Recombinant DNA Technology Quiz
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Questions and Answers

Who were the first scientists to be granted a patent for recombinant DNA technology?

  • Stanley N. Cohen and Herbert Boyer (correct)
  • Paul Berg and Herbert Boyer
  • Stanley N. Cohen and Paul Berg
  • None of the above
  • When was the first recombinant DNA molecule produced?

  • 1970
  • 1973
  • 1972 (correct)
  • 1980
  • What role did the scientists mentioned use restriction enzymes for in their work?

  • They used restriction enzymes to cut DNA at specific sites in order to splice genes. (correct)
  • They used restriction enzymes to prevent DNA from degrading.
  • They used restriction enzymes to sequence DNA.
  • They used restriction enzymes to create copies of DNA.
  • What year did the first publications on recombinant DNA technology appear?

    <p>1972 (A), 1973 (C)</p> Signup and view all the answers

    What is insertional inactivation?

    <p>A technique used to disable the expression of a gene. (D)</p> Signup and view all the answers

    What is the purpose of 'knocking out' a gene in a research setting?

    <p>To determine the biological function and importance of the gene. (C)</p> Signup and view all the answers

    What is an example of inappropriate activation of previously unexpressed host cell genes?

    <p>The activation of a gene not normally expressed in that cell type. (A)</p> Signup and view all the answers

    Which of the following is NOT a method used in recombinant DNA technology?

    <p>Gene therapy (C)</p> Signup and view all the answers

    Which of these statements BEST describes the relationship between insertional inactivation and recombinant DNA technology?

    <p>Insertional inactivation is a result of recombinant DNA technology. (C)</p> Signup and view all the answers

    Which of the following steps involves the insertion of a desired DNA sequence into a host cell?

    <p>Recombinant molecule inside host cell (D)</p> Signup and view all the answers

    What is the primary purpose of screening for clones in this process?

    <p>To identify host cells that have successfully incorporated the desired DNA sequence (D)</p> Signup and view all the answers

    What is the process of 'replicating inside the host cell' referring to?

    <p>The multiplication of the recombinant DNA molecule within the host cell (A)</p> Signup and view all the answers

    What is the main purpose of selecting recombinant colonies?

    <p>To identify colonies containing the desired DNA sequence (A)</p> Signup and view all the answers

    What happens during the 'expression of recombinant DNA' step?

    <p>The desired protein is produced (C)</p> Signup and view all the answers

    Name the process that allows for multiple copies of the recombinant molecule to be produced inside the host cell?

    <p>DNA replication (A)</p> Signup and view all the answers

    Which step involves the analysis of the recombinant DNA molecule?

    <p>Screening for clones (B)</p> Signup and view all the answers

    Which step involves the production of the desired protein encoded by the inserted gene?

    <p>Expression of recombinant DNA (C)</p> Signup and view all the answers

    What is the primary reason for the FDA's GRAS status for the genetically engineered chymosin?

    <p>It is considered a safe alternative to the traditional rennet extraction process. (C)</p> Signup and view all the answers

    What specific genetic modification is the 'golden rice' variety known for?

    <p>Enhanced nutritional content with higher levels of vitamin A. (C)</p> Signup and view all the answers

    What is the purpose of introducing the modified EPSPS gene into tobacco plants?

    <p>To produce tobacco plants that are resistant to the herbicide Roundup. (A)</p> Signup and view all the answers

    Which of the following is NOT an area where recombinant DNA technology is currently being used?

    <p>Space exploration (B)</p> Signup and view all the answers

    Which of the following is NOT a common use of recombinant DNA technology in medicine?

    <p>Production of anti-aging treatments (B)</p> Signup and view all the answers

    How does introducing a gene into a zebrafish embryo affect the fish's characteristics?

    <p>It can allow the fish to express a new protein, leading to a visible trait. (A)</p> Signup and view all the answers

    What is the primary advantage of using microbiologically produced recombinant chymosin compared to traditional rennet extracted from calves?

    <p>It is more efficient and economical. (A)</p> Signup and view all the answers

    What is the main implication of recombinant DNA technology being widely available in pharmacies, hospitals, research labs, and even pet shops?

    <p>It highlights the massive impact and widespread use of recombinant DNA technology in various sectors. (E)</p> Signup and view all the answers

    The production of transgenic sheep with the 'gene of interest' (GOI) indicates:

    <p>The use of recombinant DNA to produce valuable pharmaceutical proteins in livestock. (A)</p> Signup and view all the answers

    Which of the following statements accurately describes the role of DNA ligase in the process of joining DNA molecules?

    <p>DNA ligase joins together two DNA strands by forming phosphodiester bonds between the 5' phosphate and the 3' hydroxyl groups of adjacent nucleotides. (A)</p> Signup and view all the answers

    What is the fundamental difference between molecular cloning and polymerase chain reaction (PCR)?

