4.8 Article

Structural mechanism of helicase loading onto replication origin DNA by ORC-Cdc6

Publisher

NATL ACAD SCIENCES
DOI: 10.1073/pnas.2006231117

Keywords

DNA replication; cryo-EM; Mcm2-7 helicase; ATPase; origin recognition complex

Funding

  1. Biotechnology and Biological Sciences Research Council [BB/S001387/1, BB/N000323/1]
  2. Wellcome Trust [107903/Z/15/Z]
  3. National Institutes of Health (NIH) [GM110387, GM45436, GM131754]
  4. DFG Research Fellowship [SCHN 1524/1-1]
  5. National Science Foundation XSEDE program [CHE110042]
  6. DOE Office of Science User Facility [DE-AC05-00OR22725]
  7. BBSRC [BB/N000323/1, BB/S001387/1] Funding Source: UKRI
  8. Wellcome Trust [107903/Z/15/Z] Funding Source: Wellcome Trust

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DNA replication origins serve as sites of replicative helicase loading. In all eukaryotes, the six-subunit origin recognition com-plex (Orc1-6; ORC) recognizes the replication origin. During late M-phase of the cell-cycle, Cdc6 binds to ORC and the ORC-Cdc6 complex loads in a multistep reaction and, with the help of Cdt1, the core Mcm2-7 helicase onto DNA. A key intermediate is the ORC-Cdc6-Cdt1-Mcm2-7 (OCCM) complex in which DNA has been already inserted into the central channel of Mcm2-7. Until now, it has been unclear how the origin DNA is guided by ORC-Cdc6 and inserted into the Mcm2-7 hexamer. Here, we truncated the C-terminal winged-helix-domain (WHD) of Mcm6 to slow down the loading reaction, thereby capturing two loading intermediates prior to DNA insertion in budding yeast. In semi-attached OCCM, the Mcm3 and Mcm7 WHDs latch onto ORC-Cdc6 while the main body of the Mcm2-7 hexamer is not connected. In pre-insertion OCCM, the main body of Mcm2-7 docks onto ORC-Cdc6, and the origin DNA is bent and positioned adjacent to the open DNA entry gate, poised for insertion, at the Mcm2-Mcm5 interface. We used molecular simulations to reveal the dynamic transition from pre -loading conformers to the loaded conformers in which the loading of Mcm2-7 on DNA is complete and the DNA entry gate is fully closed. Our work provides multiple molecular insights into a key event of eukaryotic DNA replication.

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