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GartnerAnton

Gartner, Anton
DNA Damage Response and Genetic Toxicology
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The Last Chance Saloon

Author(s)
Hong, YeZhang, HongtaoGartner, Anton
Issued Date
2021-05
DOI
10.3389/fcell.2021.671297
URI
https://scholarworks.unist.ac.kr/handle/201301/55681
Citation
FRONTIERS IN CELL AND DEVELOPMENTAL BIOLOGY, v.9, pp.671297
Abstract
Accurate chromosome segregation requires the removal of all chromatin bridges, which link chromosomes before cell division. When chromatin bridges fail to be removed, cell cycle progression may halt, or cytokinesis failure and ensuing polyploidization may occur. Conversely, the inappropriate severing of chromatin bridges leads to chromosome fragmentation, excessive genome instability at breakpoints, micronucleus formation, and chromothripsis. In this mini-review, we first describe the origins of chromatin bridges, the toxic processing of chromatin bridges by mechanical force, and the TREX1 exonuclease. We then focus on the abscission checkpoint (NoCut) which can confer a transient delay in cytokinesis progression to facilitate bridge resolution. Finally, we describe a recently identified mechanism uncovered in C. elegans where the conserved midbody associated endonuclease LEM-3/ANKLE1 is able to resolve chromatin bridges generated by various perturbations of DNA metabolism at the final stage of cell division. We also discuss how LEM-3 dependent chromatin bridge resolution may be coordinated with abscission checkpoint (NoCut) to achieve an error-free cleavage, therefore acting as a "last chance saloon" to facilitate genome integrity and organismal survival.
Publisher
Frontiers Media S.A.
ISSN
2296-634X
Keyword (Author)
abscission checkpointANKLE1chromatin bridgechromothripsisLEM-3 endonucleasemicronucleiNoCut pathwayTREX1

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