Overview (from http://www.teacherweb.com/CA/NogalesHighSchool/mespinoza/h4.aspx) |
ACT 1: Initiation
- Single-strand binding proteins enter to stabilize the template strands, keeping them apart during replication.
- Helicases unwind the template DNA strands. They keep working at the replication fork to continuously open up the bubbles.
- To release the tension, as the bubbles opening up, gyrases cut the DNA, afterwards, put it back.
ACT 2: Elongation
- RNA primase enzymes begin the process by building a small complementary RNA segment called RNA primers to the origin of the strand, therefore, DNA polymerase III can add DNA nucleotides to the RNA primer.
- Nucleotides on the daughter strand can only elongate in 5' to 3' direction. This strand is called leading strand.
- On the opposite strand, which is called lagging strand, DNA polymerase III is moving away from the replication fork.
- On lagging strand, okazaki fragments are formed with series of RNA primers and short DNA fragments added by DNA polymerase III.
ACT 3: Termination
- DNA polymerase I enter. They remove the RNA nucleotides at the primers with DNA nucleotides.
- DNA ligase catalyzes the reaction of forming bonds between short DNA strands on the lagging strand.
- DNA polymerase I proofread the daughter DNA.
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