NAME: DR WAJID MAJEED KHANDAY
ROLL NO.: M.Sc , M.Phill , Ph.D , NET(3 TIMES)
ACADEMIC LECTURER
GDC BOYS SOPORE
SUPERVI
DNA REPLICATION
MECHANISM
Vocabulary
 DNA replication
 DNA helicase
 DNA polymerase
DNA Synthesis
 These subunits
are comprised of a
phosphate group,
a ribose sugar,
and one of 4
nitrogenous bases.
You should also recall that in DNA
A bonds with T and
G bonds with C.
In the first section of this unit
you learned what DNA is.
The second section you
learned what happens in
G1: the process of gene
expression; transcription
and translation.
You should also know that
DNA is a large molecule
built of billions of subunits.
Cells don’t last forever
 Every cell in an organism has
a particular life span… they
don’t last forever.
 Cells are born, grow and do
their jobs, divide, and finally
create two new daughter
cells.
 The life span is cyclical &
with every new generation
the cells that are formed
carry out the functions of the
parent cell because they are
given each an exact copy of
the parent cell’s DNA.
 The cyclical life span of a cell
is called the CELL CYCLE.
DNA Synthesis = DNA
DUPLICATION
 Every time a cell goes
through a cycle it must
DUPLICATE ITS DNA SO THAT
WHEN IT MAKES NEW BABY
CELLS THEY BOTH HAVE THE
EXACT SAME DNA.
 Happens in ‘S’ phase
 In this section we are going
explore the process of DNA
synthesis, called DNA
replication.
 This process is extremely
precise and an incredibly
important.
The Cell Cycle: The part
we’re isolating.
From single-copy of
each chromosome
•To double-copy
What’s different about these
cells?
REPLICATION
•These are identical strands of DNA
•There are two copies formed in replication (S phase) because each are destined for the
2 identical new cells that are formed, called daughter cells, after the cell divides.
•Identical DNA must be synthesized in order to achieve this.
•The process of DNA synthesis is REPLICATION.
1st
Gap Phase DNA Synthesis Phase
HOW IS DNA REPLICATED?
 There are three ways that
DNA can be duplicated…
1. Conservative: original is
left completely original.
2. Semi-conservative: new
DNA is half original and
half new.
3. Dispersive: DNA is
randomly duplicated.
The Meselson-Stahl experiment:
•Showed that DNA is replicated semi-conservatively.
•This means, the end product is one strand of original DNA and one strand of newly-
formed DNA.
SO. What is the point of
replication? The point of replication is to
produce exact copies of the
original cell’s DNA.
DNA Replication: THE STEPS
 The process of replicating DNA is broken down into three
major steps.
 Your job is to know these 3 steps and be able to
summarize what happens in each.
 The three steps are:
1. Unwinding and Separating DNA Strands
2. Adding complimentary bases
a. Leading Strand:
b. Lagging Strand: RNA Primers attach
3. Formation of Two Identical DNA molecules
DNA Replication
• Step 1:
• DNA helicases unwinds & separates
the original DNA double helix.
• These proteins wedge
themselves between the two
strands of the double helix
and break the hydrogen bonds
between the base pairs.
• Forms Replication Forks
• As the double helix unwinds,
the two complementary
strands of DNA separate from
each other and form a Y
shape.
DNA Replication
Step 2: New DNA is formed
from DNA template.
RNA Primers attach to specific
regions. New nucleotides are
added to the primer by the
enzyme DNA Polymerase
according to the base-pairing
rules.
 DNA polymerases create the
formation of the new
complimentary DNA molecule
by moving along each strand in
a 5’ to 3’ direction.
 They add nucleotides to a new
daughter compliment in a 5’ to
3’ direction only!
Primer
Primer
DNA Replication
You know that DNA is anti-
parallel because of the bi-
directionality of DNA.
One side goes 3’ to 5’.
The other 5’ to 3’.
New nucleotides can only be
added to the 3’ end of the
existing chain.
One side (the top pictured
here) is the LEADING
STRAND. It has its new
strand continuously
synthesized as helicase
unwinds more DNA.
The other side, the LAGGING
STRAND (on bottom) is
discontinuous replication
because it the bases are
oriented in the wrong
direction.
5’
5’
DNA polymerase can only
add nucleotides in a 5’ to
3’ direction.
DNA Replication
• Step 2: Leading strand
• Primers attach.
• Primers are pre-made
sequences of RNA. These
bind to complementary
regions of the original
DNA once it’s separated.
