Evidence map›Paper›PMID 9032266›Full record

ArticleMolecular and cellular biology1997

Cloning and characterization of Ras-GRF2, a novel guanine nucleotide exchange factor for Ras.

N P Fam, W T Fan, Z Wang, L J Zhang, H Chen, M F Moran

Open access · greenAbstract read
In one paragraph

Article in Molecular and cellular biology, 1997. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 47 papers.

0numbers the graph read from it
0cells of the map it votes in
47citing papers in PubMed
6.2field-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

47 citing papers in PubMed, 129 citations in OpenAlex.

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  10. RASGRF2 regulates alcohol-induced reinforcement by influencing mesolimbic dopamine neuron activity and dopamine release.Proceedings of the National Academy of Sciences of the United States of America · 2012
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  16. GEF1 is a ciliary Sec7 GEF of Tetrahymena thermophila.Cell motility and the cytoskeleton · 2009
    Article
  17. Transgenerational rescue of a genetic defect in long-term potentiation and memory formation by juvenile enrichment.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2009
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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 at 1 institution in 1 country.

N P FamBanting and Best Department of Medical Research, University of Toronto, Ontario, Canada.
W T Fan
Z Wang
L J Zhang
H Chen
M F Moran
University of Toronto · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Conversion of Ras proteins into an activated GTP-bound state able to bind effector proteins is catalyzed by specific guanine nucleotide exchange factors in response to a large number of extracellular stimuli. Here we report the isolation of mouse cDNAs encoding Ras-GRF2, a multidomain 135-kDa protein containing a COOH-terminal Cdc25-related domain that stimulates release of GDP from Ras but not other GTPases in vitro. Ras-GRF2 bound specifically to immobilized Ras lacking bound nucleotides, suggesting stabilization of the nucleotide-free form of Ras as a mechanism of catalyzing nucleotide exchange. The NH2-terminal region of Ras-GRF2 is predicted to contain features common to various signaling proteins including two pleckstrin homology domains and a Dbl homology region. Ras-GRF2 also contains an IQ motif which was required for its apparent constitutive association with calmodulin in epithelial cells ectopically expressing Ras-GRF2. Transient expression of Ras-GRF2 in kidney epithelial cells stimulated GTP binding by Ras and potentiated calcium ionophore-induced activation of mitogen-activated protein kinase (ERK1) dependent upon the IQ motif. Calcium influx caused Ras-GRF2 subcellular localization to change from cytosolic to peripheral, suggesting a possible mechanism for controlling Ras-GRF2 interactions with Ras at the plasma membrane. Epithelial cells overexpressing Ras-GRF2 are morphologically transformed and grow in a disorganized manner with minimal intercellular contacts. Northern analysis indicated a 9-kb GRF2 transcript in brain and lung, where p135 Ras-GRF2 is known to be expressed, and RNAs of 12 kb and 2.2 kb were detected in several tissues. Thus, Ras-GRF2 proteins with different domain structures may be widely expressed and couple diverse extracellular signals to Ras activation.

Indexed as

Mitogen-Activated Protein KinasesAmino Acid SequenceAnimalsCalciumCalcium-Calmodulin-Dependent Protein KinasesCalmodulinCell Cycle ProteinsCell LineCloning, MolecularCOS CellsCytoplasmDNA, ComplementaryEpithelial CellsGuanine Nucleotide Exchange FactorsGuanosine DiphosphateGuanosine TriphosphateCalciumCalcium-Calmodulin-Dependent Protein KinasesCalmodulinCell Cycle ProteinsDNA, ComplementaryGuanine Nucleotide Exchange FactorsGuanosine DiphosphateGuanosine TriphosphateHRAS protein, humanMitogen-Activated Protein Kinase 3Mitogen-Activated Protein KinasesPhosphoprotein PhosphatasesProteinsProto-Oncogene Proteins p21(ras)ras-GRF1ras Guanine Nucleotide Exchange FactorsRecombinant Fusion ProteinsRNA, Messenger

Identifiers

PMID9032266
PMCPMC231864
OpenAlexW2133852124

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.