Human ANKLE1 Is a Nuclease Specific for Branched DNA.

J Mol Biol

Cancer Research UK Nucleic Acid Structure Research Group, MSI/WTB Complex, University of Dundee, Dow Street, Dundee DD1 5EH, UK. Electronic address:

Published: October 2020

AI Article Synopsis

  • Cells must break physical connections between sister chromatids before dividing to ensure proper cell cycle progression and maintain genome integrity.
  • Eukaryotic cells use specific nucleases, like ANKLE1 in humans and LEM-3 in C. elegans, to resolve remaining DNA junctions at the end of mitosis.
  • ANKLE1 functions as a crucial enzyme that cleaves various branched DNA structures, ensuring accurate chromosome separation and successful cell division.

Article 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.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7610144PMC
http://dx.doi.org/10.1016/j.jmb.2020.08.022DOI Listing

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