MCMBP promotes the assembly of the MCM2-7 hetero-hexamer to ensure robust DNA replication in human cells

Elife. 2022 Apr 19:11:e77393. doi: 10.7554/eLife.77393.

Abstract

The MCM2-7 hetero-hexamer is the replicative DNA helicase that plays a central role in eukaryotic DNA replication. In proliferating cells, the expression level of the MCM2-7 hexamer is kept high, which safeguards the integrity of the genome. However, how the MCM2-7 hexamer is assembled in living cells remains unknown. Here, we revealed that the MCM-binding protein (MCMBP) plays a critical role in the assembly of this hexamer in human cells. MCMBP associates with MCM3 which is essential for maintaining the level of the MCM2-7 hexamer. Acute depletion of MCMBP demonstrated that it contributes to MCM2-7 assembly using nascent MCM3. Cells depleted of MCMBP gradually ceased to proliferate because of reduced replication licensing. Under this condition, p53-positive cells exhibited arrest in the G1 phase, whereas p53-null cells entered the S phase and lost their viability because of the accumulation of DNA damage, suggesting that MCMBP is a potential target for killing p53-deficient cancers.

Keywords: DNA replication; MCM2–7; MCMBP; cell biology; chromosomes; gene expression; genome instability; human; protein complex assembly.

MeSH terms

  • Adaptor Proteins, Signal Transducing / metabolism
  • Carrier Proteins* / metabolism
  • Cell Cycle Proteins / metabolism
  • DNA Damage
  • DNA Replication
  • Humans
  • Minichromosome Maintenance Complex Component 2 / genetics
  • Minichromosome Maintenance Complex Component 2 / metabolism
  • Minichromosome Maintenance Proteins / metabolism
  • Nuclear Proteins / metabolism
  • Tumor Suppressor Protein p53* / genetics

Substances

  • Adaptor Proteins, Signal Transducing
  • Carrier Proteins
  • Cell Cycle Proteins
  • MCMBP protein, human
  • Nuclear Proteins
  • Tumor Suppressor Protein p53
  • MCM2 protein, human
  • Minichromosome Maintenance Complex Component 2
  • Minichromosome Maintenance Proteins

Grants and funding

The funders had no role in study design, data collection, and interpretation, or the decision to submit the work for publication.