Slide 40
One method of introducing recombinant DNA into eukaryotic cells is electroporation, applying a brief electrical pulse to create temporary holes in plasma membranes
Alternatively, scientists can inject DNA into cells using microscopically thin needles
Once inside the cell, the DNA is incorporated into the cell’s DNA by natural genetic recombination
Slide 41
The polymerase chain reaction, PCR, can produce many copies of a specific target segment of DNA
A three-step cycle—heating, cooling, and replication—brings about a chain reaction that produces an exponentially growing population of identical DNA molecules
Slide 42
Fig. 20-8
5
Genomic DNA
TECHNIQUE
Cycle 1 yields
2
molecules
Denaturation
Annealing
Extension
Cycle 2 yields
4
molecules
Cycle 3 yields 8
molecules; 2 molecules (in white boxes) match target sequence
Target sequence
Primers
New nucleo- tides
3
3
3
3
5
5
5
1
2
3
Slide 43
Fig. 20-8a
5
Genomic DNA
TECHNIQUE
Target sequence
3
3
5
Slide 44
Fig. 20-8b
Cycle 1 yields
2
molecules
Denaturation
Annealing
Extension
Primers
New nucleo- tides
3
5
3
2
5
3
1
Slide 45
Fig. 20-8c
Cycle 2 yields
4
molecules
Slide 46
Fig. 20-8d
Cycle 3 yields 8
molecules; 2 molecules (in white boxes) match target sequence
Slide 47
Concept 20.2: DNA technology allows us to study the sequence, expression, and function of a gene
DNA cloning allows researchers to
Compare genes and alleles between individuals
Locate gene expression in a body
Determine the role of a gene in an organism
Several techniques are used to analyze the DNA of genes
Slide 48
One indirect method of rapidly analyzing and comparing genomes is gel electrophoresis