Tutorial - DNA Fingerprinting And Electrophoresis.

Tutorial - DNA FingerprintingAndElectrophoresis

Table of Contents

Introduction Pretest Part 1 – Historical Information Part 2 – Electrophoresis Equipment Setup Part 3 – Preparing DNA Sample for Electrophoresis Part 4 – Set up and run a DNA Gel Conclusion – Additional introductory resources Posttest – Administered by instructor in class

Introduction

This is an introductory tutorial on DNA Fingerprinting and Electrophoresis

During this tutorial, you will examine: Historical timeline of DNA manipulation Components of DNA manipulation Elements of electrophoresis

Pretest

Prior to continuing the tutorial, complete the pretest. Click on the “pretest” link below which will bring up a

Word document. Print out the pre-test, complete the pretest and return

it to your instructor. Then, proceed with the tutorial on electrophoresis.

PRETEST

Part 1 - What is a gene?

Each chromosome is an extremely long DNA molecule that can be thousands or millions of base pairs long.

The vast length of chromosomes posed a problem for scientists who were trying to isolate and study the stretches of DNA that make up genes.

Part 1 – Molecular Scissors – Pg 1 In 1962, Werner Arber, a

Swiss biochemist, provided the first evidence for the existence of "molecular scissors" that could cut DNA. He showed that E. coli bacteria have enzymes that recognizes and destroys foreign DNA.

Arber and his associates called this group of DNA-cutting enzymes restriction endonucleases (sometimes referred to as restriction enzymes). They showed that restriction endonucleases are specific in their snipping: a given enzyme will cut DNA only when it recognizes exactly the right sequence.

Part 1 – Molecular Scissors – Pg 2

http://opbs.okstate.edu/~petracek/CHAPTER%2029%20FIGS/Table%2029-02.JPG

Part 1 – Molecular Scissors – Pg 3 Restriction Enzyme = BamHI

Recognition Site = G G A T C CCuts = Notice the cut occurs at the arrows and follows the red line

Restriction Enzyme = HaeIIIRecognition Site = G G C CCuts = Notice the cut occurs at the arrows and follows the red line

Part 1 – Molecular Glue

Not long after Arber's discoveries, Arthur Kornberg identified the pasting mechanism for DNA, an enzyme he called ligase.

Kornberg was trying to construct artificial viral DNA from viral fragments, but had been unable to make a biologically active molecule. Once he added ligase, however, he found that the enzyme made it possible to paste the ends of DNA molecules together.

Part 1 – Cutting and Gluing DNA

RestrictionEnzyme

MolecularScissors

MolecularGlue

Part 1 – Checkup

1. Chromosomes consist of:

Long strand of DNA.2. The molecular scissors

which cut DNA into small pieces are:

Restriction endonucleases.

3. Where do these molecular scissors cut the DNA?

At a specific sequence of bases.

4. For example, what is the sequence where EcoR1 cuts?

G A A T T C

5. The molecular glue that will bind pieces of DNA together.

Ligase

Click or space bar to continue with next unit

Part 2 – Electrophoresis EquipmentWhat is Gel Electrophoresis? Electro = flow of

electricity, phoresis, from the Greek = to carry across

A gel is a colloid, a suspension of tiny particles in a medium, occurring in a solid form, like gelatin

Gel electrophoresis refers to the separation of charged particles located in a gel when an electric current is applied

Charged particles can include DNA, amino acids, peptides, etc

Part 2 – Electrophoresis EquipmentWhy “do” a gel electrophoresis? When DNA is cut by restriction enzymes, the result is a

mix of pieces of DNA of different lengths It is useful to be able to separate the pieces - i.e. for

recovering particular pieces of DNA, for forensic work or for sequencing

Part 2 – Electrophoresis EquipmentWhat is needed to do this?

Agarose - a polysaccharide made from seaweed. Agarose is dissolved in buffer and heated, then cools to a gelatinous solid with a network of cross linked molecules

Agarose is the material used to make the gel we will use.

Part 2 – Electrophoresis EquipmentWhat is needed to do this? – Pg 2

Buffer - in this case TBE

The buffer provides ions in solution to ensure electrical conductivity.

