Linked Life Data

10918068

Source:http://linkedlifedata.com/resource/pubmed/id/10918068

Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
41
pubmed:dateCreated
2000-11-13
pubmed:databankReference
pubmed:abstractText
Ras proteins operate as molecular switches in signal transduction pathways downstream of tyrosine kinases and G-protein-coupled receptors. Ras is switched from the inactive GDP-bound state to the active GTP-bound state by guanine nucleotide exchange factors (GEFs). We report here the cloning and characterization of RasGRP2, a longer alternatively spliced form of the recently cloned RapGEF, CalDAG-GEFI. A unique feature of RasGRP2 is that it is targeted to the plasma membrane by a combination of N-terminal myristoylation and palmitoylation. In vivo, RasGRP2 selectively catalyzes nucleotide exchange on N- and Ki-Ras, but not Ha-Ras. RasGRP2 also catalyzes nucleotide exchange on Rap1, but this RapGEF activity is less potent than that associated with CalDAG-GEFI. The nucleotide exchange activity of RasGRP2 toward N-Ras is stimulated by diacylglycerol and inhibited by calcium. The effects of diacylglycerol and calcium are additive but are not accompanied by any detectable change in the subcellular localization of RasGRP2. In contrast, CalDAG-GEFI is localized predominantly to the cytosol and lacks Ras exchange activity in vivo. However, prolonged exposure to phorbol esters, or growth in serum, results in localization of CalDAG-GEFI to the cell membrane and restoration of Ras exchange activity. Expression of RasGRP2 or CalDAG-GEFI in NIH3T3 cells transfected with wild type N-Ras results in an accelerated growth rate but not morphologic transformation. Thus, under appropriate growth conditions, CalDAG-GEFI and RasGRP2 are dual specificity Ras and Rap exchange factors.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Oct
pubmed:issn
0021-9258
pubmed:author
pubmed:issnType
Print
pubmed:day
13
pubmed:volume
275
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
32260-7
pubmed:dateRevised
2006-11-15
pubmed:meshHeading
pubmed-meshheading:10918068-Alternative Splicing, pubmed-meshheading:10918068-Amino Acid Sequence, pubmed-meshheading:10918068-Animals, pubmed-meshheading:10918068-Calcium, pubmed-meshheading:10918068-Cell Line, pubmed-meshheading:10918068-Cell Membrane, pubmed-meshheading:10918068-Cloning, Molecular, pubmed-meshheading:10918068-DNA-Binding Proteins, pubmed-meshheading:10918068-Diglycerides, pubmed-meshheading:10918068-Fluorescent Antibody Technique, pubmed-meshheading:10918068-Guanine Nucleotide Exchange Factors, pubmed-meshheading:10918068-Humans, pubmed-meshheading:10918068-Membrane Proteins, pubmed-meshheading:10918068-Molecular Sequence Data, pubmed-meshheading:10918068-Protein Processing, Post-Translational, pubmed-meshheading:10918068-Protein Transport, pubmed-meshheading:10918068-Recombinant Fusion Proteins, pubmed-meshheading:10918068-Substrate Specificity, pubmed-meshheading:10918068-Tetradecanoylphorbol Acetate, pubmed-meshheading:10918068-Transfection, pubmed-meshheading:10918068-rap GTP-Binding Proteins, pubmed-meshheading:10918068-ras Proteins
pubmed:year
2000
pubmed:articleTitle
Characterization of RasGRP2, a plasma membrane-targeted, dual specificity Ras/Rap exchange factor.
pubmed:affiliation
Queensland Cancer Fund Laboratory of Experimental Oncology, Department of Pathology, University of Queensland Medical School, Herston Road, Brisbane 4006, Queensland, Australia.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't