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From structure to mechanism-understanding initiation of DNA replication

期刊

GENES & DEVELOPMENT
卷 31, 期 11, 页码 1073-1088

出版社

COLD SPRING HARBOR LAB PRESS, PUBLICATIONS DEPT
DOI: 10.1101/gad.298232.117

关键词

MCM2-7; DNA replication; pre-RC; CMG; replisome; cryo-EM

资金

  1. Biotechnology and Biological Sciences Research Council [BB/M003760/1, BB/N000323/1]
  2. Medical Research Council [MC_U120085811]
  3. Wellcome Trust [107903/Z/15/Z]
  4. Biotechnology and Biological Sciences Research Council [BB/M003760/1, BB/N000323/1] Funding Source: researchfish
  5. Medical Research Council [MC_U120085811, 1583051] Funding Source: researchfish
  6. Wellcome Trust [107903/Z/15/Z] Funding Source: researchfish
  7. Wellcome Trust [107903/Z/15/Z] Funding Source: Wellcome Trust
  8. BBSRC [BB/N000323/1, BB/M003760/1] Funding Source: UKRI
  9. MRC [MC_U120085811] Funding Source: UKRI

向作者/读者索取更多资源

DNAreplication results in the doubling of the genome prior to cell division. This process requires the assembly of 50 or more protein factors into a replication fork. Here, we review recent structural and biochemical insights that start to explain how specific proteins recognize DNA replication origins, load the replicative helicase on DNA, unwind DNA, synthesize newDNAstrands, and reassemble chromatin. We focus on the minichromosome maintenance (MCM2-7) proteins, which form the core of the eukaryotic replication fork, as this complex undergoes major structural rearrangements in order to engage with DNA, regulate its DNA-unwinding activity, and maintain genome stability.

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