    <p>Molecular cloning replicates DNA within a living cell, while PCR replicates DNA in a test tube. (A)</p> Signup and view all the answers

    How do cloning vectors facilitate the formation of recombinant DNA?

    <p>Cloning vectors provide the necessary signals for replication within a living cell. (A)</p> Signup and view all the answers

    Which of these is NOT a characteristic of recombinant DNA?

    <p>Recombinant DNA can be generated via natural processes within an organism. (B)</p> Signup and view all the answers

    What is the primary function of restriction endonucleases in the process of creating recombinant DNA?

    <p>To generate DNA fragments with either blunt ends or cohesive ends. (B)</p> Signup and view all the answers

    What role does a 'nick' play in the process of DNA ligation?

    <p>A nick is a single-stranded break in a DNA molecule, which DNA ligase can seal. (A)</p> Signup and view all the answers

    Which of the following statements accurately describes the role of a cloning vector in the process of recombinant DNA technology?

    <p>Cloning vectors are small DNA molecules that can replicate within a living cell and carry foreign DNA sequences. (D)</p> Signup and view all the answers

    What is the significance of having 'cohesive ends' on DNA fragments generated by restriction endonucleases?

    <p>Cohesive ends allow for the specific pairing of DNA fragments with complementary sequences. (C)</p> Signup and view all the answers

    What is a potential advantage of using PCR over molecular cloning for amplifying DNA sequences?

    <p>All of the above are advantages of using PCR over molecular cloning. (D)</p> Signup and view all the answers

    What is a primary function of a cloning vector that is not shared by other DNA molecules?

    <p>They contain specific sequences that allow for the identification of cells containing recombinant DNA. (A)</p> Signup and view all the answers

    Which of the following is a common example of a cloning vector?

    <p>All of the above. (D)</p> Signup and view all the answers

    Which of the following is NOT a potential application of recombinant DNA technology?

    <p>Production of synthetic materials such as plastics. (C)</p> Signup and view all the answers

    Which of the following DNA sequences would most likely be recognized and cleaved by a restriction endonuclease?

    <p>All of the above. (D)</p> Signup and view all the answers

    What is the primary difference between cohesive ends and blunt ends generated by restriction endonucleases?

    <p>Cohesive ends have complementary overhangs, while blunt ends are flush with the phosphodiester backbone. (B)</p> Signup and view all the answers

    What is the significance of the term 'recombinant' in 'recombinant DNA'?

    <p>All of the above are accurate interpretations of the term 'recombinant' in relation to recombinant DNA. (D)</p> Signup and view all the answers

    What is the primary function of DNA ligase in recombinant DNA technology?

    <p>It joins two pieces of DNA together, forming phosphodiester bonds. (D)</p> Signup and view all the answers

    What is a plasmid in the context of recombinant DNA technology?

    <p>A circular DNA molecule that can replicate independently within a bacterial cell. (D)</p> Signup and view all the answers

    Which of the following is NOT a characteristic of restriction nucleases/endonucleases/enzymes used in recombinant DNA technology?

    <p>They act as vectors for carrying foreign DNA into host cells. (C)</p> Signup and view all the answers

    What is the significance of the Asilomar Conference (International Conference on Recombinant DNA Molecules) in the development of recombinant DNA technology?

    <p>It led to the development of experimental guidelines and regulations for research involving recombinant DNA. (D)</p> Signup and view all the answers

    What are cohesive ends in the context of recombinant DNA technology?

    <p>Ends of DNA fragments produced by restriction enzymes that can bind to each other due to complementary base pairing. (B)</p> Signup and view all the answers

    What is meant by the term 'chimeric DNA' in the context of recombinant DNA technology?

    <p>DNA that is composed of genetic material from two or more different species. (B)</p> Signup and view all the answers

    What is the significance of the discovery of restriction nucleases/endonucleases/enzymes in the field of recombinant DNA technology?

    <p>They allowed scientists to cut DNA at specific sequences, enabling the precise manipulation of genetic material. (D)</p> Signup and view all the answers

    What is the primary advantage of using plasmids as vectors in recombinant DNA technology?

    <p>Plasmids can replicate independently within host cells, ensuring the amplification of the inserted foreign DNA. (B)</p> Signup and view all the answers

    Which of the following is NOT a characteristic of 'wild type' genes?

    <p>They are often altered versions of genes used in research. (D)</p> Signup and view all the answers

    What is meant by the term 'gene cloning' in the context of recombinant DNA technology?

    <p>The process of creating multiple identical copies of a specific gene. (B)</p> Signup and view all the answers

    How does recombinant DNA technology differ from 'natural' genetic recombination?

