What is the difference between a knockout animal and a transgenic animal?

Short Answer

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Answer: The main difference between knockout and transgenic animals lies in the genetic modifications being made and their goals. In a knockout animal, a specific gene is disrupted or removed to study its role and function, while in a transgenic animal, new genes from a different species are introduced to provide new traits or functions for various applications.

Step by step solution

01

Define Knockout Animal

A knockout animal is a genetically modified organism (GMO) in which researchers have disrupted, or "knocked out," a specific gene to remove its function. This is usually done to study the effects of the gene's absence on the organism's development, function, and health.
02

Define Transgenic Animal

A transgenic animal is also a genetically modified organism (GMO), but in this case, researchers have introduced one or more new genes from another species into the animal's genome. This can result in the organism gaining new traits or functions that aren't typically present in its species, which can be useful in various applications such as medical research, agriculture, or industry.
03

Highlight the Key Differences

The main difference between a knockout and a transgenic animal lies in the genetic modifications being made and their goals: 1. In a knockout animal, a specific gene is disrupted or removed, preventing it from functioning. This helps researchers study the role and function of that particular gene in the organism. 2. In a transgenic animal, new genes from a different species are introduced, providing the organism with new traits or functions. This can be beneficial for various applications, such as improving disease resistance in livestock or producing proteins for medical treatments. In summary, knockout animals are used to understand the effects of removing a specific gene, while transgenic animals are used to explore the effects of introducing new genes from a different species.

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Most popular questions from this chapter

The 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?

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