Lesson 3.8.4.1.1
3.8.4.1.1 Recombinant DNA and transformation of host cells Quiz: AQA Biology, Unit 8
20 questions
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Lesson 3.8.4.1.1, Recombinant DNA and transformation of host cells: 20 multiple choice questions for the AQA Biology (7402), Unit 8: The control of gene expression, written with Revision Ninja.
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The 20 questions
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Recombinant DNA technology involves:
- Breeding two organisms that are closely related to one another in order to produce offspring with a fixed set of desirable traits
- Copying of mRNA into protein directly, without any DNA template, as occurs in the cytoplasm of every eukaryotic cell
- Transfer of fragments of DNA from one organism or species to another
- Removal of all DNA from a cell so that the cell can be grown without any genetic material for use in tissue culture experiments
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Why can DNA transferred from one species be translated in the recipient organism?
- The genetic code is universal, as are transcription and translation mechanisms
- The DNA is converted into a different genetic code first
- Recipient cells always lack their own ribosomes
- Recipient cells always translate DNA directly without mRNA
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Which enzyme converts mRNA into complementary DNA (cDNA)?
- RNA polymerase
- Reverse transcriptase
- DNA polymerase
- Restriction endonuclease
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What do restriction enzymes do in recombinant DNA technology?
- Break down proteins into amino acids
- Copy DNA by making new strands
- Cut DNA at specific base sequences
- Join DNA fragments together
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What is a gene machine?
- An enzyme that removes introns from pre-mRNA during splicing, so that the mature mRNA leaves the nucleus ready for translation
- A machine that copies genes in a cell nucleus during each division, so that every daughter cell receives an identical set of genes
- A ribosome that makes proteins from the codons of an mRNA molecule, which is the site of translation in the cytoplasm of every cell
- A device that creates a gene artificially from a known nucleotide sequence
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Why are promoter and terminator regions added to DNA fragments?
- So that the inserted gene can be transcribed in the host cell
- So that the fragment is broken down in the host cell
- So that the fragment can be copied by PCR only
- So that the fragment can be removed from a vector
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Which enzyme joins DNA fragments into a vector?
- Restriction endonuclease
- Ligase
- Reverse transcriptase
- Helicase
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A human gene is inserted into a bacterium, which then makes the human protein. Why does this work?
- Bacteria always make human proteins without DNA
- Bacteria use human ribosomes to translate the gene
- Human genes are converted to bacterial genes by a restriction enzyme
- The genetic code is universal, so the bacterial ribosomes translate the human gene
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Why is cDNA often preferred to genomic DNA when inserting a eukaryotic gene into a bacterium?
- cDNA cannot be inserted into any host cell
- cDNA is always cut by the host restriction enzyme
- cDNA has no introns, so the bacterium can express the gene
- cDNA contains more introns than genomic DNA
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What are marker genes used for in recombinant DNA technology?
- To make the vector larger for easier handling in the laboratory, so that it can be seen under a microscope during cloning work
- To remove introns from the inserted gene during cloning, so that the mature mRNA can be made directly from the vector sequence
- To speed up the rate of translation in the host cell, so that the inserted gene produces more protein in each minute of growth
- To identify cells that have taken up the vector and so are genetically modified
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What is the role of a vector in recombinant DNA technology?
- To make restriction enzymes in the host
- To carry the DNA fragment into host cells
- To destroy the DNA fragment after transfer
- To replace the host ribosomes
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What is meant by transformation of host cells?
- Conversion of host cells into pluripotent stem cells by the recombinant DNA, which then allows the host cells to form any tissue
- Destruction of host cells by a vector carrying a lethal gene, which kills the cells so that the recombinant DNA can be recovered
- Removal of the nucleus from host cells by enzymes, so that the recombinant DNA can be inserted directly into the cytoplasm
- Uptake of recombinant DNA by host cells, so their genetic material changes
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Restriction enzymes and ligases are used together to:
- Break down the vector after use
- Insert DNA fragments into vectors
- Convert DNA into protein
- Copy the vector using mRNA
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Which method creates a DNA fragment without cutting an existing DNA molecule?
- Restriction enzyme digestion of a whole genome, which cuts the existing DNA molecule at specific sites to release the required fragment
- Creating the gene in a gene machine from a nucleotide sequence
- Culturing bacteria on agar plates containing antibiotic, which selects only the cells that have taken up a plasmid carrying the gene
- Splicing of introns from pre-mRNA in the nucleus, which removes non-coding sequences from the transcript before the mRNA is exported
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A company wants to sell genetically modified seed and patents the modified gene. Which financial concern is most often raised?
- Patents make all seeds cheaper for farmers each year, because competition between companies drives the price of every crop seed down
- Patents prevent any gene from being inserted into a crop, so no company can ever create a modified seed that farmers could later use
- Patents stop any seed from being sold to farmers, which means that the modified crop is never planted outside the laboratory
- Farmers may have to buy new seed each season, creating a dependence on the company
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Which argument best balances humanitarian and environmental considerations of genetically modified crops?
- GM crops should always be grown because they have no ecological effects
- GM crops may increase food supply in poor regions, but long-term ecological effects must be assessed before use
- GM crops are irrelevant to humanitarian concerns because they are used only in rich countries
- GM crops should never be grown because all gene transfers are harmful
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How does recombinant DNA technology relate to gene therapy?
- A functional copy of a gene can be introduced into a patient's cells to correct a faulty gene
- Gene therapy removes all DNA from a patient's cells and replaces it with a copy of the genome from a healthy donor of the same age
- Gene therapy involves the reverse transcription of proteins back into DNA, so that the body's proteins can be stored in the nucleus
- Gene therapy only uses restriction enzymes to destroy genes that are expressed too strongly, so no new DNA is ever introduced into cells
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Put these steps in the most likely order: 1 cut the gene fragment with restriction enzyme, 2 join it into a plasmid vector, 3 transform host bacteria, 4 select GM cells using a marker. Which sequence is correct?
- 1, 2, 3, 4
- 4, 1, 2, 3
- 2, 1, 3, 4
- 1, 3, 2, 4
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Why must a vector carry both a promoter and a marker gene?
- The promoter copies the vector during each cell division, and the marker removes introns from the inserted gene before it is expressed
- The promoter allows transcription of the inserted gene, and the marker identifies cells that took up the vector
- The promoter destroys the inserted gene before it can be transcribed
- The promoter and marker both stop translation of the inserted gene, so that the protein is only made after the cell has been selected
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Why do ethical issues arise in the use of recombinant DNA in agriculture?
- Ethics only apply to medicine and never to agriculture, since crops and animals are not able to be affected by the methods used on them
- Ownership, environmental impact and effects on farmers and consumers must be weighed
- There are no ethical issues because all organisms are equal in value, so no one needs to consider the effects of changing their genes
- Ethics apply only to bacteria used in laboratories, because all larger organisms are regulated by agriculture ministries instead
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