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Gartner, Anton
DNA Damage Response and Genetic Toxicology
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Human ANKLE1 Is a Nuclease Specific for Branched DNA

Author(s)
Song, JunfangFreeman, Alasdair D. J.Knebel, AxelGartner, AntonLilley, David M. J.
Issued Date
2020-10
DOI
10.1016/j.jmb.2020.08.022
URI
https://scholarworks.unist.ac.kr/handle/201301/49114
Fulltext
https://www.sciencedirect.com/science/article/pii/S0022283620305167
Citation
JOURNAL OF MOLECULAR BIOLOGY, v.432, no.21, pp.5825 - 5834
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. (C) 2020 The Author(s). Published by Elsevier Ltd.
Publisher
ACADEMIC PRESS LTD- ELSEVIER SCIENCE LTD
ISSN
0022-2836
Keyword (Author)
chromosome segregationhelical junction resolutionultrafine DNA bridgesLEM-3
Keyword
HUMAN GEN1MUS81-EME1SLX1-SLX4REPAIRRESOLVASESLX4HOLLIDAY JUNCTION RESOLUTION

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