Chromatin structure restricts origin utilization when quiescent cells re-enter the cell cycle

Nucleic Acids Res. 2021 Jan 25;49(2):864-878. doi: 10.1093/nar/gkaa1148.

Abstract

Quiescent cells reside in G0 phase, which is characterized by the absence of cell growth and proliferation. These cells remain viable and re-enter the cell cycle when prompted by appropriate signals. Using a budding yeast model of cellular quiescence, we investigated the program that initiated DNA replication when these G0 cells resumed growth. Quiescent cells contained very low levels of replication initiation factors, and their entry into S phase was delayed until these factors were re-synthesized. A longer S phase in these cells correlated with the activation of fewer origins of replication compared to G1 cells. The chromatin structure around inactive origins in G0 cells showed increased H3 occupancy and decreased nucleosome positioning compared to the same origins in G1 cells, inhibiting the origin binding of the Mcm4 subunit of the MCM licensing factor. Thus, quiescent yeast cells are under-licensed during their re-entry into S phase.

Publication types

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

MeSH terms

  • Cell Cycle / genetics
  • Cell Cycle / physiology*
  • Cell Cycle Checkpoints
  • Chromatin / genetics
  • Chromatin / ultrastructure*
  • Chromatin Assembly and Disassembly
  • Chromatin Immunoprecipitation
  • DNA Replication
  • DNA, Fungal / biosynthesis
  • DNA, Fungal / genetics
  • Minichromosome Maintenance Complex Component 4 / metabolism
  • Nucleosomes / metabolism
  • Nucleosomes / ultrastructure
  • Replication Origin / genetics*
  • Saccharomyces cerevisiae / genetics*
  • Saccharomyces cerevisiae / ultrastructure
  • Saccharomyces cerevisiae Proteins / genetics
  • Saccharomyces cerevisiae Proteins / metabolism

Substances

  • Chromatin
  • DNA, Fungal
  • Nucleosomes
  • Saccharomyces cerevisiae Proteins
  • MCM4 protein, S cerevisiae
  • Minichromosome Maintenance Complex Component 4