Chapter 17: Problem 7
Restriction sites are palindromic; that is, they read the same in the \(5^{\prime}\) to \(3^{\prime}\) direction on each strand of DNA. What is the advantage of having restriction sites organized this way?
Chapter 17: Problem 7
Restriction sites are palindromic; that is, they read the same in the \(5^{\prime}\) to \(3^{\prime}\) direction on each strand of DNA. What is the advantage of having restriction sites organized this way?
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Get started for freeIn this chapter we focused on how specific DNA sequences can be copied, identified, characterized, and sequenced. At the same time, we found many opportunities to consider the methods and reasoning underlying these techniques. From the explanations given in the chapter, what answers would you propose to the following fundamental questions? (a) In a recombinant DNA cloning experiment, how can we determine whether DNA fragments of interest have been incorporated into plasmids and, once host cells are transformed, which cells contain recombinant DNA? (b) What steps make PCR a chain reaction that can produce millions of copies of a specific DNA molecule in a matter of hours without using host cells? (c) How has DNA-sequencing technology evolved in response to the emerging needs of genome scientists? (d) How can gene knockouts, transgenic animals, and geneediting techniques be used to explore gene function?
What advantages do cDNA libraries provide over genomic DNA libraries? Describe cloning applications where the use of a genomic library is necessary to provide information that a cDNA library cannot.
What is the difference between nonhomologous end-joining (NHEJ) and homology- directed repair (HDR) in the context of genome editing?
Why is genome editing by CRISPR-Cas advantageous over traditional methods for creating knockout or transgenic animals? Explain your answers.
Traditional Sanger sequencing has largely been replaced in recent years by next-generation and third-generation sequencing approaches. Describe advantages of these sequencing methods over first-generation Sanger sequencing.
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