The transcriptional co-activator p/CIP binds CBP and mediates nuclear-receptor function
Article Abstract:
The functionally conserved proteins p300 and CPB have fundamental acetylase activity and act, with other factors, to activate transcription of DNA. A new SRC family member, p/CIP, has been discovered which is a significant component of the CBP/p300 cell. Research shows that full ligand-activated gene transcription in the examined cells requires the presence of both NCoA-1 and the CBP/p/CIP complex.
Publication Name: Nature
Subject: Zoology and wildlife conservation
ISSN: 0028-0836
Year: 1997
User Contributions:
Comment about this article or add new information about this topic:
Ligand binding and co-activator assembly of the peroxisome proliferator-activated receptor-gamma
Article Abstract:
The peroxisome proliferator-activated receptor-gamma (PPAR-gamma) is an important transcription factor in adipocyte differentiation and glucose homeostasis. The x-ray crystal structure of the human apo-PPAR-gamma ligand-binding domain (LBD) is presented, revealing a large binding pocket. The ternary complex containing the PPAR-gamma LBD is described, along with 88 amino acids of human SRC-1.
Publication Name: Nature
Subject: Zoology and wildlife conservation
ISSN: 0028-0836
Year: 1998
User Contributions:
Comment about this article or add new information about this topic:
- Abstracts: Proteolytic turnover of the Gal4 transcription factor is not required for function in vivo. A putative stimulatory role for activator turnover in gene expression
- Abstracts: The strict anaerobe Bacteroides fragilis grows in and benefits from nanomolar concentrations of oxygen
- Abstracts: Atomic gas in flatland. Strong atom-field coupling for Bose-Einstein condensates in an optical cavity on a chip
- Abstracts: The synaptic vesicle cycle: a cascade of protein-protein interactions. A dual-[Ca.sup.2+]-sensor model for neurotransmitter release in a central synapse
- Abstracts: A structural change in the kinesin motor protein that drives motility. How kinesin waits between steps