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Published byCornelius Ethan Pope Modified over 8 years ago
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Learning objective SWBAT: Create a model that represents how genetic information is copied for transmission between generations and how that information is translated into poly peptides
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Central Dogma = the flow of genetic material from DNA to protein
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DNA Replication DNA replication is semiconservative. This means that, after replication, each daughter cell has one old DNA strand and one that is newly synthesized.
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If each of the 2 antiparallel strands can act as a template, they must first be separated from one another. Replication begins at sites along the DNA called origins of replication.
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The process of replication requires numerous enzymes and proteins. The double helix is untwisted and the two strands separated by helicase. This creates a replication bubble.
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Bacteria have circular DNA and a single replication bubble. Eukaryotic linear chromosomes may have 100’s or even 1000’s of these bubbles.
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At each end of the bubble is a Y-shaped region where the parent strands are being unwound by helicase called a replication fork. Single strand binding proteins then attach to the strands to prevent them from re-linking.
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As the helix unwinds, tension is created as the strands on either end of the replication forks are wound tighter. Topoisomerase relieves the tension by breaking, swiveling, and re joining the DNA. Topo = place Isomer = same composition, different structure or arrangement Ase = ENZYME
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Figure 13.12 Single-strand binding proteins Helicase Topoisomerase Primase Replication fork 5 5 5 3 3 3 RNA primer
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DNA polymerases then catalyze the elongation of the the new DNA at the replication forks by adding nucleotides matching A to T and G to C, but... 1. They can only add nucleotides; they cannot start the process. 2. They can only add to the 3´end of a growing chain, i.e. they work in a 5´to 3´direction.
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The initial nucleotide chain is actually RNA and is synthesized by RNA primase.
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Figure 13.12 Single-strand binding proteins Helicase Topoisomerase Primase Replication fork 5 5 5 3 3 3 RNA primer
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Let’s see what this looks like with a model. Please take: 2 green strands 2 white strands 1 burgundy strand Dry erase board Dry erase markers Tape – to be shared Scissors- to be shared
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Proofreading and Repair DNA ligase connects Okazaki fragments Other enzymes correct incorrectly matched nucleotides.
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While not part of this PowerPoint, you must understand: Leading vs. lagging strands Okazaki fragments
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Learning objective SWBAT: Create a model that represents how genetic information is copied for transmission between generations and how that information is translated into poly peptides
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