DNA Fingerprinting Overview - STLCC.edu :: Users` Server

DNA FINGERPRINTING MADE
EASY FOR FORENSICS
Presented by
Eilene Lyons
The St. Louis Community College – Florissant Valley
Biotechnology Program
Some slides are from a downloaded PPT presentation from The National Institute of Standards and Technology (NIST)
http://www.cstl.nist.gov/biotech/strbase/training.htm
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Where do we get the DNA?
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Blood
Semen
Saliva
Urine
Hair
Teeth
Bone
Tissue
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DNA in the Cell
chromosome
cell nucleus
Double stranded
DNA molecule
Individual
nucleotides
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REVIEW OF DNA STRUCTURE
• NUCLEOTIDE monomers – A, T, G, C
• DNA POLYMER - long chain of nucleotides
• HYRDROGEN BONDS hold two polymers
together to form a ladder
• COMPLEMENTARY nucleotides make the
steps of the ladder
– A bonds with T
– G bonds with C
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Review of Replication
Two polymers separate
Each serves as a template
DNA polymerase adds nucleotides,
but not without a primer…
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DNA: Nucleotide structure
A nucleotide is composed of a nucleobase (nitrogenous base),
a five-carbon sugar (either ribose or 2'-deoxyribose), and one to
three phosphate groups. Together, the nucleobase and sugar
comprise a nucleoside. The phosphate groups form bonds with
either the 2, 3, or 5-carbon of the sugar, with the 5-carbon site
most common. Cyclic nucleotides form when the phosphate
group is bound to two of the sugar's hydroxyl groups.[1]
Ribonucleotides are nucleotides where the sugar is ribose, and
deoxyribonucleotides contain the sugar deoxyribose.
Nucleotides can contain either a purine or pyrimidine base.
Nucleic acids are polymeric macromolecules made from
nucleotide monomers. In DNA, the purine bases are adenine
and guanine, while the pyrimidines are thymine and cytosine.
RNA uses uracil in place of thymine.
Ribose structure indicating numbering of carbon atoms
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DNA Polymerase requires a primer
WHY?
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DNA Polymerase requires the primer’s 3’OH to add the next nucleotide
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Review of DNA Replication
• POLYMERS SEPARATE - Hydrogen bonds break to
unzip the sides of the ladder
• TEMPLATE – one polymer of the DNA
• PRIMERS – complementary RNA added to the template
• NUCLEOTIDES – the monomers (A, T, G, C)
• DNA POLYMERASE – the enzyme that adds new
complementary nucleotides starting at the 3’ OH end of
the RNA primer
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Assessment 1. Name four
molecules required to make new
DNA.
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Template DNA
Primers
Nucleotides (A, T, G, C)
DNA Polymerase
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Polymerase Chain Reaction: DNA Replication in a test tube
STEP 1:
DENATURATION
HEATING TO 94C
STEP 2: PRIMER
ANNEALING
COOLING TO 58C
primer
primer
STEP 3: EXTENSION
HEATING TO 72C
primer
primer
FIGURE 3. Steps of PCR
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DNA Amplification with the
Polymerase Chain Reaction (PCR)
5’
3’
5’
3’
3’
3’
5’
5’
Starting DNA
Template
Separate
strands
(denature)
Add primers
(anneal)
Forward primer
5’
3’
5’
3’
5’
Make copies
(extend primers)
3’
3’
5’
Reverse primer
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PCR Copies DNA Exponentially
through Multiple Thermal Cycles
Original DNA target region
Thermal cycle
In 32 cycles at 100% efficiency, 1.07 billion
copies of targeted DNA region are created
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Assessment 2.
polymers
Nucleotides
complementary
ladder
steps
DNA polymerase
primers
PCR
template
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STRs are Polymorphisms
• Small Tandem Repeats
• Polymorphism: two or more distinct forms of a section of
DNA
AATT
7 repeats
8 repeats
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People are Diploid
• We inherit
polymorphisms from
our parents.
• Everyone has 2
copies of each piece
of DNA:
– One chromosome
from Mom
– One chromosome
from Dad
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The STRs used for DNA
Fingerprinting
TPOX
D3S1358
D8S1179
D5S818
FGA
CSF1PO
TH01
VWA
D7S820
AMEL
D13S317
D16S539
D18S51
D21S11
AMEL
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STRs can be replicated in
a test tube.
chromosome
cell nucleus
Double stranded
DNA molecule
Target Region for
Replication
Individual
nucleotides
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PCR Replicates STRs
Polymerase Chain
Reaction
What must be added to
the tube?
1. Template DNA
2. Primers
3. DNA Polymerase
(Taq from Thermus
aquaticus)
4. Nucleotides
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Forensics labs use
Multiplex PCR –
many STRs
copied at once
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DNA has a negative charge. If put into an electric
field, DNA will migrate towards the positive
electrode.
ROPE TRICK
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Viewing the DNA
• Stain with
ethidium bromide
– fluoresces in UV
light
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Analysis of a Single DNA
Polymorphism
• PCR results of
amplification of the
D1S80
– Range of fragment
sizes = 224 to 640 bp
400 bp
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Looking at
many
polymorphisms
at once
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Check out these sites:
• http://www.dnalc.org/ddnalc/resources/pcr.
html
• http://www.fbi.gov/hq/lab/codis/index1.htm
• http://www.cstl.nist.gov/biotech/strbase/ind
ex.htm
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DNA replication Diagram (From Wikipedia, not part of EL presentation)
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