatic mutations affect the individual's body cells only.
Step 2: Apply this to the scenario
Lung cancer develops in lung cells, which are somatic cells. These cells do not contribute genetic material to the next generation.
Step 3: Select the correct answer
Because the lung cancer mutations are in somatic cells and not gametes, they cannot be inherited by children.
Method #2Process of EliminationStep 1: Identify what needs explaining
We need to explain why a parent's cancer mutation is not passed to offspring — the key concept is which types of mutations are heritable.
Step 2: Eliminate 'cancer mutations are always recessive'
This is factually incorrect — many cancer-causing mutations are dominant (e.g. in oncogenes). Recessiveness has nothing to do with why lung cancer isn't inherited.
Step 3: Eliminate 'the immune system destroys inherited cancer mutations'
The immune system can destroy abnormal cells, but the reason the mutation is not inherited has nothing to do with the children's immune system — the mutation was never transmitted in the first place.
Step 4: Eliminate 'tobacco smoke only causes chromosomal mutations'
Tobacco smoke chemicals cause gene mutations (e.g. base changes), not exclusively chromosomal mutations. This statement is factually wrong.
Step 5: Select the correct answer
The correct explanation is that lung cancer mutations occur in somatic cells (lung cells), which do not contribute to gametes. Without being in a gamete, the mutation cannot be inherited.
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