DNA Fingerprinting: Presented by Pranab Borah Department of Herbal Science & Technology ADP College, Nagaon

DNA Fingerprinting
Presented By
Pranab Borah
Department of Herbal Science &
Technology
ADP College, Nagaon
Introduction
DNA fingerprinting is a technique that
shows the genetic makeup of living things. It
is a method of finding the difference
between the satellite DNA regions in the
genome.”
Or
DNA profiling is a process used to
determine the nucleotide sequence at a
certain part of the DNA that is unique in
all human beings.
•The process of DNA

fingerprinting was invented by Sir
Alec Jeffrey at the University of
Leicester in 1985.
Principle of DNA Fingerprinting
The DNA of every human being on the planet is 99.9% same.
However, about 0.1% or 3 x 106base pairs (out of 3 x 109 bp) of
DNA is unique in every individual.
Human genome possesses numerous small non-coding but
inheritable sequences of bases which are repeated many times.
They do not code for proteins but make-up 95% of our genetic
DNA and therefore called the ―junk DNA.
They can be separated as satellite from
the bulk DNA during density gradient
centrifugation and hence called satellite
DNA.
In satellite DNA, repetition of bases is in
tandem. Depending upon length, base
composition and numbers of tandemly
repetitive units, satellite DNAs have
subcategories like microsatellites and
mini-satellites.
Satellite DNAs show polymorphism.
The term polymorphism is used when a
variant at a locus is present with a
frequency of more than 0.01 population.
A microsatellite is a repeating sequence of 2-6 base pairs in the genome. Since it
is a type of tandem repeats with short sequences of nucleotides, microsatellites
are also known as short tandem repeats (STRs). The repeats of single
nucleotides are called single nucleotide polymorphism (SNP). Furthermore,
microsatellites occur throughout the genome. In the human genome, the
dinucleotide repeats occur in every 30, 000 base pairs.
Fig: Locus specific Microsatelite DNA sequence

Moreover, microsatellites are a highly mutative region in the genome. Unique
microsatellite sequences occur within families. Therefore, we use the analysis
of microsatellites for paternity testing. Furthermore, the extension of
trinucleotide microsatellite repeats causes severe human disorders like Fragile
X syndrome and Huntington’s disease.
Minisatellite is a repeating sequence of 10-100 base pairs in the
genome. Here, the repeating unit is somewhat large and it is called
a DNA motif. Another name for minisatellite is variable number
tandem repeats (VNTRs). The number of VNTRs is highly
variable among individuals. The repetitive unit of a minisatellite is
GC rich.
Figure 2: Minisatellites
Due to the highly variable nature of minisatellites among
individuals, scientists use them for DNA fingerprinting. They also
use minisatellites as genetic markers during the linkage analysis.
Some minisatellite sequences are involved in the formation of ras
oncogene-associated cancer.
Variations occur due to mutations. These mutations in the non-coding sequences
have piled up with time and form the basis of DNA polymorphism (variation at
genetic level arises due to mutations).
The junk DNA regions are thus made-up of length polymorphisms, which show
variations in the physical length of the DNA molecule.
At specific loci on the chromosome the number of tandem repeats varies
between individuals. There will be a certain number of repeats for any specific
loci on the chromosome.
Depending on the size of the repeat, the repeat regions are classified into two
groups. Short tandem repeats (STRs) contain 2-5 base pair repeats
and variable number of tandem repeats (VNTRs) have repeats of 9-80 base
pairs.
Short tandem repeats (STRs)
Since a child receive 50% of the DNA from its father and the
other 50% from his mother, so the number VNTRs at a particular
area of the DNA of the child will be different may be due to
insertion, deletion or mutation in the base pairs.
As a result, every individual has a distinct composition of

VNTRs and this is the main principle of DNA fingerprinting.
As single change in nucleotide may make a few more cleavage

site of a given nucleotide or might abolish some existing cleavage
site.
Thus, if DNA of any individual is digested with a restriction

enzyme, fragments pattern (sizes) will be produced and will be
different in cleavage site position.
Methods of DNA Fingerprinting
A. Restriction fragment length polymorphism (RFLP)
The first step in this process is to isolate
the DNA from the sample material to be
tested. The sample size for RFLP test must
be large enough to get the proper result.
Once the required size of the sample is

available, the DNA is isolated from the
sample and is subjected to restriction
digestion using restriction enzymes.
The digested DNA sample is

then separated by agarose gel
electrophoresis, in which the DNA is
separated based on the size.
The next step is transfer of separated DNA from
gel slab onto the nitrocellulose membrane to
hybridize with a labeled probe that is specific for
one VNTR region (radio activity labeled
complimentary sequence for VNTR region
nucleotide sequence).
This technique of transferring and hybridizing

