As biotechnology continues to change, so does its use in agriculture, industry, and medicine
National agencies and international organizations strive to set guidelines for safe and ethical practices in the use of biotechnology
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Fig. 20-UN3
Cut by same restriction enzyme, mixed, and ligated
DNA fragments from genomic DNA or cDNA or copy of DNA obtained by PCR
Vector
Recombinant DNA plasmids
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Fig. 20-UN4
G
Aardvark DNA
Plasmid
5
3
3
TCCATGAATTCTAAAGCGCTTATGAATTCACGGC
5
AGGTACTTAAGATTTCGCGAATACTTAAGTGCCG
A
C
T
T
A
A
A
G
T
T
C
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Fig. 20-UN5
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Fig. 20-UN6
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Fig. 20-UN7
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You should now be able to:
Describe the natural function of restriction enzymes and explain how they are used in recombinant DNA technology
Outline the procedures for cloning a eukaryotic gene in a bacterial plasmid
Define and distinguish between genomic libraries using plasmids, phages, and cDNA
Describe the polymerase chain reaction (PCR) and explain the advantages and limitations of this procedure
Slide 117
Explain how gel electrophoresis is used to analyze nucleic acids and to distinguish between two alleles of a gene
Describe and distinguish between the Southern blotting procedure, Northern blotting procedure, and RT-PCR
Distinguish between gene cloning, cell cloning, and organismal cloning
Describe how nuclear transplantation was used to produce Dolly, the first cloned sheep
Slide 118
Describe the application of DNA technology to the diagnosis of genetic disease, the development of gene therapy, vaccine production, and the development of pharmaceutical products
Define a SNP and explain how it may produce a RFLP
Explain how DNA technology is used in the forensic sciences
Slide 119
Discuss the safety and ethical questions related to recombinant DNA studies and the biotechnology industry