Human ANKLE1 Is a Nuclease Specific for Branched DNA

J Mol Biol. 2020 Oct 2;432(21):5825-5834. doi: 10.1016/j.jmb.2020.08.022. Epub 2020 Aug 28.

Abstract

All physical connections between sister chromatids must be broken before cells can divide, and eukaryotic cells have evolved multiple ways in which to process branchpoints connecting DNA molecules separated both spatially and temporally. A single DNA link between chromatids has the potential to disrupt cell cycle progression and genome integrity, so it is highly likely that cells require a nuclease that can process remaining unresolved and hemi-resolved DNA junctions and other branched species at the very late stages of mitosis. We argue that ANKLE1 probably serves this function in human cells (LEM-3 in Caenorhabditis elegans). LEM-3 has previously been shown to be located at the cell mid-body, and we show here that human ANKLE1 is a nuclease that cleaves a range of branched DNA species. It thus has the substrate selectivity consistent with an enzyme required to process a variety of unresolved and hemi-resolved branchpoints in DNA. Our results suggest that ANKLE1 acts as a catch-all enzyme of last resort that allows faithful chromosome segregation and cell division to occur.

Keywords: LEM-3; chromosome segregation; helical junction resolution; ultrafine DNA bridges.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Cycle
  • Cell Line
  • Chromosome Segregation
  • DNA / chemistry
  • DNA / metabolism*
  • Endonucleases / analysis
  • Endonucleases / metabolism*
  • Humans
  • Insecta
  • Nucleic Acid Conformation

Substances

  • DNA
  • ANKLE1 protein, human
  • Endonucleases