Campbell Biology in Focus, 2e (Urry)
Chapter 14 Gene Expression: From Gene to Protein
14.1 Multiple-Choice Questions
1) Garrod hypothesized that inherited diseases such as alkaptonuria, the inability to metabolize
the chemical alkapton, occur because
A) metabolic enzymes require vitamin cofactors, and affected individuals have significant
nutritional deficiencies.
B) many metabolic enzymes use DNA as a cofactor, and affected individuals have mutations that
prevent their enzymes from interacting efficiently with DNA.
C) certain metabolic reactions are carried out by ribozymes, and affected individuals lack key
splicing factors.
D) genes dictate the production of specific enzymes, and affected individuals have genetic
defects that cause them to lack certain enzymes.
2) Garrod’s information about the enzyme alteration resulting in alkaptonuria led to further
understanding of these types of metabolic pathways 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.
3) The nitrogenous base adenine is found in all members of which of the following groups of
molecules?
A) proteins, triglycerides, and testosterone
B) proteins, ATP, and DNA
C) ATP, RNA, and DNA
D) glucose, ATP, and DNA
E) proteins, carbohydrates, and ATP