Two subunits of human ORC are dispensable for DNA replication and proliferation

Elife. 2016 Dec 1:5:e19084. doi: 10.7554/eLife.19084.

Abstract

The six-subunit Origin Recognition Complex (ORC) is believed to be an essential eukaryotic ATPase that binds to origins of replication as a ring-shaped heterohexamer to load MCM2-7 and initiate DNA replication. We have discovered that human cell lines in culture proliferate with intact chromosomal origins of replication after disruption of both alleles of ORC2 or of the ATPase subunit, ORC1. The ORC1 or ORC2-depleted cells replicate with decreased chromatin loading of MCM2-7 and become critically dependent on another ATPase, CDC6, for survival and DNA replication. Thus, either the ORC ring lacking a subunit, even its ATPase subunit, can load enough MCM2-7 in partnership with CDC6 to initiate DNA replication, or cells have an ORC-independent, CDC6-dependent mechanism to load MCM2-7 on origins of replication.

Keywords: CDC6; DNA replication; ORC; cell biology; human.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Cell Cycle Proteins
  • Cell Line
  • DNA / metabolism
  • DNA Replication*
  • Humans
  • Minichromosome Maintenance Proteins / metabolism
  • Nuclear Proteins
  • Origin Recognition Complex / genetics
  • Origin Recognition Complex / metabolism*
  • Protein Binding
  • Replication Origin*

Substances

  • CDC6 protein, human
  • Cell Cycle Proteins
  • Nuclear Proteins
  • ORC1 protein, human
  • ORC2 protein, human
  • Origin Recognition Complex
  • DNA
  • Minichromosome Maintenance Proteins