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Molecular cloning of xSRC-3, a novel transcription coactivator from Xenopus, that is related to AIB1, p/CIP, and TIF2.

Abstract
Nuclear receptors regulate transcription by binding to specific DNA response elements of target genes. Herein, we report the molecular cloning and characterization of a novel Xenopus cDNA encoding a transcription coactivator xSRC-3 by using retinoid X receptor (RXR) as a bait in the yeast two-hybrid screening. It belongs to a growing coactivator family that includes a steroid receptor coactivator amplified in breast cancer (AIB1), p300/ CREB-binding protein (CBP)-interacting protein (p/ CIP), and transcriptional intermediate factor 2 (TIF2). It also interacts with a series of nuclear receptors including retinoic acid receptor (RAR), thyroid hormone receptor (TR), and orphan nuclear receptors [hepatocyte nuclear receptor 4 (HNF4) and constitutive androstane receptor (CAR)]. However, it does not interact with small heterodimer partner (SHP), an orphan nuclear receptor known to antagonize ligand-dependent transactivation of other nuclear receptors. In CV-1 cells, cotransfection of xSRC-3 differentially stimulates ligand-induced transactivation of RXR, TR, and RAR in a dose-dependent manner. Interestingly, xSRC-3 is highly expressed in adult liver and early stages of oocyte development, suggesting that studies of xSRC-3 may lead to better understanding of the roles nuclear receptors play in oocyte development as well as liver-specific gene expression.
AuthorsH J Kim, S K Lee, S Y Na, H S Choi, J W Lee
JournalMolecular endocrinology (Baltimore, Md.) (Mol Endocrinol) Vol. 12 Issue 7 Pg. 1038-47 (Jul 1998) ISSN: 0888-8809 [Print] United States
PMID9658407 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • NCOA2 protein, human
  • NCOA3 protein, Xenopus
  • Nuclear Receptor Coactivator 2
  • Oncogene Proteins
  • Receptors, Retinoic Acid
  • Receptors, Thyroid Hormone
  • Recombinant Fusion Proteins
  • Retinoid X Receptors
  • Trans-Activators
  • Transcription Factors
  • Xenopus Proteins
  • Acetyltransferases
  • Histone Acetyltransferases
  • NCOA1 protein, human
  • NCOA3 protein, human
  • Nuclear Receptor Coactivator 1
  • Nuclear Receptor Coactivator 3
Topics
  • Acetyltransferases
  • Alternative Splicing
  • Amino Acid Sequence
  • Animals
  • Binding Sites
  • Cell Nucleus (metabolism)
  • Cloning, Molecular
  • Female
  • Gene Expression
  • Histone Acetyltransferases
  • Humans
  • Molecular Sequence Data
  • Mutagenesis
  • Nuclear Receptor Coactivator 1
  • Nuclear Receptor Coactivator 2
  • Nuclear Receptor Coactivator 3
  • Oncogene Proteins
  • Receptors, Retinoic Acid (metabolism)
  • Receptors, Thyroid Hormone (metabolism)
  • Recombinant Fusion Proteins
  • Retinoid X Receptors
  • Saccharomyces cerevisiae (genetics)
  • Sequence Homology
  • Trans-Activators (chemistry, genetics, metabolism)
  • Transcription Factors (chemistry, metabolism)
  • Transcriptional Activation
  • Xenopus
  • Xenopus Proteins

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