Initiation of DNA replication requires actin dynamics and formin activity

EMBO J. 2017 Nov 2;36(21):3212-3231. doi: 10.15252/embj.201796585. Epub 2017 Oct 5.

Abstract

Nuclear actin regulates transcriptional programmes in a manner dependent on its levels and polymerisation state. This dynamics is determined by the balance of nucleocytoplasmic shuttling, formin- and redox-dependent filament polymerisation. Here, using Xenopus egg extracts and human somatic cells, we show that actin dynamics and formins are essential for DNA replication. In proliferating cells, formin inhibition abolishes nuclear transport and initiation of DNA replication, as well as general transcription. In replicating nuclei from transcriptionally silent Xenopus egg extracts, we identified numerous actin regulators, and disruption of actin dynamics abrogates nuclear transport, preventing NLS (nuclear localisation signal)-cargo release from RanGTP-importin complexes. Nuclear formin activity is further required to promote loading of cyclin-dependent kinase (CDK) and proliferating cell nuclear antigen (PCNA) onto chromatin, as well as initiation and elongation of DNA replication. Therefore, actin dynamics and formins control DNA replication by multiple direct and indirect mechanisms.

Keywords: DNA replication; actin; cyclin‐dependent kinase; formin; nuclear transport.

MeSH terms

  • Actins / genetics*
  • Actins / metabolism
  • Active Transport, Cell Nucleus / genetics
  • Animals
  • Cell Line, Tumor
  • Cell Nucleus / metabolism
  • Chromatin / chemistry
  • Chromatin / metabolism*
  • Complex Mixtures / chemistry
  • Cytoplasm / metabolism
  • DNA Replication*
  • Epithelial Cells / cytology
  • Epithelial Cells / metabolism
  • Fetal Proteins / genetics*
  • Fetal Proteins / metabolism
  • Formins
  • Gene Expression Regulation
  • HeLa Cells
  • Humans
  • Karyopherins / genetics
  • Karyopherins / metabolism
  • Microfilament Proteins / genetics*
  • Microfilament Proteins / metabolism
  • Nuclear Localization Signals
  • Nuclear Proteins / genetics*
  • Nuclear Proteins / metabolism
  • Proliferating Cell Nuclear Antigen / genetics
  • Proliferating Cell Nuclear Antigen / metabolism
  • Signal Transduction
  • Transcription, Genetic*
  • Xenopus laevis
  • Zygote / chemistry
  • ran GTP-Binding Protein / genetics
  • ran GTP-Binding Protein / metabolism

Substances

  • Actins
  • Chromatin
  • Complex Mixtures
  • Fetal Proteins
  • Formins
  • Karyopherins
  • Microfilament Proteins
  • Nuclear Localization Signals
  • Nuclear Proteins
  • Proliferating Cell Nuclear Antigen
  • ran GTP-Binding Protein