BIOSC 0160 Lecture Notes - Lecture 3: Dna Clamp, Okazaki Fragments, Dna Mismatch Repair
Document Summary
Enzyme dna helicase uses e from atp hydrolysis to unwind and separate the strands and single-strand binding proteins bind to the unwound strands to keep them from reassociating into a double helix. Two template strands available for complementary base pairing. The two dna strands grow differently at the replication fork. The dna at the replication for opens up like a zipper in one direction. The 3" end template strand(leading strand) is able to have a 5" strand synthesized continuously. The 5" template strand (lagging strand) end synthesizes backwards, but the new strand can only synthesize to the point where the zipper closes again so it forms in okazaki fragments. Synthesis of the lagging strand requires the synthesis of relatively small, discontinuous stretches of dna (100-200 nucleotides in eukaryotes, 1000-2000 nucleotides in prokaryotes. Leading strand only needs one primer, but each okazaki fragment requires its own primer to be synthesized by the primase.