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A. T
hey have a higher GC content compared to other nuclear genes.
B. T
hey have a different base composition compared to other nuclear genes.
C. There are no repetitive sequences.
E. T
hey are transcribed by RNA polymerases I and III.
2. You were asked to choose a method to separate a mixture of eukaryotic polymerases. Which of
the following methods would you choose?
A. c hromatography
B. w
estern blotting
C. S1 nuclease assay
D. DNase 1 footprinting
3. An antibody was produced and used in an immunohistochemical assay to detect the location of
RNA polymerase I in a thin section of a liver biopsy. The section was stained with the antibody
that had been labeled with a fluorescent tag, then viewed under a fluorescent microscope. State
where you would expect to find positive staining if the enzyme is present.
A. r ough endoplasmic reticulum
B. n
ucleoplasm
C. nucleolus
D. endoplasmic reticulum
E. r ibosomes
A. t RNA
B. s nRNA
C. hnRNA
A. α
-amanitin
B. D
MS
C. heparin
D. ammonium sulfate
E. n
one of the choices are correct.
A. 7
SL RNA
B. 5
SrRNA
C. snRNA
E. 7
SL RNA, 5SrRNA, and snRNA
7. A new mutant cell line was developed and found to be defective in polymerase III activity. Which
of the following is likely to be observed in this cell line?
A. T
here will be an overabundance of secreted proteins.
B. S
plicing function is impaired.
C. There will be an overproduction of 7 SL RNA.
D. There will be an overabundance of secreted proteins and splicing function is impaired are
correct.
E. T
here will be an overabundance of secreted proteins, splicing function is impaired, and there
will be an overproduction of 7 SL RNA are correct.
8. Which of the following is ideal to study the function of the subunits of polymerase II?
A. B
reak the enzymes into component parts and gradually reassemble them.
B. U
se mutational analysis.
C. Conduct DNA binding assays.
D. Break the enzymes into component parts and gradually reassemble them and use mutational
analysis are correct.
E. U
se mutational analysis and conduct DNA binding assays are correct.
9. One effect of the deletion of the hRPB1 subunit of RNA polymerase II is
A. l oss of the oligosaccharide-binding domain.
D. non-viable cells.
E. e xtended CTD.
10. Which of the following subunits are common in all three yeast polymerases?
A. R
pb2
B. R
pd8
C. Rpd10
E. b
oth B. Rpd8 and C. Rpd10
A. R
pb2
B. R
pb3
C. Rpb4
D. Rpd8
E. R
pd10
12. Which of the following subunits, when combined, are orthologs of the prokaryotic alpha dimer?
A. R
pb2 and rpb3
B. R
pb3 and rpb11
C. Rpb8 and rpb10
E. R
pb10 and rpb12
13. Which of the following would you choose to study the role of polymerase subunits in elongation?
A. e
pitope tagging
B. i mmunoprecipitation
C. in vitro transcription
D. western blotting
E. D NAase footprinting
A. T
he clamp does not come in contact with the RNA:DNA complex.
B. P
rocessivity is slowed by the closing of the clamp.
C. The clamp closes over the RNA:DNA hybrid in the enzyme's cleft.
D. Five loops in the clamps play a role in the movement of the enzyme.
E. T
he active site of the enzyme lies at the end of pore 2.
A. I t binds to Rpb3 to facilitate melting of the DNA promoter.
B. I t extends the dock region of polymerase, making it easier for transcription factors to bind.
D. It binds to Rpb3 to facilitate melting of the DNA promoter and it extends the dock region of
polymerase, making it easier for transcription factors to bind are correct.
E. I t extends the dock region of polymerase, making it easier for transcription factors to bind and
it binds to DNA and facilitate elongation are correct.
16. Which of the following is not a part of the core class II promoter?
A. T
ATA box
B. u
pstream element
C. BRE
D. DPE
E. I nr
17. Which of the following techniques would you use to study the role of the BRE?
A. S
1 nuclease protection analysis
B. l inker scanning mutations
C. X-ray crystallography
A. S
p1
B. D
PE
C. TBP
D. CTF
E. T
FB
19. Predict a possible effect of deleting the enhancers region of the polymerase I gene.
A. r educed transcription of ribosomes
20. Eukaryotic ribosomal RNA genes are transcribed by RNA polymerase II.
True False
21. Compared to other nuclear genes, ribosomal genes differ in their base compositions.
True False
22. Roeder and Rutter showed that there are four polymerases operating in the eukaryotic cell.
True False
23. Based on studies on Saccharomyces cerevisiae, there are at least 12 subunits in RNA
polymerase II.
True False
24. Epitope tagging is an efficient way to immunoprecipate and isolate an entire polymerase
complex.
True False
25. Mutational studies have shown that yeast Rpb3 is homologous to the alpha-subunit of E. coli.
True False
26. The product of the RPB1 gene in yeast assists polymerase IIA in binding DNA.
True False
27. Study of yeast polymerase II has revealed a deep cleft that can accept a linear DNA template
from one end to the other.
