The proteasome controls ESCRT-III-mediated cell division in an archaeon

Science. 2020 Aug 7;369(6504):eaaz2532. doi: 10.1126/science.aaz2532.

Abstract

Sulfolobus acidocaldarius is the closest experimentally tractable archaeal relative of eukaryotes and, despite lacking obvious cyclin-dependent kinase and cyclin homologs, has an ordered eukaryote-like cell cycle with distinct phases of DNA replication and division. Here, in exploring the mechanism of cell division in S. acidocaldarius, we identify a role for the archaeal proteasome in regulating the transition from the end of one cell cycle to the beginning of the next. Further, we identify the archaeal ESCRT-III homolog, CdvB, as a key target of the proteasome and show that its degradation triggers division by allowing constriction of the CdvB1:CdvB2 ESCRT-III division ring. These findings offer a minimal mechanism for ESCRT-III-mediated membrane remodeling and point to a conserved role for the proteasome in eukaryotic and archaeal cell cycle control.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Archaeal Proteins / chemistry
  • Archaeal Proteins / physiology*
  • Bortezomib / chemistry
  • Bortezomib / pharmacology
  • Cell Division*
  • Endosomal Sorting Complexes Required for Transport / chemistry
  • Endosomal Sorting Complexes Required for Transport / physiology*
  • Models, Molecular
  • Proteasome Endopeptidase Complex / chemistry
  • Proteasome Endopeptidase Complex / physiology*
  • Proteasome Inhibitors / chemistry
  • Proteasome Inhibitors / pharmacology
  • Proteolysis
  • Sulfolobus acidocaldarius / cytology*
  • Sulfolobus acidocaldarius / drug effects
  • Sulfolobus acidocaldarius / enzymology

Substances

  • Archaeal Proteins
  • Endosomal Sorting Complexes Required for Transport
  • Proteasome Inhibitors
  • Bortezomib
  • Proteasome Endopeptidase Complex