The document discusses DNA technology and polymerase chain reaction (PCR). It begins by explaining DNA sequencing techniques like Sanger sequencing. It then describes the development of PCR by Kary Mullis in 1985. PCR allows for rapid amplification of specific DNA sequences and has revolutionized fields like forensics, ancient DNA analysis, disease detection, and more. It works by cycling between high and low temperatures to denature and copy DNA using primers and DNA polymerase. The document outlines the components and steps of PCR and factors that influence it.

1. 1
Chapter 5 : DNA TECHNOLOGY

2. BIO 300
BIOLOGICAL TECHNIQUES AND SKILLS
SARINI BINTI AHMAD WAKID
FACULTY OF APPLIED SCIENCE
Chapter 5 : DNA TECHNOLOGY
2

3. CHAPTER 5
TECHNIQUES in DNA TECHNOLOGY
Chapter 5 : DNA TECHNOLOGY
3

4. DNA SEQUENCING

The ultimate level of analysis is determination
of the actual sequence of bases in a DNA
molecule. The development of sequencing
has paralleled the advancement of molecular
biology. The genomics was born out of the
ability to determine the sequence of an entire
genome relatively rapid.
Chapter 5 : DNA TECHNOLOGY
4

5. Idea

To generate a set of nested fragments that
each begin with the same sequence and end
in a specific base. When this set of fragments
is separated by high resolution gel
electrophoresis, the results is a “ladder” of
fragments in which each band consist of
fragments that end in a specific base. By
starting with the shortest fragments, one can
read the sequence by moving up the ladder.
Chapter 5 : DNA TECHNOLOGY
5

6. ENZYMATIC SEQUENCING


Developed by Fredrick Sanger, who also was
the first to determine the complete sequence
of a protein.
This method uses dideoxynucleotides as chain
terminators in DNA synthesis reactions. A
dideoxynucleotides has H in place of OH at
both the 2’ position and at the 3’ position.
Chapter 5 : DNA TECHNOLOGY
6

7. AUTOMATED SEQUENCING

The technique of enzymatic sequencing is
very powerful, but it is also labor intensive and
takes a significant amount of time. It requires
a series of enzymatic manipulations, time for
electrophoresis, then time to expose the gel to
film.
Chapter 5 : DNA TECHNOLOGY
7

8. PCR
Polymerase Chain Reaction
Chapter 5 : DNA TECHNOLOGY
8

9. Review: The structure of DNA
Helix
Complementary Base Pairing 9
Chapter 5 : DNA TECHNOLOGY

10. Review: The structure of DNA
Unzipping
Antiparallel Strands
Chapter 5 : DNA TECHNOLOGY
10

11. Review: Genome Sizes








Pine: 68 billion bp
Corn: 5.0 billion bp
Soybean: 1.1 billion bp
Human: 3.4 billion bp
Housefly: 900 million bp
Rice: 400 million bp
E. coli: 4.6 million bp
HIV: 9.7 thousand bp
11
Chapter 5 : DNA TECHNOLOGY http://www.cbs.dtu.dk/databases/DOGS/abbr_table.txt

12. Just How Big Is 3.4 Billion?




Human genome is 3.4 B bp
If the bases were written in standard
10-point type, on a tape measure...
...The tape would stretch for 5,366
MILES!
Identifying a 500bp sequence in a
genome would be like finding a
section of this tape measure only 4
feet long!
Chapter 5 : DNA TECHNOLOGY
12

13. The Problem...


How do we identify and detect a specific
sequence in a genome?
TWO BIG ISSUES:

There are a LOT of other sequences in a genome
Y
ICIT that we’re not interested in detecting.
ECIF
SP
 The amount of DNA in samples we’re interested in is
ION
TVERY small.
A
FIC
PLI
AM
PCR solves BOTH of these issues!!!
Chapter 5 : DNA TECHNOLOGY
13

14. PCR
- a method for amplifying (copying) small
amount of DNA in nearly any amount
required, starting with a small initial quantity.
- an in vitro or cell-free method for
synthesizing DNA.
- it was invented in 1985 by Kary Mullis
(received the Nobel Prize for chemistry in
1993).
Chapter 5 : DNA TECHNOLOGY
14