• Primers serve as tethers
from which replication
can proceed from the 3’
end.
• DNA Polymerase attaches
free nucleotides to the 3’
end of the primer.
• On the leading strand
there is one primer and
the newly forming DNA
follows the replication
fork as the new DNA is
synthesized.
Primer
DNA Replication
• Step 2: Lagging strand
• The lagging strand creates a particular problem for replication.
• Since DNA can only be synthesized from the 3’ end of the
primers, the lagging strand would be left incomplete.
• Multiple primers attach to the lagging strand as the replication
fork moves forward, creating what are known as “Okasaki
Fragments”
• These are usually 1-2000 nucleotides long.
DNA Replication
• Step 2: Lagging strand
• If you notice, the Okazaki Fragments are not joined
together.
• A special enzyme, call ligase, joins Okasaki
fragments together to form one continuous
molecule.
Ligase
Ligase
DNA Replication
Step 3:
 The process completes
when all the original bases
have been paired with a
new complementary
nucleotide.
 Each double-stranded DNA
helix is made of one new
strand of DNA and one
original strand of DNA.
Summary
 What is DNA replication?
 Why does it happen?
 Know the steps…
 On your handout, label:
Where is…
a. Leading Strand
b. Lagging Strand
c. Okazaki fragments
d. DNA Ligase
e. Replication Fork
f. DNA Polymerase
g. All 3’ & 5’ ends.
h. Where helicase should be
Replication Proteins
• Replication involves many proteins that form a machine-like
complex of moving parts.
• These proteins play a key role in making sure that the process is
flawless.
• DNA Helicase unwinds DNA carefully so it doesn’t get torn.
• Ligase is a protein that ensures proper bonding of growing
Okasaki fragments.
• DNA polymerase adds complimentary nucleotides.
• DNA polymerase also has a “proofreading” function.
• During DNA replication, errors sometime occur and the wrong
nucleotide is added to the new strand.
• This could lead to cancer if not detected.
• If a mismatch occurs, the DNA polymerase has the amazing
ability of being able to backtrack, remove the incorrect
nucleotide, and replace it with the correct one.
• This decreases the chances of the wrong DNA being made,
lessening our chances of CANCER!
Replication v Transcription
 Based upon what you’ve learned about transcription and
replication, shoulder partner share and come up with a
similarity between transcription and replication.
 WHAT IS THE SIMILARITY BETWEEN TRANSCRIPTION &
REPLICATION?
 Similarities: transcription and replication both use DNA as
the template for copying.
 SHOULDER PARTNER AND ANSWER: WHAT IS A CRITICAL
DIFFERENCE BETWEEN REPLICATION AND TRANSCRIPTION?
 Differences:
 In transcription, a new molecule of mRNA is made from
the template DNA by using the enzyme RNA polymerase.
 In DNA replication, a new molecule of DNA is made from
the template DNA by using the enzyme DNA polymerase.
Objectives
Primary
 Compare the process of DNA replication in
prokaryotes and in eukaryotes.
 Identify the features of prokaryotic and Eukaryotic
replication on an illustration.
Secondary
 Compare the number of nucleotides replicated in
eukaryotes and prokaryotes by calculating the
rates of replication.
Prokaryotic and Eukaryotic
Replication
 All cells have chromosomes, but eukaryotes and
prokaryotes replicate their chromosomes
differently.
 The main difference between prokaryote and
eukaryote replication is how many start sites
each have.
 Eukaryotes have hundreds of start sites.
 The start sites then regulate how replication
proceeds in each organism type.
Prokaryotic DNA Replication
 Recall the structure of prokaryotic DNA.
 Does anyone remember what the
structure is?
 Prokaryotic cells usually have a single
chromosome which is a closed loop
attached to the inner cell membrane.
 Replication in prokaryotes begins at a
single site along the loop. This site is
called the origin of replication.
Prokaryotic Replication
 Two replication forks begin at the
origin of replication.
 Replication occurs in opposite
directions until the forks meet on the
opposite side of the loop.
 The result is two identical loops of
DNA.
Eukaryotic Replication
 Eukaryotic cells often have several chromosomes which
are linear and contain both DNA and protein.
 How many chromosomes do humans have?
 What are the proteins called that hold DNA in nucleosomes?
 Eukaryotic replication starts at many sites along the
chromosome.
 This process allows eukaryotic cells to replicate their
DNA faster than prokaryotes.
Eukaryotic Replication
 Two distinct replication forks form at each start site and
replication occurs in opposite directions.
