Evidence map›Paper›PMID 9878064›Full record

ArticleThe EMBO journal1999

Integration of a growth-suppressing BTB/POZ domain protein with the DP component of the E2F transcription factor.

S de la Luna, K E Allen, S L Mason, N B La Thangue

Open access · bronzeAbstract read
In one paragraph

Article in The EMBO journal, 1999. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
2.6field-weighted citation impact, top 10% 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

26 citing papers in PubMed, 85 citations in OpenAlex.

  1. Review
  2. The role of inner nuclear membrane protein emerin in myogenesis.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2025
    Review
  3. The Role of Emerin in Cancer Progression and Metastasis.International journal of molecular sciences · 2021
    Review
  4. Article
  5. Article
  6. Article
  7. Double abdomen in a short-germ insect: Zygotic control of axis formation revealed in the beetleProceedings of the National Academy of Sciences of the United States of America · 2018
    Article
  8. Diseases of the Nucleoskeleton.Comprehensive Physiology · 2016
    Review
  9. Article
  10. Article
  11. Emerin in health and disease.Seminars in cell & developmental biology · 2014
    Review
  12. Article
  13. Article
  14. The nuclear envelope at a glance.Journal of cell science · 2010
    Article
  15. Review
  16. Article
  17. Article
  18. Article
  19. Review
  20. Multiple roles for emerin: implications for Emery-Dreifuss muscular dystrophy.The anatomical record. Part A, Discoveries in molecular, cellular, and evolutionary biology · 2006
    Review
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

4 authors at 1 institution in 1 country.

S de la LunaDivision of Biochemistry and Molecular Biology, Davidson Building, University of Glasgow, Glasgow G12 8QQ, UK.
K E Allen
S L Mason
N B La Thangue
University of Glasgow · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Transcription factor E2F plays an important role in orchestrating early cell cycle progression through its ability to co-ordinate and integrate the cell cycle with the transcription apparatus. Physiological E2F arises when members of two distinct families of proteins interact as E2F-DP heterodimers, in which the E2F component mediates transcriptional activation and the physical interaction with pocket proteins, such as the tumour suppressor protein pRb. In contrast, a discrete role for the DP subunit has not been defined. We report the identification and characterization of DIP, a novel mammalian protein that can interact with the DP component of E2F. DIP was found to contain a BTB/POZ domain and shows significant identity with the Drosophila melanogaster germ cell-less gene product. In mammalian cells, DIP is distributed in a speckled pattern at the nuclear envelope region, and can direct certain DP subunits and the associated heterodimeric E2F partner into a similar pattern. DIP-dependent growth arrest is modulated by the expression of DP proteins, and mutant derivatives of DIP that are compromised in cell cycle arrest exhibit reduced binding to the DP subunit. Our study defines a new pathway of growth control that is integrated with the E2F pathway through the DP subunit of the heterodimer.

Indexed as

Carrier ProteinsCell Cycle ProteinsDrosophila ProteinsTrans-ActivatorsAmino Acid SequenceAnimalsCell CycleCell LineDimerizationDNA-Binding ProteinsDrosophila melanogasterE2F Transcription FactorsGrowth InhibitorsHumansIntercellular Signaling Peptides and ProteinsMiceArid4a protein, mouseCarrier ProteinsCell Cycle ProteinsDNA-Binding ProteinsDP-interacting protein, mouseDp transcription factor, DrosophilaDrosophila ProteinsE2F Transcription Factorsgcl protein, DrosophilaGcl protein, mouseGrowth InhibitorsIntercellular Signaling Peptides and ProteinsNuclear ProteinsRetinoblastoma-Binding Protein 1Trans-ActivatorsTranscription Factor DP1Transcription Factors

Identifiers

PMID9878064
PMCPMC1171116
OpenAlexW2143496370

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.