Evidence map›Paper›PMID 11046156›Full record

ArticleMolecular and cellular biology2000

A family of LIM-only transcriptional coactivators: tissue-specific expression and selective activation of CREB and CREM.

G M Fimia, D De Cesare, P Sassone-Corsi

Open access · greenAbstract readComparative Study
In one paragraph

Article in Molecular and cellular biology, 2000. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 78 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
78citing papers in PubMed, 3 pooled it
6.5field-weighted citation impact, top 3% 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

78 citing papers in PubMed, 3 syntheses or guidelines pooled it, 188 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Article
  5. Article
  6. Article
  7. The roles of FHL2 in cancer.Clinical and experimental medicine · 2023
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  12. The Roles of FHL3 in Cancer.Frontiers in oncology · 2022
    Review
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  14. Review
  15. Article
  16. Review
  17. Article
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18 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

3 authors at 3 institutions in 1 country.

G M FimiaInstitut de Génétique et de Biologie Moléculaire et Cellulaire, CNRS-INSERM, Université Louis Pasteur, 67404 Illkirch-Strasbourg, France.
D De Cesare
P Sassone-Corsi
Centre National de la Recherche Scientifique · FRInserm · FRInstitut de génétique et de biologie moléculaire et cellulaire · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Transcription factors of the CREB family control the expression of a large number of genes in response to various signaling pathways. Regulation mediated by members of the CREB family has been linked to various physiological functions. Classically, activation by CREB is known to occur upon phosphorylation at an essential regulatory site (Ser133 in CREB) and the subsequent interaction with the ubiquitous coactivator CREB-binding protein (CBP). However, the mechanism by which selectivity is achieved in the identification of target genes, as well as the routes adopted to ensure tissue-specific activation, remains unrecognized. We have recently described the first tissue-specific coactivator of CREB family transcription factors, ACT (activator of CREM in testis). ACT is a LIM-only protein which associates with CREM in male germ cells and provides an activation function which is independent of phosphorylation and CBP. Here we characterize a family of LIM-only proteins which share common structural organization with ACT. These are referred to as four-and-a-half-LIM-domain (FHL) proteins and display tissue-specific and developmentally regulated expression. FHL proteins display different degrees of intrinsic activation potential. They provide powerful activation function to both CREB and CREM when coexpressed either in yeast or in mammalian cells, specific combinations eliciting selective activation. Deletion analysis of the ACT protein shows that the activation function depends on specific arrangements of the LIM domains, which are essential for both transactivation and interaction properties. This study uncovers the existence of a family of tissue-specific coactivators that operate through novel, CBP-independent routes to elicit transcriptional activation by CREB and CREM. The future identification of additional partners of FHL proteins is likely to reveal unappreciated aspects of tissue-specific transcriptional regulation.

Indexed as

Muscle ProteinsRepressor ProteinsAmino Acid MotifsAmino Acid SequenceAnimalsCOS CellsCyclic AMP Response Element-Binding ProteinCyclic AMP Response Element ModulatorDNA-Binding ProteinsHomeodomain ProteinsIntracellular Signaling Peptides and ProteinsLIM Domain ProteinsLIM-Homeodomain ProteinsMaleMiceMolecular Sequence Dataactivator of CREM in testis (ACT)Cyclic AMP Response Element-Binding ProteinCyclic AMP Response Element ModulatorDNA-Binding ProteinsFhl2 protein, mouseFhl3 protein, mouseFHL4 protein, mouseFhl5 protein, mouseHomeodomain ProteinsIntracellular Signaling Peptides and ProteinsLIM Domain ProteinsLIM-Homeodomain ProteinsMuscle ProteinsRepressor ProteinsTranscription Factors

Identifiers

PMID11046156
PMCPMC102166
OpenAlexW2131223814

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.