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Replisomes are the protein assemblies that replicate DNA. They function as molecular motors to catalyze template-mediated polymerization of nucleotides, unwinding of DNA, the synthesis of RNA primers, and the assembly of proteins on DNA. The replisome of bacteriophage T7 contains a minimum of proteins, thus facilitating its study. This review describes the molecular motors and coordination of their activities, with emphasis on the T7 replisome. Nucleotide selection, movement of the polymerase, binding of the processivity factor, unwinding of DNA, and RNA primer synthesis all require conformational changes and protein contacts. Lagging-strand synthesis is mediated via a replication loop whose formation and resolution is dictated by switches to yield Okazaki fragments of discrete size. Both strands are synthesized at identical rates, controlled by a molecular brake that halts leading-strand synthesis during primer synthesis. The helicase serves as a reservoir for polymerases that can initiate DNA synthesis at the replication fork. We comment on the differences in other systems where applicable.
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Supplemental Movie 1: Animation of Figure 8. Collision release of the replication loop. In this frame from an animation by Steve Moskowitz at Advanced Medical Graphics, the lagging strand polymerase is in the process of releasing the completed Okazaki fragment as a result of its collision with the 5'-end of the previously synthesized Okazaki fragment.
Download movie file (MOV) Supplemental Movie 2: Animation of Figure 9. Signaling release of the replication loop. In this frame from an animation by Steve Moskowitz at Advanced Medical Graphics, the lagging strand polymerase is in the process of releasing the nascent Okazaki fragment as a result of signaling by the primase upon synthesizing a dinucleotide (circle) at a primase recognition sequence. Download movie file (MOV)