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DNA REPLICATION DNA REPLICATION Guided By- Dr.Cletus D’Souza Dept. Of Biochemistry Presented By- Narayan Prahlad V VIth Semester Dept.of Molecular Biology
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Dna replication and enzymes involved in dna replication

Aug 09, 2015

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Page 1: Dna replication and enzymes involved in dna replication

DNA REPLICATIONDNA REPLICATION

Guided By-Dr.Cletus D’SouzaDept. Of Biochemistry

Presented By-Narayan Prahlad VVIth SemesterDept.of Molecular Biology

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ContentsContents

Introduction Chemistry of DNA Synthesis Extension of 3’-OH of Primer Enzymes involved in replication Mechanism of Replication Proof Reading Conclusion Reference Acknowledgement

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INTRODUCTIONINTRODUCTION

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Chemistry of DNA SynthesisChemistry of DNA Synthesis

• Requires 4 Deoxynucleoside Triphosphates (dGTP,dCTP,dATP,dTTP).• Have three Phosphate groups-attached via 5’-OH & 2’ deoxyribose.

• Second essential substrate- Primer:Template Junction• Primer- Should have exposed 3’-OH.

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Extension of 3’-OH of PrimerExtension of 3’-OH of Primer

• New chain grows-extension of 3’ end of primer-Phosphodiester bond is formed by SN2 mechanism.

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EnzymesEnzymes

DNA Polymerase-• Mainly catalyses DNA synthesis.• Multimolecular forms of this enzyme- DNA Pol-I, DNA Pol-II, DNA

Pol-III DNA Pol-I: Polymerase Activity. 5’ to 3’ Exonuclease Activity-Used to remove primer and replace with DNA. DNA Pol-III: Core replication enzyme. Holoenzyme Has proof reading capabilities(3’ to 5’ exonuclease activity).

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Polymerase Polymerase

clamp loader

Sliding clamp

3'-5' exonuclease

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DNA Pol-III

• The fingers and the thumb are composed-helices. • The incoming dNTP is in red (for the base and the deoxyribose) and yellow (for the triphosphate moiety). • The template strand of the DNA is shown in dark gray, and the primer strand is shown in light gray.

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Continued..Continued..

Helicase-• Hexameric assembly of 6 identical subunits.• Uses ATP (Hydrolysis)-unwind DNA.

Sliding Clamp-• Part of DNA Pol-III (β-Subunit).• Encircles and slides along DNA-tethering it to

template.

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Continued..Continued.. Single Strand DNA Binding Protein (SSB)-• Tertamer of identical subunits.• Binds to ssDNA-preventing it from recoiling.

DNA Primase-• Synthesis of Oligoribonucleotide(Primer) -extended by DNA Pol-III.

Ligase-• Seals the gaps between Okazaki fragments-forming a

continuous strand.

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Mechanism of ReplicationMechanism of Replication

STEP-1 -UnwindingUnwinding of DNA by Helicase of DNA by Helicase

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• Step-2- Binding of SSBs to ssDNABinding of SSBs to ssDNA

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• Step-3

Binding of TopoisomeraseBinding of Topoisomerase

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• Step-4Action of DNA Pol-IIIAction of DNA Pol-III

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Sliding ClampSliding Clamp

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Thrombone ModelThrombone Model

• In order to explain synthesis on lagging strand-Thrombone model was proposed.

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Synthesis of DNA on Lagging Synthesis of DNA on Lagging StrandStrand

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Action of DNA Pol-I & LigaseAction of DNA Pol-I & Ligase

• DNA Pol-I replaces RNA fragments with DNA and fills the gaps.

• Ligase joins the fragments –Phosphodiester bonds and forms a continuous strand.

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Proof ReadingProof Reading

• DNA Pol-3.

• When a mismatched nucleotide comes-rate of addition of nucleotide by polymerase slows down.

• Exonuclease catalytic site in DNA Pol-3.

• Error rate- 1 in 1010 bp added, occasionally- 1 in 105 .

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ConclusionConclusion

• DNA replication is a very important phase in cell cycle.• Replication is a must so as to ensure the equal distribution of

genetic material to daughter cells.• Thus all enzymes have to coordinate well in order for

replication to occur successfully.

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ReferencesReferences

• Molecular Biology of Gene by Watson;7th edition; Cold Spring Harbour Laboratory Press, Cold Spring Harbour New York.

• Biochemistry 5th edition by Lubert Stryer;W.H Freeman Company.

• Molecular Cell Biology by Lodish;6th edition;W.H Freeman and Company;New York.

• http://sites.fas.harvard.edu/~biotext/animations/replication1.swf

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AcknowledgementAcknowledgement

• I would like thank my guide Dr.Cletus D’Souza for his valuable guidance.

• I would also like to thank our course coordinator Dr.N.S Devaki for providing me this opportunity to present this seminar.

Thank You all for your patient listening.

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