DNA Evidence How is DNA used to solve crimes?
-
Upload
stephanie-little -
Category
Documents
-
view
217 -
download
0
description
Transcript of DNA Evidence How is DNA used to solve crimes?
DNA Evidence How is DNA used to solve crimes?
T. Trimpe 1/31/12 What is DNA? What makes up DNA? Double
Helix
DNA stands for deoxyribonucleic acid and contains genetic
information. It is found on chromosomes located in the nucleus of
our cells. What makes up DNA? The sides or backbone of the DNA
molecule are made up of sugar (deoxyribose) and phosphate
molecules. The rungs that form the middle of the molecule are made
up of pairs of nucleotides or nitrogen bases. Adenine (A) pairs
with thymine (T), while guanine (G) always pairs with cytosine (C).
The order of the bases determines the genetic code. Double Helix
1/31/12 DNA Image: How is DNA used as evidence?
Only one-tenth of a single percent of DNA (about 3 million bases)
differs from one person to the next. Scientists can use these
variable regions to generate a DNA profile of an individual, using
samples from blood, bone, hair, and other body tissues and
products. In criminal cases, this generally involves obtaining
samples from crime-scene evidence and a suspect, extracting the
DNA, and analyzing it for the presence of a set of specific DNA
regions (markers). If the sample profiles don't match, the person
did not contribute the DNA at the crime scene. If the patterns
match, the suspect may have contributed the evidence sample.
1/31/12 How is DNA used as evidence?
Each persons DNA is different from other people (except identical
twins). DNA collected from a crime scene can either link a suspect
to the evidence or eliminate a suspect, similar to the use of
fingerprints. DNA can identify a victim through DNA from relatives,
even when no body can be found. DNA can link crime scenes together
by linking the same perpetrator to different scenes locally,
statewide, and across the nation. DNA can place an individual at a
crime scene, in a home, or in a room where the suspect claimed not
to have been. DNA can refute a claim of self-defense and put a
weapon in the suspect's hand. It can change a story from an alibi
to one of consent. 1/31/12 DNA Strand Image & information: What
factors affect DNA evidence?
Several factors can affect the DNA left at a crime scene, such as
environmental factors (e.g., heat, sunlight, moisture, bacteria,
and mold). Therefore, not all DNA evidence will result in a usable
DNA profile. Further, DNA testing cannot identify when the suspect
was at the crime scene or for how long. What is CODIS? CODIS stands
for COmbined DNA Index System, which is an electronic database of
DNA profiles that can identify suspects. DNA profiles from
individuals convicted of certain crimes, such as rape, murder, and
child abuse, are entered into CODIS and help officers identify
possible suspects when no prior suspect existed. Did you know? Each
human cell contains three billion DNA base pairs. Our unique DNA
amounts to 0.1% or 3 million base pairs. 1/31/12 DNA information:
Which three statements below are true?
True or False? Which three statements below are true? 1. The DNA in
a man's blood is the same as the DNA in his skin cells and saliva.
2. Each person's DNA is different from every other individual's. 3.
DNA can be found in all the cells in our bodies except the blood
cells. 4. DNA can have forensic value even if it is decades old. 5.
DNA evidence was first used to get a conviction in a trial in 1987.
Watch the video segment from NOVA: "The Killer's Trail" and be
ready to answer the questions on the next slide. 1/31/12 History of
Forensic DNA Analysis
DNA typing, introduced in the mid-1980s, has revolutionized
forensic science and the ability of law enforcement to match
perpetrators with crime scenes. Thousands of cases have been closed
and innocent suspects freed with guilty ones punished because of
the power of a silent biological witness at the crime scene. 'DNA
fingerprinting' or DNA typing (profiling) was first described in
1985 by an English geneticist named Alec Jeffreys, who found that
certain regions of DNA contained DNA sequences that were repeated
over and over again next to each other. He also discovered that the
number of repeated sections present in a sample could differ from
individual to individual. By developing a technique to examine the
length variation of these DNA repeat sequences, Dr. Jeffreys
created the ability to perform human identity tests. 1/31/12
Restriction Fragment Length Polymorphism
These DNA repeat regions became known as VNTRs, which stands for
Variable Number of Tandem Repeats. The technique used by Dr.