15. PCR History
In what has been called by some the greatest achievement of
modern molecular biology, Kary B. Mullis developed the
polymerase chain reaction (PCR) in 1983. PCR allows the
rapid synthesis of designated fragments of DNA. Using the
technique, over one billion copies can be synthesized in a
matter of hours.
PCR is valuable to scientists by assisting gene mapping, the
study of gene functions, cell identification, and to forensic
scientists in criminal identification. Cetus Corporation, Mullis'
employer at the time of his discovery, was the first to
commercialize the PCR process. In 1991, Cetus sold the PCR
patent to Hoffman-La Roche for a price of $300 million. It is
currently an indispensable tool for molecular biologists and
the development of genetic engineering.
Chapter 5 : DNA TECHNOLOGY
15

16. Idea


Simple
Two primers are used that complimentary to the
opposite strands of a DNA sequence, oriented
toward each other. When DNA polymerase acts
on these primers and the sequence of interest,
the primers produce complementary strands,
each containing the other primer. If this
procedure is done cyclically, the result is a large
quantity of a sequence corresponding to the
DNA that lies between the two primers.
Chapter 5 : DNA TECHNOLOGY
16

17. Chapter 5 : DNA TECHNOLOGY
17

18. PCR Machine / Thermocycler
Chapter 5 : DNA TECHNOLOGY
18

19. PCR

Components of PCR
 Template DNA
 primers
 dNTPs (dATP, dTTP, dCTP & dGTP)
 Taq DNA polymerase
 MgCl
2

PCR buffer, pH 8
Chapter 5 : DNA TECHNOLOGY
19

20. PCR

Three major phases in PCR:
 Denaturing –high temperature (94ºC)
 Annealing of primers –low temperature(55ºC)
 Extension – synthesis – intermediate
temperature (72ºC)

The total time to perform a standard PCR is
approximately 4 hours.
Chapter 5 : DNA TECHNOLOGY
20

21. Chapter 5 : DNA TECHNOLOGY
21

22. Chapter 5 : DNA TECHNOLOGY
22

23. Factors influencing PCR





Quality of template DNA
Concentration of template DNA
Primers
Concentration of MgCl2
Annealing temperature
Chapter 5 : DNA TECHNOLOGY
23

24. Quality of template DNA
- should be free of proteases that could
degrade the DNA polymerase.
- template DNA with high levels of
proteins or salts should be diluted or
cleaned up to reduce inhibition of DNA
polymerase activity.
Chapter 5 : DNA TECHNOLOGY
24

25. Concentration of template DNA
- highly concentrated template DNA may
yield nonspecific product or inhibit the
reaction.
- it is rare that template DNA concentration
is too low.
Chapter 5 : DNA TECHNOLOGY
25

26. Primers
- select primers with a random base
distribution and GC content similar to
template DNA being amplified.
- avoid sequences with secondary
structure, especially at the 3’ end.
- check primers for complementary and
avoid primers with 3’ overlaps to reduce
primer-dimer artifacts.
- design so the base at the 3’ end of the
primer is a G or C to enhance specificity.
Chapter 5 : DNA TECHNOLOGY
26

27. Concentration of MgCl2
- MgCl2 concentration is very important.
- excess Mg2+ promotes production of
nonspecific product and primer-dimer
artifacts.
- insufficient Mg2+ reduces yield.
Chapter 5 : DNA TECHNOLOGY
27

28. Annealing temperature
- annealing temperature depends on length
and GC content of primers (55ºC good for
primers 20 nucleotides long; 50%).
- Higher annealing temperatures may be
needed to increase primer specificity.
Chapter 5 : DNA TECHNOLOGY
28

29. Some Uses of PCR






Forensic DNA detection
Identifying transgenic plants
Detection and quantification of
viral infection
Cloning
Detection of ancient DNA
Gene expression analysis
Chapter 5 : DNA TECHNOLOGY
29

30. Uses of PCR: Ancient DNA
Archaeologists have happily seized on PCR
and are applying it in an amazing variety of
ways. It is helping, for example, to launch a
new chapter in the colorful and controversial
story of the 2000-year-old Dead Sea Scrolls,
which are written on parchment made out of
skins from goats and gazelles. Researchers are
analyzing the parchment fragments to try to
identify individual animals they came from.
The hope is that the genetic information will
guide them in piecing together the 10,000
particles of scrolls that remain.
Chapter 5 : DNA TECHNOLOGY
http://www.faseb.org/opar/bloodsupply/pcr.html
30