    <p>Recombinant DNA technology involves the deliberate creation of new DNA molecules in the laboratory, while natural genetic recombination occurs within organisms through natural processes. (A)</p> Signup and view all the answers

    What is the primary reason for the universal nature of DNA structure across all organisms?

    <p>All organisms share a common ancestor. (D)</p> Signup and view all the answers

    Why is the production of insulin using recombinant DNA technology considered a significant breakthrough?

    <p>It allowed for the mass production of insulin, making it more affordable and accessible to patients. (B)</p> Signup and view all the answers

    What is the primary reason why the potential hazards of recombinant DNA technology raised concerns in the early 1970s?

    <p>The possibility of creating new and potentially dangerous pathogens. (C)</p> Signup and view all the answers

    What is the key difference between blunt ends and cohesive ends produced by restriction enzymes?

    <p>Blunt ends are unable to bind to each other, while cohesive ends can bind due to their complementary base sequences. (D)</p> Signup and view all the answers

    Flashcards

    Cohen

    A researcher who helped create recombinant DNA technology and received its first patent with Boyer.

    Boyer

    A researcher at UCSF who collaborated with Cohen to produce recombinant DNA and patented the technology.

    Recombinant DNA

    DNA formed by combining DNA from different species using restriction enzymes.

    First recombinant DNA molecule

    Produced in 1972 by Cohen and Boyer, marking a milestone in genetic engineering.

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    First patent on recombinant DNA

    The first patent granted for recombinant DNA technology was in 1980, held by Cohen and Boyer.

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    Screening for clones

    The process of identifying host cells with desired recombinant DNA inserts.

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    Recombinant molecule

    A DNA molecule formed by combining DNA from different sources within a host cell.

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    Host cell

    A living cell used to replicate recombinant DNA molecules.

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    Recombinant colonies

    Groups of cells that have successfully taken up recombinant DNA.

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    Replicate

    To make copies of the recombinant molecule within the host cell.

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    Molecule analysis

    The examination of recombinant molecules to confirm their structure and function.

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    Expression of recombinant DNA

    The process by which a host cell transcribes and translates the recombinant DNA into proteins.

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    Selection process

    The method used to identify successful recombinant colonies from unsuccessful ones.

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    DNA ligase

    An enzyme that joins the ends of DNA strands together.

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    Cohesive ends

    Overhanging ends of DNA that can base pair with complementary sequences.

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    Blunt ends

    Straight-cut ends of DNA that do not have overhangs.

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    Genetic recombination

    Natural process of mixing existing DNA sequences in organisms.

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    Chemical synthesis of DNA

    Artificial creation of DNA sequences in the lab.

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    Cloning vector

    A DNA molecule used to replicate specific DNA sequences in cells.

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    Molecular cloning

    Replicating DNA within a living cell.

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    Polymerase chain reaction (PCR)

    Technique to amplify DNA in a test tube without living cells.

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    Plasmids

    Circular DNA molecules used as vectors in cloning.

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    Viruses as vectors

    Use of viral DNA to carry foreign genes into host cells.

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    Restriction endonucleases

    Enzymes that cut DNA at specific sequences.

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    Foreign DNA

    DNA from another organism inserted into a host.

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    Identifying recombinant DNA

    Methods used to find cells that contain recombinant DNA.

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    Insertional inactivation

    A technique in recombinant DNA that disables gene expression by inserting a plasmid.

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    Knockout genes

    A method to inactivate genes to study their functions and importance in organisms.

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    Gene expression effects

    Modification of gene expression by recombinant DNA can lead to undesired outcomes.

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    Recombinant DNA consequences

    In some cases, recombinant DNA can produce harmful effects even when not expressed.

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    Unexpressed host genes

    Previously inactive genes in host cells that can be inappropriately activated by recombinant DNA.

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    Cohen & Boyer

    Researchers recognized for pioneering recombinant DNA technology and awarded the Nobel Prize in Chemistry in 1980.

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    Recombinant DNA technology

    Takes DNA from different sources to create new genetic combinations, allowing for gene manipulation.

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    Gene cloning

    The process of making multiple identical copies of a gene by replicating it in host cells.

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    Restriction nuclease

    Enzymes that cut DNA at specific sequences, helping create fragments for cloning.

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    1980 Nobel Prize

    Awarded to Cohen & Boyer for their work on recombinant DNA.

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    DNA cloning

    The production of multiple identical copies of a specific gene or DNA segment.

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    Experimental guidelines

    Developed during the Asilomar Conference to address safety in recombinant DNA experiments.

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    First human hormone produced

    Insulin produced using recombinant DNA technology in 1978.

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    First animal vaccine

    Developed in 1982 using recombinant DNA technology.

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    Chymosin

    An enzyme used to curdle milk, produced recombinantly for cheese making.

