1. Genetic Engineering Techniques
Restriction Enzymes
DNA Recombination
DNA Insertion
DNA Sequencing
Transgenic Bacteria, Plants, and Animals
Cloning
Gel electrophoresis

2. Genetic Engineering Techniques
Restriction Enzymes:
Genes can be cut at specific DNA sequences by proteins known as Restriction Enzymes
Each recognizes and cuts DNA at a particular sequence (area of Bases)
They are INCREDIBLY accurate, they will ONLY cut the area that they recognize
This amazing ability allows us to cut DNA into fragments so that we can isolate it, separate it, and/or analyze it.

4. Restriction Enzyme
A restriction enzyme is an enzyme that cuts double-stranded DNA at a specific recognition nucleotide sequences (A, T, C, G) known as restriction sites.
Such enzymes, found in bacteria, are thought to have evolved to provide a defense mechanism against invading viruses.
Restriction enzymes are required when removing or replacing genes
They are also very important in the creation of recombinant DNA

5. Genetic Engineering Techniques
Restriction Enzymes
DNA Recombination
DNA Insertion
DNA Sequencing
Transgenic Bacteria, Plants, and Animals
Cloning
Gel electrophoresis

6. Genetic Engineering Techniques
DNA RECOMBINANT:
Literally means “combined DNA”
DNA fragments cannot function all by themselves.
They must be part of the genetic material of living things cells before the genes they contain can be activated.
In this, second step of genetic engineering, the DNA fragment must be put into a hosts cells

7. Genetic Engineering Techniques
DNA RECOMBINANTS:
DNA fragments (cut by restriction enzymes) may be combined with bacterial DNA so that they can later be inserted into a bacterial cell
The small, circular DNA molecules in bacteria (called plasmids) can be removed and cut with a restriction enzyme.
The cut ends are sticky to the foreign fragment, and can allow for the formation of a recombinant DNA molecule

8. DNA Recombination
DNA recombination is sometimes called gene splicing, because the genes are “cut & pasted”
The new DNA strand created is considered to be artificial, because it would not normally occur in nature
Benefit of all life using the exact same DNA
Not the same thing as “natural” genetic recombination
This how we engineer drugs to combat bacterial resistance (like MRSA) and how we are able to make non-human organisms make things like human insulin

9. Genetic Engineering Techniques
DNA INSERTION:
During the first 2 steps of genetic engineering, DNA fragments containing the desired gene are obtained and then inserted into DNA that has been removed from the recipient cell (the cell where the DNA is going.)
Forming recombinant DNA (New DNA)

10. DNA Insertion & Cloning
To insert the DNA into LIVING cells it is easiest to use bacteria
Bacteria in a solution of salt and the desired DNA will eventually take up the DNA in its own DNA.
This is considered DNA insertion
These new bacteria are then cultured (grown) into a large colony.
The technical term for a large number of cells grown from a single cells Clone.
So this is DNA cloning.
You don’t HAVE to use bacteria but it is the easiest.

12. Genetic Engineering Techniques
Restriction Enzymes
DNA Recombination
DNA Insertion
DNA Sequencing
Transgenic Bacteria, Plants, and Animals
Cloning
Gel electrophoresis

13. Genetic Engineering Techniques
DNA sequencing:
Sequencing DNA is when you read the nitrogenous bases (ATCG) along the length of the DNA fragment.
Only one strand of the double helix is used to sequence the DNA
need multiples of the used strand (So you clone it)
The DNA’s bases are tagged using different chemical treatments that break the pieces and reveal the Base sequence.
By tagging the bases, we are able see the order of A, T, C, & G and are then able to read the base sequence

14. Genetic Engineering Techniques
Restriction Enzymes
DNA Recombination
DNA Insertion
DNA Sequencing
Transgenic Bacteria, Plants, and Animals
Cloning
Gel electrophoresis

15. Gel electrophoresis
During gel electrophoresis, DNA is cut with a restriction enzyme into small pieces
Because DNA has a slight negative charge, different charges are placed at either end of a gel containing tray.
When the DNA is placed into the tray it will slowly move across the gel (towards the +)
Because the pieces are different sizes they move at different speeds (large = slower).

16. DNA Fingerprinting
The amazing complexity of the human genome ensures that NO TWO INDIVIDUALS are exactly the same.
This biological theory allows for a powerful new tool in criminal investigations
Now, finding bodily fluids and/or skin cells at the scene of a crime or on a victim can link a suspect to a crime with amazing reliability.

17. Electrophoresis

18. Electrophoresis
- side
+ side

19. Genetic Engineering Techniques
Restriction Enzymes
DNA Recombination
DNA Insertion
DNA Sequencing
Transgenic Bacteria, Plants, and Animals
Cloning
Gel electrophoresis

20. Genetic Engineering Techniques
Transgenic (means gene from across species)
It is now possible to insert genes from one organism into another.
Organisms that contain such foreign genes are said to be Transgenic.
Trans- across or moved genes
Requires many of the already mentioned genetic engineering techniques (most of them)
This allows us to create organisms with foreign traits

21. This transgenic animal is the result of placing jellyfish genes in an albino rabbit, and then bathing it in UV light

22. Transgenic Plants
It is through the process of genetic engineering that we have most of the plants that we use for food.
Not only can we selectively breed more productive organisms, but we can use transgenic organisms to make plants that are resistant to diseases, insects, drought, winds, etc.