Evidence map›Paper›PMID 11571645›Full record

ArticleOncogene2001

Cloning and characterization of a novel transcription factor involved in cellular proliferation arrest: PATF.

P Crisanti, G Raguenez, C Blancher, B Neron, A Mamoune, B Omri

Abstract read
PubMed Publisher
In one paragraph

Article in Oncogene, 2001. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. 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

6 authors.

P CrisantiDéveloppement, Vieillissement et Pathologie de la Rétine, INSERM U450, Affiliée CNRS, Association Claude Bernard, 29 rue Wilhem, 75016 Paris, France. plassiaz@infobiogen.fr
G Raguenez
C Blancher
B Neron
A Mamoune
B Omri

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cell cycle withdrawal involves several transcription factors such as E2Fs members that play a key role in cell growth control. Here we describe a novel putative bZIP transcription factor isolated from the retina and involved in neuronal proliferation arrest at the terminal differentiation: PATF (Proliferation Arrest Transcription Factor). We show that PATF associates with E2F4 protein and interacts with the E2F consensus site. PATF expression increases with establishment of quiescent state. Furthermore, the nuclear PATF localization like E2F4, depends on cell growth arrest. The decrease of PATF amount, using a retroviral antisense strategy, results in pursued neuroretina cell mitosis. Our results indicate that PATF could be a new molecular signal implicated in the final neuronal cell cycle withdrawal.

Indexed as

Avian ProteinsAmino Acid SequenceAnimalsBase SequenceBasic-Leucine Zipper Transcription FactorsCell DivisionCell NucleusChick EmbryoCloning, MolecularConsensus SequenceDNA, AntisenseDNA-Binding ProteinsE2F4 Transcription FactorEye ProteinsHumansMolecular Sequence DataAvian ProteinsBasic-Leucine Zipper Transcription FactorsDNA, AntisenseDNA-Binding ProteinsE2F4 Transcription FactorEye Proteinsproliferation arrest transcription factor, Coturnix japonicaRNA, MessengerTranscription Factors

Identifiers

PMID11571645

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.