Chapter 18 - Regulation of Gene Expression - Multiple Choice Flashcards
Complete the concept map to help you review the mechanisms by which bacteria regulate their gene expression in response to varying metabolic needs.
a. operons
b. promoter
c. operator
d. negative control
e. repressor
f. inactive
g. active
h. corepressor
i. inducer
j. anabolic
k. activate
l. inactivate
m. catabolic
n. cAMP
o. lack of glucose
Inducible enzymes
a. are usually involved in anabolic pathways.
b. are produced when a small molecule inactivates the repressor protein.
c. are produced when an activator molecule enhances the attachment of RNA polymerase with the operator.
d. are regulated by inherently inactive repressor molecules.
e. are regulated almost entirely by feedback inhibition.
b. are produced when a small molecule inactivates the repressor protein.
In E. coli, tryptophan switches off the trp operon by
a. inactivating the repressor protein.
b. inactivating the gene for the first enzyme in the pathway by feedback inhibition.
c. binding to the repressor and increasing the latter’s affinity for the operator.
d. binding to the operator.
e. binding to the promoter.
c. binding to the repressor and increasing the latter’s affinity for the operator.
In the control of the gene expression in bacteria, a regulatory gene
a. has its own promoter.
b. is transcribed continuously.
c. is not contained in the operon it controls.
d. codes for repressor proteins.
e. is or does all of the above.
e. is or does all of the above.
A mutation that reders nonfunctional the product of a regulatory gene for a repressible operon would result in
a. continuous transcription of the genes of the operon.
b. complete blocking of the attachment of RNA polymerase to the promoter.
c. irreversible binding of the repressor to the operator.
d. no difference in transcription rate when an activator protein was present.
e. negative control of transcription.
a. continuous transcription of the genes of the operon.
The control of gene expression is more complex in eukaryotic cells because
a. DNA is associated with protein.
b. gene expression differentiates specialized cells.
c. the chromosomes are linear and more numerous.
d. operons are controlled by more than one promoter region.
e. inhibitory or activitating molecules may help regulate transcription.
b. gene expression differentiates specialized cells.
DNA methylation of cytosine residues
a. initiates the acetylation of histones.
b. may be a mechanism of epigenic inheritance when methylation patterns are repeated in daughter cells.
c. occurs in the promoter region and enhances binding of RNA polymerase.
d. is a signal for proteasomes to degrade a protein.
e. may be related to the transformation of proto-oncogenes to oncogenes.
b. may be a mechanism of epigenic inheritance when methylation patterns are repeated in daughter cells.
Which of the following in not true of enhancers?
a. They may be located thousands of nucleotides upstream from the genes they affect.
b. When bound with activators, they interact with the promoter region and other transcription factors to produce an initiation complex.
c. They may complex with steroid-activated receptor proteins, which selectively activate specific genes.
d. They may coordinate the transcription of enzymes involved in the same metabolic pathway when they contain the same combination of control elements.
e. Each gene may have several enhancers, and each enhancer may be associated with and regulate several genes.
e. Each gene may have several enhancers, and each enhancer may be associated with and regulate several genes.
Which of the following is not an example of the control of gene expression that occurs after transcription?
a. mRNA stored in the cytoplasm needing activation of translation initiation factors
b. the length of time mRNA lasts before it is degraded
c. rRNA genes amplified in multiple copies in the genome
d. alternative RNA splicing before mRNA exits from the nucleus
e. splicing or modification of a polypeptide
c. rRNA genes amplified in multiple copies in the genome
Which of the following might a proto-oncogene code for?
a. DNA polymerase
b. RNA polymerase
c. receptor proteins for growth factors
d. an enhancer
e. transcription factors that inhibit cell division genes
c. receptor proteins for growth factors
A gene can develop into an oncogene when
a. it is present in more copies than normal.
b. it underoges a translocation that removes it from its normal control region.
c. a mutation results in a more active or resistant protein.
d. a mutation in a contol element increases expression.
e. any of the above occur.
e. any of the above occur.
A tumor-suppressor gene could cause the onset of cancer if
a. both alleles have mutations that decrease the activity of the gene product.
b. only one allele has a mutation that alters the gene product.
c. it is inherited in mutated form from a parent.
d. a proto-oncogene has also become an oncogene.
e. both a and d have happened.
e. both a and d have happened.
A eukaryotic gene typically has all of the following associated with it except
a. a promoter.
b. an operator.
c. enhancers.
d. introns and exons.
e. control elements.
b. an operator.
What is apoptosis?
a. a cell suicide program that may be initiated by p53 protein in response to DNA damage
b. metastasis, or the spread of cancer cells to a new location in the body
c. the transformation of a normal cell to a cancer cell
d. the mutation of a G protein into a hyperactive form
e. the transformation of a proto-oncogene to an oncogene by a point mutation
a. a cell suicide program that may be initiated by p53 protein in response to DNA damage
Which of the following would you expect to find as part of a receptor protein that binds with a steroid hormone?
a. a TATA box
b. a domain that binds to DNA and protein-binding domains
c. an activated operator region that allows attachment of RNA polymerase
d. an enhancer sequence located at some distance upstream or downstream from the promoter
e. transmembrane domains that facilitate its localization in a plasma membrane
b. a domain that binds to DNA and protein-binding domains