Forensics:
The
Following Term Paper was prepared for a Forensics
class I took at Durham Technical
Community College. Circa 1992. I received a Grade of
4.0 for same.
THE FUTURE OF
DNA FINGERPRINTING
by
Jesse R. Duke
Introduction
The image that most
of us have of the American courtroom is that of an arena of truth. When into
this arena walks science, we often lean a little forward in our seats. We expect
our hero to pull from his bag the proper weapon to shred the murky darkness and
allow the truth to shine.
Recently, science
has added a powerful new weapon to his bag of arms. This new gadget is known
metaphorically as DNA fingerprinting (D f/p). D f/p has already been used in
thousands of criminal cases since 1987.(1 Until recently, the use and impact of
D f/p has met with little resistance. However, recent studies and friction
within the scientific community have many sending up red flags. Also, the
catcalls of criticism, for a multitude of reasons, signals a crisis in the
works. Further, using the Frye "general acceptance" standard, recent
use of D f/p as evidence has met with mixed results.(2 This suggest that Frye
alone may not be adequate to deal with modern forensic issues.
In a sense, the
current debate over D f/p is a microcosm of the present relationship of science
to law. The resolution of this debate, and the correctness of current Frye
standard interpretations will lay the cornerstone for the future of science in
the courtroom.
At Issue
Ever since Watson
and Crick first unraveled the mystery of the structure and function of the
chemical we know as DNA, most of us have been satisfied with the simple
knowledge that it is the blue-print of life, and self-replicates to allow living
things to grow and reproduce. However, since that discovery, the place of DNA in
science has rapidly gone from the pure science of knowing to aggressive
application. In fact, "tool DNA" has been used for such diverse ends
as fooling bacteria into making miracle drugs, to confirming a petrified leaf 18
million years old was indeed a magnolia
There are currently
two techniques used to perform D f/p analysis. The first is restriction fragment
length polymorphism or (RFLP). The use of RFLP rests on the knowledge that 99%
of the 3.3 billion base pairs in human DNA are the same among all humans. Most
of the remaining 33 million base pairs, that make-up the variant 1%, are what we
normally think of as our gene traits (color, shape, and size etc.).(4
Unfortunately, extraction of these "genes" and their analysis is
beyond our current ability. After you account for "genes", a small
fraction of this 1% is regions of non-sense along the DNA strand. Known as core
sequences, these areas repeat a pattern of base pair combinations over and over
again like a "stuck phonograph". The number of repeats is highly
variable for the total population. Thus, if you extract five or more of these
segments from an individual's DNA, the chance of another person (other than an
identical twin) having the same combination becomes astronomical. Cellmark
Diagnostics, (a commercial company that provides D f/p services) claims the
chance to be 1 in 30 billion.(5 The RFLP technique entails placing a drop of DNA
core sequence extract in a gel and applying electrical voltage across it. The
current pushes the segments Through the gel. In a given amount of time, small
fragments (less repeats) are pushed farther than larger fragments. After
development, what you have is a strip of film with dark bands where different
sized fragments came to rest. In theory each individual's pattern of bands and
their spacing is unique. Thus, the fingerprint of that person's DNA.(6 RFLP was
adopted by the FBI in 1989 and is performed by two commercial companies in the
U.S..(7
The other, newer, D
f/p technique is polymerase chain reaction
DNA can be thought
of as a "twisted zipper" and each tooth, on one side, has a
counterpart on the other side. The "trick" of DNA is that when it
unzips and separates during mitosis, it is able to use "spare parts"
floating in the medium to build the counter tooth. Thus, the whole missing side
is rebuilt. This occurs for both halves of the zipper so we end up with two
complete zippers. This process of unzipping and rebuilding in duplication is
closely guarded in living creatures so that duplication only occurs as a cell is
ready to divide and needs two sets of DNA to share. The power of PCR is that, in
a test tube, we add plenty of spare parts, simulate conditions of mitosis,
remove the regulating safe guard factors, and if into this environment we place
a single strand of DNA ... we can have a billion fold replication in one
afternoon.(9 This amplification of DNA is often very important to forensic
investigation because biological crime scene evidence is often scant and in poor
condition when it reaches the lab. To conduct RFLP analysis requires upwards of
500 nanograms (.0000005 grams) of DNA.(10 This is a fantastically small amount
to try to contemplate. 1 gram equals about one fifth the weight of a nickel.
