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Unit 3: DNA Evidence
Objective 1: Identify the structure and function of a DNA molecule. 1. Students should be able to label the parts of a nucleotide and understand function of DNA 2. Understand the concept of base pairing as it relates to the double helix structure of DNA 3. Describe the difference between nuclear and mitochondrial DNA 4. Contrast DNA strands that code for the production of proteins with strands that contain
repeating base sequences (ie exons and introns, SNPs)
Objective 2: Describe the procedures for obtaining biological samples and how they are used in criminal law.
1. List the necessary procedures for proper preservation of biological evidence for laboratory DNA analysis
2. Understand how CODIS is used in criminal investigations 3. Understand what prompted the Innocence Project and what it does today
Objective 3: Describe advancements in technology used to obtain a DNA fingerprint. 1. Explain the technology of PCR and gel electrophoresis and how it applies to forensics DNA
typing 2. Contrast the newest DNA typing technique, STRs with previous DNA technology 3. Be able to match SNPs from suspects to those found at a crime scene in a simulated lab
experience
Key Terms:
Deoxyribonucleic Acid (DNA)
Complimentary Base Pairing
Mitochondrial DNA (mtDNA)
Nucleotide
Substrate Control
Buccal Cells
Epithelial Cells
Sequencing
Polymerase Chain Reaction (PCR)
Primer
Restriction Fragment Length
Polymorphisms (RFLP)
Gel Electrophoresis
Restriction Enzymes
DNA Ladder
Short Tandem Repeats (STR)
Y-STR
Loci
Nuclear DNA
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DNA Evidence Unit
Date Topic
2/25 Structure and Function of DNA Notes and The Double Helix Movie
2/26 DNA Extraction Lab
2/27 Introduction to DNA Analysis: DNA Typing Annotated Reading
2/28 Introduction to RFLP’s and Gel Electrophoresis Notes and RFLP Simulation
3/1 Who Killed Rockina? Lab
3/4 Gel Electrophoresis-Hector’s Dolphin Lab
3/5 Introduction to STR’s and STR Case Study
3/6 Finish STR Case Study
3/7 Who Dun It? STR Lab
3/8 911 Case Study and Annotation
3/11 Unit Review
3/12 DNA Evidence Unit Multiple Choice Test
3/13 Guest Speaker
3/14 DNA Evidence Unit Performance Assessment
3/15 DNA Evidence Unit Performance Assessment
2/25/19
Objective: Students will be able to describe the basic structure of DNA and how it is collected at a crime
scene.
Warm-Up:
1. What are two things that I want you to know by the end of this unit?
2. When is your unit test?
Structure of DNA
What is DNA?
Stands for: _______________________________
Carries our genetic material from one generation to the next in ______________
DNA is arranged in a ___________________ -two strands are twisted around each other like a
winding staircase.
If you unwind a single human chromosome of DNA, it will be about ___________
What does our DNA do?
Only about ___________________________________ is made up of our genes.
Up until recently, scientists believed that the rest of our DNA was noncoding-they thought these
sequences were “_________”!
However, a research project called Encode studied these sections and found:
o Parts of the DNA that don’t code for genes contain about ______________
__________________________________________________________:
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Determine when the gene turns on and off
_____________________________________________________
Switches for a variety of diseases
Affects every cell, but can do so at different times in our lifetime
Can be sequenced and used for identification purposes in crime cases
Examples:
• Instructions for the cells to be different types of cells (brain cell vs liver
cell)
• Instructions for pancreas cell to make insulin after a meal
• Instructions for cells to reproduce to replace dead or damaged cells (like
skin cells replacing those that sloughed off).
Structure
Nucleic Acids: ____________________________________________________
________________________________________________________________
o Nucleotides are made up of 3 things:
A phosphate group (same on all nucleotides)
5 Carbon sugar molecule (same on all nucleotides)
_____________________________ (Different on each nucleotide)
Adenine (A) (__________________: 2 rings of
Guanine (G) Carbon and Nitrogen)
Thymine (T) (__________________: single ring of
Cytosine (C) Carbon and Nitrogen)
o The phosphate of one nucleotide is attached to the sugar of the next nucleotide with a
__________________________ (strong)
o The base pairs on each strand of DNA are bound together with ________
______________ (weak)
Base pairing:
Purines are always paired with Pyrimidines
o __________ always pairs with _____________ (forms 2 hydrogen bonds)
o ___________ always pairs with ___________ (forms 3 hydrogen bonds)
This is called ___________________________-the sequence on one strand determines the
sequence on the other.
DNA has a direction-it is polar! We call the strands anti-parallel
o It goes from the 5’ end to the 3’ end.
o The opposite strand also goes from the 5’ to the 3’ end,
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Mitochondrial DNA
The in our cells also contains its own DNA (mtDNA) that tells the
mitochondria what to do and how to replicate.
