Chen Yonggang Zhejiang University Schools of Medicine Biochemistry

Chen Yonggang

Zhejiang University

Schools of Medicine

Biochemistry

Central dogma

replication

transcription translation

DNA RNA Protein

DNA Replication

.

DNA Replication-Conservation of Information

• DNA replication must be carried out every time a cell divides

• Procaryotic growth involves cell division• Mitosis in eucaryotes involves cell division• DNA replication is template driven and

synthesizes DNA in a semi-conservative manner

dNTP + DNAn DNAn+1 +PPi

DNA is replicated in a semi-conservative manner

• Messelson & Stahl showed, using 15N-labelled DNA that the products of replication had intermediate density

McKee 18.2

15Nstrand A strand B

15N14N

15N 15N14N 14N14N 14N

15N 15N14N14N14N14N 14N14N

Each separated DNA strand is duplicated to give two

new double helices.

DNA semiconservative replication

Each DNA strand serves as a template for the synthesis of a new strand, producing two new DNA molecules , each with one new strand and one old strand, this is semiconservative replication.

The process which appeared simple initially is complex

• Replication occurs just prior to cell division• The E coli chromosome is a single circular

DNA double helix associated with proteins in a nucleoid

• The E coli chromosome is negatively supercoiled and thus is quite compact and inaccessible

McKee 17.16

To allow the replication to occur supercoiling must be relaxed

• A type I (single strand breaking) topoisomerase cleaves and relaxes the negative supercoiling ahead of the replication complex

• The topoisomerase has a central hole through which the double helix passes. An intermediate is an enzyme-linked 3’OH

• dnaA is displaced providing access for the next component needed for replication

The first step in replication involves oriC

• OriC is a 245 bp region, the origin of E coli replication

• OriC contains 3 tandem repeats of a 13 bp sequence beginning in GATC and rich in AT bp

• These repeats are weakly H-bonded and serve to provide 4 binding sites for a protein, dnaA, a start signal for replication

• Replication proceeds in two directions - bidirectional

dnaA allows binding of two other important proteins

• dnaB is a DNA helicase which carries out the ATP- driven unwinding of the DNA double helix

• dnaC is an important accessory protein which binds and is soon released

• Together the three proteins utilize ATP to bend and separate the two strands of the bacterial chromosome

SSB, a single strand binding tetramer stabilizes the initiation complex

McKee 18.7

DNA replication involves many enzymes

• An RNA primase binds to the SSB stabilized melted helix

• Since DNA polymerases require a primer and only extend that primer, the RNA primase (dnaG) in association with other proteins (primosome) synthesizes a 5-7 nucleotide primer using information from the template strand

At the replication fork two strands are managed differently

• The 5’ end of the primer(leading strand) is extended continuously by DNA polymerase III in a 5’→3’ direction by dNTPs

• The primer on the lagging strand is also extended 5’→3’ by DNA polymerase III, in a discontinuous manner

• Thus primer is made once on the leading strand and every 1000 nucleotides on the lagging strand

The replication fork

McKee 18.6

DNA Polymerase III holoenzyme contains 10 distinct types of subunits

• DNA Polymerase III is the primary replicase in E. coli

• It has polymerase and 3’→5’ exonuclease activities

• It functions as a dimer• It has great fidelity, only 1 error in 1010 bp• It is highly processive, sticking to the DNA for the

entire trip through the chromosome• It has a rapid biosynthetic rate, synthesizing 1000

nt/sec

The Pol III synthesizes DNA from dNTPs

McKee 18.3

The Dimer moves in one direction and synthesizes 5’→3’ • The leading strand is synthesized by

addition of 5’-dNTPs in response to the template

• The looped lagging strand is synthesized in Okazaki fragments using 5’-dNTPs

• The lagging strand must be pieced together using DNA Polymerase I

DNA polymerase III forms phosphodiester bonds

• 2’-deoxynucleoside 5’ triphosphates are the activated intermediates needed for synthesis

• Information from the parental strand provides the information for 5’→3’ synthesis (parental strand is read 3’→5’)

• Thus each parental strand serves as the template for synthesis of a complementary strand

Synthesis of a phosphodiester bond

OBASE1OP

O

O

CHAIN

OH

P

O

O

O O OP

O

O

OBASE2OP

O

O

OH

..nucleophilic attack

OBASE1OP

O

O

CHAIN

O

OBASE2OP

O

OH

O

new phospho-diesterbond

DNA Polymerase III is at the center of Replication

McKee 18.8

Top-down view of replication

While DNA polymerase III does the replicating, DNAP I cleans up• Pol I(100kd) is a monomer of about 10%

the size of Pol III(900kd)

