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Synthesis of DNA. June.21.2010. DNA synthesis occurs by the process of replication. During replication, each of the two parental strands of DNA serves as a template for the synthesis of a Complementary strand. Each molecule generated by the replication process contains
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Synthesis of DNA June.21.2010
DNA synthesis occurs by the process of replication. During replication, each of the two parental strands of DNA serves as a template for the synthesis of a Complementary strand.
Each molecule generated by the replication process contains one intact parental strand and one newly synthesized strand.
In eukaryotes, DNA replication occurs during the S phase of the cell cycle The cell divides during the next phase (M), and each daughter cell receives an exact copy of the DNA of the parent cells.
Cultured MDCK cells Day 3 Day 1
1953 article in Nature Watson and Crick
Double helix structure of DNA “It has not escaped our notice that the specific pairing we have postulated immediately suggests a possible copying mechanism for the genetic material.” Watson & Crick
Directionality of DNA • You need to number the carbons! • it matters! nucleotide PO4 N base 5 CH2 This will beIMPORTANT!! O 1 4 ribose 3 2 OH
5 The DNA backbone PO4 • Putting the DNA backbone together • refer to the 3 and 5 ends of the DNA • the last trailing carbon base CH2 5 O 4 1 C 3 2 O P –O O Sounds trivial, but…this will beIMPORTANT!! O base CH2 5 O 4 1 2 3 OH 3
Anti-parallel strands • Nucleotides in DNA backbone are bonded from phosphate to sugar between 3 & 5 carbons • DNA molecule has “direction” • complementary strand runs in opposite direction 5 3 3 5
hydrogen bonds covalent phosphodiester bonds Bonding in DNA 5 3 3 5 ….strong or weak bonds? How do the bonds fit the mechanism for copying DNA?
Base pairing in DNA • Purines • adenine (A) • guanine (G) • Pyrimidines • thymine (T) • cytosine (C) • Pairing • A : T • 2 bonds • C : G • 3 bonds
Copying DNA • Replication of DNA • base pairing allows each strand to serve as a template for a new strand • new strand is 1/2 parent template & 1/2 new DNA
Let’s meetthe team… DNA Replication • Large team of enzymes coordinates replication
Replication: 1st step • Unwind DNA • helicase enzyme • unwinds part of DNA helix • stabilized by single-stranded binding proteins helicase single-stranded binding proteins replication fork
Definitions • Template strands: The old strands which are now separated from each other. • New strands: The growing complementary nucleotide sequences that allow for forming the two double helix structures • Note that replication is direction specific.
5 DNA Elongation PO4 • Works only 5’ to 3’ • This means that the 5’ end of the nucleotide links on to the 3’ end of the DNA (or RNA primer) • The NEW strand only grows 5’ to 3’ base CH2 5 O 4 1 C 3 2 O P –O O O base CH2 5 O 4 1 2 3 OH 3
3 3 3 3 3 3 DNA polymerase III 5 5 5 5 5 5 Starting DNA synthesis: RNA primers Limits of DNA polymerase III • can only build onto 3 end of an existing DNA strand growing replication fork primase RNA RNA primer • built by primase • serves as starter sequence for DNA polymerase III
Okazaki ligase 3 3 3 3 3 3 3 5 5 5 5 5 5 5 Leading & Lagging strands Limits of DNA polymerase III • can only build onto 3 end of an existing DNA strand Okazaki fragments Lagging strand growing replication fork Leading strand Lagging strand • Okazaki fragments • joined by ligase • “spot welder” enzyme DNA polymerase III Leading strand • continuous synthesis
direction of replication Replication fork DNA polymerase III lagging strand DNA polymerase I 3’ primase Okazaki fragments 5’ 5’ ligase SSB 3’ 5’ 3’ helicase DNA polymerase III 5’ leading strand 3’ SSB = single-stranded binding proteins
DNA polymerase III 3 3 3 3 3 3 3 3 3 3 3 growing replication fork growing replication fork 5 5 5 5 5 5 5 5 5 5 5 5 5 5 5 5 Replication fork / Replication bubble leading strand lagging strand leading strand lagging strand leading strand lagging strand
Replication: 2nd step • Build daughter DNA strand • add new complementary bases • DNA polymerase III But… We’re missing something! What? Where’s theENERGYfor the bonding! DNA Polymerase III
ligase 3 3 3 3 5 5 5 5 Replacing RNA primers with DNA DNA polymerase I • removes sections of RNA primer and replaces with DNA nucleotides DNA polymerase I growing replication fork RNA But DNA polymerase I still can only build onto 3 end of an existing DNA strand
Fast & accurate! • It takes E. coli <1 hour to copy 5 million base pairs in its single chromosome • divide to form 2 identical daughter cells • Human cell copies its 6 billion bases & divide into daughter cells in only few hours • remarkably accurate • only ~1 error per 100 million bases • ~30 errors per cell cycle
1 2 3 4 What does it really look like?
