Figure 1.
Inactive double hexamers of the replicative helicase core Mcm2–7 are loaded onto origins at the end of mitosis/G1 phase (origin licensing). Origins are activated during S phase with the assembly of the active replicative helicase, also known as CMG (Cdc45-Mcm2–7-GINS), which involves the recruitment of GINS and Cdc45 to the Mcm2–7 complex. While double hexamers of Mcm2–7 encircle dsDNA, CMGs encircle ssDNA and translocate in an ‘N-terminus first' direction thus passing each other within the origin (origin firing). Replisomes are built around CMGs and they progress through the chromatin unwinding DNA and promoting DNA synthesis in a semi-discontinuous way (elongation). Replication forks from neighbouring origins finally converge, leading to complete replication of sister chromatids (termination).
Simplified model of eukaryotic DNA replication.

Inactive double hexamers of the replicative helicase core Mcm2–7 are loaded onto origins at the end of mitosis/G1 phase (origin licensing). Origins are activated during S phase with the assembly of the active replicative helicase, also known as CMG (Cdc45-Mcm2–7-GINS), which involves the recruitment of GINS and Cdc45 to the Mcm2–7 complex. While double hexamers of Mcm2–7 encircle dsDNA, CMGs encircle ssDNA and translocate in an ‘N-terminus first' direction thus passing each other within the origin (origin firing). Replisomes are built around CMGs and they progress through the chromatin unwinding DNA and promoting DNA synthesis in a semi-discontinuous way (elongation). Replication forks from neighbouring origins finally converge, leading to complete replication of sister chromatids (termination).

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