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2.7/7.1 Replication
Question | Answer |
---|---|
cell cycle phase of DNA replication | S phase |
Meselson and Stahl | showed DNA replication is semiconservative by tracking heavy and normal nitrogen isotopes during replication |
phrase used to describe DNA replication | semiconservative |
describe semiconservative | strands unwind and new nucleotides are added this means the new DNA has one old strand and one new strand |
origin of replication in eukaryotes | 1000s bubbles/all eventually meet |
origin of replication in prokaryotes | 1 bubble/replication in both directions |
direction of DNA replication | 5' to 3' on the leading strand and 3' to 5' on the lagging strand |
process of DNA replication pt. 1 | -DNA helicase breaks hydrogen bonds at origins of replication -single strand binding proteins prevent strands from rewinding -replication bubble is created with 2 replication forks |
PCR's purpose | useful when a larger amount of DNA is needed ex. crime scenes |
step by step process of PCR | denaturation: heat DNA sample to separate it, annealing: DNA primers attach to opposite ends, elongation: DNA Taq polymerase copies the strands |
DNA helicase | unwinds DNA by breaking hydrogen bonds |
primerase | creates RNA primer |
DNA polymerase III | adds DNA nucleotides in the 5'to 3' direction |
DNA polymerase I | replaces RNA primers with DNA |
DNA ligase | links all DNA nucleotides |
DNA gyrase | straightens the strand after it's unwound |
single strand binding proteins | prevent DNA strands from unwinding |
Okazaki fragments | short 5' to 3' segments of DNA that are added by DNA polymerase III |
leading vs. lagging strands | the leading strand is 5' to 3' while the lagging is 3' to 5'. Leading strand is continuous while the lagging is discontinuous. Leading has a single primer while lagging has multiple primers. |
process of DNA replication pt. 2 | -primerase creates RNA primer -DNA polymerase III adds complementary DNA nucleotides in 5' to 3' |
process of DNA replication pt. 3 | -leading strand adds DNA nucleotides continously in 5' to 3' direction -lagging strand uses okazaki fragments after which DNA polymerase I replaces RNA primer with DNA and DNA ligase links them |