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Questions and Answers
Who were the first scientists to be granted a patent for recombinant DNA technology?
Who were the first scientists to be granted a patent for recombinant DNA technology?
When was the first recombinant DNA molecule produced?
When was the first recombinant DNA molecule produced?
What role did the scientists mentioned use restriction enzymes for in their work?
What role did the scientists mentioned use restriction enzymes for in their work?
What year did the first publications on recombinant DNA technology appear?
What year did the first publications on recombinant DNA technology appear?
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What is insertional inactivation?
What is insertional inactivation?
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What is the purpose of 'knocking out' a gene in a research setting?
What is the purpose of 'knocking out' a gene in a research setting?
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What is an example of inappropriate activation of previously unexpressed host cell genes?
What is an example of inappropriate activation of previously unexpressed host cell genes?
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Which of the following is NOT a method used in recombinant DNA technology?
Which of the following is NOT a method used in recombinant DNA technology?
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Which of these statements BEST describes the relationship between insertional inactivation and recombinant DNA technology?
Which of these statements BEST describes the relationship between insertional inactivation and recombinant DNA technology?
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Which of the following steps involves the insertion of a desired DNA sequence into a host cell?
Which of the following steps involves the insertion of a desired DNA sequence into a host cell?
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What is the primary purpose of screening for clones in this process?
What is the primary purpose of screening for clones in this process?
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What is the process of 'replicating inside the host cell' referring to?
What is the process of 'replicating inside the host cell' referring to?
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What is the main purpose of selecting recombinant colonies?
What is the main purpose of selecting recombinant colonies?
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What happens during the 'expression of recombinant DNA' step?
What happens during the 'expression of recombinant DNA' step?
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Name the process that allows for multiple copies of the recombinant molecule to be produced inside the host cell?
Name the process that allows for multiple copies of the recombinant molecule to be produced inside the host cell?
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Which step involves the analysis of the recombinant DNA molecule?
Which step involves the analysis of the recombinant DNA molecule?
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Which step involves the production of the desired protein encoded by the inserted gene?
Which step involves the production of the desired protein encoded by the inserted gene?
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What is the primary reason for the FDA's GRAS status for the genetically engineered chymosin?
What is the primary reason for the FDA's GRAS status for the genetically engineered chymosin?
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What specific genetic modification is the 'golden rice' variety known for?
What specific genetic modification is the 'golden rice' variety known for?
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What is the purpose of introducing the modified EPSPS gene into tobacco plants?
What is the purpose of introducing the modified EPSPS gene into tobacco plants?
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Which of the following is NOT an area where recombinant DNA technology is currently being used?
Which of the following is NOT an area where recombinant DNA technology is currently being used?
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Which of the following is NOT a common use of recombinant DNA technology in medicine?
Which of the following is NOT a common use of recombinant DNA technology in medicine?
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How does introducing a gene into a zebrafish embryo affect the fish's characteristics?
How does introducing a gene into a zebrafish embryo affect the fish's characteristics?
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What is the primary advantage of using microbiologically produced recombinant chymosin compared to traditional rennet extracted from calves?
What is the primary advantage of using microbiologically produced recombinant chymosin compared to traditional rennet extracted from calves?
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What is the main implication of recombinant DNA technology being widely available in pharmacies, hospitals, research labs, and even pet shops?
What is the main implication of recombinant DNA technology being widely available in pharmacies, hospitals, research labs, and even pet shops?
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The production of transgenic sheep with the 'gene of interest' (GOI) indicates:
The production of transgenic sheep with the 'gene of interest' (GOI) indicates:
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Which of the following statements accurately describes the role of DNA ligase in the process of joining DNA molecules?
Which of the following statements accurately describes the role of DNA ligase in the process of joining DNA molecules?
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What is the fundamental difference between molecular cloning and polymerase chain reaction (PCR)?
What is the fundamental difference between molecular cloning and polymerase chain reaction (PCR)?
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How do cloning vectors facilitate the formation of recombinant DNA?
How do cloning vectors facilitate the formation of recombinant DNA?
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Which of these is NOT a characteristic of recombinant DNA?
Which of these is NOT a characteristic of recombinant DNA?
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What is the primary function of restriction endonucleases in the process of creating recombinant DNA?
What is the primary function of restriction endonucleases in the process of creating recombinant DNA?
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What role does a 'nick' play in the process of DNA ligation?
What role does a 'nick' play in the process of DNA ligation?
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Which of the following statements accurately describes the role of a cloning vector in the process of recombinant DNA technology?
Which of the following statements accurately describes the role of a cloning vector in the process of recombinant DNA technology?
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What is the significance of having 'cohesive ends' on DNA fragments generated by restriction endonucleases?
What is the significance of having 'cohesive ends' on DNA fragments generated by restriction endonucleases?
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What is a potential advantage of using PCR over molecular cloning for amplifying DNA sequences?
What is a potential advantage of using PCR over molecular cloning for amplifying DNA sequences?
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What is a primary function of a cloning vector that is not shared by other DNA molecules?
What is a primary function of a cloning vector that is not shared by other DNA molecules?
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Which of the following is a common example of a cloning vector?
Which of the following is a common example of a cloning vector?
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Which of the following is NOT a potential application of recombinant DNA technology?
Which of the following is NOT a potential application of recombinant DNA technology?
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Which of the following DNA sequences would most likely be recognized and cleaved by a restriction endonuclease?
