dna polymerase summary 1.dna replication is semi-conservative. 2.dna polymerase enzymes are...
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DNA polymerase summary
1. DNA replication is semi-conservative.2. DNA polymerase enzymes are specialized for
different functions.3. DNA pol I has 3 activities: polymerase, 3’-->5’
exonuclease & 5’-->3’ exonuclease.4. DNA polymerase structures are conserved.5. But: Pol can’t start and only synthesizes DNA 5’--
>3’!6. Editing (proofreading) by 3’-->5’ exo reduces
errors.7. High fidelity is due to the race between addition
and editing.8. Mismatches disfavor addition by DNA pol I at 5
successive positions. The error rate is ~1/109.
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Replication fork summary
1. DNA polymerase can’t replicate a genome.Problem Solution
ATP?No single stranded template Helicase
+The ss template is unstable SSB (RPA (euks))
-No primer Primase
(+)No 3’-->5’ polymerase Replication forkToo slow and distributive SSB and sliding
clamp -
2. Replication fork is organized around an asymmetric, DNA- polymerase III dimer.
3. Both strands made 5’-->3’.4. “Leading strand” is continuous; “lagging strand”
is discontinuous.
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DNA polymerase can’t replicate a genome!
1. No single stranded template2. The ss template is unstable3. No primer4. No 3’-->5’ polymerase5. Too slow and distributive
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Solution: the replication fork
1. No single-stranded template2. The ss template is unstable3. No primer4. No 3’-->5’ polymerase5. Too slow and distributive
Schematic drawing of a replication fork
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DNA polymerase holoenzyme
QuickTime™ and aDV - PAL decompressor
are needed to see this picture.
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DNA replication factors were discovered using “temperature sensitive” mutations
1. No single stranded template2. The ss template is unstable3. No primer4. No 3’-->5’ polymerase.5. Too slow in vitro.
Mutations that inactivate the DNA replication machinery are lethal.
Temperature sensitive (conditional) mutations allow isolation of mutations in essential genes.
37 ºC
42 ºC
42 ºC,Mutant geneoverexpressed
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A hexameric replicative helicase unwinds DNA ahead of the replication fork
1. No single stranded template2. The ss template is unstable3. No primer4. No 3’-->5’ polymerase.5. Too slow in vitro.
Replicative DNA helicase is called DnaB in E. coli.
DnaB couples ATP binding and hydrolysis to DNA strand separation.
Helicase assay
ds DNA
ss DNA
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SSB (or RPA) cooperatively binds ss DNA template
1. No single stranded template2. The ss template is unstable3. No primer4. No 3’-->5’ polymerase.5. Too slow in vitro.
SSB (single-strand binding protein (bacteria)) or RPA (Replication Protein A (eukaryotes)): No ATP used.Filament is substrate for DNA pol.
ds DNA
ss DNA + SSB
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SSB tetramer structure
1. No single stranded template2. The ss template is unstable3. No primer4. No 3’-->5’ polymerase.5. Too slow in vitro.
SSB (bacteria) and RPA (eukaryotes)
form tetramers.The C-terminus of SSB binds replication factors (primase, clamp loader (chi subunit))
ds DNA
ss DNA + SSB
N
C
N
C
N
C
N
C
Conservation Positive potential
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1. No single stranded template2. The ss template is unstable3. No primer4. No 3’-->5’ polymerase.5. Too slow in vitro.
DNA synthesis is primed by a short RNA segment
Primase makes about 10-base RNA. The product is a RNA/DNA hybrid.RNA primer has a free 3’OH.
Uses ATP, which ends up across from T in the RNA/DNA hybrid.
Primase: DNA-dependent RNA polymerase
Start preference for CTG on template
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DnaG primase defines a distinct polymerase family (DNA dependent RNA pol)
Map ofsurfac
e charg
e
Ribbondiagram
Model of “primosome”:DnaB helicase + DnaG primase
DnaB helicase
DnaG primase
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Primase passes the primed template to DNA polymerase
Lagging strand:
discontinuous
Leading strand:
continuous
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1. No single stranded template2. The ss template is unstable3. No primer4. No 3’-->5’ polymerase.5. Too slow in vitro.
DNA pol III “holoenzyme” is asymmetric
DNA pol III holoenzyme:A molecular machine
binds SSB opens clamp ()
SynthesizesLaggingStrand
SynthesizesLeadingStrand
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Pol III dimer couples leading and lagging strand synthesis
Leadingstrand
Laggingstrand
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Replication fork
1. No single stranded template2. The ss template is unstable3. No primer4. No 3’-->5’ polymerase5. Too slow and distributive
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Replication fork
1. No single stranded template2. The ss template is unstable3. No primer4. No 3’-->5’ polymerase5. Too slow and distributive
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Sliding clamp wraps around DNA
N
C
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Sliding clamps are structurally conserved
“Palm”
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Summary of the replication fork
“Palm”
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Synthesis of Okazaki fragments by pol III holoenzyme
When pol III reaches the primer of the previous Okazaki fragment, clamp loader removes 2 from the DNA template. As a result, the pol III on the lagging strand falls off the template.
Clamp loader places 2 on the next primer-template.
