Linked Life Data

20534573

Source:http://linkedlifedata.com/resource/pubmed/id/20534573

Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
22
pubmed:dateCreated
2010-6-10
pubmed:abstractText
Ras/MAPK signaling is often aberrantly activated in human cancers. The downstream effectors are transcription factors, including those encoded by the ETS gene family. Using cell-based assays and biophysical measurements, we have determined the mechanism by which Ras/MAPK signaling affects the function of Ets1 via phosphorylation of Thr38 and Ser41. These ERK2 phosphoacceptors lie within the unstructured N-terminal region of Ets1, immediately adjacent to the PNT domain. NMR spectroscopic analyses demonstrated that the PNT domain is a four-helix bundle (H2-H5), resembling the SAM domain, appended with two additional helices (H0-H1). Phosphorylation shifted a conformational equilibrium, displacing the dynamic helix H0 from the core bundle. The affinity of Ets1 for the TAZ1 (or CH1) domain of the coactivator CBP was enhanced 34-fold by phosphorylation, and this binding was sensitive to ionic strength. NMR-monitored titration experiments mapped the interaction surfaces of the TAZ1 domain and Ets1, the latter encompassing both the phosphoacceptors and PNT domain. Charge complementarity of these surfaces indicate that electrostatic forces act in concert with a conformational equilibrium to mediate phosphorylation effects. We conclude that the dynamic helical elements of Ets1, appended to a conserved structural core, constitute a phospho-switch that directs Ras/MAPK signaling to downstream changes in gene expression. This detailed structural and mechanistic information will guide strategies for targeting ETS proteins in human disease.
pubmed:grant
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Jun
pubmed:issn
1091-6490
pubmed:author
pubmed:issnType
Electronic
pubmed:day
1
pubmed:volume
107
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
10026-31
pubmed:dateRevised
2011-3-3
pubmed:meshHeading
pubmed-meshheading:20534573-Amino Acid Sequence, pubmed-meshheading:20534573-Animals, pubmed-meshheading:20534573-CREB-Binding Protein, pubmed-meshheading:20534573-Conserved Sequence, pubmed-meshheading:20534573-Humans, pubmed-meshheading:20534573-MAP Kinase Signaling System, pubmed-meshheading:20534573-Mice, pubmed-meshheading:20534573-Models, Molecular, pubmed-meshheading:20534573-Molecular Dynamics Simulation, pubmed-meshheading:20534573-Molecular Sequence Data, pubmed-meshheading:20534573-NIH 3T3 Cells, pubmed-meshheading:20534573-Nuclear Magnetic Resonance, Biomolecular, pubmed-meshheading:20534573-Phosphorylation, pubmed-meshheading:20534573-Protein Binding, pubmed-meshheading:20534573-Protein Conformation, pubmed-meshheading:20534573-Protein Interaction Domains and Motifs, pubmed-meshheading:20534573-Proto-Oncogene Protein c-ets-1, pubmed-meshheading:20534573-Recombinant Proteins, pubmed-meshheading:20534573-Sequence Homology, Amino Acid, pubmed-meshheading:20534573-Signal Transduction, pubmed-meshheading:20534573-Static Electricity, pubmed-meshheading:20534573-ras Proteins
pubmed:year
2010
pubmed:articleTitle
Ras signaling requires dynamic properties of Ets1 for phosphorylation-enhanced binding to coactivator CBP.
pubmed:affiliation
Department of Oncological Sciences, University of Utah School of Medicine, Huntsman Cancer Institute, University of Utah, Salt Lake City, UT, 84112, USA.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't, Research Support, N.I.H., Extramural