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The lagging strand is the strand of new DNA whose direction of synthesis is opposite to the direction of the growing replication fork. Because of its orientation, replication of the lagging strand is more complicated as compared to that of the leading strand.
This asymmetry is due to the formation of the replication fork and its division into nascent leading and lagging strands. The leading strand is synthesized continuously and in juxtapose to the leading strand; the lagging strand is replicated through short fragments of polynucleotide (Okazaki fragments) in a 5' to 3' direction. [6]
After around 20 nucleotides, elongation is taken over by Pol ε on the leading strand and Pol δ on the lagging strand. [103] Polymerase δ (Pol δ): Highly processive and has proofreading, 3'->5' exonuclease activity. In vivo, it is the main polymerase involved in both lagging strand and leading strand synthesis. [104]
Lagging strands, in contrast, are synthesized discontinuously: primers are placed on the template every ~200 nucleotides and extended to form short Okazaki fragments. For simplicity, this diagram does not show the replacement of primers with DNA or the synthesis of telomeres at the chromosome ends.
The lagging strand moves away from the replication fork in the 3' to 5' direction and consists of small fragments called Okazaki fragments. DNA polymerase makes the lagging strand by using a new RNA primer for each Okazaki fragment it encounters. Overall, the leading strand only uses one RNA primer, while the lagging strand uses a new RNA ...
The dimerisation of the replicative polymerases solves the problems related to efficient synchronisation of leading and lagging strand synthesis at the replication fork, but the tight spatial-structural coupling of the replicative polymerases, while solving the difficult issue of synchronisation, creates another challenge: dimerisation of the ...
The leading strand is continuously synthesized and is elongated during this process to expose the template that is used for the lagging strand (Okazaki fragments). During the process of DNA replication, DNA and RNA primers are removed from the lagging strand of DNA to allow Okazaki fragments to bind to.
1 γ unit (also dnaX) which acts as a clamp loader for the lagging strand Okazaki fragments, helping the two β subunits to form a unit and bind to DNA. The γ unit is made up of 5 γ subunits which include 3 γ subunits, 1 δ subunit , and 1 δ' subunit . The δ is involved in copying of the lagging strand.