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Vitamin D-interacting protein 205 (DRIP205) coactivation of estrogen receptor alpha (ERalpha) involves multiple domains of both proteins.

Abstract
Vitamin D-interacting protein 205 (DRIP205) is a mediator complex protein that anchors the complex to the estrogen receptor (ER) and other nuclear receptors (NRs). In ZR-75 breast cancer cells treated with 17beta-estradiol (E2) and transfected with a construct containing three tandem estrogen responsive elements (pERE(3)), DRIP205 coactivates ERalpha-mediated transactivation. DRIP205Delta587-636 is a DRIP205 mutant in which both NR boxes within amino acids 587-636 have been deleted and, in parallel transfection studies, DRIP205Delta587-636 also coactivates ERalpha. Moreover, both wild-type and variant DRIP205 also colocalize with ERalpha in the nuclei of transfected cells. Extensive deletion analysis of DRIP205 shows that multiple domains of this protein play a role in coactivation of ERalpha and in interactions with ERalpha. Coactivation of ERalpha by DRIP205 does not require NR boxes, and variants with deletion of N-terminal (amino acids 1-639) and C-terminal (amino acids 576-1566) significantly coactivate ERalpha. DRIP205 resembles p160 coactivators that also interact with multiple regions of ERalpha; however, unlike p160 coactivators, DRIP205 coactivation of ERalpha does not require NR boxes.
AuthorsQian Wu, Robert Burghardt, Stephen Safe
JournalThe Journal of biological chemistry (J Biol Chem) Vol. 279 Issue 51 Pg. 53602-12 (Dec 17 2004) ISSN: 0021-9258 [Print] United States
PMID15471764 (Publication Type: Journal Article)
Chemical References
  • Estrogen Receptor alpha
  • Estrogens
  • MED1 protein, human
  • Mediator Complex Subunit 1
  • Oligonucleotides
  • Receptors, Estrogen
  • Transcription Factors
  • DNA Restriction Enzymes
Topics
  • Animals
  • Blotting, Western
  • COS Cells
  • Cell Line, Tumor
  • Cell Nucleus (metabolism)
  • Cloning, Molecular
  • DNA Restriction Enzymes (pharmacology)
  • Estrogen Receptor alpha (metabolism)
  • Estrogens (metabolism)
  • Gene Deletion
  • Humans
  • Mediator Complex Subunit 1
  • Mutation
  • Oligonucleotides (chemistry)
  • Plasmids (metabolism)
  • Protein Binding
  • Protein Structure, Tertiary
  • Receptors, Estrogen (metabolism)
  • Response Elements
  • Transcription Factors (metabolism)
  • Transcriptional Activation
  • Transfection

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