DNA onto nitrocellulose membrane is known as
southern blotting, a most widely used DNA
detection technique by molecular biologists.
After the hybridization with the radioactive probes,

the X- ray film is developed form the southern
blotting and only the areas where the radioactive
probe binds will show up on the film.
Now these bands when compared with the other

known samples, will give the final result of the
DNA fingerprinting.
Advantages
The RFLP is considered to be more accurate than the PCR,
mainly because the size of the sample used more, use of a
fresh DNA sample, and no amplification contamination.
Limitation
The RFLP, however, require longer time period to complete
the analysis and is costly.
B. Polymerase Chain Reaction (PCR) amplification of short
tandem repeats (STRs)
Thousands of copies of a particular variable region are amplified
by PCR which forms the basis of this detection.
STR with a known repeat sequence is amplified and separated

using gel-electrophoresis. The distance migrated by the STR is
examined.
For the amplification of STRs using PCR, a short synthetic DNA, called
primers are specially designed to attach to a highly conserved common
nonvariable region of DNA that flanks the variable region of the DNA.
By comparing the STR sequence size amplified by PCR with the other
known samples, will give the final result of the DNA fingerprinting.
Advantages
Small amount of specimen is sufficient for the test.
Takes a shorter time to complete.
Less costly.
Limitation
Less accurate than RFLP.
Possibility of amplification contamination.
Applications of DNA Fingerprinting
•DNA Fingerprinting is used by scientists to distinguish between
individuals of the same species using only samples of their DNA. It is
a primary method for identifying an individual.
•Forensic Science:
Biological materials used for
DNA profiling are: Blood, Hair,
Saliva, Semen, Body tissue cells
etc. DNA isolated from the
evidence sample can be
compared through VNTR
(Variable number of tandem
repeats) prototype. It is useful in
solving crimes like murder and
rape.
•Paternity and Maternity Determination:
A Person accedes to his or

her VNTRs from his or her
parents. Parent-child VNTR
prototype analysis has been
used to solve disputed cases.
This information can also be
used in inheritance cases,
immigration cases.
•Personal Identification:
It utilizes the concept of using DNA fingerprints as a sort
of genetic bar code to pinpoint individuals.
•Diagnosis of Inherited Disorders:
It is also useful in diagnosing inherited disorders in both
prenatal and newborn babies. These disorders may include
cystic fibrosis, hemophilia, Huntington’s disease, familial
Alzheimer’s, sickle cell anemia, thalassemia, and many others.
•Development of Cures for Inherited Disorders:
By studying the
DNA fingerprints of
relatives who have a
history of some
particular disorder,
DNA prototypes
associated with the
disease can be
ascertained.
•Detection of AIDS:
By comparing the band of HIV “RNA” (converted to DNA

using RTPCR) with the bands form by the man’s blood,
person suffering with AIDS can be identified.
•Breeding Program:
Breeders conventionally use the phenotype to
evaluate the genotype of a plant or an animal.As it
is difficult to make out homozygous or
heterozygous dominance from appearance, the
DNA fingerprinting allows a fastidious and precise
determination of genotype. It is basically useful in
breeding race horses and hunting dogs.
References
•https://nptel.ac.in/courses/102103017/pdf/lecture%2038.pdf
•http://www.indiastudychannel.com/resources/155090-The-
principles-techniques-application-DNA-fingerprinting.aspx
•https://www.biologyexams4u.com/2014/05/dna-fingerprinting-
procedure.html#.W4QNuPkzbIU
•https://web.wpi.edu/Pubs/E-project/Available/E-project-011306-
130417/unrestricted/IQP.pdf
•http://www.yourarticlelibrary.com/dna/dna-fingerprinting-
principles-and-techniques-of-dna-fingerprinting/12211.

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DNA Fingerprinting

•The process of DNA

Fig: Locus specific Microsatelite DNA sequence

As a result, every individual has a distinct composition of

As single change in nucleotide may make a few more cleavage

Thus, if DNA of any individual is digested with a restriction

Once the required size of the sample is

The digested DNA sample is

This technique of transferring and hybridizing

After the hybridization with the radioactive probes,

Now these bands when compared with the other

STR with a known repeat sequence is amplified and separated

A Person accedes to his or

By comparing the band of HIV “RNA” (converted to DNA

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