Lagging Strand Synthesis and Genomic Stability

Abstract

In eukaryotic cells, DNA replication starts at many origins in each chromosome during S phase of cell cycle. Each origin is activated at different time points in S phase, which takes place once and only once per cell cycle. In yeast and most likely higher eukaryotes, the origin-recognition complex (ORC) and several other initiation factors play a pivotal role in activation and regulation of replication origins. Briefly, the ORC-bound origins are sequentially activated and deactivated along the progression of cell cycle. The prereplicative complex (pre-RC) is formed by loading the replicative helicase MCM complex onto the ORC-bound origins with the aid of Cdc6 and Cdt1. This complex is activated by S-phase cyclin dependent kinases (Cdks) when cells enter S phase. The elevated levels of Cdk activities lead to removal of some initiation proteins such as Cdc6 by proteolysis, allowing the pre-RC to be further activated for subsequent DNA synthesis. The irreversible removal of initiation factors is a major mechanism to ensure DNA to be replicated once and only once per cell cycle. The assembly of replication initiation complex and its activation are well reviewed in many literatures (Sclafani & Holzen, 2007; Remus & Diffley, 2009; Araki, 2010). Activation of origins leads to the establishment of bidirectional replication forks for the DNA synthesis of leading and lagging strands.