Of the three billion nucleotides in human DNA, more than 99%
are identical among individuals. The remaining 1%, however, adds up to a
significant amount of code variations between individuals, making each person's
DNA profile as unique as a fingerprint. Due to the large number of possible
variations, no two people (with the exception of identical twins) have the same
DNA sequence.
For every 1,000 nucleotides inherited, there is one site of
variation, or polymorphism. DNA polymorphisms change the length of the DNA
fragments produced by the digestion of restriction enzymes, so the exact number
and size of fragments produced by a specific restriction enzyme digestion
varies from person to person. The resulting fragments, called Restriction Fragment
Length Polymorphisms (RFLPs), can be separated, and their size determined, by
electrophoresis.
Most of the DNA in a chromosome is not used for the genetic
code; it is uncertain what, if any, use this DNA may have. Because these
regions are not essential to an organism's development, it is more likely that
changes will be found in these nonessential regions. The regions that contain
nucleotide sequences that repeat from 20 to 100 times (e.g., GTCAGTCAGTCAGTCA)
are the strands cut by restriction enzymes to create RFLPs.
The difference in the fragments can be quantified to create
a "DNA fingerprint". Distinct RFLP patterns can be used to trace the
inheritance of chromosomal regions with genetic disorders or to identify the
origin of a blood sample in a criminal investigation. Scientists have
identified more than 3,000 RFLPs in the human genetic code, many of which are
highly variable among individuals. It is this large number of variable yet
identifiable factors that allows scientists to identify individuals by the
number and size of their various RFLPs.
This technique is being used more and more frequently in
legal matters. Using DNA fingerprinting, the identity of a person who has
committed a violent crime can be determined from minute quantities of DNA left at
the scene of the crime in the form of blood, semen, hair, or saliva. The DNA
fingerprint matched to a suspect can be accurate to within one in 10 billion
people, which is almost twice the total population in the world. Certain
limitations in the technique prevent two samples from being identified as a
"perfect match", yet it is possible to measure the statistical
probability of two samples coming from the same individual based on the number
of known RFLPs that exist in a given population.
DNA fingerprinting has many other applications, since half
of a person's genome comes from each parent, DNA fingerprinting can be used to
determine familial relationships. It has a much higher certainty than a blood
test when used to determine fatherhood in a paternity suit. DNA fingerprinting
can be used to track hereditary diseases passed down family lines, as well as
to find the closest possible matches for organ transplants. It can also be used
to ascertain the level of inbreeding of endangered animals, aiding in the development
of breeding programs to increase animals' genetic health and diversity.
Students use micropipettes to load their samples into agar rose gels |
The gels are placed in the electrophoresis apparatus and submerged in a buffer. Once this is done the micropipette is used to load the wells in the gel |