CH17 Flashcards
A frameshift mutation could result from A) a base insertion only. B) a base deletion only. C) a base substitution only. D) deletion of three consecutive bases. E) either an insertion or a deletion of a base.
E
Suppose that a mutation alters the formation of a tRNA such that it still attaches to the same amino acid (phe) but its anticodon loop has the sequence AAU that binds to the mRNA codon UUA (that usually specifies leucine leu).
A) The modified tRNA will cause this mRNA to make only nonfunctioning product.
B) The tRNA-leu will not be able to enter the site of the ribosome to bind to the UUA.
C) One mutated tRNA molecule will be relatively inconsequential because it will compete with many “normal” ones.
D) The tRNA will be so unstable that it will not participate in translation.
E) The mutated tRNA will result in an amino acid variant in all copies of the protein.
Answer: A
C
In eukaryotic cells, transcription cannot begin until
A) the two DNA strands have completely separated and exposed the promoter.
B) several transcription factors have bound to the promoter.
C) the 5’ caps are removed from the mRNA.
D) the DNA introns are removed from the template.
E) DNA nucleases have isolated the transcription unit.
B
50) The most commonly occurring mutation in people with cystic fibrosis is a deletion of a single codon. This results in A) a base-pair substitution. B) a nucleotide mismatch. C) a frameshift mutation. D) a polypeptide missing an amino acid. E) a nonsense mutation.
D
45) Which of the following types of mutation, resulting in an error in the mRNA just after the AUG start of translation, is likely to have the most serious effect on the polypeptide product?
A) a deletion of a codon
B) a deletion of two nucleotides
C) a substitution of the third nucleotide in an ACC codon
D) a substitution of the first nucleotide of a GGG codon
E) an insertion of a codon
B
The TATA sequence is found only several nucleotides away from the start site of transcription. This most probably relates to which of the following?
A) the number of hydrogen bonds between A and T in DNA
B) the triplet nature of the codon
C) the ability of this sequence to bind to the start site
D) the supercoiling of the DNA near the start site
E) the 3-D shape of a DNA molecule
A
The genetic code is essentially the same for all organisms. From this, one can logically assume which of the following?
A) A gene from an organism can theoretically be expressed by any other organism.
B) All organisms have experienced convergent evolution.
C) DNA was the first genetic material.
D) The same codons in different organisms translate into the different amino acids.
E) Different organisms have different numbers of different types of amino acids.
A
Which of the following provides some evidence that RNA probably evolved before DNA?
A) RNA polymerase uses DNA as a template.
B) RNA polymerase makes a single-stranded molecule.
C) RNA polymerase does not require localized unwinding of the DNA.
D) DNA polymerase uses primer, usually made of RNA.
E) DNA polymerase has proofreading function.
D
The nitrogenous base adenine is found in all members of which group?
A) proteins, triglycerides, and testosterone
B) proteins, ATP, and DNA
C) ATP, RNA, and DNA
D) α glucose, ATP, and DNA
E) proteins, carbohydrates, and ATP
C
An experimenter has altered the 3’ end of the tRNA corresponding to the amino acid methionine in such a way as to remove the 3’ AC. Which of the following hypotheses describes the most likely result?
A) tRNA will not form a cloverleaf.
B) The nearby stem end will pair improperly.
C) The amino acid methionine will not bind.
D) The anticodon will not bind with the mRNA codon.
E) The aminoacylsynthetase will not be formed.
C
What is the effect of a nonsense mutation in a gene?
A) It changes an amino acid in the encoded protein.
B) It has no effect on the amino acid sequence of the encoded protein.
C) It introduces a premature stop codon into the mRNA.
D) It alters the reading frame of the mRNA.
E) It prevents introns from being excised.
C
Which of the following mutations is most likely to cause a phenotypic change?
A) a duplication of all or most introns
B) a large inversion whose ends are each in intergenic regions
C) a nucleotide substitution in an exon coding for a transmembrane domain
D) a single nucleotide deletion in an exon coding for an active site
E) a frameshift mutation one codon away from the 3’ end of the nontemplate strand
D
Which component is not directly involved in translation? A) mRNA B) DNA C) tRNA D) ribosomes E) GTP
B
Which of the following variations on translation would be most disadvantageous for a cell?
A) translating polypeptides directly from DNA
B) using fewer kinds of tRNA
C) having only one stop codon
D) lengthening the half-life of mRNA
E) having a second codon (besides AUG) as a start codon
A
During splicing, which molecular component of the spliceosome catalyzes the excision reaction? A) protein B) DNA C) RNA D) lipid E) sugar
C
