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Published byShawn Gallagher Modified over 9 years ago
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Who are these two famous characters of science?
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Mendel (1865): Inheritance
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T.H. Morgan (1910): genes linked on chromosomes Chromosomes are made of DNA and proteins DNA and proteins are the two candidates for the genetic material
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Griffith(1928): bacterial work- streptococcus pneumoniae Transformation: change in genotype and phenotype due to assimilation of external substance (DNA) by a cell
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Avery and team(MacLeod and McCarty)(1944): transformation agent was DNA
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Hershey and Chase(1952): determine that DNA is the hereditary material and not proteins:
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Chargaff(1950): found “peculiar regularity” in the ratios of nucleotide bases within a single species: A = 30.3% T = 30.3% C= 19.9% G = 19.5% Chargaff rules: A= T, C= G
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Watson & Crick(Wilkins, Franklin)(1953): The Double Helix
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Basic Unit of Nucleic Acids = nucleotide Sugar/ phosphate backbone Nitrogen base
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5 carbon sugar = ribose Phosphate group Phosphodiester bond
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In DNA there are four(make up the interior of the molecule): Adenine Thymine Cytosine Guanine Two groups: Purines: double ringed structures Adenine and Guanine Pyrimidines: single ringed structures Thymine and Cytosine
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5’ to 3’ 5’ with the phosphate group 3’ with the –OH group
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Inward facing nitrogen base will pair with their complementary base A will pair with T (two H- bonds) G will pair with G (three H- bonds) A double ringed structure will always pair with a single ringed structure to maintain width.
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DNA strands are oriented in the opposite directions
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Van der Waals attractions play a role in holding the DNA molecule together
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Proposed the semiconservative model of DNA replication:
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DNA polymerase Helicase Primase DNA ligase Topoisomerase
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Sites where DNA replication begins Prokaryotes: one origin Replication proceeds in two directions Humans: hundreds maybe thousands of origins Replication proceeds in two directions
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Replication bubble: unwinding and separation of the DNA strand Replication fork: Y- shaped region at each end of the bubble
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1. 2. 3. 4. ?’?’?’?’ ?’?’?’?’ ?’?’?’?’ ?’?’?’?’ 5.
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Elongation catalyzed by DNA polymerase E. coli bacteria adds nucleotides at a rate of 500/sec Humans add nucleotides at a rate of 50/sec Nucleoside triphosphate:
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Antiparallel elonagation: 5’ – 3’ direction Leading strand Lagging strand Okazaki fragments E. coli fragments: 1000- 2000 nucleotides Human fragments: 100 -200
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Meselson & Stahl replication semiconservative; Expt: varying densities of radioactive nitrogen
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Briefly describe the role of the following enzymes involved in DNA replication: DNA polymerase I DNA polymerase III Helicase DNA ligase Topoisomerase Primase
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1. 2. 3. 4. ?’?’?’?’ ?’?’?’?’ ?’?’?’?’ ?’?’?’?’ 5.
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How many primers are needed for the leading strand? How many primers are needed for the lagging strand?
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DNA replication ensures continuity of hereditary information:
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1. Enzymes of DNA replication work as part of a large complex: 2. Replication process is probably a stationary process DNA polymerase “reels- in” the parent DNA Lagging strand may may be looped
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Pairing errors occur at the rate of 1 out of every 100, 000 base pairs DNA polymerase proof reads each nucleotide Incorrectly paired nucleotides are immediately removed and replaced
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Mismatch pair: Repaired by the action of nuclease(one of many different DNA repair enzymes) Removes nucleotides damaged by chemicals or the environment
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Telomeres= nucleotide sequences at the ends of the DNA molecule Contain a repeated unit TTAGGG Do not contain genes No nucleotides added Protects the molecule from the replication process Triggers apoptosis May contribute to the aging process
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Catalyzes the lengthening of the telomeres in eukaryotic germ cells
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