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DNA and DNA Replication Chapter 12 – Part 1 CP Biology Paul VI Catholic High School
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12-1 DNA I.HISTORICAL BACKGROUND 1. Hammerling Experiment: Joachim Hammerling 1930’s Acetabularia mediterranea Acetabularia crenulata Hammerling Experiment video clip
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12-1 DNA
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2. Frederick Griffith (1928) Streptococcus pneumonia Smooth-pathogenic Rough-non-pathogenic Transforming Factor I.Historical Background: 12-1 DNA Griffith experiment video clip
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12-1 DNA
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I.HISTORICAL BACKGROUND: 3. Oswald Avery (1944): Revisited Griffith’s experiment Utilized “digesting” enzymes Localized “Transforming Factor” to DNA 12-1 DNA
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Oswald Avery 1944 12-1 DNA
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I. Historical Background: 4. Hershey-Chase (1952) Utilized T 2 Bacteriophages DNA containing viruses Used radioisotopes 32 P and 35 S Corroborated work of Avery 12-1 DNA Hershey-Chase experiment video clip
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Alfred Hershey Martha Chase 12-1 DNA
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T 2 Bacteriophage 12-1 DNA
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Phoebus Levene 12-1 DNA
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II. Chemistry of DNA: 1. Phoebus Levene (1920’s) a. DNA composed of: PO 4 5 Carbon Sugar (deoxyribose) Nitrogen containing base Purine (adenine, guanine) “double ringed” base Pyrimidine (cytosine, thymine) “single-ringed” base 12-1 DNA
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adenine guanine cytosinethymine 12-1 DNA
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Nucleotide 12-1 DNA
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Phosphodiester Bond 12-1 DNA
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II. Chemistry of DNA: 1. Phoebus Levene: b. NUCLEOTIDES are the monomers of the DNA molecule c. DNA has intrinsic directionality One end ALWAYS has 5’PO 4 One end ALWAYS has 3’OH 12-1 DNA
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Erwin Chargaff 12-1 DNA
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II. Chemistry of DNA: 2. Erwin Chargaff CHARGAFF’S RULE: Amount of adenine is ALWAYS equal to amount of thymine Amount of cytosine is ALWAYS equal to amount of guanine 12-1 DNA Short HHMI video clip
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Chargaff’s Rule 12-1 DNA
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III. Structure of DNA: A. Contribution of 1. James Watson & Francis Crick 2. Maurice Wilkins 3. Rosalind Franklin B. Double Helix Model 1. Antiparallel Strands 2. Complementarity of bases 3. 10 bp per turn of helix 12-1 DNA
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James Watson Francis Crick 12-1 DNA Secrets of the Sequence video clip
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Rosalind Franklin Maurice Wilkins 12-1 DNA
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Diffraction Study 1952 Diffraction Study 1953 12-1 DNA
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X-Ray study DNA 1953 12-1 DNA
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DOUBLE HELIX 12-1 DNA
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10 bp per turn 3.4 nm per turn 3.4Å between bp 1Å = 0.1nm (1X10 -10 m) 12-1 DNA
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Antiparallel arrangement of helices 12-1 DNA
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Complement Base Pairing A pairs with T G pairs with C 12-1 DNA
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12- 2 DNA Replication
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IV. Replication Process Summary: A. Opening the Double Helix B. Building the Primer C. Assembling Complementary Strands D. Removing the Primer E. Joining of Okazaki Fragments 12- 2 DNA Replication Video and DNA Replication Worksheet
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IV. Replication Process: A. Opening the Double Helix: 1. Initiating Replication Replication origin 2. Unwinding the Duplex Helicase 3. Stabilizing Complementary Strand Single Strand Binding Protein 4. Relieving the torque Topoisomerase (“swivelase”) 12- 2 DNA Replication
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Helicase unwinds the double strand 12- 2 DNA Replication
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Topoisomerase I and II Topoisomerase I and II video
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Topoisomerases relieve the torque generated by the unwinding of the helix 12- 2 DNA Replication
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Direction of synthesis Building the primer 12- 2 DNA Replication
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RNA Polymerase (Primase) 12- 2 DNA Replication
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B. Building the Primer: RNA Polymerase (Primase) “Primasome” C. Assembling the Complementary Strands DNA Polymerase III D. Removing the Primer DNA Polymerase II (Rnase H) E. Joining Okazaki Fragments DNA Ligase 12- 2 DNA Replication
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Removal of RNA primer By RNAse H 12- 2 DNA Replication
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Synthesis of Lagging Strand 12- 2 DNA Replication
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Part 1 – DNA’s Discovery video clip DNA – The Secret of Photo 51 (NOVA video 55 min)
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