 This process forms replication “bubbles” along the DNA
molecule.
 Replication bubbles continue to get larger as more of the
DNA is copied.
 The replication bubbles keep growing until they join
together with other bubbles and complete replication.
 Replication is complete when two identical complementary
strands of DNA is formed.
Eukaryotic Replication
Original DNA
Replication bubbles
Replication bubbles joining
Original + new DNA
New + original DNA
Prokaryotic and Eukaryotic
Replication
 Even the smallest eukaryotic chromosomes are often 10
times the size of a prokaryotic chromosome. Eukaryotic
chromosomes are so long that it would take 33 days to
replicate a typical human chromosome if there were only
one origin of replication.
 As such, evolution has allowed Human chromosomes to
replicate in about 100 sections that are 100,000 nucleotides
long, each section with its own starting point.
Remember, the 46 human chromosomes laid end to end would measure
≈ 2m. Bacterial chromosomes measure ≈ 0.25cm!
 Because eukaryotic cells have multiple replication forks
working at the same time, an entire human chromosome can
be replicated much faster, in only about 8 hours.
 Bacteria replicate their small genomes in minutes…
In-class Activity: Replication Comparison
A
B
C
D
E
F
G
What is the difference between prokaryotic replication & eukaryotic
replication?
•Why are they different?
Summary
 In DNA replication, the DNA molecule unwinds, and the
two sides split. Then, new bases are added to each side
until two identical sequences result.
 The replication of DNA involves many proteins that
form a machinelike complex of moving parts.
 In prokaryotic cells, replication starts at a single site. In
eukaryotic cells, replication starts at many sites along
the chromosome.
Replication concept Check
1. What is the purpose, outcome of DNA replication AND what stage does it happen in
the cell cycle?
To create an identical, duplicate copy of original DNA,
“S”
2. What enzyme is responsible for “unzipping” the DNA double helix?
DNA Helicase
3. What enzyme is responsible for adding nucleotides to the “unzipped” DNA?
DNA polymerase
4. What is the enzyme responsible for bonding the fragments on the lagging strand?
Ligase
5. (Review) What is the enzyme responsible for creating mRNA copies of genes in DNA?
RNA polymerase
6. What is the enzyme responsible for “proofreading” the newly made DNA, checking for
mismatched base-pairs?
DNA polymerase
Summary… The More Complex
Version
DNA Replication in eukaryotes and prokaryotes

DNA Replication in eukaryotes and prokaryotes

  • 1.
    NAME: DR WAJIDMAJEED KHANDAY ROLL NO.: M.Sc , M.Phill , Ph.D , NET(3 TIMES) ACADEMIC LECTURER GDC BOYS SOPORE SUPERVI DNA REPLICATION MECHANISM
  • 2.
    Vocabulary  DNA replication DNA helicase  DNA polymerase
  • 3.
    DNA Synthesis  Thesesubunits are comprised of a phosphate group, a ribose sugar, and one of 4 nitrogenous bases. You should also recall that in DNA A bonds with T and G bonds with C. In the first section of this unit you learned what DNA is. The second section you learned what happens in G1: the process of gene expression; transcription and translation. You should also know that DNA is a large molecule built of billions of subunits.
  • 4.
    Cells don’t lastforever  Every cell in an organism has a particular life span… they don’t last forever.  Cells are born, grow and do their jobs, divide, and finally create two new daughter cells.  The life span is cyclical & with every new generation the cells that are formed carry out the functions of the parent cell because they are given each an exact copy of the parent cell’s DNA.  The cyclical life span of a cell is called the CELL CYCLE.
  • 5.
    DNA Synthesis =DNA DUPLICATION  Every time a cell goes through a cycle it must DUPLICATE ITS DNA SO THAT WHEN IT MAKES NEW BABY CELLS THEY BOTH HAVE THE EXACT SAME DNA.  Happens in ‘S’ phase  In this section we are going explore the process of DNA synthesis, called DNA replication.  This process is extremely precise and an incredibly important.
  • 6.
    The Cell Cycle:The part we’re isolating. From single-copy of each chromosome •To double-copy
  • 7.
    What’s different aboutthese cells? REPLICATION •These are identical strands of DNA •There are two copies formed in replication (S phase) because each are destined for the 2 identical new cells that are formed, called daughter cells, after the cell divides. •Identical DNA must be synthesized in order to achieve this. •The process of DNA synthesis is REPLICATION. 1st Gap Phase DNA Synthesis Phase
  • 8.