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    Genetically engineered chymosin

    Chymosin produced through recombinant DNA technology, cheaper than traditional methods.

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    Golden Rice

    A genetically modified rice that produces beta-carotene, a vitamin A precursor.

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    Transgenic sheep

    Sheep genetically modified to produce a specific gene of interest (GOI).

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    EPSPS

    An enzyme that helps plants resist herbicides, modified for Roundup tolerance.

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    Fluorescent zebrafish

    Zebrafish engineered to fluoresce in response to environmental toxins.

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    GRAS status

    Generally Recognized As Safe; FDA designation for approved substances.

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    Recombinant proteins

    Proteins produced from genetically modified organisms using recombinant DNA.

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    Biotechnology applications

    Uses of recombinant DNA technology in medicine, agriculture, and research.

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    Study Notes

    Recombinant DNA Technology

    • Recombinant DNA is a form of artificial DNA created by combining two or more DNA sequences that do not naturally occur together.
    • It involves cloning and creating chimeric genes.
    • Recombinant DNA technology involves joining DNA molecules from different species in a host organism to create new genetic combinations beneficial to science, medicine, agriculture, and industry.
    • Recombinant organisms contain a different combination of alleles from their parents. Recombinant viruses are formed by recombining genetic material.

    Recombinant DNA Technology: Key Figures

    • Stanley N. Cohen and Herbert Boyer were among the first to produce recombinant DNA molecules and received the first patent on recombinant DNA technology.
    • Paul Berg also contributed significantly and was awarded a Nobel Prize in Chemistry in 1980 for his work on the biochemistry of nucleic acids, with a focus on recombinant DNA.
    • Researchers used restriction enzymes to cut DNA from different species, then fused the cut strands together.

    Recombinant DNA Technology: Timeline

    • 1972: DNA ligase joins two fragments, creating the first recombinant DNA molecules.
    • 1972 and 1973: First publications on recombinant DNA.
    • 1974: A world moratorium on some recombinant experiments due to safety concerns.
    • 1975: Development of experimental guidelines for recombinant DNA technology discussed at the Asilomar Conference.
    • 1978: First human hormone (insulin) produced by recombinant DNA technology.
    • 1980: First patent on recombinant DNA technology awarded to Stanley N. Cohen and Herbert Boyer.

    Recombinant DNA Technology: Plasmids

    • Plasmids are extra-chromosomal genetic elements found in bacteria.
    • They are circular DNA molecules that can replicate independently within a host cell.
    • Plasmids frequently carry antibiotic resistance genes (e.g., tetracycline, ampicillin, kanamycin).
    • The expression of these marker genes can help identify host cells carrying the vectors.

    Plasmids and Recombinant DNA Technology

    • Plasmids are crucial for cloning. A foreign DNA fragment is inserted into a plasmid vector during recombinant DNA construction.
    • The gene in question becomes inactivated by the foreign DNA fragment insertion (if positioned at the designated cleavage site).
    • The host DNA is cleaved (using restriction endonucleases).
    • Compatibility (sticky ends produced by cleavage) is crucial, allowing DNA fragments from different sources to stick together via annealing.
    • Recombinant plasmid, containing the gene of interest, is introduced to a bacterial cell.

    Gene Cloning

    • A clone is a collection of identical molecules or cells derived from an original molecule or cell
    • Gene cloning is creating multiple copies of a gene.
    • Recombinant DNA technology enables gene manipulation.

    DNA Sequencing

    • DNA sequencing determines the order of nucleotide bases in a DNA molecule.
    • Recombinant DNA technology has led to faster and more efficient DNA sequencing methods.

    Important Methods in Gene Cloning

    • Restriction enzymes (nucleases): Cut DNA at specific sequences. This creates sticky or blunt ends allowing the insertion of foreign DNA into a plasmid or similar vector.
    • DNA ligase: Joins DNA fragments together.
    • Polymerase chain reaction (PCR): Amplifies DNA sequences to produce copies.
    • These techniques allow recombinant DNA technology to be used for various applications, including drug development and disease diagnosis.

    Recombinant DNA Applications

    • Medicine: Production of therapeutic proteins (e.g., insulin, growth hormone).
    • Agriculture: Creation of crops with enhanced traits (e.g., pest resistance).
    • Industry: Production of enzymes and other useful compounds.
    • Forensics: DNA fingerprinting in crime investigations and determining paternity.
    • Basic Biology: Studying gene structure and function to understand the workings of organisms.

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    Description

    Test your knowledge on the pioneers of recombinant DNA technology and the fundamental concepts surrounding it. This quiz covers key milestones, techniques, and implications in the field of genetic engineering. Whether you're a student or a science enthusiast, challenge yourself and learn more about the origins of this groundbreaking technology.

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