DNA Mutations, Damage, and Repair Mechanisms
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Genetics › DNA Mutations, Damage, and Repair Mechanisms
Which of the following statements is not true about genetic mutations?
All mutations cause a loss-of-function of the protein product.
Mutations can cause a gain-of-function of the protein product.
Mutations can have no effect on the function of the protein product.
Some mutations can cause lethality.
A mutation can be inherited.
Explanation
Mutations can cause a huge variety of effects, including proteins that don't work (loss-of-function) and proteins that are too active (gain-of-function). Not all mutations are loss-of-function. Mutations can be inherited or from environmental factors, and many times a mutation will mean nothing at all for the organism.
A(n) mutation causes a gene to have a premature stop codon. This means that translation of the protein will never be complete, because the machinery stops too early.
nonsense
missense
point
inversion
duplication
Explanation
A nonsense mutation will cause the protein to never be completed because of a premature stop codon, hence the protein "never makes sense," ie nonsense. Missense will make a protein with the incorrect amino acid sequence. A point mutation can cause a nonsense mutation, but is not the best answer, as it is vague. The other two mutations also theoretically can cause a nonsense mutation, but nonsense is most specific answer.
Which of the following mutation would be most deleterious?
A insertion of two bases in the splice site
Insertion of three bases in a coding region of mRNA
Deletion of one base int he 3'UTR
A change of one base in the wobble position in a coding region of mRNA
An insertion of one base in an intron
Explanation
The most deleterious mutation would be a frameshift mutation. This would attained by inserting or deleting multiples of 1 or 2 bases in any important coding regions (exons, splice site, translation start site). Inserting or deleting multiples of 3 bases would not cause a frameshift mutation. A mutation in 3' UTR or intron would essentially have minimal effects. A mutation in the wobble position would most likely not change the amino acid.
A T G C C T G G A T A G C T A
T A C G G A C C T A T C G A T
The original strand of DNA is written above. Which of the following choices represents a possible frameshift mutation?
A T G C T G G A T A G C T
T A C G A C C T A T C G A
A T G C C T G G G T A G C T A
T A C G G A C C C A T C G A T
A T G G G A T A G C T A
T A C C C T A T C G A T
A T G C A T G G A T A G C T A
T A C G T A C C T A T C G A T
Explanation
Recall that a frameshift mutation occurs when part of one or more codons in lost in such a way that the entire sequence of codons "shifts," making the transcribed mRNA translate as a different pattern of amino acids during protein synthesis. This is a big problem, since it means that a sequence of DNA coding for a specific protein now likely codes for a completely, fundamentally different one.
The correct answer is:
A T G C T G G A T A G C T A
T A C G A C C T A T C G A T
Compare to the original DNA, and note where one base pair was removed:
A T G C C T G G A T A G C T A
T A C G G A C C T A T C G A T
The codons on a piece of mRNA transcribed from the top strand of the non-mutated form would read:
UAC GGA CCU AUC GAU
However, mRNA transcribed from the mutated DNA would read:
UAC GAC CUA UCG AT\[ \] (we don't know the last codon, since the next base pair is not given)
This is a serious issue. The non-mutated form codes for these first four amino acids...
tyr gly pro ile
...while the mutated form codes for these first four amino acids:
tyr asp leu ser
Clearly, frameshift mutations can be very dangerous.
What refers to chromosomes in which the centromere is off to one side?
sub-metacentric
metacentric
acrocentric
lop-centric
Explanation
Sub-metacentric is when the the centromere is off to one side. Metacentric is when the centromere is in the middle. Acrocentric is when the centromere is at one end. Lop-centric is not a real thing.
If a nucleic acid is added into the RNA sequence, what type of mutation is this?
insertion
point mutation
deletion
addition
Explanation
It is an insertion because a nucleic acid was added to the sequence.
What is the name for a mutation that occurs when one nucleic acid in the sequence is switched with another?
point mutation
Insertion
deletion
frame shift
Explanation
Point mutations occur when one nucleic base is swapped for a different nucleic base.