Evidence map›Paper›PMID 22134138›Full record

ArticleCell cycle (Georgetown, Tex.)2011

Artemis interacts with the Cul4A-DDB1DDB2 ubiquitin E3 ligase and regulates degradation of the CDK inhibitor p27.

Yiyi Yan, Xiaoshan Zhang, Randy J Legerski

Open access · bronzeAbstract read
In one paragraph

Article in Cell cycle (Georgetown, Tex.), 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
1.1field-weighted citation impact, top 22% 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

20 citing papers in PubMed, 30 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. [Targeting Cullin-RING E3 ligases for anti-cancer therapy: efforts on drug discovery].Zhejiang da xue xue bao. Yi xue ban = Journal of Zhejiang University. Medical sciences · 2020
    Review
  10. Emerging Roles of DDB2 in Cancer.International journal of molecular sciences · 2019
    Review
  11. The emerging role for Cullin 4 family of E3 ligases in tumorigenesis.Biochimica et biophysica acta. Reviews on cancer · 2019
    Review
  12. Article
  13. Review
  14. Article
  15. Article
  16. Review
  17. Article
  18. Article
  19. Cullin-RING Ligases as attractive anti-cancer targets.Current pharmaceutical design · 2013
    Review
  20. 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

3 authors at 1 institution in 1 country.

Yiyi YanDepartment of Genetics, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Xiaoshan Zhang
Randy J Legerski
The University of Texas MD Anderson Cancer Center · US

Funding

Recognition and processing of complex lesions by components from multiple DNAP01CA097175 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI NAIRN, RODNEY S · 2004 to 2014
$15.3M
The Role of Artemis in Cellular Responses to DNA DamageR01CA096574 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI LEGERSKI, RANDY J · 2004 to 2008
$1.5M
NCI NIH HHS CA096574NCI NIH HHS CA097175NCI NIH HHS P01 CA097175NCI NIH HHS R01 CA096574
6 · The paper itself

Abstract

Artemis, a member of the SNM1 gene family, is a multifunctional phospho-protein that has been shown to have important roles in V(D)J recombination, DNA double strand break repair, and stress-induced cell-cycle checkpoint regulation. We show here that Artemis interacts with the Cul4A-DDB1 E3 ubiquitin ligase via a direct interaction with the substrate-specificity receptor DDB2. Furthermore, Artemis also interacts with the CDK inhibitor and tumor suppressor p27, a substrate of the Cul4A-DDB1 ligase, and both DDB2 and Artemis are required for the degradation of p27 mediated by this complex. We also show that the regulation of p27 by Artemis and DDB2 is important for cell cycle progression in normally proliferating cells and in response to serum deprivation. These findings thus define a function for Artemis as an effector of Cullin-based E3 ligase-mediated ubiquitylation, demonstrate a novel pathway for the regulation of p27, and show that Cul4A-DDB1(DDB2-Artemis) regulates G1 phase cell cycle progression in mammalian cells.

Indexed as

G1 PhaseCell NucleusCullin ProteinsCyclin-Dependent Kinase Inhibitor p27DNA-Binding ProteinsEndonucleasesEscherichia coliHEK293 CellsHeLa CellsHumansMultiprotein ComplexesNuclear ProteinsProtein Interaction MappingRNA, Small InterferingSubstrate SpecificityTransfectionCDKN1B protein, humanCUL4A protein, humanCullin ProteinsCyclin-Dependent Kinase Inhibitor p27DCLRE1C protein, humanDDB1 protein, humanDDB2 protein, humanDNA-Binding ProteinsEndonucleasesMultiprotein ComplexesNuclear ProteinsRNA, Small InterferingUbiquitin-Protein Ligases

Identifiers

PMID22134138
PMCPMC3272290
OpenAlexW1966698287

What OpenQuestion holds

Textmetadata
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.