Evidence map›Paper›PMID 32978522›Full record

ArticleOncogene2020

The Greatwall kinase safeguards the genome integrity by affecting the kinome activity in mitosis.

Xavier Bisteau, Joann Lee, Vinayaka Srinivas, Joanna H S Lee, Joanna Niska-Blakie, Gifford Tan, Shannon Y X Yap, Kevin W Hom, Cheng Kit Wong, Jeongjun Chae and 6 more

Open access · hybridAbstract read
In one paragraph

Article in Oncogene, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.8field-weighted citation impact, top 28% 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

8 citing papers in PubMed, 20 citations in OpenAlex.

  1. Article
  2. Article
  3. Phosphoregulation of RAD51AP1 function in homology-directed repair.bioRxiv : the preprint server for biology · 2025
    Article
  4. IL-22 regulates MASTL expression in intestinal epithelial cells.American journal of physiology. Gastrointestinal and liver physiology · 2024
    Article
  5. Article
  6. Article
  7. Article
  8. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

16 authors at 4 institutions in 5 countries.

Xavier BisteauInstitute of Molecular and Cell Biology (IMCB), A*STAR (Agency for Science, Technology and Research), Singapore, 138673, Republic of Singapore. xbisteau@ulb.ac.be.ORCID http://orcid.org/0000-0002-8896-5098
Joann LeeInstitute of Molecular and Cell Biology (IMCB), A*STAR (Agency for Science, Technology and Research), Singapore, 138673, Republic of Singapore.
Vinayaka SrinivasProgram in Cancer and Stem Cell Biology, Duke-NUS Graduate Medical School, Singapore, 169857, Republic of Singapore.
Joanna H S LeeInstitute of Molecular and Cell Biology (IMCB), A*STAR (Agency for Science, Technology and Research), Singapore, 138673, Republic of Singapore.
Joanna Niska-BlakieInstitute of Molecular and Cell Biology (IMCB), A*STAR (Agency for Science, Technology and Research), Singapore, 138673, Republic of Singapore.
Gifford TanInstitute of Molecular and Cell Biology (IMCB), A*STAR (Agency for Science, Technology and Research), Singapore, 138673, Republic of Singapore.
Shannon Y X YapInstitute of Molecular and Cell Biology (IMCB), A*STAR (Agency for Science, Technology and Research), Singapore, 138673, Republic of Singapore.
Kevin W HomInstitute of Molecular and Cell Biology (IMCB), A*STAR (Agency for Science, Technology and Research), Singapore, 138673, Republic of Singapore.
Cheng Kit WongInstitute of Medical Biology, A*STAR, Singapore, 138648, Republic of Singapore.
Jeongjun ChaeDepartment of Health Sciences and Technology, SAIHST, Sungkyunkwan University, Seoul, 06351, Korea.
Loo Chien WangInstitute of Molecular and Cell Biology (IMCB), A*STAR (Agency for Science, Technology and Research), Singapore, 138673, Republic of Singapore.
Jinho KimSamsung Genome Institute, Samsung Medical Center, Gangnam-gu, Seoul, 06351, Korea.
Giulia RancatiInstitute of Medical Biology, A*STAR, Singapore, 138648, Republic of Singapore.
Radoslaw M SobotaInstitute of Molecular and Cell Biology (IMCB), A*STAR (Agency for Science, Technology and Research), Singapore, 138673, Republic of Singapore.ORCID http://orcid.org/0000-0002-2455-2526
Chris S H TanInstitute of Molecular and Cell Biology (IMCB), A*STAR (Agency for Science, Technology and Research), Singapore, 138673, Republic of Singapore.
Philipp KaldisInstitute of Molecular and Cell Biology (IMCB), A*STAR (Agency for Science, Technology and Research), Singapore, 138673, Republic of Singapore. philipp.kaldis@med.lu.se.ORCID http://orcid.org/0000-0002-7247-7591
Agency for Science, Technology and Research · SGDuke-NUS Medical School · SGSamsung Medical Center · KRSungkyunkwan University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Progression through mitosis is balanced by the timely regulation of phosphorylation and dephosphorylation events ensuring the correct segregation of chromosomes before cytokinesis. This balance is regulated by the opposing actions of CDK1 and PP2A, as well as the Greatwall kinase/MASTL. MASTL is commonly overexpressed in cancer, which makes it a potential therapeutic anticancer target. Loss of Mastl induces multiple chromosomal errors that lead to the accumulation of micronuclei and multilobulated cells in mitosis. Our analyses revealed that loss of Mastl leads to chromosome breaks and abnormalities impairing correct segregation. Phospho-proteomic data for Mastl knockout cells revealed alterations in proteins implicated in multiple processes during mitosis including double-strand DNA damage repair. In silico prediction of the kinases with affected activity unveiled NEK2 to be regulated in the absence of Mastl. We uncovered that, RAD51AP1, involved in regulation of homologous recombination, is phosphorylated by NEK2 and CDK1 but also efficiently dephosphorylated by PP2A/B55. Our results suggest that MastlKO disturbs the equilibrium of the mitotic phosphoproteome that leads to the disruption of DNA damage repair and triggers an accumulation of chromosome breaks even in noncancerous cells.

Indexed as

AnimalsCDC2 Protein KinaseChromosome BreakageChromosome SegregationDNA-Binding ProteinsDNA Breaks, Double-StrandedDNA RepairFibroblastsGene Knockout TechniquesHEK293 CellsHumansMiceMice, TransgenicMicrotubule-Associated ProteinsMitosisNIMA-Related KinasesCDC2 Protein KinaseCdk1 protein, mouseDNA-Binding Proteinsgreatwall protein, mouseMicrotubule-Associated ProteinsNek2 protein, mouseNIMA-Related KinasesPpp2r2a protein, mouseProtein Phosphatase 2Protein Serine-Threonine KinasesRad51ap1 protein, mouseRNA-Binding Proteins

Identifiers

PMID32978522
PMCPMC7605441
OpenAlexW3087809066

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.