Mitochondrial DNA comes from our
o This is because the portion of sperm that is able to penetrate the egg does not contain
mitochondria.
Mitochondrial DNA is much more than nuclear DNA and therefore might
be to find and analyze at a crime scene.
However, since the DNA comes from our mother, it is in all children
produced by the same woman.
Collection of Biological Materials
Arriving at a Crime Scene
When biological materials are found at a crime scene, the first step is to
the investigator and the sample from by taking precautionary
measures.
A scientist should always assume that biological materials are contagious and should wear the
following protective gear:
o Latex or Nitrile Gloves
o Face Mask
o Boot Covers
o Eye Protection
o Lab coat/Coveralls
Once the investigator has on the proper protective gear, and
sketches of the blood should be taken at the scene.
A substrate control should also be collected at the scene.
o A is a piece of the material that is close to but not
part of the biological material being collected.
Collecting Evidence
Possible sources of DNA:
o Blood
o Semen
o Sweat
o Skin
o Saliva
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o Buccal swabs: a swab is used to collect cheek cells out of your mouth
Collecting DNA Samples:
o Biological materials should be placed in a or well
ventilated box to discourage the growth of bacteria.
o Dried blood is swabbed with a that has been dipped in
distilled water. The Qtip then goes into a well ventilated for transport.
o that contains blood is packaged in an airtight container
and immediately . This is to discourage the growth of
bacteria that is naturally in the soil.
Types of DNA Analysis
DNA Analysis Techniques
Before any analysis can be done, the DNA sample has to be amplified, or copied, through a
process called Polymerase Chain Reaction ( ).
After enough of the sample is created, we can use one of the two techniques to analyze the
sample.
o Restriction Fragment Length Polymorphism ( ): a sample of DNA is separated
using gel electrophoresis based on the size of the DNA fragments.
o Short Tandem Repeats ( ): looks at the non-coding part of our genome and
counts how many times a specific sequence of nucleotides repeats.
2/26/19
Objective: Students will be able to extract DNA from wheat germ and observe it with the naked eye.
Warm-Up:
1. Where is DNA located in a cell? What are the barriers that you must get through in order to
remove DNA from a cell?
2. Why is protective wear necessary when collecting biological evidence from a crime scene?
3. Why do we want to inhibit the growth of bacteria when collecting blood from a crime scene?
Vocabulary Scramble: use the definition to unscramble the vocabulary word. Then, draw a picture of
the word. (5 words on the next page)
Word Scramble Definition Picture
oucdlnetie The components of this monomer are: phosphate, sugar, and a nitrogen base.
oetmplnyimcar sabe aiipngr
A-T and C-B, therefore the sequence on one strand determines the sequence on the paired strand.
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itdohocalmnri adn
This type of DNA is passed down from the mother only and is found outside the nucleus of the cell.
uclcba Cheek cells
ecuesgnqin A procedure used to determine the order of the base pairs that make up a DNA molecule.
utbestrsa ronlcto
A piece of the material that is close to but not part of the biological material being collected and is used for comparison.
palheiteli Skin cells.
2/27/19
Objective: Students will be able to explain the technology of PCR and gel electrophoresis and how it
applies to forensics DNA typing.
Warm-Up:
Read pages 369-371 in the textbook and answer the following questions.
1. What are the steps of DNA replication?
2. What enzyme proofreads the growing DNA for mismatched pairs?
3. Why was PCR a huge advancement in the field of DNA analyzation?
Read pages 382-384 and answer the following questions.
1. What enzyme starts the process of PCR?
2. How many times can a strand of DNA be amplified by PCR?
3. Fill in the chart about the specifics of PCR.
Temperature (⁰C) Enzymes Used What is happening?
94
60
72
7
2/28/19
Objective: Students will be able to explain the technology of PCR and gel electrophoresis and how it
applies to forensics DNA typing.
Warm-Up:
1. How are nuclear DNA and Mitochondrial DNA similar? How are they different?
2. What is an advantage to processing mitochondrial DNA rather than nuclear DNA from a crime
scene? What is a disadvantage?
PCR and RFLP’s
Polymerase Chain Reaction (PCR)
A method of making of a piece of DNA.
o It takes about 3 hours to make 1 billion copies of a single DNA molecule.
You need:
o sample to amplify
o Many copies of 2 specific olignoculeotide
These primers are synthetically made and are specific to the section of DNA you
wish to copy.
o DNA
o : “Taq DNA Polymerase”
Found in geysers of Yellowstone National Park
Steps in Copying DNA
1. A DNA molecule is placed in a small .
2. Taq DNA polymerase, , and nucleotide base are added.
3. The DNA is -usually to around 90 C.
a. This breaks the hydrogen bonds between the two strands of DNA so they
are .