Which of the following DNA sequences would most likely be recognized and cleaved by a restriction endonuclease?
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What is the primary difference between cohesive ends and blunt ends generated by restriction endonucleases?
What is the primary difference between cohesive ends and blunt ends generated by restriction endonucleases?
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What is the significance of the term 'recombinant' in 'recombinant DNA'?
What is the significance of the term 'recombinant' in 'recombinant DNA'?
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What is the primary function of DNA ligase in recombinant DNA technology?
What is the primary function of DNA ligase in recombinant DNA technology?
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What is a plasmid in the context of recombinant DNA technology?
What is a plasmid in the context of recombinant DNA technology?
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Which of the following is NOT a characteristic of restriction nucleases/endonucleases/enzymes used in recombinant DNA technology?
Which of the following is NOT a characteristic of restriction nucleases/endonucleases/enzymes used in recombinant DNA technology?
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What is the significance of the Asilomar Conference (International Conference on Recombinant DNA Molecules) in the development of recombinant DNA technology?
What is the significance of the Asilomar Conference (International Conference on Recombinant DNA Molecules) in the development of recombinant DNA technology?
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What are cohesive ends in the context of recombinant DNA technology?
What are cohesive ends in the context of recombinant DNA technology?
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What is meant by the term 'chimeric DNA' in the context of recombinant DNA technology?
What is meant by the term 'chimeric DNA' in the context of recombinant DNA technology?
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What is the significance of the discovery of restriction nucleases/endonucleases/enzymes in the field of recombinant DNA technology?
What is the significance of the discovery of restriction nucleases/endonucleases/enzymes in the field of recombinant DNA technology?
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What is the primary advantage of using plasmids as vectors in recombinant DNA technology?
What is the primary advantage of using plasmids as vectors in recombinant DNA technology?
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Which of the following is NOT a characteristic of 'wild type' genes?
Which of the following is NOT a characteristic of 'wild type' genes?
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What is meant by the term 'gene cloning' in the context of recombinant DNA technology?
What is meant by the term 'gene cloning' in the context of recombinant DNA technology?
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How does recombinant DNA technology differ from 'natural' genetic recombination?
How does recombinant DNA technology differ from 'natural' genetic recombination?
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What is the primary reason for the universal nature of DNA structure across all organisms?
What is the primary reason for the universal nature of DNA structure across all organisms?
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Why is the production of insulin using recombinant DNA technology considered a significant breakthrough?
Why is the production of insulin using recombinant DNA technology considered a significant breakthrough?
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What is the primary reason why the potential hazards of recombinant DNA technology raised concerns in the early 1970s?
What is the primary reason why the potential hazards of recombinant DNA technology raised concerns in the early 1970s?
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What is the key difference between blunt ends and cohesive ends produced by restriction enzymes?
What is the key difference between blunt ends and cohesive ends produced by restriction enzymes?
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Flashcards
Cohen
Cohen
A researcher who helped create recombinant DNA technology and received its first patent with Boyer.
Boyer
Boyer
A researcher at UCSF who collaborated with Cohen to produce recombinant DNA and patented the technology.
Recombinant DNA
Recombinant DNA
DNA formed by combining DNA from different species using restriction enzymes.
First recombinant DNA molecule
First recombinant DNA molecule
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First patent on recombinant DNA
First patent on recombinant DNA
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Screening for clones
Screening for clones
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Recombinant molecule
Recombinant molecule
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Host cell
Host cell
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Recombinant colonies
Recombinant colonies
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Replicate
Replicate
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Molecule analysis
Molecule analysis
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Expression of recombinant DNA
Expression of recombinant DNA
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Selection process
Selection process
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DNA ligase
DNA ligase
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Cohesive ends
Cohesive ends
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Blunt ends
Blunt ends
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Genetic recombination
Genetic recombination
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Chemical synthesis of DNA
Chemical synthesis of DNA
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Cloning vector
Cloning vector
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Molecular cloning
Molecular cloning
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Polymerase chain reaction (PCR)
Polymerase chain reaction (PCR)
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Plasmids
Plasmids
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Viruses as vectors
Viruses as vectors
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Restriction endonucleases
Restriction endonucleases
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Foreign DNA
Foreign DNA
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Identifying recombinant DNA
Identifying recombinant DNA
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Insertional inactivation
Insertional inactivation
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Knockout genes
Knockout genes
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Gene expression effects
Gene expression effects
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Recombinant DNA consequences
Recombinant DNA consequences
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Unexpressed host genes
Unexpressed host genes
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Cohen & Boyer
Cohen & Boyer
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Recombinant DNA technology
Recombinant DNA technology
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Gene cloning
Gene cloning
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Restriction nuclease
Restriction nuclease
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1980 Nobel Prize
1980 Nobel Prize
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DNA cloning
DNA cloning
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Experimental guidelines
Experimental guidelines
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First human hormone produced
First human hormone produced
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First animal vaccine
First animal vaccine
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Chymosin
Chymosin
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Genetically engineered chymosin
Genetically engineered chymosin
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Golden Rice
Golden Rice
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Transgenic sheep
Transgenic sheep
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EPSPS
EPSPS
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Fluorescent zebrafish
Fluorescent zebrafish
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GRAS status
GRAS status
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Recombinant proteins
Recombinant proteins
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Biotechnology applications
Biotechnology applications
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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.