Evidence map›Paper›PMID 19282287›Full record

ArticleThe Journal of biological chemistry2009

Ikaros stability and pericentromeric localization are regulated by protein phosphatase 1.

Marcela Popescu, Zafer Gurel, Tapani Ronni, Chunhua Song, Ka Ying Hung, Kimberly J Payne, Sinisa Dovat

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 63 papers.

0numbers the graph read from it
0cells of the map it votes in
63citing papers in PubMed
5.9field-weighted citation impact, top 4% 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

63 citing papers in PubMed, 90 citations in OpenAlex.

  1. Article
  2. NSUN7-mediated mJournal of translational medicine · 2025
    Article
  3. Article
  4. Article
  5. Review
  6. Regulation of cancer progression by CK2: an emerging therapeutic target.Medical oncology (Northwood, London, England) · 2024
    Review
  7. IKAROS in Acute Leukemia: A Positive Influencer or a Mean Hater?International journal of molecular sciences · 2023
    Review
  8. Review
  9. Review
  10. Article
  11. Review
  12. Antitumor Activity of the Novel BTK Inhibitor TG-1701 Is Associated with Disruption of Ikaros Signaling in Patients with B-cell Non-Hodgkin Lymphoma.Clinical cancer research : an official journal of the American Association for Cancer Research · 2021
    Article
  13. Pathogenic germlineCold Spring Harbor molecular case studies · 2021
    Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Review
  20. Article

3 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

7 authors at 2 institutions in 1 country.

Marcela PopescuDepartment of Pediatrics, University of Wisconsin, Madison, Wisconsin 53792-4108.
Zafer GurelDepartment of Pediatrics, University of Wisconsin, Madison, Wisconsin 53792-4108.
Tapani RonniDepartment of Pediatrics, University of Wisconsin, Madison, Wisconsin 53792-4108.
Chunhua SongDepartment of Pediatrics, University of Wisconsin, Madison, Wisconsin 53792-4108.
Ka Ying HungDepartment of Pediatrics, University of Wisconsin, Madison, Wisconsin 53792-4108.
Kimberly J PayneCenter for Health Disparities and Molecular Medicine and Department of Pathology and Human Anatomy, Loma Linda University School of Medicine, Loma Linda, California 92350.
Sinisa DovatDepartment of Pediatrics, University of Wisconsin, Madison, Wisconsin 53792-4108. Electronic address: dovat@wisc.edu.
University of Wisconsin–Madison · USLoma Linda University · US

Funding

INSTITUTIONAL CTSA (UW-MADISON): CLINICAL TRIALSUL1RR025011 · NCRR · UNIVERSITY OF WISCONSIN-MADISON · PI DREZNER, MARC KENNETH · 2007 to 2011
$29.5M
RESEARCH TRAINING IN HEMATOLOGYT32HL007899 · NHLBI · UNIVERSITY OF WISCONSIN-MADISON · PI Jane Ellen Churpek · 1998 to 2026
$8.2M
Clinical Academic Oncologist Training ProgramK12CA087718 · NCI · UNIVERSITY OF WISCONSIN-MADISON · PI ALBERTINI, MARK R · 2000 to 2008
$3.8M
IL-7 in Human B1 and B2 Lymphocyte DifferentiationK01DK066163 · NIDDK · LOMA LINDA UNIVERSITY · PI PAYNE, KIMBERLY J · 2004 to 2008
$626k
The Role of Zinc Finger Genes in Cellular ProliferationK22CA111392 · NCI · UNIVERSITY OF WISCONSIN-MADISON · PI DOVAT, SINISA · 2005 to 2007
$488k
NCI NIH HHS K12 CA 087718NCI NIH HHS K12 CA087718NCI NIH HHS K22 CA 111392NCRR NIH HHS 1UL1RR025011NHLBI NIH HHS T32 HL007899NHLBI NIH HHS T32 HL07899NIDDK NIH HHS 5K01 DK066163
6 · The paper itself

Abstract

Ikaros encodes a zinc finger protein that is involved in gene regulation and chromatin remodeling. The majority of Ikaros localizes at pericentromeric heterochromatin (PC-HC) where it regulates expression of target genes. Ikaros function is controlled by posttranslational modification. Phosphorylation of Ikaros by CK2 kinase determines its ability to bind DNA and exert cell cycle control as well as its subcellular localization. We report that Ikaros interacts with protein phosphatase 1 (PP1) via a conserved PP1 binding motif, RVXF, in the C-terminal end of the Ikaros protein. Point mutations of the RVXF motif abolish Ikaros-PP1 interaction and result in decreased DNA binding, an inability to localize to PC-HC, and rapid degradation of the Ikaros protein. The introduction of alanine mutations at CK2-phosphorylated residues increases the half-life of the PP1-nonbinding Ikaros mutant. This suggests that dephosphorylation of these sites by PP1 stabilizes the Ikaros protein and prevents its degradation. In the nucleus, Ikaros forms complexes with ubiquitin, providing evidence that Ikaros degradation involves the ubiquitin/proteasome pathway. In vivo, Ikaros can target PP1 to the nucleus, and a fraction of PP1 colocalizes with Ikaros at PC-HC. These data suggest a novel function for the Ikaros protein; that is, the targeting of PP1 to PC-HC and other chromatin structures. We propose a model whereby the function of Ikaros is controlled by the CK2 and PP1 pathways and that a balance between these two signal transduction pathways is essential for normal cellular function and for the prevention of malignant transformation.

Indexed as

Models, BiologicalAmino Acid MotifsAnimalsCell Line, TumorCell NucleusCell Transformation, NeoplasticCentromereDNAHumansIkaros Transcription FactorMicePhosphorylationPoint MutationProtein BindingProtein Phosphatase 1Protein StabilityDNAIkaros Transcription FactorIKZF1 protein, humanProtein Phosphatase 1UbiquitinZfpn1a1 protein, mouse

Identifiers

PMID19282287
PMCPMC2679487
OpenAlexW2090936301

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.