Evidence map›Paper›PMID 7600583›Full record

ArticleCell1995

The Rho family GTPases RhoA, Rac1, and CDC42Hs regulate transcriptional activation by SRF.

C S Hill, J Wynne, R Treisman

Open access · bronzeAbstract read
PubMed Publisher
In one paragraph

Article in Cell, 1995. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 455 papers.

0numbers the graph read from it
0cells of the map it votes in
455citing papers in PubMed
44.1field-weighted citation impact, top 1% 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

455 citing papers in PubMed, 1,271 citations in OpenAlex.

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395 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

3 authors at 1 institution in 1 country.

C S HillTranscription Laboratory, Imperial Cancer Research Fund Laboratories, London, England.
J Wynne
R Treisman
The Honourable Society of Lincoln's Inn · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The c-fos serum response element (SRE) forms a ternary complex with the transcription factors SRF (serum response factor) and TCF (ternary complex factor). By itself, SRF can mediate transcriptional activation induced by serum, lysophosphatidic acid, or intracellular activation of heterotrimeric G proteins. Activated forms of the Rho family GTPases RhoA, Rac1, and CDC42Hs also activate transcription via SRF and act synergistically at the SRE with signals that activate TCF. Functional Rho is required for signaling to SRF by several stimuli, but not by activated CDC42Hs or Rac1. Activation of the SRF-linked signaling pathway does not correlate with activation of the MAP kinases ERK, SAPK/JNK, or MPK2/p38. Functional Rho is required for regulated activity of the c-fos promoter. These results establish SRF as a nuclear target of a novel Rho-mediated signaling pathway.

Indexed as

Gene Expression RegulationGenes, fos3T3 CellsAnimalsBase SequenceBinding Sitescdc42 GTP-Binding ProteinCell Cycle ProteinsCell LineGTP-Binding ProteinsGTP PhosphohydrolasesHumansMiceMolecular Sequence Datarac GTP-Binding ProteinsRecombinant Proteinscdc42 GTP-Binding ProteinCell Cycle ProteinsGTP-Binding ProteinsGTP Phosphohydrolasesrac GTP-Binding ProteinsRecombinant ProteinsrhoA GTP-Binding ProteinTranscription Factors

Identifiers

PMID7600583
OpenAlexW2053257956

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.