Mcm10 and And-1/CTF4 recruit DNA polymerase α to chromatin for initiation of DNA replication

By Wenge Zhu, C. Ukomadu, S. Jha, T. Senga, S. Dhar, J. Wohlschlegel, L. Nutt, S. Kornbluth, Anindya Dutta. 2007

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The MCM2-7 helicase complex is loaded on DNA replication origins during the G1 phase of the cell cycle to license the origins for replication in S phase. How the initiator primase–polymerase complex, DNA polymerase (pol ), is brought to the origins is still unclear. We show that And-1/Ctf4 (Chromosome transmission fidelity 4) interacts with Mcm10, which associates with MCM2-7, and with the p180 subunit of DNA pol . And-1 is essential for DNA synthesis and the stability of p180 in mammalian cells. In Xenopus egg extracts And-1 is loaded on the chromatin after Mcm10, concurrently with DNA pol , and is required for efficient DNA synthesis. Mcm10 is required for chromatin loading of And-1 and an antibody that disrupts the Mcm10–And-1 interaction interferes with the loading of And-1 and of pol , inhibiting DNA synthesis. And-1/Ctf4 is therefore a new replication initiation factor that brings together the MCM2-7 helicase and the DNA pol –primase complex, analogous to the linker between helicase and primase or helicase and polymerase that is seen in the bacterial replication machinery. The discovery also adds to the connection between replication initiation and sister chromatid cohesion.

Subfields: Cancer Research, Molecular Biology

View Paper: https://www.semanticscholar.org/paper/de77a2d310223a9f9fefca593f36a9f7e709d8b0