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Title: PRIC320, a transcription coactivator, isolated from peroxisome proliferator-binding protein complex

Journal Article · · Biochemical and Biophysical Research Communications
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  1. Department of Pathology, Northwestern University, Feinberg School of Medicine, Chicago, IL 60611 (United States)

Ciprofibrate, a potent peroxisome proliferator, induces pleiotropic responses in liver by activating peroxisome proliferator-activated receptor {alpha} (PPAR{alpha}), a nuclear receptor. Transcriptional regulation by liganded nuclear receptors involves the participation of coregulators that form multiprotein complexes possibly to achieve cell and gene specific transcription. SDS-PAGE and matrix-assisted laser desorption/ionization reflection time-of-flight mass spectrometric analyses of ciprofibrate-binding proteins from liver nuclear extracts obtained using ciprofibrate-Sepharose affinity matrix resulted in the identification of a new high molecular weight nuclear receptor coactivator, which we designated PRIC320. The full-length human cDNA encoding this protein has an open-reading frame that codes for a 320 kDa protein containing 2882 amino acids. PRIC320 contains five LXXLL signature motifs that mediate interaction with nuclear receptors. PRIC320 binds avidly to nuclear receptors PPAR{alpha}, CAR, ER{alpha}, and RXR, but only minimally with PPAR{gamma}. PRIC320 also interacts with transcription cofactors CBP, PRIP, and PBP. Immunoprecipitation-immunoblotting as well as cellular localization studies confirmed the interaction between PPAR{alpha} and PRIC320. PRIC320 acts as a transcription coactivator by stimulating PPAR{alpha}-mediated transcription. We conclude that ciprofibrate, a PPAR{alpha} ligand, binds a multiprotein complex and PRIC320 cloned from this complex functions as a nuclear receptor coactivator.

OSTI ID:
20798934
Journal Information:
Biochemical and Biophysical Research Communications, Vol. 343, Issue 2; Other Information: DOI: 10.1016/j.bbrc.2006.02.160; PII: S0006-291X(06)00414-1; Copyright (c) 2006 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved; Country of input: International Atomic Energy Agency (IAEA); ISSN 0006-291X
Country of Publication:
United States
Language:
English