Molecular Cloning of xSRC-3, a Novel Transcription Coactivator from Xenopus, That Is Related to AIB1, p/CIP, and TIF2
- 1 July 1998
- journal article
- Published by The Endocrine Society in Molecular Endocrinology
- Vol. 12 (7) , 1038-1047
- https://doi.org/10.1210/me.12.7.1038
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 stimula...Keywords
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