4. The temperature is to about 55 C
a. This allows the specific to bind to the DNA strand at the appropriate
sequence.
b. The primers act like bookends-only the DNA sequence the primers
will be .
5. The temperature is again to around 70 C.
a. This allows the Taq DNA polymerase to new bases to the separated strands.
6. The cycle is repeated many times over the next few hours to create many copies of the DNA.
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Restriction Fragment Length Polymorphism (RFLP)
Restriction enzymes are used to “ ” the strand of DNA at a specific nucleotide
sequence.
o Each person has unique DNA and therefore, the location of the specific sequence will be
different for each person.
o The result is many of DNA that are all different .
We can use a technique called to separate these fragments
and analyze the DNA.
Uses:
o Genome mapping, localization of genetic disease genes, determination of risk for a
disease, genetic fingerprinting (who does the DNA belong to), and paternity testing.
Gel Electrophoresis
What is it?
A method used to and analyze DNA, RNA and proteins based on their size
and charge.
o The phosphate groups are charged so they will be attracted to the
positive electrode.
How does it Work?
1. is added to a container hooked up to an electric current generator.
2. Samples of the DNA, RNA, or protein are added to the at one end of the gel.
3. The is turned on.
4. are pulled through the gel in ladders based on their .
a. particles move father than large particles and are found near
the .
b. Negative DNA moves toward the positive electrode.
5. is used to stain the material based on what you want to see.
How to Read a Gel
The sample in each well will separate into well defined “lines” of DNA. Each line is called
a .
o Each band contains a large number of DNA fragments of the
that have all traveled as a group to the same position.
Together, all the bands are called a .
We can compare the DNA ladder of each sample to a slot that
contains fragments of a .
We can also compare the different bands to each other to get a “ ”
3/1/19
Objective: Students will be able to explain the technology of PCR and gel electrophoresis and how it
applies to forensics DNA typing.
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Warm-Up:
These are the results of a DNA test from a crime scene.
1. Circle the smallest fragment in the control ladder. Box the largest fragment in the control
ladder.
2. Highlight the alleles in sample 2 that match the victim.
3. Is the suspect guilty of the crime? Explain how you know.
Vocabulary Dice
Roll two dice. The first dice tells you the vocabulary word. The second dice tells you the task. Switch
back and forth with your partner until the teacher calls time.
Vocabulary Words
1. PCR 2. Primer 3. RFLP 4. Gel Electrophoresis 5. Restriction Enzymes 6. DNA Ladder
Activity
1. Give the definition in your own words. 2. Draw a picture of the word. 3. Pair the word with another vocabulary
word and explain why you paired them together.
4. Give an example of the word. 5. Use the word in a sentence. 6. Explain how you are going to remember
the word.
3/4/19
Objective: Students will be able to describe the process of PCR and identify an unknown sample by
mimicking how an enzyme will cut the DNA and how it will travel through the agros gel in gel
electrophoresis.
Sample 1 is the victim’s DNA.
Sample 2 is a sample collected from
the crime scene. It is a mixture of the
victim’s DNA and the killer’s DNA.
Sample 3 is the suspect’s DNA.
Sample 4 is the control.
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Warm-Up:
Mr. and Mrs. Smith just gave birth to fraternal
twins-Bob and Jane. Unfortunately, a fire alarm
caused the entire nursery to evacuate the building.
Six children were on their way to their parents and
were carried out of the building in the arms of
nurses. When the parents, children, nurses, and
doctors were allowed back into the building, they
discovered that they weren’t sure which child
belonged to who. The doctor took DNA samples
from Mr. and Mrs. Smith and the six unknown
children. Use the gel results to answer the questions.
1. Which of the six children are Mr. and Mrs. Smith’s twins? How do you know?
2. What do the bands in the gel represent?
3. How does the DNA get fragmented?
3/5/19
Objective: Students will be able to explain the technology of Short Tandem Repeats and how it applies
to forensics DNA typing.
Warm-Up:
Read pages 374-381 and answer the following questions.
1. Define RFLP in your own words.
2. How is electrophoresis used with these fragments?
3. Briefly describe the process of gel electrophoresis.
4. What distinction does RFLP DNA typing have? (pg 380)
5. What is the significance of the dress on page 381?
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Short Tandem Repeats
DNA Identification
99% of each human’s DNA is indistinguishable
Yet, no two people (except identical twins!) share exactly the same arrangement of base pairs
What are STR’s?
Looking at the intron region of DNA
o The coding part of the DNA tells our bodies what to do so it is the for
most individuals.
o We call these regions variable number of tandem repeats ( )
o The VNTR’s are in common locations on a set chromosome. We call these locations loci.
We get one set of chromosomes from so the number of STR’s will be
different on each chromosome.
o So each STR has numbers!
o Although siblings with the same parents get their genes from the same “gene pool”,
crossing over allows for a unique set of genes in each person.
