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Gel electrophoresis can distinguish between the _____ of different DNA fragments.


A) sequences
B) charge
C) sizes

D) A) and C)
E) None of the above

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Restriction enzymes recognize certain DNA sequences and:


A) cut straight through both strands of DNA.
B) cut through the DNA, leaving some overhang at both ends.
C) will alternate between cutting straight through both strands of DNA and leaving some overhang at both ends.
D) some of them will cut straight through, while others will leave an overhang at both ends of the cut.

E) A) and B)
F) C) and D)

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DNA replication of small circular molecules usually starts at a single origin of replication and proceeds bidirectionally (that is, with two replication forks proceeding in opposite directions from the origin of replication). How would the time required for replication be affected if replication of such a molecule were unidirectional rather than bidirectional?

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The time required for replicat...

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Mitochondria contain their own double-stranded, circular DNA and replicate on their own. Why don't they suffer the same consequences as our cells in terms of limited division?


A) Because they have high telomerase activity.
B) Shortening of the DNA is only a problem with nuclear DNA; shortening of mitochondrial DNA isn't catastrophic.
C) Because mitochondrial DNA is circular, it doesn't shorten when it replicates.
D) Since mitochondrial DNA only contains a few genes, it can last a lot longer.
E) Because they have high telomerase activity and their DNA is circular and so doesn't shorten in replication.

F) A) and D)
G) A) and C)

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Denaturation of DNA is a necessary step in Southern blotting procedure because it separates double stranded DNA into single stranded DNA.

A) True
B) False

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The oligonucleotide primers used in the polymerase chain reaction are typically 20-30 nucleotides in length or longer; however, for purposes of this problem let's assume that six nucleotides is long enough. You wish to amplify the fragment shown below (the raised dots indicate several kilobases of DNA sequence not shown) and decide to design primers corresponding to the regions that are shown in bold. What primer sequences would you use? 5 '-TCAAACTTGCATGTG \cdots GAGCCATGTGGCACAAA-3' 3'-AGTTTGAACGTACAG \cdots CTCGGTACACCGTGTTT-5 '


A) 5'-GCAAGT-3' and 5'-TGCCAC-3'
B) 5'-ACTTGC-3' and 5'-GTGGCA-3'
C) 5'-GCAAGT-3' and 5'-GTGGCA-3'
D) 5'-ACTTGC-3' and 5'-TGCCAC-3'

E) B) and C)
F) A) and C)

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In addition to introducing mutations in a gene, DNA editing by means of CRISPR can also correct mutations in a gene.

A) True
B) False

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One of the first uses of DNA renaturation (hybridization) was to determine the degree of similarity in DNA between different pairs of species; this technique provides a measure of how closely the species are related evolutionarily. In renaturation studies, the genetic similarity between two samples is measured by determining the:


A) number and locations of bands on an electrophoresis gel.
B) number of restriction sites in each of the samples.
C) temperature at which the two samples form duplexes.
D) rate at which PCR amplifies the two samples.
E) nucleotide sequences of each sample.

F) C) and D)
G) C) and E)

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As a piece of linear DNA is replicated, the leading strand will have _____ RNA primer(s) and the lagging strand will have _____ RNA primer(s) .


A) one; one
B) one; two
C) one; many
D) many; one
E) many; many

F) C) and E)
G) B) and C)

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What is the benefit of using Taq polymerase in PCR?


A) Because it is taken from bacteria that live in high temperatures, it doesn't have a proofreading function.
B) Because it is taken from bacteria, this enzyme works much more efficiently than other types of DNA polymerase.
C) Because it is taken from bacteria that live in high temperatures, it stays active during denaturation steps of the reaction
D) Because it is taken from bacteria, it makes fewer mistakes.
E) None of the other answer options is correct.

F) C) and D)
G) A) and E)

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Which of the following statements is TRUE regarding DNA replication?


A) Only the lagging strand gets shortened during replication.
B) Only the leading strand gets shortened during replication.
C) Both strands get shortened at the same end during replication.
D) Both strands get shortened at opposite ends during replication.
E) Only the lagging strand gets shortened after every other round of replication.

F) B) and C)
G) A) and C)

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Which of the following enzymes is necessary to produce recombinant DNA?


A) helicase
B) Taq polymerase
C) primase
D) DNA ligase
E) topoisomerase

F) B) and C)
G) All of the above

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The enzyme responsible for replacing RNA primers with DNA is a type of:


A) DNA polymerase.
B) helicase.
C) topoisomerase II.
D) DNA ligase.
E) DNA replicase.

F) A) and E)
G) C) and E)

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The fact that DNA replication occurs in virtually the same way in all organisms reflects:


A) its origin early in the history of life.
B) its multiple origins in different lineages of organisms.
C) the laws of thermodynamics.
D) the fact that mutations are generally harmful.
E) the universal genetic code.

F) B) and D)
G) D) and E)

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A student in a biology laboratory designs oligonucleotide primers to carry out the polymerase chain reaction. However when ordering the sequences, she reverses the 3' and 5' ends. The vendor synthesizes the sequences as ordered and returns them to the student. Will they produce an amplified product? Please explain your answer.

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They will not work. In fact, they will n...

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A cell with a defect in the proofreading function of DNA polymerase is observed to have a rate of incorporation of incorrect bases into newly synthesized DNA that is 100 times greater than a cell with a nondefective, normal DNA polymerase. Estimate from this number what fraction of incorrect nucleotide incorporations are corrected by the proofreading function of DNA polymerase in the cell with normal DNA polymerase.


A) 0) 9 percent
B) 9) 0 percent
C) 99.0 percent
D) 99.9 percent

E) B) and D)
F) None of the above

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_____ moves outward from the origin of replication and breaks hydrogen bonds between DNA nucleotides.


A) RNA primase
B) Helicase
C) Topoisomerase II
D) DNA polymerase

E) A) and D)
F) All of the above

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Forensic technicians unearth a skeleton from a shallow grave. They extract a tiny amount of DNA from the pulp found in the teeth. How could they obtain sufficient DNA for an analysis of the victim's genes?


A) subject the DNA to gel electrophoresis
B) use a nucleic acid probe
C) subject the specimen to amniocentesis
D) use the polymerase chain reaction
E) subject the DNA to restriction enzymes

F) A) and D)
G) A) and E)

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Using PCR, a student wants to amplify a sequence of known DNA from a genomic DNA sample. The two primers are both designed to pair with sequences that have a 40% GC content. Using a particular set of denaturation temperatures, annealing temperatures, and extension temperatures, the experiment does not produce the expected single DNA fragment of a single known size, but instead a set of fragments of varied sizes. Which of the following could account for these results?


A) The annealing temperature was too low so that the primers can bind with multiple genomic sequences that contain some mismatched bases.
B) The denaturation temperature was too high so that the primers can bind with each other as well as with multiple genomic sites containing mismatches.
C) The extension temperature was too low so that many fragments were terminated before the full fragment was replicated.

D) A) and B)
E) A) and C)

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The enzyme that catalyzes the addition of new nucleotides to a growing DNA strand is:


A) DNA polymerase.
B) helicase.
C) topoisomerase II.
D) DNA ligase.
E) DNA replicase.

F) C) and D)
G) A) and E)

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