31. Uses of PCR: Disease Detection
PCR can also be more accurate than standard tests.
It is making a difference, for example, in a painful,
serious, and often stubborn misfortune of
childhood, the middle ear infection known as otitis
media. The technique has detected bacterial DNA
in children's middle ear fluid, signaling an active
infection even when culture methods failed to
detect it. Lyme disease, the painful joint
inflammation caused by bacteria transmitted
through tick bites, is usually diagnosed on the basis
of symptom patterns. But PCR can zero in on the
disease organism's DNA contained in joint fluid,
permitting speedy treatment that can prevent
serious complications.
Chapter 5 : DNA TECHNOLOGY
http://www.faseb.org/opar/bloodsupply/pcr.html
31

32. Uses of PCR: Endangered Species
Researchers have used the technique to aid in
reducing illegal trade in endangered species, and
products made from them. Because PCR is a
relatively low-cost and portable technology, and
likely to become more so, it is adaptable for field
studies of all kinds in the developing countries. It is
also a tool for monitoring the release of genetically
engineered organisms into the environment.
Chapter 5 : DNA TECHNOLOGY
http://www.faseb.org/opar/bloodsupply/pcr.html
32

33. Uses of PCR: Forensic DNA
The technique's unparallelled ability to identify and
copy the tiniest amounts of even old and damaged
DNA has proved exceptionally valuable in the law,
especially the criminal law. PCR is an
indispensable adjunct to forensic DNA typingcommonly called DNA fingerprinting.
Chapter 5 : DNA TECHNOLOGY
http://www.faseb.org/opar/bloodsupply/pcr.html
33

34. Uses of PCR: Proving Innocence
DNA typing is only one of many pieces of evidence
that can lead to a conviction, but it has proved
invaluable in demonstrating innocence. Dozens of
such cases have involved people who have spent
years in jail for crimes they did not commit. Many
people have been freed because of the power of
PCR. Even when evidence such as semen and
blood stains is years old, PCR can make unlimited
copies of the tiny amounts of DNA remaining in
the stains for typing.
Chapter 5 : DNA TECHNOLOGY
http://www.faseb.org/opar/bloodsupply/pcr.html
34

35. Uses of PCR: Disease Detection
The method is especially useful for searching out
disease organisms that are difficult or impossible to
culture, such as many kinds of bacteria, fungi, and
viruses, because it can generate analyzable
quantities of the organism's genetic material for
identification. It can, for example, detect the AIDS
virus sooner during the first few weeks after
infection than the standard ELISA test. PCR looks
directly for the virus's unique DNA, instead of the
method employed by the standard test, which looks
for indirect evidence that the virus is present by
searching for antibodies the body has made against
it.
Chapter 5 : DNA TECHNOLOGY
http://www.faseb.org/opar/bloodsupply/pcr.html
35

36. Uses of PCR: Ancient DNA
Archaeologists are finding that PCR can
illuminate human cultural practices as well as
human biology. Analyzing pigments from
4000-year-old rock paintings in Texas, they
found one of the components to be DNA,
probably from bison. The animals did not live
near the Pecos River at that time, so the paleoartists must have gone to some effort to obtain
such an unusual ingredient for their paint.
Taking so much trouble suggests that the
paintings were not simply decorations, but had
religious or magical significance.
Chapter 5 : DNA TECHNOLOGY
http://www.faseb.org/opar/bloodsupply/pcr.html
36

37. Uses of PCR: Disease Detection
PCR can even diagnose the diseases of the past.
Former vice president and presidential candidate
Hubert H. Humphrey underwent tests for bladder
cancer in 1967. Although the tests were negative,
he died of the disease in 1978. In 1994, researchers
compared a 1976 tissue sample from his cancerridden bladder with his 1967 urine sample. With
the help of PCR amplification of the small amount
of DNA in the 27-year-old urine, they found
identical mutations in the p53 gene, well-known for
suppressing tumors, in both samples. "Humphrey's
examination in 1967 may have revealed the
cancerous growth if the techniques of molecular
biology were as well understood then as they have
become," the researchers said.
Chapter 5 : DNA TECHNOLOGY
http://www.faseb.org/opar/bloodsupply/pcr.html
37

38. Uses of PCR: Gene Expression Analysis
The Human Genome Project has identified tens of
thousands of genes in the human genome. A key
questions is: what do these genes do? Part of the
answer comes from determining when the genes are
turned on and off, and what affects the level of
gene expression. Quantitative PCR is a key
component of determining the levels of gene
expression, and is a critical tool in cancer research,
disease studies, and developmental biology.
DNA
RNA
GENEX Analysis
Chapter 5 : DNA TECHNOLOGY
Enzymes
Biology
38

39. THANK YOU
Chapter 5 : DNA TECHNOLOGY
39