Exam 3 Flashcards
The MutHLS repair system removes DNA around mismatched base pairs. How does the MutHLS repair system know which DNA strand to remove?
- The Mut repair system indiscriminately removes either DNA strand
- The Mut repair system interacts with DNA polymerase and thus knows which strand is the new one
- The Mut repair system recognizes methylated DNA and removes the DNA strand that is unmethylated
- The Mut repair system recognizes methylated DNA and removes the DNA strand that is methylated
- The Mut repair system remoes teh strand of DNA that contains uracil
The Mut repair system recognizes methylated DNA and removes the DNA strand that is unmethylated
In Von Neumann’s analogy
- the genes represent hardware
- a viral protein coat is software
- the cell’s enzymes represent hardware
- the cell’s enzymes represent software
- the genes are the software
- A and D
- C and E
- H. none of these answers is correct
C and E
- the cell’s enzymes represent hardware
- the genes are the software
What is the order of development described by Dyson from earliest to latest?
- pathogen > symbiont > parasite > integrated component
- integrated component > symbiont > parasite > pathogen
- pathogen > parasite > symbiont > integrated component
- nucleic acid > clay > protein > membranes
- none of the above
pathogen > parasite > symbiont > integrated component
Which has a lower error rate?
- reproduction as used by Dyson
- replication
- metabolism
- parasitic infection
- the average student taking this exam
replication
(he sometimes calls it modern replication)
Where in a protein would you expect the mutation rate to be highest?
- α helices
- β strands
- in the active site
- in the loops
- none of the above, as all regions would show the same rate
in the loops
Modification of DNA by methylases in bacteria is used
- To identify “self’ DNA and recognize “foreign” DNA
- To regulate the expression of certain genes
- To identify the original DNA strand in mismatch repair
- To mark DNA to be cut by restriction enzymes
- Two of the above
Two of the above
- The role of nick translation in DNA replication is
- to replace the RNA primer bases by the appropriate DNA bases
- to connect pieces of DNA to one another (ligation).
- to help unwind the double helix.
- to generate high energy phosphate bonds.
- none of the above.
to replace the RNA primer bases by the appropriate DNA bases
Splicing mRNA in eukaryotes
- Removes the introns
- Removes the exons
- Always involves folding of the mRNA
- Always involves proteins
- Two of the above
Two of the above
Which of the following is not true of translation initiation?
- Starts with a methionine-tRNA
- Needs a ribosome binding site on the mRNA
- Requires GTP
- The large subunit of the ribosome binds the mRNA first
- Two of the above are not true
The large subunit of the ribosome binds the mRNA first
When amino acids are attached to tRNAs,
- the N-terminal end is attached to the 2’ or 3’ hydroxyl of the ribose at the 3’ end of the tRNA.
- the N-terminal end is attached to the 5’ hydroxyl of the ribose at the 3’ end of the tRNA.
- the C-terminal end is attached to the 2’ or 3’ hydroxyl of the ribose at the 3’ end of the tRNA.
- the C-terminal end is attached to the 5’ hydroxyl of the ribose at the 3’ end of the tRNA.
- None of the above
the C-terminal end is attached to the 2’ or 3’ hydroxyl of the ribose at the 3’ end of the tRNA.
How are amino acids attached to tRNAs,
- the N-terminal end is attached to the 2’ or 3’ hydroxyl of the tRNA.
- the N-terminal end is attached to the 5’ hydroxyl of the tRNA.
- the C-terminal end is attached to the 2’ or 3’ hydroxyl of the tRNA.
- the C-terminal end is attached to the 5’ hydroxyl of the tRNA.
- None of the above
the C-terminal end is attached to the 2’ or 3’ hydroxyl of the tRNA.
When amino acids are attached to tRNAs,
- the N-terminal end is attached to the 2’ or 3’ hydroxyl of the ribose at the 3’ end of the tRNA.
- the N-terminal end is attached to the 5’ hydroxyl of the ribose at the 3’ end of the tRNA.
- the C-terminal end is attached to the 2’ or 3’ hydroxyl of the ribose at the 3’ end of the tRNA.
- the C-terminal end is attached to the 5’ hydroxyl of the ribose at the 3’ end of the tRNA.
- None of the above
the C-terminal end is attached to the 2’ or 3’ hydroxyl of the ribose at the 3’ end of the tRNA.
