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Replication of DNA
Dr. V.P.Acharya
Hi! Let’s dive into the central dogma
CENTRAL DOGMA
The Flow of Information: DNA → RNA → Protein
A gene is expressed in two steps:
DNA is transcribed to RNA
Then RNA is translated into protein
DNA- major store of genetic
information
To transfer genetic information from
parent to daughter cell, DNA must be
duplicated.
DNA duplication– DNA
REPLICATION
DNA→DNA
 Semi- conservative replication
Different models of DNA replication
Salient features of replication
Each strand serves as a template/mould,
over which a new complementary strand is
synthesized
Base-pairing rule is maintained
Polymerization from 5’-3’ direction
Old DNA is not degraded but conserved
DNA polymerase synthesises a new
complementary strand
Requisites for replication
Substrates
4 deoxyribonucleotides; dNTP
Template
2 separated DNA strands
Enzymes
DNA polymerases
DNA topoisomerases
RNA Primer
Steps of DNA replication
Identification of origin of replication
Unwinding of dsDNA to provide an ssDNA
template
Formation of replication fork
Initiation of DNA synthesis and elongation
Formation of replication bubbles with
ligation of the newly synthesised DNA
segments
Reconstitution of chromatin structure
3 stages of replication
Initiation
Elongation
Termination
Initiation
Replication starts with recognition of ori
(origin of replication)
Single site of ori– bacteria
Multiple sites– mammals
dnaA protein binds to ori
↓
Local denaturation & unwinding of an
adjacent A-T rich region
dnaB / Helicase– Binds to ori and unwinds
& separates the strands using ATP
↓
Replication fork formed
Topoisomerases– Relieve supercoils
Type I– Breaks one strand of DNA
Type II– Breaks both strands
Introduces negative supercoils
SSB (Single strand binding protein)-
Stabilizes the separated strands and
prevents reannealing.
Mammals- SSB counterpart is RFA
(replication factor)
dnaC protein– reqd. for dnaB binding
at ori
dnaG / Primase– Complexes with
proteins to form PRIMOSOME
↓
RNA primer synthesis
RNA Primer
RNA primer
10-200 nucleotides long
Primase in prokaryotes
DNAP α- eukaryotes
Nucleophilic attack by 3’- OH group of the
RNA primer on the phosphate of the first
entering deoxynucleotide triphosphate
Action of Helicase
Uses energy from ATP to
unwind the duplex DNA
SSB
SSB SSB
SSB
Replication fork
Components of replication fork
DNA helicase
Primase
DNA polymerase
SSB
Elongation
After RNA primers laid down, 2 DNA
polymerase III complexes attach
Leading strand & lagging strand
DNA chain which runs in 3’-5’ direction
copied by DNAP III in 5’-3’ direction in a
continuous manner
Okazaki fragments on lagging strand
DNAP I– removes RNA primers and fills in
the gap between okazaki fragments
Ligase– joins the segments
Okazaki fragments
Short stretches of 150-250bp (eukaryotes)
Found on lagging strand during DNA
replication
Later gap is filled by DNAP I and joined by
DNA ligase enzymes
Found in both eukaryotes and prokaryotes
Approx. 250 per replication fork
DNA polymerase complex
3 bacterial and 5 eukaryotic DNAP
Properties of DNAP
Chain elongation– 100
nucleotides/sec in mammals
Proof reading-- rectification
Processivity– How many nucleotides
are to be added before it dislodges
Proteins involved in replication
Termination
ter binding protein – binds to the sequence
↓
prevents helicase from
further action
↓
termination of replication
Which factor triggers DNA
replication???
