9010223

Source:http://linkedlifedata.com/resource/pubmed/id/9010223

Download in:

Switch to

Custom View

Named Graph Language Inference

Statements in which the resource exists as a subject.
Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0086860, umls-concept:C0439855, umls-concept:C0542341, umls-concept:C0808900, umls-concept:C0812446, umls-concept:C0908880, umls-concept:C0969709, umls-concept:C1414314, umls-concept:C1521761, umls-concept:C1564656
pubmed:issue	2
pubmed:dateCreated	1997-2-21
pubmed:abstractText	The ETS gene products are a family of transcriptional regulatory proteins that contain a highly conserved and structurally unique DNA binding domain, termed the ETS domain. Several ETS proteins bind to DNA as monomers, however it has been shown that the DNA binding activity is enhanced or modulated in the presence of other factors. By differential display and whole genome PCR techniques, we have recently shown that the Erg1 gene is a target for ETS proteins. The Egr1 promoter contains multiple ETS binding sites, three of which exist as parts of two serum response elements (SREI and SREII). The SRE is a cis-element that regulates the expression of many growth factor responsive genes. ELK1 and SAP1a have been shown to form ternary complexes with SRF on the SRE located in the c-fos promoter. Similarly, we examined whether the ELK1, SAP1a, FLI1, EWS-FLI1, ETS1, ETS2, PEA3 and PU.1 proteins can form ternary complexes with SRF on the Egr1 SREI and II. Our results demonstrate that indeed ELK1, SAPla, FLI1 and EWS-FLI1 are able to form ternary complexes with SRF on Egr1 SREs. In addition, ELK1 and SAP1a can also form quarternary complexes on the Egr1 SREI. However, the proteins ETS1, ETS2, PEA3 and PU.1 were unable to form ternary complexes with SRF on either the Egr1 or c-fos SREs. Our data demonstrate that FLI1 and EWS-FLI1 constitute new members of a subgroup of ETS proteins that can function as ternary complex factors and further implicate a novel function for these ETS transcription factors in the regulation of the Egr1 gene. By amino acid sequence comparison we found that, in fact, 50% of the amino acids present in the B-box of SAP1a and ELK1, which are required for interaction with SRF, are identical to those present in both FLI1 (amino acids 231- 248) and EWS-FLI1 proteins. This B-box is not present in ETS1, ETS2, PEA3 or PU.1 and these proteins were unable to form ternary complexes with SRF and Egrl-SREs or c-fos SRE. Furthermore, deletion of 194 amino terminal amino acids of FLI1 did not interfere with its ability to interact with SRF, in fact, this truncation increased the stability of the ternary complex. The FLI1 protein has a unique R-domain located next to the DNA binding region. This R-domain may modulate the interaction with SRF, providing a mechanism that would be unique to FLI1 and EWS-FLI1, thus implicating a novel function for these ETS transcription factors in the regulation of the Egr1 gene.
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/8711562
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/DNA-Binding Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Heterogeneous-Nuclear..., http://linkedlifedata.com/resource/pubmed/chemical/Nuclear Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Proto-Oncogene Protein c-ets-1, http://linkedlifedata.com/resource/pubmed/chemical/Proto-Oncogene Protein c-fli-1, http://linkedlifedata.com/resource/pubmed/chemical/Proto-Oncogene Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Proto-Oncogene Proteins c-ets, http://linkedlifedata.com/resource/pubmed/chemical/RNA-Binding Protein EWS, http://linkedlifedata.com/resource/pubmed/chemical/Ribonucleoproteins, http://linkedlifedata.com/resource/pubmed/chemical/Serum Response Factor, http://linkedlifedata.com/resource/pubmed/chemical/Trans-Activators, http://linkedlifedata.com/resource/pubmed/chemical/Transcription Factors, http://linkedlifedata.com/resource/pubmed/chemical/ets-Domain Protein Elk-1, http://linkedlifedata.com/resource/pubmed/chemical/ets-Domain Protein Elk-4
pubmed:status	MEDLINE
pubmed:month	Jan
pubmed:issn	0950-9232
pubmed:author	pubmed-author:HodgeD RDR, pubmed-author:KolbJJ, pubmed-author:PapasT STS, pubmed-author:RHIMJ SJS, pubmed-author:RobinsonLL, pubmed-author:WatsonD KDK
pubmed:issnType	Print
pubmed:day	16
pubmed:volume	14
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	213-21
pubmed:dateRevised	2006-11-15
pubmed:meshHeading	pubmed-meshheading:9010223-Animals, pubmed-meshheading:9010223-Base Sequence, pubmed-meshheading:9010223-Binding Sites, pubmed-meshheading:9010223-DNA-Binding Proteins, pubmed-meshheading:9010223-Heterogeneous-Nuclear Ribonucleoproteins, pubmed-meshheading:9010223-Molecular Sequence Data, pubmed-meshheading:9010223-Nuclear Proteins, pubmed-meshheading:9010223-Polymerase Chain Reaction, pubmed-meshheading:9010223-Proto-Oncogene Protein c-ets-1, pubmed-meshheading:9010223-Proto-Oncogene Protein c-fli-1, pubmed-meshheading:9010223-Proto-Oncogene Proteins, pubmed-meshheading:9010223-Proto-Oncogene Proteins c-ets, pubmed-meshheading:9010223-RNA-Binding Protein EWS, pubmed-meshheading:9010223-Rabbits, pubmed-meshheading:9010223-Ribonucleoproteins, pubmed-meshheading:9010223-Serum Response Factor, pubmed-meshheading:9010223-Trans-Activators, pubmed-meshheading:9010223-Transcription Factors, pubmed-meshheading:9010223-ets-Domain Protein Elk-1, pubmed-meshheading:9010223-ets-Domain Protein Elk-4
pubmed:year	1997
pubmed:articleTitle	FLI1 and EWS-FLI1 function as ternary complex factors and ELK1 and SAP1a function as ternary and quaternary complex factors on the Egr1 promoter serum response elements.
pubmed:affiliation	Center for Molecular and Structural Biology, Medical University of South Carolina, Charleston 29425, USA.
pubmed:publicationType	Journal Article, Research Support, Non-U.S. Gov't