Evidence map›Paper›PMID 10918599›Full record

ArticleOncogene2000

Identification of E2F-3B, an alternative form of E2F-3 lacking a conserved N-terminal region.

Y He, M K Armanious, M J Thomas, W D Cress

Abstract read
PubMed Publisher
In one paragraph

Article in Oncogene, 2000. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed
2.5field-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

40 citing papers in PubMed, 78 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Transcription factor E2F3a regulatesCancer cell international · 2018
    Article
  6. Article
  7. MicroRNA-34a: A Key Regulator in the Hallmarks of Renal Cell Carcinoma.Oxidative medicine and cellular longevity · 2017
    Article
  8. Expression and prognostic value of E2F activators in NSCLC and subtypes: a research based on bioinformatics analysis.Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine · 2016
    Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. Article
  15. Article
  16. miR-210: the master hypoxamir.Microcirculation (New York, N.Y. : 1994) · 2012
    Review
  17. Curcumin Induces Downregulation of E2F4 Expression and Apoptotic Cell Death in HCT116 Human Colon Cancer Cells; Involvement of Reactive Oxygen Species.The Korean journal of physiology & pharmacology : official journal of the Korean Physiological Society and the Korean Society of Pharmacology · 2010
    Article
  18. MiR-210--micromanager of the hypoxia pathway.Trends in molecular medicine · 2010
    Review
  19. Role of microRNA-23b in flow-regulation of Rb phosphorylation and endothelial cell growth.Proceedings of the National Academy of Sciences of the United States of America · 2010
    Article
  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

4 authors at 3 institutions in 1 country.

Y HeH. Lee Moffitt Cancer Center and Research Institute, Department of Biochemistry and Molecular Biology, University of South Florida, College of Medicine, Tampa 33612, USA.
M K Armanious
M J Thomas
W D Cress
Florida College · USMolecular Oncology (United States) · USUniversity of South Florida · US

Funding

STRUCTURE, FUNCTION AND REGULATION OF E2F FAMILYR29CA078214 · NCI · UNIVERSITY OF SOUTH FLORIDA · PI CRESS, WILLIAM D · 1997 to 2001
$215k
NCI NIH HHS CA78214
6 · The paper itself

Abstract

We have identified a novel form of the full-length E2F-3 protein that we term E2F-3B. In contrast to full-length E2F-3, which is expressed only at the G1/S boundary, E2F-3B is detected throughout the cell cycle with peak levels in GO where it is associated with Rb. Transfection and in vitro translation experiments demonstrate that a protein identical to E2F-3B in size and iso-electric point is produced from the E2F-3 mRNA via the use of an alternative translational start site. This alternative initiation codon was mapped by mutagenesis to codon 102, an ACG codon. Mutation of the ACG codon at position 102 abolished E2F-3B expression, whereas the conversion of ACG 102 to a consensus ATG led to the expression of a protein indistinguishable from E2F-3B. Given these results, E2F-3B is missing 101 N-terminal amino acids relative to full-length E2F-3. This region includes a moderately conserved sequence of unknown function that is present only in the growth-promoting E2F family members, including E2F-1, 2 and full-length E2F-3. These observations make E2F-3B the first example of an E2F gene giving rise to two different protein species and also suggest that E2F-3 and E2F-3B may have opposing roles in cell cycle control.

Indexed as

Alternative SplicingConserved Sequence3T3 CellsAnimalsDeoxycholic AcidDown-RegulationE2F3 Transcription FactorHL-60 CellsHumansMiceMice, Inbred BALB CProtein BiosynthesisProtein IsoformsResting Phase, Cell CycleRetinoblastoma ProteinTranscription FactorsDeoxycholic AcidE2F3 protein, humanE2f3 protein, mouseE2F3 Transcription FactorProtein IsoformsRetinoblastoma ProteinTranscription Factors

Identifiers

PMID10918599
OpenAlexW2324510594

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.