External signals are delivered to cells
during the G1 phase of the cell cycle and
activate the synthesis of cyclins
Cyclins form complexes with cyclin-
dependent kinases (CDK)
Cascade of reaction
Synthesis of S phase proteins like DNAP
and thymidylate synthase
Eukaryotic replication
Binding of origin recognition complex(ORC)
to origins of replication during G1 phase
↓
ORC serves as a platform for highly
complicated pre-RC complex formation
↓
Converted to RC by CDK and Dbf4-
dependent kinase
↓
DNA polymerase α- primase
complex synthesizes first primer
2 characteristic features
Histone complexes
Telomeres- repeated end sequences of
(TTAGGG)n and have typical sizes of 15–20 kb
at birth
↓
In somatic cells it is shortened after each cycle
↓
Germline and cancer cells have telomerases
↓
extend the 5′ end of lagging strands
Telomerase
Reverse transcriptase
Contains an RNA template
Telomerase over-activity- cancer
Under-activity- ageing
Modification after replication
Methylation of DNA
At C5 of C
Catalysed by DNA methyl transferase
Methylation occurs at G-C rich region of
promoter sequence
>90% methyl C s are in CpG dinucleotides
Methylated areas- transcriptionally silent
Aberrant methylation- cancer, ageing, ROS
dependent damage
Difference between prokaryotic and eukaryotic
replication
Features Prokaryotes Eukaryotes
RNA primer
length
~50 nucleotides 9 nucleotides
DNAP 3; I,II,III 5; α,β,γ,ε,δ
Number of
origin
Single Many
Okazaki
fragments
1000-2000
nucleotides
~250
nucleotides
Rate of
replication
~500
nucleotides/sec
~100
nucleotides/sec
DNA replicates once and once only
Pre-replicative sequence is formed-
ORC-DNA complex with Cdc6 and Cdt1 at
G1-S phase
New nucleosomes are assembled behind
the replication fork
Inhibitors of DNA replication
Topoisomerase II (DNA gyrase) inhibitor
Novobiocin– prevents ATP binding to gyrase
Nalidixic acid & Ciprofloxacin- interfere with the
breakage and rejoining of DNA chains
Camptothecin– inhibits human topoisomerase I
Nucleotide analogues– 2,3 dioxyinosine,
Cytarabine
Zidovudine, Acyclovir- terminate DNA chain
elongation
Be like the stem cell-differentiate yourself
from others
WWW.VPACHARYA.COM
For more ppt on Medical Biochemistry
please visit my website

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Replication of dna

  • 2. Hi! Let’s dive into the central dogma
  • 3. CENTRAL DOGMA The Flow of Information: DNA → RNA → Protein A gene is expressed in two steps: DNA is transcribed to RNA Then RNA is translated into protein
  • 4. DNA- major store of genetic information To transfer genetic information from parent to daughter cell, DNA must be duplicated. DNA duplication– DNA REPLICATION DNA→DNA  Semi- conservative replication
  • 5. Different models of DNA replication
  • 6.
  • 7. Salient features of replication Each strand serves as a template/mould, over which a new complementary strand is synthesized Base-pairing rule is maintained Polymerization from 5’-3’ direction Old DNA is not degraded but conserved DNA polymerase synthesises a new complementary strand
  • 8. Requisites for replication Substrates 4 deoxyribonucleotides; dNTP Template 2 separated DNA strands Enzymes DNA polymerases DNA topoisomerases RNA Primer
  • 9. Steps of DNA replication Identification of origin of replication Unwinding of dsDNA to provide an ssDNA template Formation of replication fork Initiation of DNA synthesis and elongation Formation of replication bubbles with ligation of the newly synthesised DNA segments Reconstitution of chromatin structure
  • 10. 3 stages of replication Initiation Elongation Termination
  • 11. Initiation Replication starts with recognition of ori (origin of replication) Single site of ori– bacteria Multiple sites– mammals dnaA protein binds to ori ↓ Local denaturation & unwinding of an adjacent A-T rich region
  • 12.
  • 13. dnaB / Helicase– Binds to ori and unwinds & separates the strands using ATP ↓ Replication fork formed Topoisomerases– Relieve supercoils Type I– Breaks one strand of DNA Type II– Breaks both strands Introduces negative supercoils SSB (Single strand binding protein)- Stabilizes the separated strands and prevents reannealing.
