Exam 12: Dna Replication and Manipulation

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What features of DNA make it possible to make recombinant DNA in the lab?

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Incorrect nucleotides are sometimes incorporated into DNA during the process of replication. In the sequences shown here, the template strand is shown on top and the replicating daughter strand at the bottom. The nucleotide shown in bold is incorrect in that its base does not undergo pairing with the base in the template strand. In the situation shown in (A) the proofreading function of DNA polymerase removes the incorrect nucleotide from the daughter strand and replaces it with the correct one, but in situation (B) the polymerase has moved on and the incorrect nucleotide cannot be repaired. Can you explain why the error in situation (B) cannot be fixed by DNA polymerase? (A) 3 '-GAAACTGCCATG-5 ' 5 '-CTTTGG (B) 3 '-GAAACTGCCATG-5 ' 5 '-CTTTGGC

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If you were able to find a drug that could inhibit the reactivation of telomerase activity in cancer cells, the cancer cells would:

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DNA polymerase is the enzyme that separates the two strands of DNA during DNA replication.

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Which of the following reasons explains why bacteria can continually divide?

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The technique of Sanger sequencing takes advantage of the fact that dideoxynucleotides (nucleotides in which the 3 hydroxyl group is absent) act as:

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All four dideoxynucleotides can be present in a single Sanger sequencing reaction and still be distinguished because:

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Imagine that a doctor is culturing cells from a malignant melanoma and from a normal skin sample. How would you expect these two cell populations to differ?

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Energy is required in order to add a nucleotide to the growing strand of DNA during replication. From where does that energy come?

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Sheep that produce a human protein in their milk used to treat a human disorder is an example of a genetically modified organism.

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A solution of DNA fragments of known sizes is sometimes placed in one of the wells during electrophoresis and used for size comparison.

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Which of the following statements is TRUE regarding origins of replication?

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What is the name of the class of enzymes that recognizes and cuts a specific sequence of DNA?

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What feature of double-stranded DNA makes it necessary to have a leading strand and a lagging strand during replication?

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The BIGGEST remaining obstacle for personal genome sequencing is still:

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You discover a virus with a number of unusual properties, and decide to assign it the name virus U238. The genome of U238 consists of double-stranded DNA. To study the mode of DNA replication in U238, you carry out a Meselson-Stahl type of experiment, and first observe that viral DNA containing only normal "light" nitrogen (14N) has a density of 1.715 gm/cm3. You then allow the virus to replicate in the presence of nucleotides containing "heavy" nitrogen (15N) until both strands of its genome are "heavy." At this point the density of the viral DNA is 1.722 gm/cm3. You allow the virus with "heavy" DNA to undergo one round of replication in the presence of only "light" nucleotides, and you observe that half of the viral progeny have DNA with a density of 1.722 gm/cm3 and the other half of the viral progeny have DNA with a density of 1.715 gm/cm3. How would you interpret these results?

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In gel electrophoresis, DNA fragments are separated based on:

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What is the result of DNA ligase's action?

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What feature is shared by restriction fragments produced by the restriction enzymes BclI (TGATCA) and BglII (AGATCT)? (The downward arrow denotes the site of cleavage in each strand.)

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As in the development of computer hardware, interest in large-scale DNA sequencing has stimulated the development of sequencing devices that:

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