Not only is the agarose dissolved in buffer, but the gel slab is submerged (submarine gel) in buffer after hardening

Part 2 – Electrophoresis EquipmentWhat is needed to do this? – Pg 3 Also needed are a

power supply and a gel chamber

Gel chambers come in a variety of models, from commercial through home-made, and a variety of sizes

Part 2 – Electrophoresis EquipmentHow does it work? DNA is an organic acid, and is negatively charged

(remember, DNA for Negative) When the DNA is exposed to an electrical field, the

particles migrate toward the positive electrode Smaller pieces of DNA can travel faster in a given time

than larger pieces because smaller fragments do not experience as much resistance when traveling through the gel.

Part 2 – Electrophoresis EquipmentApparatus Diagram

Gel

Wells

GelBox

PositiveElectrode

(red)

Part 2 – Electrophoresis EquipmentApparatus – Another Example

Agarose gel block

Positive electrode

DNA loaded inwells in the agarose

Black backgroundTo make loading wells easier

Comb

Buffer

Part 2 – Checkup – Page 1

1. A suspension, gelatin like, used to separate DNA fragments gel

2. Name of the material used to make our gels. agarose

3. Liquid containing ions which promote electrical conductivity buffer

4. Name the apparatus containing the gel slab and buffer.

gel chamber5. What charge does DNA

possess? negative

6. DNA will migrate toward which terminal in a gel chamber?

positive

Click or hit the space bar to continue to the next page


7. Why do large fragments move slower? because they are

bigger


Part 3 – Preparing DNA Sample for Electrophoresis – DNA Extraction – Page 1

1. DNA can be extracted from almost any human tissue. Buccal cells from inside cheek for paternity tests. Sources of DNA at crime scene: blood, semen,

hair follicle, saliva. DNA extracted from evidence is compared to DNA

from known individuals


2. Extracted DNA molecules are combined with restriction enzymes (endonucleases) and allowed to react with each other. Restriction enzymes are produced by bacteria

as a defense against viruses. These enzymes cut DNA at specific base

sequences called recognition sites. Results in smaller pieces of DNA called

RFLP’s.


An EcoR1 restriction enzyme


RF stands for Restriction Fragments. Those are the fragments that were cut by restriction enzymes.

L stands for Length, and refers to the length of the restriction fragment.

P stands for Polymorphisms, a Greek term for “many shapes”. The lengths of some of the restriction fragments differ greatly between individuals.

RFLP = Restriction Fragment Length Polymorphism

3. RFLP Analysis:


Electrophoresis of these RFLP’s produce different patterns of DNA bands.

With 3 billion base pairs in the human genome, however, RFLP analysis would produce a “smear” of many similar sized fragments.

smear

Part 3 – Preparing DNA Sample for Electrophoresis – DNA Extraction – Page 6 Molecular biologists have identified regions of the human

genome where restriction fragment lengths are highly variable between individuals.


VNTR stands for ‘variable number of tandem repeats. A tandem repeat is a short sequence of DNA that is

repeated at a specific chromosomal locus. Tandem repeats are interspersed throughout the

human genome. The number of repeats at a given place on a certain

chromosome is highly variable from one person to another.

The number of such repeats is usually different on the paternal and maternal members of the same person’s chromosome pair.

VNTR alleles are highly variable regions of human DNA.


Red boxes represent the repeat unit and the blue lollipops represent cut sites for a restriction endonuclease. (Here 3 different variants, may be 50 in reality).


Analysis of a VNTR locus most commonly results in a two-band pattern, one band inherited from each parent.

A one-band pattern can occur if the size of the two parental bands are the same or nearly the same.

For our simple example of three different alleles designated A, B, and C illustrated above, six unique DNA profiles are possible.


The possible genotypes are AA, BB, CC, AB, BC, and AC

Part 3 – Preparing DNA Sample for Electrophoresis – DNA Extraction – Page 11 The RFLP markers most commonly used for DNA profile

analysis are found on chromosomes 1, 2, 4, 5, 10 and 17.