  • 14. Mammals- SSB counterpart is RFA (replication factor) dnaC protein– reqd. for dnaB binding at ori dnaG / Primase– Complexes with proteins to form PRIMOSOME ↓ RNA primer synthesis
  • 16. RNA primer 10-200 nucleotides long Primase in prokaryotes DNAP α- eukaryotes Nucleophilic attack by 3’- OH group of the RNA primer on the phosphate of the first entering deoxynucleotide triphosphate
  • 17. Action of Helicase Uses energy from ATP to unwind the duplex DNA SSB SSB SSB SSB
  • 19. Components of replication fork DNA helicase Primase DNA polymerase SSB
  • 20. Elongation After RNA primers laid down, 2 DNA polymerase III complexes attach Leading strand & lagging strand DNA chain which runs in 3’-5’ direction copied by DNAP III in 5’-3’ direction in a continuous manner Okazaki fragments on lagging strand DNAP I– removes RNA primers and fills in the gap between okazaki fragments Ligase– joins the segments
  • 21.
  • 22. Okazaki fragments Short stretches of 150-250bp (eukaryotes) Found on lagging strand during DNA replication Later gap is filled by DNAP I and joined by DNA ligase enzymes Found in both eukaryotes and prokaryotes Approx. 250 per replication fork
  • 23. DNA polymerase complex 3 bacterial and 5 eukaryotic DNAP
  • 24. Properties of DNAP Chain elongation– 100 nucleotides/sec in mammals Proof reading-- rectification Processivity– How many nucleotides are to be added before it dislodges
  • 25. Proteins involved in replication
  • 27. ter binding protein – binds to the sequence ↓ prevents helicase from further action ↓ termination of replication
  • 28. Which factor triggers DNA replication??? External signals are delivered to cells during the G1 phase of the cell cycle and activate the synthesis of cyclins Cyclins form complexes with cyclin- dependent kinases (CDK) Cascade of reaction Synthesis of S phase proteins like DNAP and thymidylate synthase
  • 29. Eukaryotic replication Binding of origin recognition complex(ORC) to origins of replication during G1 phase ↓ ORC serves as a platform for highly complicated pre-RC complex formation ↓ Converted to RC by CDK and Dbf4- dependent kinase ↓ DNA polymerase α- primase complex synthesizes first primer
  • 30. 2 characteristic features Histone complexes Telomeres- repeated end sequences of (TTAGGG)n and have typical sizes of 15–20 kb at birth ↓ In somatic cells it is shortened after each cycle ↓ Germline and cancer cells have telomerases ↓ extend the 5′ end of lagging strands
  • 31. Telomerase Reverse transcriptase Contains an RNA template Telomerase over-activity- cancer Under-activity- ageing
  • 32. Modification after replication Methylation of DNA At C5 of C Catalysed by DNA methyl transferase Methylation occurs at G-C rich region of promoter sequence >90% methyl C s are in CpG dinucleotides Methylated areas- transcriptionally silent Aberrant methylation- cancer, ageing, ROS dependent damage
  • 33. Difference between prokaryotic and eukaryotic replication Features Prokaryotes Eukaryotes RNA primer length ~50 nucleotides 9 nucleotides DNAP 3; I,II,III 5; α,β,γ,ε,δ Number of origin Single Many Okazaki fragments 1000-2000 nucleotides ~250 nucleotides Rate of replication ~500 nucleotides/sec ~100 nucleotides/sec
  • 34. DNA replicates once and once only Pre-replicative sequence is formed- ORC-DNA complex with Cdc6 and Cdt1 at G1-S phase New nucleosomes are assembled behind the replication fork
  • 35. Inhibitors of DNA replication Topoisomerase II (DNA gyrase) inhibitor Novobiocin– prevents ATP binding to gyrase Nalidixic acid & Ciprofloxacin- interfere with the breakage and rejoining of DNA chains Camptothecin– inhibits human topoisomerase I Nucleotide analogues– 2,3 dioxyinosine, Cytarabine Zidovudine, Acyclovir- terminate DNA chain elongation
  • 36. Be like the stem cell-differentiate yourself from others
  • 37. WWW.VPACHARYA.COM For more ppt on Medical Biochemistry please visit my website