Evidence map›Paper›PMID 20980823›Full record

ArticleCell cycle (Georgetown, Tex.)2010

A novel role for greatwall kinase in recovery from DNA damage.

Aimin Peng, Tomomi M Yamamoto, Michael L Goldberg, James L Maller

Abstract read
In one paragraph

Article in Cell cycle (Georgetown, Tex.), 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
–field-weighted citation impact
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

30 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. The ATM-E6AP-MASTL axis mediates DNA damage checkpoint recovery.bioRxiv : the preprint server for biology · 2023
    Article
  5. Article
  6. Article
  7. Review
  8. Molecular Basis of the Mechanisms Controlling MASTL.Molecular & cellular proteomics : MCP · 2020
    Article
  9. Review
  10. Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. The Oncogenic Functions of MASTL Kinase.Frontiers in cell and developmental biology · 2018
    Review
  17. Article
  18. Article
  19. Article
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

4 authors.

Aimin PengHoward Hughes Medical Institute, Department of Pharmacology, University of Colorado School of Medicine, Aurora, USA. Aimin.Peng@unmc.edu
Tomomi M Yamamoto
Michael L Goldberg
James L Maller

Funding

Greatwall Kinase and the Mitotic Control of Phosphatase ActivityR01GM048430 · NIGMS · CORNELL UNIVERSITY ITHACA · PI GOLDBERG, MICHAEL L · 1992 to 2017
$6.6M
Howard Hughes Medical InstituteNIGMS NIH HHS GM48430NIGMS NIH HHS R01 GM048430
6 · The paper itself

Abstract

Activation of the DNA damage response (DDR) is critical for genomic integrity and tumor suppression. The occurrence of DNA damage quickly evokes the DDR through ATM/ATR-dependent signal transduction, which promotes DNA repair and activates the checkpoint to halt cell cycle progression. The "turn off" process of the DDR upon satisfaction of DNA repair, also known as "checkpoint recovery", involves deactivation of DDR elements, but the mechanism is poorly understood. Greatwall kinase (Gwl) has been identified as a key element in the G(2)/M transition and helps maintain M phase through inhibition of PP 2A/B55δ, the principal phosphatase for Cdk-phosphorylated substrates. Here we show that Gwl also promotes recovery from DNA damage and is itself directly inhibited by the DNA damage response (DDR). In Xenopus egg extracts, immunodepletion of Gwl increased the DDR to damaged DNA, whereas addition of wild type, but not kinase dead Gwl, inhibited the DDR. The removal of damaged DNA from egg extracts leads to recovery from checkpoint arrest and entry into mitosis, a process impaired by Gwl depletion and enhanced by Gwl overexpression. Moreover, activation of Cdk1 after the removal of damaged DNA is regulated by Gwl. Collectively, these results defines Gwl as a new regulator of the DDR, which plays an important role in recovery from DNA damage.

Indexed as

DNA DamageDNA RepairAnimalsCarboxylic Ester HydrolasesCDC2 Protein KinaseCell DivisionG2 PhaseMitosisPhosphorylationProtein Serine-Threonine KinasesXenopus laevisXenopus ProteinsCarboxylic Ester HydrolasesCDC2 Protein KinaseMASTL protein, Xenopusprotein phosphatase methylesterase-1Protein Serine-Threonine KinasesXenopus Proteins

Identifiers

PMID20980823
PMCPMC3055187

What OpenQuestion holds

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Registered trials

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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.