• It has three activities– It is a DNA polymerase– It is a 3’→5’ exonuclease– It is a 5’→3’ exonuclease

• It is a processing and proofreading enzyme

The three activities are on one polypeptide

• The larger fragment(Klenow fragment) of 67kd contains the polymerase and the 3’→5’ exonuclease activity

• The smaller, 36kd contains the 5’→3’ exonuclease activity

As Pol III finishes, Pol I goes to work

• The 5’→3’ exonuclease removes the RNA primer• The polymerase synthesizes DNA to fill the gap• Errors in Pol III synthesis are removed by 3’→5’

exonuclease• The function of DNA Pol II is not understood,

although it apperas to be similar to Pol I

Supercoiling was taken out by dnaB, DNA gyrase replaces it

• Following synthesis of the strands, excision of RNA, replacement by DNA using Pol I, the supercoiling can be reinstated

• DNA gyrase, an ATP- linked, energy requiring enzyme introduces negative supercoils to restore the original twist in the leading strand

DNA ligase seals the Okazaki fragments and the completed double

helical DNA• DNA polyI removes the primers and fills the gaps, DNA

ligase seals the nicks and Okazaki fragments are connected

• Pyrophosphate cleavage drives the reaction to completion• Termination occurs at a ter region and is mediated by a

binding protein TBP• A type II(double stranded) topoisomerase is probably

involved in helix dissociation(the two daughter DNA molecules separate)

Enzymes and proteins involved in DNA replication

1, Topoisomerase

2, dnaA 1 : recognize the origin of replication

dnaB(helixase):unwind double helix

dnaC

3, SSB

4, Primase

5, DNA polymeraseIII, DNA polymeraseI

6, Ligase

Happy Birthday

•Samar and Barry

Eucaryotic Replication is similar to that of procaryotes

• Both have initiation, elongation and termination phases and are bidirectional

• Both involve multiple DNA polymerases• Both involve multiple copies of the primary

replicase which replicates strands differently• Replication rate is slower, but replication is rapid

due to multiple replicons• Both require topoisomerases to unwind and

rewind the DNA• Both require ligases

Eucaryotic replication is distinct from that of procaryotes

• There are 5 polymerases(α,β,γ,δ,ε)• The chromosomes are linear• There are multiple ori, and replication units• Replication only occurs during the S phase

of the cell cycle• Telomeres restrict the number of times a

replicon can be expressed

Initiation of replication occurs at multiple ori

• A large complex of proteins assembles at an ori (Origin Recognition Complex-ORC)

• Details not for testing– A complex with helicase activity must bind and be

activated– Replication Protein A (RPA ) binds and separates the

strands(like SSB in E.coli)– RFC(replication factor C– a clamp loading factor) and

PCNA(proliferating cell nuclear antigen) allows binding of Pol to both the leading and lagging strand

Binding of initiation factors to the lagging strand differs

• Pol is the main eucaryotic replication polymerase (Details not for testing)– Replication protein A(RPA) binds to the single strands

– Pol a and a primase complex binds to the lagging strand

– An RNA primer and 15-30 dNTPs are synthesized

• Pol binds and replicates one nucleosomes worth of Okazaki fragment

Finishing and sealing of the lagging strand is different

• Specific protein factors are important in finishing up replication (details not for testing)– DNA polymerase remove the primers and DNA

polymerase excise errors

– Topoisomerases induce supercoiling

– DNA ligase seals the breaks

– Chromosomes segregate

• Replication bubbles merge• Telomeres determine the end of replication

Eukaryotic DNA polymerases• Eukaryotes have at least 15 DNA Polymerases (5 most

important):Pol α: acts as a primase (synthesizing a RNA primer), and

then as a DNA Pol elongating that primer with DNA nucleotides. After a few hundred nucleotides elongation is taken over by Pol δ and ε.

Pol β: is implicated in repairing DNA. Pol γ: replicates mitochondrial DNA. Pol δ: is the main polymerase in eukaryotes, it is highly

processive and has 3'→5' exonuclease activity. Pol ε: may substitute for Pol δ in lagging strand synthesis,

however the exact role is uncertain.

Telomeres are GC rich self-complementary sequences at

chromosome ends

• Telomerase maintains the telomeres

• Telomeres are repeat structures with a terminal loop

• At each replication the telomeres are modified using an integral RNA template

• Loss of telomeres limits replication

• Cancer cells lose control of their telomeres

Telomeres

The structure at the ends of linear eukaryotic

chromosomes, generally consist of many tandem copies of a short oligonucleotide

sequence.

Supercoiled DNA in Prokaryote

Structure of Nucleosome

Negative and positive supercoil