This alone is a small weight by our everyday standards. Now picture a small
bedroom 10ft. by 10ft. by 8 feet high filled completely with water. This
represents 800 cubic feet of water. Now, one gram is to 500 nanograms as 800
cubic feet of water is to four tenths of an ounce. With PCR technology we can
often get results with only 1 nanogram or one five hundredth of this amount.
Argument
Almost all
concerned parties agree that D f/p, when properly applied, is a most valuable
technique of individual identification. Victor A. McKusick chaired a two year
NRC study of D f/p and recently commented that D f/p was a "valid means of
convicting the guilty and freeing the innocent".(11 In addition, The much
criticized position of Lifecodes(l of 2 major commercial interest in D f/p) that
there is only a 1 in 10 billion chance of finding two identical sets of D f/p,
has met with recent support from a Yale University study.(12
Yet, the future of
D f/p is in no way certain and the disjunction of science to law, that D f/p has
come to symbolize, has become a mass media circus. At the center of this cyclone
lie the origins of D f/p. The technology of D f/p was developed in a vacuum.
Scant little objective scientific study of D f/p has been published and almost
no articles on the technique have appeared. This lack of information is due
mainly to the motivations of the three principles that provide D f/p services (Cellmark
Diagnostics, Lifecodes, and the FBI). Of these three, the first two are
commercial outfits that have patented their own RFLP methods and regard raw data
and data base information as trade secrets.(13 As for the FBI, it too is
reluctant to publish or disclose raw data citing it's "privilege against
self-criticism". Further, the FBI stands nearly alone in opposing
independent proficiency testing.(14 This unwillingness to publish and submit to
peer review is a breach of science methodology that extends back to Robert Hooke
and the 1600's.
In addition,
current standards of evidence allows novel forensic methods to be used without
scientific verification.(15 The Frye standard uses an adversarial system that
usually requires experts to take a side in a criminal case, and usually involves
payment of the expert to maintain his side's position regardless. The objective
is to help his side to victory.(16 The Frye standard stems from a 1923 ruling
that
Many have called
for reform of both evidence standards, and D f/p technology. The loudest cries
are for universal standards, lab certification, an end to trade secrets, more
resources for both DNA insult and data base research, and better education and
training of lab personnel.(18 Add to this list reexamination of the Frye
standard and the development of PCR technology in the public domain.
Summation
The current status
of DNA fingerprinting reminds me of a line from The Tale of Two Cities ...
"it was the best of times, it was the worst of times ... ". When
science drew from his bag of arms DNA fingerprinting, it laid open the
relationship of science to law and the cancer of discourse has presented itself
in fullness. How we proceed to rid ourselves of it's ugliness will make all the
difference.
BIBLIOGRAPHY
Cherfas, Jeremy.
"Ancient DNA: still busy after death" Science, 9-20-91, pp. 1354-1356
Notes: 3
Lampton,
Christopher. DNA Fingerprinting Impact Books, New York 1991 Notes: 12, 16
Neufeld, Peter J.
Colman, Neville. "When Science Takes the Witness Stand": Scientific
American, 5-90 pp. 46-53 Notes: 1, 2, 4, 5, 13, 14, 15, 17
Reynolds, Rebecca.
Sensabaugh, George. Edwards, Blake "Analysis of Genetic Markers in Forensic
DNA Samples Using the Polymerase Chain Reaction" Analytical Chemistry,
1-1-91, pp. 2-15 Notes: 6, 7, 8, 9, 10, 18
,"Report Shows
Genetic Fingerprinting To Be Reliable In Court": The Herald Sun, 4-14-92 p.
A7 A.P. Wire Service Report, Washington, D.C. Notes: 11