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Ch. 15 - Recombinant DNA Technology and Its Applications
Sanders - Genetic Analysis: An Integrated Approach 3rd Edition
Sanders3rd EditionGenetic Analysis: An Integrated ApproachISBN: 9780135564172Not the one you use?Change textbook
Chapter 15, Problem 12

Compare and contrast methods for making transgenic plants and transgenic Drosophila.

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Step 1: Define what transgenic organisms are—organisms that have had foreign DNA introduced into their genome to express new traits—and explain that both transgenic plants and Drosophila are created to study gene function or improve traits.
Step 2: Describe common methods for making transgenic plants, such as Agrobacterium-mediated transformation, where the bacterium Agrobacterium tumefaciens transfers a gene of interest into plant cells, and biolistic (gene gun) methods, which physically deliver DNA into plant cells.
Step 3: Explain methods for making transgenic Drosophila, focusing on microinjection of DNA directly into early embryos, often using P-element transposons to integrate the foreign DNA into the fly genome.
Step 4: Compare the two approaches by highlighting that plant transformation often relies on bacterial vectors or physical delivery due to plant cell walls, while Drosophila transformation uses direct embryo injection and transposon-mediated integration because of the animal’s developmental biology.
Step 5: Contrast the efficiency, technical challenges, and typical applications of each method, noting that plant transformation can be slower and requires tissue culture, whereas Drosophila transformation is relatively rapid but limited to certain genomic insertion sites.

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Key Concepts

Here are the essential concepts you must grasp in order to answer the question correctly.

Transgenic Plant Production Methods

Transgenic plants are commonly created using Agrobacterium-mediated transformation or biolistic (gene gun) methods. Agrobacterium transfers a DNA segment (T-DNA) into the plant genome, mainly effective in dicots, while biolistics physically delivers DNA into plant cells and can be used for monocots. Both methods require tissue culture to regenerate whole plants from transformed cells.
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Transgenic Drosophila Production Methods

Transgenic Drosophila are typically generated by microinjecting DNA into early embryos, where the DNA integrates into the germline. Techniques include P-element mediated transformation, which uses transposons to insert DNA, and more recent methods like CRISPR/Cas9 for targeted genome editing. These methods allow stable inheritance of the transgene in fly populations.
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Comparison of Transformation Techniques

While both plants and Drosophila require DNA integration into the genome, plant methods often rely on bacterial vectors or physical delivery and tissue culture regeneration, whereas Drosophila methods involve direct embryo injection and transposon-mediated insertion. Differences arise from organism biology, such as cell wall presence in plants and developmental stages accessible for transformation.
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Related Practice
Textbook Question
Chimeric gene-fusion products can be used for medical or industrial purposes. One idea is to produce biological therapeutics for human medical use in animals from which the products can be easily harvested—in the milk of sheep or cattle, for example. Outline how you would produce human insulin in the milk of sheep.
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Textbook Question
Why are diseases of the blood simpler targets for treatment by gene therapy than are many other genetic diseases?
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Textbook Question

Injection of double-stranded RNA can lead to gene silencing by degradation of RNA molecules complementary to either strand of the dsRNA. Could RNAi be used in gene therapy for a defect caused by a recessive allele? A dominant allele? If so, what might be the major obstacle to using RNAi as a therapeutic agent?

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Textbook Question
It is often desirable to insert cDNAs into a cloning vector in such a way that all the cDNA clones will have the same orientation with respect to the sequences of the plasmid. This is referred to as directional cloning. Outline how you would directionally clone a cDNA library in the plasmid vector pUC18.
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Textbook Question
A major advance in the 1980s was the development of technology to synthesize short oligonucleotides. This work both facilitated DNA sequencing and led to the advent of the development of PCR. Recently, rapid advances have occurred in the technology to chemically synthesize DNA, and sequences up to 10 kb are now readily produced. As this process becomes more economical, how will it affect the gene-cloning approaches outlined in this chapter? In other words, what types of techniques does this new technology have potential to supplant, and what techniques will not be affected by it?
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Textbook Question

The bacteriophage lambda genome can exist in either a linear form or a circular form.

How many fragments will be formed by restriction enzyme digestion with XhoI alone, with XbaI alone, and with both XhoI and XbaI in the linear and circular forms of the lambda genome?

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