Jeffreys to examine the VNTRs was called Restriction Fragment
Length Polymorphism (RFLP) because it involved the use of a
restriction enzyme to cut the regions of DNA surrounding the VNTRs.
The past 15 years have seen tremendous growth in the use of DNA
evidence in crime scene investigations as well as paternity
testing. Today over 150 public forensic laboratories and several
dozen private paternity testing laboratories conduct hundreds of
thousands of DNA tests annually in the United States. The number of
laboratories around the world conducting DNA testing will continue
to grow as the technique gains in popularity within the law
enforcement community. 1/31/12 Polymerase Chain Reaction
The evolution of DNA testing advanced significantly when Dr. Kary
Mullis discovered that DNA could be copied in the laboratory much
as it is in the natural world. The copying process, known as
Polymerase Chain Reaction (PCR), uses an enzyme (polymerase) to
replicate DNA regions in a test tube. By repeating the copying
process, a small number of DNA molecules can be reliably increased
up to billions within several hours. RFLP analysis requires a
biological sample about the size of a quarter, but PCR can be used
to reproduce millions of copies of the DNA contained in a few skin
cells. Since PCR analysis requires only a minute quantity of DNA,
it can enable the laboratory to analyze highly degraded evidence
for DNA. On the other hand, because the sensitive PCR technique
replicates any and all of the DNA contained in an evidence sample,
greater attention to contamination issues is necessary when
identifying, collecting, and preserving DNA evidence. 1/31/12 Short
Tandem Repeats Short Tandem Repeat (STR) technology is a forensic
analysis that evaluates specific regions (loci) that are found on
nuclear DNA. The variable nature of the STR regions that are
analyzed for forensic testing intensifies the discrimination
between one DNA profile and another. The likelihood that any two
individuals (except identical twins) will have the same 13-loci DNA
profile can be as high as 1 in 1 billion or greater. The Federal
Bureau of Investigation (FBI) has chosen 13 specific STR loci to
serve as the standard for CODIS to ensure that all forensic
laboratories are uniform. If the CODIS index is to be used in the
investigative stages of unsolved cases, DNA profiles must be
generated by using STR technology and the specific 13 core STR loci
selected by the FBI. 1/31/12 Sources of DNA Evidence
Since only a few cells can be sufficient to obtain useful DNA
information to help your case, this list identifies some common
items of evidence that you may need to collect, the possible
location of the DNA on the evidence, and the biological source
containing the cells. Remember that just because you cannot see a
stain does not mean there are not enough cells for DNA typing.
1/31/12 Mitochondrial DNA Mitochondrial DNA (mtDNA) analysis allows
forensic laboratories to develop DNA profiles from evidence that
may not be suitable for RFLP or STR analysis. While RFLP and PCR
techniques analyze DNA extracted from the nucleus of a cell, mtDNA
technology analyzes DNA found in a different part of the cell, the
mitochondrion. Old remains and evidence lacking nucleated cells
--such as hair shafts, bones, and teeth--that are unamenable to STR
and RFLP testing may yield results if mtDNA analysis is performed.
It is important to note that all maternal relatives (for example, a
person's mother or maternal grandmother) have identical mtDNA. This
enables unidentified remains to be analyzed and compared to the
mtDNA profile of any maternal relative for the purpose of aiding
missing persons or unidentified remains investigations. 1/31/12
Steps of DNA Analysis Following collection of biological material
from a crime scene or paternity investigation, the DNA is first
extracted from its biological source material. After isolating the
DNA from its cells, specific regions are copied with a technique
known as the polymerase chain reaction, or PCR. PCR produces
millions of copies for each DNA segment of interest and thus
permits very minute amounts of DNA to be examined. Multiple STR
regions can be examined simultaneously to increase the
informativeness of the DNA test. The resulting PCR products are
then separated and detected in order to characterize the STR region
being examined. The separation methods used today include slab gel
and capillary electrophoresis (CE). 1/31/12 What is
Electrophoresis?
Electrophoresis has proved to be an invaluable tool in the analysis
of crime scene evidence, especially in the area of DNA
fingerprinting. Electrophoresis involves the separation of
chemicals along a solid medium in the presence of an applied
potential difference. In electrophoresis, chemicals such as blood
proteins, DNA or inorganic ions can be separated according to
differences in their mass and/or charge. The solid medium used in
electrophoresis is usually an agarose or polyacrylamide gel.
1/31/12