Chapter 17: Problem 17
What is the difference between a knockout animal and a transgenic animal?
Chapter 17: Problem 17
What is the difference between a knockout animal and a transgenic animal?
All the tools & learning materials you need for study success - in one app.
Get started for freeThe CRISPR-Cas system has great potential but also raises many ethical issues about its potential applications because theoretically it can be used to edit any gene in the genome. What do you think are some of the concerns about the use of CRISPR. Cas on humans? Should CRISPR-Cas applications be limited for use on only certain human genes but not others? Explain your answers.
In 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?
Gene targeting and genome editing are both techniques for removing or modifying a particular gene, each of which can produce the same ultimate goal. Describe some of the differences between the experimental methods used for these two techniques.
The human insulin gene contains a number of sequences that are removed in the processing of the mRNA transcript. Bacterial cells cannot excise these sequences from mRNA transcripts, yet this gene can be cloned into a bacterial cell and produce insulin. Explain how this is possible.
If you performeda PCR experimentstarting withonly onecopy of double-stranded DNA, approximately how many DNA molecules would be present in the reaction tube after 15 cycles of amplification?
What do you think about this solution?
We value your feedback to improve our textbook solutions.