Evidence map›Paper›PMID 23260667›Full record

ArticleCell reports2012

MORC2 signaling integrates phosphorylation-dependent, ATPase-coupled chromatin remodeling during the DNA damage response.

Da-Qiang Li, Sujit S Nair, Kazufumi Ohshiro, Anupam Kumar, Vasudha S Nair, Suresh B Pakala, Sirigiri Divijendra Natha Reddy, Rajendra P Gajula, Jeyanthy Eswaran, L Aravind and 1 more

Open access · goldAbstract read
In one paragraph

Article in Cell reports, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 86 papers.

0numbers the graph read from it
0cells of the map it votes in
86citing papers in PubMed
2.0field-weighted citation impact, top 14% 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

86 citing papers in PubMed, 139 citations in OpenAlex.

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  11. Emerging roles of the chromatin remodeler MORC2 in cancer metabolism.Medical oncology (Northwood, London, England) · 2024
    Review
  12. Article
  13. Article
  14. Review
  15. TRIM28 in cancer and cancer therapy.Frontiers in genetics · 2024
    Review
  16. Article
  17. Article
  18. Review
  19. Article
  20. Review

26 more citing papers are in PubMed but not listed here.

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

11 authors at 3 institutions in 1 country.

Da-Qiang LiDepartment of Biochemistry and Molecular Biology, The George Washington University, Washington, DC 20037, USA. bcmdql@gwu.edu
Sujit S Nair
Kazufumi Ohshiro
Anupam Kumar
Vasudha S Nair
Suresh B Pakala
Sirigiri Divijendra Natha Reddy
Rajendra P Gajula
Jeyanthy Eswaran
L Aravind
Rakesh Kumar
George Washington University · USNational Institutes of Health · USThe University of Texas MD Anderson Cancer Center · US

Funding

Pak1 Signaling and Targets in Breast Cancer ProgressionR01CA090970 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI KUMAR, RAKESH · 2001 to 2014
$3.5M
Role of PAK1-MORC2 Pathway in Breast CancerR01CA139573 · NCI · GEORGE WASHINGTON UNIVERSITY · PI KUMAR, RAKESH · 2009 to 2010
$649k
Intramural NIH HHSNCI NIH HHS CA139573NCI NIH HHS CA90970NCI NIH HHS R01 CA090970NCI NIH HHS R01 CA139573
6 · The paper itself

Abstract

Chromatin dynamics play a central role in maintaining genome integrity, but how this is achieved remains largely unknown. Here, we report that microrchidia CW-type zinc finger 2 (MORC2), an uncharacterized protein with a derived PHD finger domain and a conserved GHKL-type ATPase module, is a physiological substrate of p21-activated kinase 1 (PAK1), an important integrator of extracellular signals and nuclear processes. Following DNA damage, MORC2 is phosphorylated on serine 739 in a PAK1-dependent manner, and phosphorylated MORC2 regulates its DNA-dependent ATPase activity to facilitate chromatin remodeling. Moreover, MORC2 associates with chromatin and promotes gamma-H2AX induction in a PAK1 phosphorylation-dependent manner. Consequently, cells expressing MORC2-S739A mutation displayed a reduction in DNA repair efficiency and were hypersensitive to DNA-damaging agent. These findings suggest that the PAK1-MORC2 axis is critical for orchestrating the interplay between chromatin dynamics and the maintenance of genomic integrity through sequentially integrating multiple essential enzymatic processes.

Indexed as

Chromatin Assembly and DisassemblyDNA DamageAdenosine TriphosphatasesAmino Acid SubstitutionDNA RepairHeLa CellsHumansMutation, Missensep21-Activated KinasesPhosphorylationProtein Structure, TertiaryTranscription FactorsAdenosine TriphosphatasesMORC2 protein, humanp21-Activated KinasesPAK1 protein, humanTranscription Factors

Identifiers

PMID23260667
PMCPMC3554793
OpenAlexW2041519802

What OpenQuestion holds

Textmetadata
LicenceTDM
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.