These RFLP markers are named after their locations on these chromosomes.

For example, the marker on chromosome 2 is called D2S44 (section 44 of chromosome 2).

These chromosomal locations are also referred to as DNA loci (plural) or locus (singular).


When profiles form a single VNTR locus from unrelated individuals are compared, the profiles are normally different.

However, it is possible for two individuals to have the same profile at one or two loci.

But the chance of more than one person having the same DNA profile at 4, 5, or 6 different VNTR loci is extremely small.

DNA profiles vary from person to person.

Part 3 – Checkup – Page 11. What human cell(s) can

we extract DNA? From almost any

cell.2. What is used to cut the

DNA into fragments? Restriction

enzymes.3. How does a restriction

enzyme know where to cut the DNA? Looks for specific

sequence of bases, called recognition sites

4. The resulting small pieces of DNA are called?

RFLP’s5. What is the recognition

site (sequence of bases) for EcoR1?

G A A T T C6. What does RFLP stand

for? Restriction

Fragment Length Polymorphism

Click or hit the space bar to continue to the next page of checkup questions

Part 3 – Checkup – Page 27. When you electrophores

these fragments, what results?

Different patterns of DNA bands

8. If you electrophores all human DNA, what results?

A smear of indistinguishable bands.

9. What have scientists found that seems more unique among individuals?

Regions of human DNA fragments that are highly variable

10. These highly variable areas are called what?

VNTR’s11. What does VNTR stand for?

Variable number of tandem repeats

12. Can you expect the VNTR’s at a location to be different from one person to another?

Yes, the repeats at a given place on a certain chromosome is highly variable from on person to the next.

Click or hit the space bar to continue to the next page of checkup questions


12. What chromosomes are usually tested for VNTR’s? Chromosomes 1,

2, 4, 5, 10 and 17.13. When analyzing DNA

from different individuals, why use several chromosomes? More samples

used from an individual, the less chance there will be duplication.


Part 4 – Set up and run a DNA GelPage 11. DNA is prepared by

digestion with restriction enzymes

2. Agarose is made to an appropriate thickness (the higher the % agarose, the slower the big fragments run) and “melted” in the microwave

3. The gel chamber is set up, the ‘comb’ is inserted

4. The agarose may have a DNA ‘dye’ added (or it may be stained later). The agarose is poured onto the gel block and cooled

Part 4 – Set up and run a DNA GelPage 25. The comb is

removed, leaving little “wells”.

6. Buffer is poured over the gel, covering it completely.

7. The DNA samples are loaded into the wells using a micropipette

Part 4 – Set up and run a DNA GelPage 38. Gel box top is secured.

9. Terminal cords are attached to appropriate terminals.

10. The power source is turned on and the gel is run.

Part 4 – Checkup

1. What happens when the percent of agarose used in the gel is changed? High the

percentage, slower the fragments will move.

2. Why is a comb used when preparing the gel? Makes the wells in

the gel

3. What is the micropipette used for?

Load DNA samples into the wells

Click here to return to the contents pageOr click anywhere else or hit space bar to go to the next page

Conclusion

Video Clip – Sam Sheppard Case – Application of DNA fingerprinting (Viewing video instruction: when web page appears: (1) click on “view” button, (2) On “required registration” screen, click on “Take a Test Drive” button, (3) Click on “view” button again.) Note: If you do not have sound, click on the “captions on” option. This will show the text as the video plays.)

Use of DNA in Identification – Link to more detailed explanation of using DNA when comparing evidence DNA with suspect DNA.

How can RFLP’s help find faulty genes? – Link to a description of another practical use of RFLPs

DNA Fingerprinting, Genetics and Crime: DNA Testing and the Courtroom – A seminar by geneticist and evolutionary biologist Julian Adams of the University of Michigan explains the principles, procedures and issues involved with the use of DNA as a tool in the identification of individuals.

DNA Fingerprinting

THE END

Tutorial - DNA Fingerprinting And Electrophoresis.

Documents

Transcript of Tutorial - DNA Fingerprinting And Electrophoresis.