    HOW IS DNAREPLICATED?  There are three ways that DNA can be duplicated… 1. Conservative: original is left completely original. 2. Semi-conservative: new DNA is half original and half new. 3. Dispersive: DNA is randomly duplicated. The Meselson-Stahl experiment: •Showed that DNA is replicated semi-conservatively. •This means, the end product is one strand of original DNA and one strand of newly- formed DNA.
  • 9.
    SO. What isthe point of replication? The point of replication is to produce exact copies of the original cell’s DNA.
  • 10.
    DNA Replication: THESTEPS  The process of replicating DNA is broken down into three major steps.  Your job is to know these 3 steps and be able to summarize what happens in each.  The three steps are: 1. Unwinding and Separating DNA Strands 2. Adding complimentary bases a. Leading Strand: b. Lagging Strand: RNA Primers attach 3. Formation of Two Identical DNA molecules
  • 11.
    DNA Replication • Step1: • DNA helicases unwinds & separates the original DNA double helix. • These proteins wedge themselves between the two strands of the double helix and break the hydrogen bonds between the base pairs. • Forms Replication Forks • As the double helix unwinds, the two complementary strands of DNA separate from each other and form a Y shape.
  • 12.
    DNA Replication Step 2:New DNA is formed from DNA template. RNA Primers attach to specific regions. New nucleotides are added to the primer by the enzyme DNA Polymerase according to the base-pairing rules.  DNA polymerases create the formation of the new complimentary DNA molecule by moving along each strand in a 5’ to 3’ direction.  They add nucleotides to a new daughter compliment in a 5’ to 3’ direction only! Primer Primer
  • 13.
    DNA Replication You knowthat DNA is anti- parallel because of the bi- directionality of DNA. One side goes 3’ to 5’. The other 5’ to 3’. New nucleotides can only be added to the 3’ end of the existing chain. One side (the top pictured here) is the LEADING STRAND. It has its new strand continuously synthesized as helicase unwinds more DNA. The other side, the LAGGING STRAND (on bottom) is discontinuous replication because it the bases are oriented in the wrong direction. 5’ 5’ DNA polymerase can only add nucleotides in a 5’ to 3’ direction.
  • 14.
    DNA Replication • Step2: Leading strand • Primers attach. • Primers are pre-made sequences of RNA. These bind to complementary regions of the original DNA once it’s separated. • Primers serve as tethers from which replication can proceed from the 3’ end. • DNA Polymerase attaches free nucleotides to the 3’ end of the primer. • On the leading strand there is one primer and the newly forming DNA follows the replication fork as the new DNA is synthesized. Primer
  • 16.
    DNA Replication • Step2: Lagging strand • The lagging strand creates a particular problem for replication. • Since DNA can only be synthesized from the 3’ end of the primers, the lagging strand would be left incomplete. • Multiple primers attach to the lagging strand as the replication fork moves forward, creating what are known as “Okasaki Fragments” • These are usually 1-2000 nucleotides long.
  • 17.
    DNA Replication • Step2: Lagging strand • If you notice, the Okazaki Fragments are not joined together. • A special enzyme, call ligase, joins Okasaki fragments together to form one continuous molecule. Ligase Ligase
  • 18.
    DNA Replication Step 3: The process completes when all the original bases have been paired with a new complementary nucleotide.  Each double-stranded DNA helix is made of one new strand of DNA and one original strand of DNA.
  • 19.
    Summary  What isDNA replication?  Why does it happen?  Know the steps…  On your handout, label: Where is… a. Leading Strand b. Lagging Strand c. Okazaki fragments d. DNA Ligase e. Replication Fork f. DNA Polymerase g. All 3’ & 5’ ends. h. Where helicase should be
  • 20.
    Replication Proteins • Replicationinvolves many proteins that form a machine-like complex of moving parts. • These proteins play a key role in making sure that the process is flawless. • DNA Helicase unwinds DNA carefully so it doesn’t get torn. • Ligase is a protein that ensures proper bonding of growing Okasaki fragments. • DNA polymerase adds complimentary nucleotides. • DNA polymerase also has a “proofreading” function. • During DNA replication, errors sometime occur and the wrong nucleotide is added to the new strand. • This could lead to cancer if not detected. • If a mismatch occurs, the DNA polymerase has the amazing ability of being able to backtrack, remove the incorrect nucleotide, and replace it with the correct one. • This decreases the chances of the wrong DNA being made, lessening our chances of CANCER!
  • 21.