True False
28. The catalytic center of polymerase II contains Na+ ions.
True False
29. Enhancers and repressors can be tissue-specific based on the types of DNA-binding proteins that
are present in the cell.
True False
10 Key
1. Which of the statements about ribosomal genes is incorrect?
A. They have a higher GC content compared to other nuclear genes.
A. chromatography
B. western blotting
C. S1 nuclease assay
D. DNase 1 footprinting
A. rough endoplasmic reticulum
B. nucleoplasm
C. nucleolus
D. endoplasmic reticulum
E. ribosomes
A. tRNA
B. snRNA
C. hnRNA
A. α-amanitin
B. DMS
C. heparin
D. ammonium sulfate
A. 7SL RNA
B. 5SrRNA
C. snRNA
7. A new mutant cell line was developed and found to be defective in polymerase III activity.
Which of the following is likely to be observed in this cell line?
A. There will be an overabundance of secreted proteins.
D. There will be an overabundance of secreted proteins and splicing function is impaired are
correct.
E. There will be an overabundance of secreted proteins, splicing function is impaired, and
there will be an overproduction of 7 SL RNA are correct.
A. Break the enzymes into component parts and gradually reassemble them.
D. Break the enzymes into component parts and gradually reassemble them and use
mutational analysis are correct.
E. Use mutational analysis and conduct DNA binding assays are correct.
A. loss of the oligosaccharide-binding domain.
D. non-viable cells.
E. extended CTD.
10. Which of the following subunits are common in all three yeast polymerases?
A. Rpb2
B. Rpd8
C. Rpd10
A. Rpb2
B. Rpb3
C. Rpb4
D. Rpd8
E. Rpd10
A. Rpb2 and rpb3
13. Which of the following would you choose to study the role of polymerase subunits in
elongation?
A. epitope tagging
B. immunoprecipitation
C. in vitro transcription
D. western blotting
E. DNAase footprinting
A. The clamp does not come in contact with the RNA:DNA complex.
C. The clamp closes over the RNA:DNA hybrid in the enzyme's cleft.
D. Five loops in the clamps play a role in the movement of the enzyme.
A. It binds to Rpb3 to facilitate melting of the DNA promoter.
B. It extends the dock region of polymerase, making it easier for transcription factors to bind.
D. It binds to Rpb3 to facilitate melting of the DNA promoter and it extends the dock region of
polymerase, making it easier for transcription factors to bind are correct.
E. It extends the dock region of polymerase, making it easier for transcription factors to bind
and it binds to DNA and facilitate elongation are correct.
16. Which of the following is not a part of the core class II promoter?
A. TATA box
B. upstream element
C. BRE
D. DPE
E. Inr
A. S1 nuclease protection analysis
C. X-ray crystallography
A. Sp1
B. DPE
C. TBP
D. CTF
E. TFB
19. Predict a possible effect of deleting the enhancers region of the polymerase I gene.
A. reduced transcription of ribosomes
FALSE
Blooms Level: 1. Remember
Section: 10.01
Weaver - Chapter 10 #20
21. Compared to other nuclear genes, ribosomal genes differ in their base compositions.
TRUE
Blooms Level: 1. Remember
Section: 10.01
Weaver - Chapter 10 #21
22. Roeder and Rutter showed that there are four polymerases operating in the eukaryotic cell.
FALSE
Blooms Level: 1. Remember
Section: 10.01
Weaver - Chapter 10 #22
23. Based on studies on Saccharomyces cerevisiae, there are at least 12 subunits in RNA
polymerase II.
TRUE
Blooms Level: 1. Remember
Section: 10.01
Weaver - Chapter 10 #23
24. Epitope tagging is an efficient way to immunoprecipate and isolate an entire polymerase
complex.
TRUE
Blooms Level: 2. Understand
Section: 10.01
Weaver - Chapter 10 #24
25. Mutational studies have shown that yeast Rpb3 is homologous to the alpha-subunit of E. coli.
TRUE
Blooms Level: 1. Remember
Section: 10.01
Weaver - Chapter 10 #25
26. The product of the RPB1 gene in yeast assists polymerase IIA in binding DNA.
TRUE
Blooms Level: 2. Understand
Section: 10.01
Weaver - Chapter 10 #26
27. Study of yeast polymerase II has revealed a deep cleft that can accept a linear DNA template
from one end to the other.
TRUE
Blooms Level: 2. Understand
Section: 10.01
Weaver - Chapter 10 #27
28. The catalytic center of polymerase II contains Na+ ions.
FALSE
Blooms Level: 2. Understand
Section: 10.01
Weaver - Chapter 10 #28
29. Enhancers and repressors can be tissue-specific based on the types of DNA-binding proteins
that are present in the cell.
TRUE
Blooms Level: 2. Understand
Section: 10.03
Weaver - Chapter 10 #29
10 Summary
Category # of Questions
Blooms Level: 1. Remember 11
Blooms Level: 2. Understand 11
Blooms Level: 3. Apply 2
Blooms Level: 4. Analyze 2
Blooms Level: 5. Evaluate 3
Section: 10.01 24
Section: 10.02 3
Section: 10.03 2
Weaver - Chapter 10 29