Repeats are bp long (for example: CTTG-4bp)
3 to 100+ repeats arranged head-to-tail (CTTGCTTGCTTGCTTGCTTG…)
The number of repeats in a row in the population.
Y STR’s
Short Tandem Repeats found on the
o These are passed down through the paternal side and there is very little variation from
generation to generation.
Used for:
o -since females don’t have a Y chromosome, if
there is one present, it has to come from a male
o Used to distinguish between
o Ancestry Testing for Males
Analyzing STR’s
1. Locate a sample to test.
2. Use to amplify the desired DNA sequence.
3. Use to separate the different lengths of STR’s.
4. Compare the of STR’s in each loci to known samples to determine a match.
Results
We use STR loci to evaluate a DNA sample.
The more STR’s at a given loci that are the same, the more the sample
came from that .
o It is common to share the same number of STR’s at 1 or 2 loci
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Reading Results
2 ways:
o A computerized
o A with the loci across the top and the number of repeats at each loci
Remember-you have two of each chromosome so you will have 2 numbers for
each loci.
3/6/19
Objective: Students will be able to contrast the newest DNA typing technique, STR’s, with previous DNA
technology (RFLP) and be able to match SNP’s from suspects to samples found at a crime scene in a
simulated lab experience.
Warm-Up:
Read pages 384-388 and answer the following questions.
1. Explain what STR’s are.
2. What are two advantages for using STR’s?
3. How many CODIS STR’s are there?
4. What does this tell forensic scientists and how accurate is it?
Read pages 390-392 and answer the following questions.
1. How is sex identification done using STR’s?
2. Is DNA typing becoming acceptable as truth in courts?
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3/7/19
Objective: Students will be able to contrast the newest DNA typing technique, STR’s, with previous DNA
technology (RFLP) and be able to match SNP’s from suspects to samples found at a crime scene in a
simulated lab experience.
Warm-Up:
Karen has four children: three daughters (Tiffany, Melissa, and Amanda) and one son (Steve).
1. Predict the STR’s for Steve using the table below. Remember, you get one chromosome from
each parent.
2. A body was found in the woods and forensic scientists have the following DNA data for the
missing person. Is this person Steve? Why or why not?
STR Body STR Body STR Body
D3S1358 16,18 D18S51 18,18 TPOX 8,10
vWA 17,18 D5S818 11,12 CSF1PO 12,12
FGA 22,24 D13S317 8,8
AMEL XX D7S820 9,10
D8S1179 13,15 D16S539 12,12
D21S11 28,28 THO1 8,9
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3/8/19
Objective: Students will be able to apply their knowledge of DNA, PCR, Gel Electrophoresis and the two
different analyzation techniques (RFLP and STR) to a real-life case study.
Warm-Up:
The 15-STR locus DNA profile of a missing person, James Dittman, is given in the following table.
STR Loci Allele
D3S1358 15
THO1 6, 9.3
D21S11 27
D18S51 15, 16
PENTA E 10
D5S818 11
D13S317 10, 13
D7S820 9, 10
D16S539 11, 12
CSF1PO 13
PENTA D 12, 13
AMELOGENIN XY
vWA 17, 19
D8S1179 10, 13
TPOX 8, 12
FGA 21
Decomposing remains were found deep in the woods near the missing person’s house. DNA from these
remains was extracted, amplified, and analyzed at 15 STR loci. Compare the resulting STR readout to
determine whether the remains could belong to James Dittman. If not, at which STR loci do the profiles
differ?
Vocabulary Builder
Define the following vocabulary words. Then, write a sentence using the word but instead of writing the
word, draw a picture in its place.
EXAMPLE Word: Noble Gases Definition: The elements in group 8A or 18 including Helium, Neon, Argon, Krypton, Xenon, and Radon.
Sentence: The are called noble because they contain 8 valence electrons and do not react with other elements.
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Word: STR Definition: Sentence:
Word: Y-STR Definition: Sentence:
Word: Loci Definition: Sentence:
Word: Nuclear DNA Definition: Sentence:
3/11/19
Objective: Students will be able to demonstrate their knowledge of DNA and analyzation techniques on
a unit review.
Warm-Up:
1. Go back to the front page of this packet and read through the essential outcomes. Put a
question mark next to the topics that you still have questions about. Put a check mark next to
the topics that you feel confident about.
2. How are you going to go about learning those topics that have a question mark next to them?
3/12/19
Objective: Students will be able to demonstrate their knowledge of DNA and analyzation techniques on
a unit test.
Warm-Up:
1. None
3/13/19-Guest Speaker
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3/14/19
Objective: Students will be able to describe the components of blood and how it is used to analyze a
crime scene.
Warm-Up:
1. None
3/15/19
Objective: Students will be able to demonstrate their knowledge of DNA and analyzation techniques on
a unit test.
Warm-Up:
1. Turn your work into the basket.