The Last Chance Saloon

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 severin...

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Main Authors: Ye Hong, Hongtao Zhang, Anton Gartner
Format: Article
Language:English
Published: Frontiers Media S.A. 2021-05-01
Series:Frontiers in Cell and Developmental Biology
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fcell.2021.671297/full
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spelling doaj-5308c14ff6254ad59216ad35003698332021-05-14T04:29:31ZengFrontiers Media S.A.Frontiers in Cell and Developmental Biology2296-634X2021-05-01910.3389/fcell.2021.671297671297The Last Chance SaloonYe Hong0Hongtao Zhang1Anton Gartner2Shandong Provincial Key Laboratory of Animal Cell and Developmental Biology, School of Life Sciences, Shandong University, Qingdao, ChinaShandong Provincial Key Laboratory of Animal Cell and Developmental Biology, School of Life Sciences, Shandong University, Qingdao, ChinaCenter for Genomic Integrity, Institute for Basic Science, Ulsan, South KoreaAccurate 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.https://www.frontiersin.org/articles/10.3389/fcell.2021.671297/fullchromatin bridgeabscission checkpointNoCut pathwayTREX1LEM-3 endonucleaseANKLE1
collection DOAJ
language English
format Article
sources DOAJ
author Ye Hong
Hongtao Zhang
Anton Gartner
spellingShingle Ye Hong
Hongtao Zhang
Anton Gartner
The Last Chance Saloon
Frontiers in Cell and Developmental Biology
chromatin bridge
abscission checkpoint
NoCut pathway
TREX1
LEM-3 endonuclease
ANKLE1
author_facet Ye Hong
Hongtao Zhang
Anton Gartner
author_sort Ye Hong
title The Last Chance Saloon
title_short The Last Chance Saloon
title_full The Last Chance Saloon
title_fullStr The Last Chance Saloon
title_full_unstemmed The Last Chance Saloon
title_sort last chance saloon
publisher Frontiers Media S.A.
series Frontiers in Cell and Developmental Biology
issn 2296-634X
publishDate 2021-05-01
description 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.
topic chromatin bridge
abscission checkpoint
NoCut pathway
TREX1
LEM-3 endonuclease
ANKLE1
url https://www.frontiersin.org/articles/10.3389/fcell.2021.671297/full
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