Becker's World of the Cell (9th Edition)
Becker's World of the Cell (9th Edition)
9th Edition
ISBN: 9780321934925
Author: Jeff Hardin, Gregory Paul Bertoni
Publisher: PEARSON
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Chapter 17, Problem 17.4PS

QUANTITATIVE Still More DNA Replication. Suppose you are given a new temperature-sensitive bacterial mutant that grows normally at 37°C but cannot replicate its chromosomes properly at 42°C. To investigate the nature of the underlying defect, you incubate the cells at 42°C with radioactive substrates required for DNA synthesis. After 1 hour you find that the cell population has doubled its DNA content, suggesting that DNA replication can still occur at 42°C. Moreover, centrifugation reveals that all of this DNA has the same large molecular weight as does the original DNA present in the cells. When the DNA is denatured, however, you discover that 75% of the resulting single-stranded DNA has a molecular weight that is half that of the original double-stranded DNA, and the remaining 25% of the DNA has a much lower molecular weight. Based on the preceding results, what gene do you think is defective in these cells? Explain how such a defect would account for the experimental results that you observed.

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Draw a replication bubble. Be sure to label the directionality of all strands of DNA. For one of the two replication forks, draw and label all of the proteins required the text describes as being important for DNA synthesis, and label the leading and lagging strands.
to 4 minutes) The schematic diagram below shows organization of the DNA replication fork. Match parts of the diagram (labeled A-F) with the corresponding term from the answer list (designated 31 parental duplex 5' 3' fork progression v A 1Lagging strand 2. An Okazaki tragment 3.Site of action of DNA topoisomerase 4 Leading strand 5. Site of action of DNA helicCase 6.Site of action of DNA ligase
Which statements are true? Explain why or why not.1 The different cells in your body rarely havegenomes with the identical nucleotide sequence.2 In E. coli, where the replication fork travels at 500nucleotide pairs per second, the DNA ahead of the fork—in the absence of topoisomerase—would have to rotate atnearly 3000 revolutions per minute.3 In a replication bubble, the same parental DNAstrand serves as the template strand for leading-strandsynthesis in one replication fork and as the template forlagging-strand synthesis in the other fork.4 When bidirectional replication forks from adja-cent origins meet, a leading strand always runs into a lag-ging strand.5 DNA repair mechanisms all depend on the exis-tence of two copies of the genetic information, one in eachof the two homologous chromosomes
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