1. Announcements 1. First lab report deadline extended by one week: X-linked cross lab report due 11/ 5,6. 2. Bookstore is closed Sundays. Buy your bluebook early. 3. Get lab overview for PCR lab - quiz in lab next week. 4. If your transformation did not work, look at plates in lab refrigerator, both group “A” and “B”; make counts from these plates. Lab assignment due 10/29, 30 (extra week). 5. Group B presentations in lab 10/29, 30 - get sources approved. 6. Problems to look over Ch. 11: 4, 5, 8, 15. Ch. 12: 3, Insights, 1.

2. 3. DNA Replication is Semiconservative Review of Last Lecture 1. Structure of DNA 2. Analytical analysis of nucleic acids

3. Learning check 1. Match the bases with the nucleic acid: UracilRNA ThymineDNA Cytosine Guanine Adenine 2. Match the sugars with the nucleic acid: RiboseDNA 2-deoxyriboseRNA

4. The sequence of the dwarf gene in garden peas is as follows: 5’ - A G C T A C G T -3’ 3’ - T C G A T G C A -5’ Write the RNA sequence transcribed from the top strand of DNA, 5’- 3’. Learning check, revisited

5. Outline of Lecture 21 I. Discussion: Watson and Crick paper II. Bacterial DNA replication III. Many complex issues to resolve during DNA replication - DNA helix must be unwound, RNA primer needed - Synthesis is both continuous and discontinuous - Proofreading is critical IV. Eukaryotic DNA replication is similar, more complex V. The “end” problem and telomerase VI. DNA Recombination

7. I. Bacterial DNA Replication begins at a Single Origin and Proceeds Bidirectionally Origin of Replication

8. DNA Polymerase I can Synthesize DNA Arthur Kornberg et al. (1957) discovered the enzyme from E. coli that could synthesize DNA in vitro (in tube) Requires template DNA strand, primer, MgCl2, and 4 dNTPs Monomers are added 5’ to 3’

9. 5’ to 3’ Addition of Monomers

10. Skepticism regarding pol I as the enzyme that replicates DNA in vivo 1. Pol I slower in vitro than rate of replication observed in vivo 2. Pol I could degrade DNA 3. Pol I replicated ss DNA better than ds DNA 4. A mutant E. coli strain was isolated that had defective pol I activity, but still duplicated DNA and reproduced. - mutant was sensitive to UV light and radiation A second enzyme must exist to replicate DNA Pol I may perform a different function in vivo

11. Bacterial DNA polymerases I, II and III pol I –most abundant (400/cell) and very stable –RNA primer removal, polymerase, exonuclease pol II –unknown abundance –Polymerase, exonuclese, DNA repair? pol III –low abundance (15/cell) –Polymerase, exonuclease, DNA replication Pol III is very complex, many subunits

12. II. Problems of DNA Synthesis Unwinding double-stranded helix Tension must be relieved Priming Antiparallel strands RNA primer removal Backbone joining Proofreading

13. Steps of DNA Synthesis -how “problems” are solved (1)Denaturation and Unwinding (2) Priming and Initiation (3) Continuous and Discontinuous Synthesis - Including Proofreading and Error Correction (4) Removal of Primer (5) Ligation of nicks in backbone

14. Steps of DNA Synthesis: (1)Denaturation and Unwinding of DNA DnaA, DnaB, DnaC proteins are helicases which bind origin and separate strands Single-strand binding protein (SSBP) keeps strands apart DNA gyrase, a type of DNA topoisomerase, cuts to relax supercoiling DnaA DnaB,C

15. (2) Priming and Initiation of Synthesis RNA Primase makes RNA primer on DNA template, does not need free 3’ -OH DNA Polymerase III extends primer with DNA DNA Polymerase I removes RNA primer, replaces with DNA 5’ 3’

16. Directionality of DNA synthesis III

17. Proofreading occurs as polymerase moves along; if incorrect base pairing, base is removed and replaced. STEP 3 3’-5’

18. (3) Continuous and Discontinuous Synthesis Continuous on Leading Strand. Discontinuous on Lagging Strand creates Okazaki fragments. (5) DNA ligase joins nicks in backbone. 53535353 3535 (4) Pol I removes primer

19. Model for DNA replication Action at the Replication Fork: Two Polymerases act as a Dimer

20. III. Multiple Replication Forks During Eukaryotic DNA Synthesis

21. When, during the cell cycle, can new replication origins be formed? G1 S G2 Pre-replicationreplicationpost replication ARSs complexDNA synthesisDNA synthesis Into ORCscompleted Pre-RCs can formNo new pre-RCsNo new pre-RCs ARS = autonomously replicating sequence = origin ORC = origin recognition complex Pre-RC = pre-replication complex

22. Eukaryotic DNA Polymerases EnzymeLocationFunction Pol  (alpha) NucleusDNA replication –includes RNA primase activity, starts DNA strand Pol  (gamma)NucleusDNA replication –replaces Pol  to extend DNA strand, proofreads Pol  (epsilon)NucleusDNA replication –similar to Pol , shown to be required by yeast mutants Pol  (beta)NucleusDNA repair Pol  (zeta)NucleusDNA repair Pol  (gamma)MitochondriaDNA replication

23. IV. The Eukaryotic Problem of Telomere Replication RNA primer near end of chromosome on lagging strand can’t be replaced with DNA since DNA polymerase must add to a primer sequence.

24. Solution to Problem: Telomerase Telomerase enzyme adds TTGGGG repeats to end of lagging strand template. Contains RNA strand that base- pairs with repeat. Forms hairpin turn primer on lagging strand for polymerase to extend from, which is later removed. Age-dependent decline in telomere length in somatic cells, not in stem cells, cancer cells.

25. V. Recombination at the Molecular Level Breakage and joining also directed by enzymes. Homologous recombination occurs during synapsis in meiosis I, general recombination in bacteria, and viral genetic exchange. Molecular mechanism proposed by Holliday and Whitehouse (1964). Depends on complementary base pairing.

26. DNA Recombination (12.20a-f) Heteroduplex DNA Holliday structure Can occur all the way to the end or second pair of nicks can create internal recombinant fragment.

27. DNA Recombination (12-20f-g) EM Evidence for Mechanism

28. DNA Recombination (12.20h-i) Exonuclease nicking Nicks here would create noncrossover duplexes