Proofreading during the elongation step of translation occurs
- During insertion of the tRNA carrying the new amino acid into the ribosome
- Just before peptide bond formation
- Just after pepetide bond formation
- During the translocation step to move the peptide from one site to another
- None of the above; there is no proofreading during translation
Just before peptide bond formation
Reverse transcriptase
- Is the enzyme responsible for degrading mRNA
- Is an enzyme that works with RNA polymerase to proofread the new message
- Makes an RNA copy of RNA
- Makes a DNA copy of RNA
- None of the above
Makes a DNA copy of RNA
What is the major role of DNA polymerase III?
- Repair of damaged DNA
- Fills in gaps between Okazaki fragments
- Synthesizes the majority of new DNA at replication forks
- The role of DNA polymerase III is not known
- None of the above
Synthesizes the majority of new DNA at replication forks
The lac operon is controlled by
- A repressor
- An activator
- Attenuation
- Both a repressor and activator
- Both attenuation and a repressor
Both a repressor and activator
Peptidyl transferase
- is needed for initiation of translation.
- is needed for elongation during translation
- is needed for termination of translation.
- is not needed for translation
- two of the above
is needed for elongation during translation
An iducible operon is one that is
- normally not transcribed unless a co-activator or an inducer is present that can interact with regulatory proteins to allow transcription
- normally transcribed unless an inhibitor or a corepressor is present that can interact with regulatory proteins to allow transcription
- only occurs with negatively controlled operons
- only occurs with positively controlled operons
normally not transcribed unless a co-activator or an inducer is present that can interact with regulatory proteins to allow transcription
Several different glycosylases can be involved in DNA repair. What do these enzymes do?
- Cleave the phosphate-sugar DNA backbone leaving a 5’ phosphate and a 3’ hydroxyl
- Cleave the phosphate-sugar DNA backbone leaving a 5’ hydroxyl and a 3’ phosphate
- Removes the sugar directly from the DNA backbone leaving an apyrimidinic site
- Removes the base attached to a sugar in the DNA backbone
- None of the above
Removes the base attached to a sugar in the DNA backbone
Which of the following contributes to the specificity with which regulatory proteins bind to particular DNA sequences?
- broad electrostatic attraction between DNA phosphates and positively charged protein side chains
- hydrogen bonding interactions between polar protein side chains and the parts of bases exposed to the solvent in the major groove
- hydrophobic interactions between the DNA riboses and hydrophobic amino acid side chains
- complementarity between the protein and the DNA sequence to which it binds.
- more than one of the above
more than one of the above
The binding reaction between the E. coli lac repressor and the lac operon can be represented by the dissociation reaction RO ⇔ R + 0. Kd, the dissociation equilibrium constant, for this reaction is 10-10 M. Kd for dissociation of the repressor from other E. coli DNA sequences is 10-4 M. This means that
- The repressor binds a million times more tightly to the operator than to other parts of the DNA.
- The repressor binds 10,000 times more tightly to the operator than to other parts of the DNA.
- The repressor binds a million times less tightly to the operator than to other parts of the DNA.
- The repressor binds 10,000 times less tightly to the operator than to other parts of the DNA.
- None of the above
The repressor binds a million times more tightly to the operator than to other parts of the DNA.
Binding of the lac repressor to the lac promoter in E. coli DNA
- stops RNA polymerase from elongating the operon’s mRNA
- occurs only when the lactose concentration is high
- prevents binding of RNA polymerase to the DNA
- causes the RNA polymerase to act as a hydrolase rather than as a polymerase
- E. more than one of the above.
prevents binding of RNA polymerase to the DNA
Leucine zippers
- are protein regions which prevent protein-protein interactions when these would interfere with gene regulation.
- are protein-protein interaction domains which interact with DNA polymerase
- are protein-protein interaction domains which help regulate RNA polymerase activity
- are a synthetic material used in certain types of clothing
- none of the above.
are protein-protein interaction domains which help regulate RNA polymerase activity
When the concentrations of both glucose and lactose are high,
- transcription of the lac operon is stimulated because lactose binding to the repressor causes it to dissociate from the operator.
- transcription of the lac operon is stimulated because glucose binds to the repressor, causing it to dissociate from the operator.
- the RNA polymerase will be stimulated because the elevated glucose concentration will produce an elevated cAMP concentration which, in turn, will bind to the catabolite gene activator protein (CAP), causing CAP to stimulate RNA polymerase transcription of the lac operon
- the RNA polymerase will not be stimulated by CAP, because the lowered cAMP concentration caused by elevated glucose will not allow much cAMP to bind to CAP, and that, in turn, will prevent CAP binding to the DNA
- None of the above
- the RNA polymerase will not be stimulated by CAP, because the lowered cAMP concentration caused by elevated glucose will not allow much cAMP to bind to CAP, and that, in turn, will prevent CAP binding to the DNA


