Campbell’s Biology, 9e (Reece et al.)
Chapter 17 From Gene to Protein
The text for Chapter 17 has remained largely unchanged from the previous edition. However, one-third
of the following questions are new, and considerably more are at the skill level of analysis and
application.
Multiple-Choice Questions
1) 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
2) Garrod hypothesized that “inborn errors of metabolism” such as alkaptonuria occur because
A) metabolic enzymes require vitamin cofactors, and affected individuals have significant nutritional
deficiencies.
B) enzymes are made of DNA, and affected individuals lack DNA polymerase.
C) many metabolic enzymes use DNA as a cofactor, and affected individuals have mutations that
prevent their enzymes from interacting efficiently with DNA.
D) certain metabolic reactions are carried out by ribozymes, and affected individuals lack key splicing
factors.
E) genes dictate the production of specific enzymes, and affected individuals have genetic defects that
cause them to lack certain enzymes.
3) Garrod’s information about the enzyme alteration resulting in alkaptonuria led to further elucidation
of the same pathway in humans. Phenylketonuria (PKU) occurs when another enzyme in the pathway is
altered or missing, resulting in a failure of phenylalanine (phe) to be metabolized to another amino acid:
tyrosine. Tyrosine is an earlier substrate in the pathway altered in alkaptonuria. How might PKU affect
the presence or absence of alkaptonuria?
A) It would have no effect, because PKU occurs several steps away in the pathway.
B) It would have no effect, because tyrosine is also available from the diet.
C) Anyone with PKU must also have alkaptonuria.
D) Anyone with PKU is born with a predisposition to later alkaptonuria.
E) Anyone with PKU has mild symptoms of alkaptonuria.