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Replication fork summary
1. DNA polymerase can’t replicate a genome.Solution
ATP?No single stranded template Helicase
+The ss template is unstable SSB (RPA (euks))
-No primer Primase
(+)No 3’-->5’ polymerase Replication forkToo slow and distributive SSB and sliding
clamp -
2. Replication fork is organized around an asymmetric, DNA- polymerase III dimer.
3. Both strands made 5’-->3’.4. “Leading strand” is continuous; “lagging strand”
is discontinuous.
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Replication fork summary
1. DNA polymerase can’t replicate a genome.Problem Solution
ATP?No single stranded template Helicase
+The ss template is unstable SSB (RPA (euks))
-No primer Primase
(+)No 3’-->5’ polymerase Replication forkToo slow and distributive SSB and sliding
clamp - Sliding clamp can’t get on Clamp loader
(/RFC) +Lagging strand contains RNAPol I 5’-->3’ exo,
RNAseH -Lagging strand is nicked DNA ligase
+Helicase introduces positive Topoisomerase II
+supercoils
2. DNA replication is fast and processive
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Sliding clamp wraps around DNA
N
C
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/RFC clamp loader complex puts the clamp on DNA
6. Sliding clamp can’t get on7. Lagging strand contains RNA8. Lagging strand is nicked9. Helicase introduces + supercoils
complex -- bacteriaRFC -- eukaryotes(Replication Factor C)
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RFC reaction
1. RFC + clamp + ATP opens clamp2. Ternary complex + DNA/RNA --> Closed clamp + RFC + ADP + Pi
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Schematic drawing of the RFC:PCNA complex on the primer:template
RFC contains 5 similar subunits that spiral around DNA.The RFC helix tracks the DNA or DNA/RNA helix
RFC
PCNA
DNA:RNA
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RFC:PCNA crystal structure
RFC:PCNA crystal structure
RFC
PCNA
DNA:RNA
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SSB opens hairpins, maintains processivity andmediates exchange of factors on the lagging strand
1. No single stranded template2. The ss template is unstable3. No primer4. No 3’-->5’ polymerase.5. Too slow in vitro.
SSB (bacteria) and RPA (eukaryotes) form tetramers.The C-terminus of SSB binds replication factors (Primase, Clamp loader (chi subunit))
SSB:DNAbinds primase
Primer:template:SSBBinds clamp loader
Clamp loader exchanges with pol III on the clamp
Primase - to - pol III switch
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Synthesis of Okazaki fragments by pol III holoenzyme
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DNA polymerase 5’-->3’ exonuclease or RNase Hremove RNA primers
DNA polymerase I 5’-->3’ exo creates ss template.Pol works on the PREVIOUS Okazaki fragment!
6. Sliding clamp can’t get on7. Lagging strand contains RNA8. Lagging strand is nicked9. Helicase introduces + supercoils
OR RNaseH cleaves RNA:DNA --> ssDNA + rNMPs primer
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DNA polymerase 5’-->3’ exonuclease or RNase Hremove RNA primers
DNA polymerase I 5’-->3’ exo creates ss template.Pol works on the PREVIOUS Okazaki fragment!
6. Sliding clamp can’t get on7. Lagging strand contains RNA8. Lagging strand is nicked9. Helicase introduces + supercoils
OR RNaseH cleaves RNA:DNA --> ssDNA + rNMPs primer
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DNA ligase seals the nicks
1. Adenylylate theenzyme
2. Transfer AMP tothe PO4 at the nick
3. Seal nick, releasingAMP
Three steps in the DNA ligase reaction
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Maturation of Okazaki fragments
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All tied up in knots
6. Sliding clamp can’t get on7. Lagging strand contains RNA8. Lagging strand is nicked9. Helicase introduces + supercoils
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“Topological” problems in DNA can be lethal
•Gene misexpression
•Chromosome breakage
•Cell death
(+) supercoils
(-) supercoils
(+) supercoils
precatenanes
catenanes
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Topoisomerases control chromosome topologyCatenanes/knots
Relaxed/disentangled
•Major therapeutic target - chemotherapeutics/antibacterials
•Type II topos transport one DNA through another
Topos
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Topoisomerases cut one strand (I) or two (II)
Topoisomerase I - Cuts ssDNA region (1A (proks)) or nicks DNA (1B (euks))
Topoisomerase II - Cuts DNA and passes one duplex through the other!
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Topoisomerase II is a dimer that makes two staggered cuts
Tyr OH attacks PO4 and forms a covalent intermediate
Structural changes in the protein open the gap by 20 Å!
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ATPase DNA Binding/Cleavage
GyrAGyrB
Type IIA topoisomerases comprise a homologous superfamily
Gyrase(proks)
Topo II(euks)
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Type IIA topoisomerase mechanism
• “Two-gate” mechanism
• Why is the reaction directional?
• What are the distinct conformational states?
ADP
G-segment
T-segment
QuickTime™ and a decompressor
are needed to see this picture.
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Summary of the replication fork
“Palm”
“Fingers” “Thumb”
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Accessory factors summary
1. DNA polymerase can’t replicate a genome.Solution
ATP?No single stranded template Helicase
+The ss template is unstable SSB (RPA (euks))
-No primer Primase
(+)No 3’-->5’ polymerase Replication forkToo slow and distributive SSB and sliding
clamp - Sliding clamp can’t get on Clamp loader
(/RFC) +Lagging strand contains RNAPol I 5’-->3’ exo,
RNAseH -Lagging strand is nicked DNA ligase
+Helicase introduces positive Topoisomerase II
+supercoils
2. DNA replication is fast and processive