Evidence map›Paper›PMID 33355621›Full record

ArticleThe Journal of cell biology2021

An ATM-Chk2-INCENP pathway activates the abscission checkpoint.

Eleni Petsalaki, George Zachos

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of cell biology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
1.3field-weighted citation impact, top 19% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

22 citing papers in PubMed, 27 citations in OpenAlex.

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  16. Mechanics and regulation of cytokinetic abscission.Frontiers in cell and developmental biology · 2022
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

2 authors at 1 institution in 1 country.

Eleni PetsalakiDepartment of Biology, University of Crete, Heraklion, Greece.
George ZachosDepartment of Biology, University of Crete, Heraklion, Greece.
University of Crete · GR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

During cell division, in response to chromatin bridges, the chromosomal passenger complex (CPC) delays abscission to prevent chromosome breakage or tetraploidization. Here, we show that inhibition of ATM or Chk2 kinases impairs CPC localization to the midbody center, accelerates midbody resolution in normally segregating cells, and correlates with premature abscission and chromatin breakage in cytokinesis with trapped chromatin. In cultured human cells, ATM activates Chk2 at late midbodies. In turn, Chk2 phosphorylates human INCENP-Ser91 to promote INCENP binding to Mklp2 kinesin and CPC localization to the midbody center through Mklp2 association with Cep55. Expression of truncated Mklp2 that does not bind to Cep55 or nonphosphorylatable INCENP-Ser91A impairs CPC midbody localization and accelerates abscission. In contrast, expression of phosphomimetic INCENP-Ser91D or a chimeric INCENP protein that is targeted to the midbody center rescues the abscission delay in Chk2-deficient or ATM-deficient cells. Furthermore, the Mre11-Rad50-Nbs1 complex is required for ATM activation at the midbody in cytokinesis with chromatin bridges. These results identify an ATM-Chk2-INCENP pathway that imposes the abscission checkpoint by regulating CPC midbody localization.

Indexed as

Cell Cycle CheckpointsCytokinesisSignal TransductionAtaxia Telangiectasia Mutated ProteinsAurora Kinase BCell ProliferationCheckpoint Kinase 2ChromatinChromosomal Proteins, Non-HistoneChromosome SegregationGreen Fluorescent ProteinsHeLa CellsHumansKinesinsMRE11 Homologue ProteinMultiprotein ComplexesAtaxia Telangiectasia Mutated ProteinsATM protein, humanAurora Kinase BCheckpoint Kinase 2CHEK2 protein, humanChromatinChromosomal Proteins, Non-HistoneGreen Fluorescent ProteinsINCENP protein, humanKIF20A protein, humanKinesinsMRE11 Homologue ProteinMRE11 protein, humanMultiprotein Complexes

Identifiers

PMID33355621
PMCPMC7769160
OpenAlexW3117205546

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.