Energy of Replication Where does energy for bonding usually come from? We comewith our ownenergy! energy YourememberATP!Are there other waysto get energyout of it? energy Are thereother energynucleotides?You bet! And weleave behind anucleotide! CTP ATP TTP GTP AMP ADP GMP TMP CMP modified nucleotide
Energy of Replication • The nucleotides arrive as nucleosides • DNA bases with P–P–P • P-P-P = energy for bonding • DNA bases arrive with their own energy source for bonding • bonded by enzyme: DNA polymerase III ATP GTP TTP CTP
3 5 Replication energy DNA Polymerase III • Adding bases • can only add nucleotides to 3 end of a growing DNA strand • need a “starter” nucleotide to bond to • strand only grows 53 DNA Polymerase III energy DNA Polymerase III energy DNA Polymerase III energy B.Y.O. ENERGY! The energy rulesthe process 3 5
ligase 5 3 5 3 need “primer” bases to add on to energy no energy to bond energy energy energy energy energy energy 3 5 3 5
3 3 3 3 5 5 5 5 Houston, we have a problem! Chromosome erosion All DNA polymerases can only add to 3 end of an existing DNA strand DNA polymerase I growing replication fork DNA polymerase III RNA Loss of bases at 5 endsin every replication • chromosomes get shorter with each replication • limit to number of cell divisions?
3 3 3 3 5 5 5 5 Telomeres Repeating, non-coding sequences at the end of chromosomes = protective cap • limit to ~50 cell divisions growing replication fork telomerase Telomerase • enzyme extends telomeres • can add DNA bases at 5 end • different level of activity in different cells • high in stem cells & cancers -- Why? TTAAGGG TTAAGGG TTAAGGG
Roger Kornberg 2006 Arthur Kornberg 1959 DNA polymerases • DNA polymerase III • 1000 bases/second! • main DNA builder • DNA polymerase I • 20 bases/second • editing, repair & primer removal DNA polymerase III enzyme
Editing & proofreading DNA • 1000 bases/second = lots of typos! • DNA polymerase I • proofreads & corrects typos • repairs mismatched bases • removes abnormal bases • repairs damage throughout life • reduces error rate from 1 in 10,000 to 1 in 100 million bases
Energy of Replication Where does energy for bonding usually come from? We comewith our ownenergy! YourememberATP!Are there other waysto get energyout of it? energy And weleave behind anucleotide! ATP GTP TTP ATP ADP AMP GMP TMP AMP modified nucleotide
3 5 energy Replication DNA Polymerase III • Adding bases • can only add nucleotides to 3 end of the growing DNA strand • need a primer nucleotide to bond to • strand grows 53 B.Y.O. ENERGY! The energy rulesthe process 3 5
5 3 5 3 no energyto bond 3 5 5 3
ligase 5 3 5 3 energy 3 5 3 5
3 3 3 3 5 5 5 5 Houston, we have a problem! Chromosome erosion DNA polymerases can only add to 3 end of an existing DNA strand DNA polymerase I growing replication fork DNA polymerase III Loss of bases at 5 endsin every replication • chromosomes get shorter with each replication • limit to number of cell divisions?
direction of replication Replication fork 3’ 5’ 5’ 3’ 5’ 3’ 5’ 3’
DNA synthesis in prokaryotes • Replication is bidirectional. • Replication is semi-conservative.
Bidirectional replication of a circular chromosome Replication begins at the point of origin (oriC) and proceeds in both directions at the same time.
Unwinding of Parental Strands Topoisomerases:can break phosphodiester bonds and rejoin them relieve the supercoiling of the parental duplex caused by unwinding. DNA gyrase is a major topoisomerase in bacterial cells.