mbb 407/511 lecture 19: prokaryotic dna replication (part i) nov. 12, 2004
TRANSCRIPT
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MBB 407/511
Lecture 19:Prokaryotic DNA Replication
(Part I)
Nov. 12, 2004
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V. cDNA Libraries (converting mRNA into “complementary DNA”
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I. Why Study DNA Replication?
1) To understand cancer
2) To understand aging
3) To understand diseases related to DNA repair
a) Bloom’s Syndromeb) Xeroderma Pigmentosumc) Werner’s Syndrome
Keith Richards (of the Rolling Stones)
Example of premature agingNOT caused by a hereditary disease
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II. Historical Background
A. 1953 Watson and Crick: DNA Structure Predicts a Mechanism of Replication“It has no escaped our notice that the specific pair we have postulated immediately suggests a possible copying mechanism for the genetic material.”
B. 1958 Meselson and Stahl: DNA Replication is Conservative
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The Meselson-Stahl Experiment“the most beautiful experiment in biology.”
Three potential DNA replication models and their predicted outcomes The actual data!
1/4 old:3/4 new
1/2 hybids:1/2 new
Allhybrids
1/2 old:1/2 new
Allhybrids
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III. General Features of DNA Replication
1. requires a DNA template and a primer with a 3’ OH end. (DNA synthesis cannot initiate de novo)
2. requires dNTPs.
3. occurs in a 5’ to 3’ direction.
DNA Synthesis:
Short RNA moleculesact as primersin vivo
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Replication of the E. coli Chromosome is Bidirectional
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Replication of the E. coli Chromosome is Semidiscontinuous
Replicates continuously
DNA synthesis is going in same direction as replication fork
Because of the anti-parallel structure of the DNA duplex, new DNA must be synthesized in the direction of fork movement in both the 5’ to 3’ and 3’ to 5’ directions overall.
Replicates discontinuously
DNA synthesis is going in opposite direction as replication fork
However all known DNA polymerases synthesize DNA in the 5’ to 3’ direction only.
The solution is semidiscontinuous DNA replication.
Joined by DNA ligase
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“Now this end is called the thagomizer,after the late Thag Simmons.”
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IV. DNA Polymerases of E. coli
The first DNA polymerase was discovered by Arthur Kornberg in 1957 → DNAPolymera se I
A. . E coli DNA Pol I has 3 enzymatic activities:
1) 5’ → 3’ DNA polymeraseKlenow Fragment
2) 3’ → 5’ exoncuclease (For proofrea )ding
3) 5’ → 3’ DNA exonucleas (e To edit out sections of damaged DN )A
1 323
Hans Klenow showed tha t limited proteolysis wit h eithe r subtilisi n o r trypsi n will cleavePol I into t wo biologicall yacti vefragments.
Facts abou t DNA Synthesis Erro r Rate :s—DNA polymera seinserts one incorrec tnucleoti defor eve 10ry 5 nucleotides added.—Proofreading exonucleas es decrease the appearance of an incorrect paired base t o onei ne 10very 7 nucleotides added.—Actua l error rate observed i n a typical cell is one mistake i n every 1010 nucleotidesadded.—Error rat efor RNA Polymerase is 1/105 nucleotides.
aa 928Klenow Fragment
5’ to 3’ E .xo5’ to 3’ Pol & 3’ to 5’ Exo
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Model for the Interaction of Klenow Fragment with DNA
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How the Proofreading Activity of Klenow Fragment Works
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DNA Polymerase I can Perform “Nick Translation”
They act together to edit out
sections of damaged DNA
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The 5’ to 3’ Exonuclease and 5’ to 3 Polymerase of Pol I Result in “NickTranslation”:
5’ 3’ 3’ 5’
I
5’ 3’ 3’ 5’
5’ → 3’ exonuclea se edits damage dDNA
Newly synthesized. DNA
DNA Polymerase I
+
5’ -dNMPs
nick
nick
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B. Processivity
DNA Polymerases Can be Processive or Distributive
Processivity is continuous synthesis by polymerase without dissociationfrom the template.
A DNA polymerase that is Distributive will dissociate from the templateafter each nucleotide addition.
Processive Polymerization
Distributive Polymerization
1 nucleotide
Used inDNAReplication
Suitable forDNA Repair
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Proc. Dist.
How to Measure Processivity
dATPdCTP
dGTP[32P]-dTTP
ssDNAtemplate
M13Mg2+
5 min. @ 37oC
STOP w/ EDTA
DNA Pol
Polyacrylamide Gel
Processivity experimentsrequire a large excess oftemplate to Pol to preventreassociation to the sametemplate.
primer
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DNA Pol III is highly “processive” DNA Pol I is” distributive”
Pol I & II – main DNA repair enzymePol III – main DNA replication enzyme
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DNA Pol I
RNA
Okazaki fragment
>10 kb
1 kb
Roles of DNA Pol III and Pol I in E. coli
Pol III—main DNA replication enzyme. It exists as a dimer to coordinate the synthesis of both the leading and lagging strands at the replication fork.
Pol I—repair enzyme to remove RNA primers that initiate DNA synthesis on both strands. It is need predominantly for maturation of Okazaki fragments.
1) Removes RNA primers (5’3’ Exo)2) Replaces the RNA primers with DNA (5’3’ Pol & 3’5’ Exo proofreading)
RNA primer replaced withDNA by Pol I’s nick translatiton activity
Okazaki fragment