    Replication v Transcription Based upon what you’ve learned about transcription and replication, shoulder partner share and come up with a similarity between transcription and replication.  WHAT IS THE SIMILARITY BETWEEN TRANSCRIPTION & REPLICATION?  Similarities: transcription and replication both use DNA as the template for copying.  SHOULDER PARTNER AND ANSWER: WHAT IS A CRITICAL DIFFERENCE BETWEEN REPLICATION AND TRANSCRIPTION?  Differences:  In transcription, a new molecule of mRNA is made from the template DNA by using the enzyme RNA polymerase.  In DNA replication, a new molecule of DNA is made from the template DNA by using the enzyme DNA polymerase.
  • 22.
    Objectives Primary  Compare theprocess of DNA replication in prokaryotes and in eukaryotes.  Identify the features of prokaryotic and Eukaryotic replication on an illustration. Secondary  Compare the number of nucleotides replicated in eukaryotes and prokaryotes by calculating the rates of replication.
  • 23.
    Prokaryotic and Eukaryotic Replication All cells have chromosomes, but eukaryotes and prokaryotes replicate their chromosomes differently.  The main difference between prokaryote and eukaryote replication is how many start sites each have.  Eukaryotes have hundreds of start sites.  The start sites then regulate how replication proceeds in each organism type.
  • 24.
    Prokaryotic DNA Replication Recall the structure of prokaryotic DNA.  Does anyone remember what the structure is?  Prokaryotic cells usually have a single chromosome which is a closed loop attached to the inner cell membrane.  Replication in prokaryotes begins at a single site along the loop. This site is called the origin of replication.
  • 25.
    Prokaryotic Replication  Tworeplication forks begin at the origin of replication.  Replication occurs in opposite directions until the forks meet on the opposite side of the loop.  The result is two identical loops of DNA.
  • 26.
    Eukaryotic Replication  Eukaryoticcells often have several chromosomes which are linear and contain both DNA and protein.  How many chromosomes do humans have?  What are the proteins called that hold DNA in nucleosomes?  Eukaryotic replication starts at many sites along the chromosome.  This process allows eukaryotic cells to replicate their DNA faster than prokaryotes.
  • 27.
    Eukaryotic Replication  Twodistinct replication forks form at each start site and replication occurs in opposite directions.  This process forms replication “bubbles” along the DNA molecule.  Replication bubbles continue to get larger as more of the DNA is copied.  The replication bubbles keep growing until they join together with other bubbles and complete replication.  Replication is complete when two identical complementary strands of DNA is formed.
  • 28.
    Eukaryotic Replication Original DNA Replicationbubbles Replication bubbles joining Original + new DNA New + original DNA
  • 29.
    Prokaryotic and Eukaryotic Replication Even the smallest eukaryotic chromosomes are often 10 times the size of a prokaryotic chromosome. Eukaryotic chromosomes are so long that it would take 33 days to replicate a typical human chromosome if there were only one origin of replication.  As such, evolution has allowed Human chromosomes to replicate in about 100 sections that are 100,000 nucleotides long, each section with its own starting point. Remember, the 46 human chromosomes laid end to end would measure ≈ 2m. Bacterial chromosomes measure ≈ 0.25cm!  Because eukaryotic cells have multiple replication forks working at the same time, an entire human chromosome can be replicated much faster, in only about 8 hours.  Bacteria replicate their small genomes in minutes…
  • 30.
    In-class Activity: ReplicationComparison A B C D E F G What is the difference between prokaryotic replication & eukaryotic replication? •Why are they different?
  • 31.
    Summary  In DNAreplication, the DNA molecule unwinds, and the two sides split. Then, new bases are added to each side until two identical sequences result.  The replication of DNA involves many proteins that form a machinelike complex of moving parts.  In prokaryotic cells, replication starts at a single site. In eukaryotic cells, replication starts at many sites along the chromosome.
  • 32.
    Replication concept Check 1.What is the purpose, outcome of DNA replication AND what stage does it happen in the cell cycle? To create an identical, duplicate copy of original DNA, “S” 2. What enzyme is responsible for “unzipping” the DNA double helix? DNA Helicase 3. What enzyme is responsible for adding nucleotides to the “unzipped” DNA? DNA polymerase 4. What is the enzyme responsible for bonding the fragments on the lagging strand? Ligase 5. (Review) What is the enzyme responsible for creating mRNA copies of genes in DNA? RNA polymerase 6. What is the enzyme responsible for “proofreading” the newly made DNA, checking for mismatched base-pairs? DNA polymerase
  • 33.
    Summary… The MoreComplex Version