Characterization of the fasting-induced adipose factor FIAF, a novel peroxisome proliferator-activated receptor target gene.
Details
Serval ID
serval:BIB_4B2A552A1FDC
Type
Article: article from journal or magazin.
Collection
Publications
Institution
Title
Characterization of the fasting-induced adipose factor FIAF, a novel peroxisome proliferator-activated receptor target gene.
Journal
Journal of Biological Chemistry
ISSN
0021-9258[print], 0021-9258[linking]
Publication state
Published
Issued date
2000
Volume
275
Number
37
Pages
28488-28493
Language
english
Notes
Publication types: Journal Article ; Research Support, Non-U.S. Gov't
Publication Status: ppublish
Publication Status: ppublish
Abstract
Fasting is associated with significant changes in nutrient metabolism, many of which are governed by transcription factors that regulate the expression of rate-limiting enzymes. One factor that plays an important role in the metabolic response to fasting is the peroxisome proliferator-activated receptor alpha (PPARalpha). To gain more insight into the role of PPARalpha during fasting, and into the regulation of metabolism during fasting in general, a search for unknown PPARalpha target genes was performed. Using subtractive hybridization (SABRE) comparing liver mRNA from wild-type and PPARalpha null mice, we isolated a novel PPARalpha target gene, encoding the secreted protein FIAF (for fasting induced adipose factor), that belongs to the family of fibrinogen/angiopoietin-like proteins. FIAF is predominantly expressed in adipose tissue and is strongly up-regulated by fasting in white adipose tissue and liver. Moreover, FIAF mRNA is decreased in white adipose tissue of PPARgamma +/- mice. FIAF protein can be detected in various tissues and in blood plasma, suggesting that FIAF has an endocrine function. Its plasma abundance is increased by fasting and decreased by chronic high fat feeding. The data suggest that FIAF represents a novel endocrine signal involved in the regulation of metabolism, especially under fasting conditions.
Keywords
Adipose Tissue/metabolism, Amino Acid Sequence, Angiopoietins, Animals, Base Sequence, Blood Proteins/analysis, Blood Proteins/genetics, Fasting, Mice, Molecular Sequence Data, RNA, Messenger/analysis, Receptors, Cytoplasmic and Nuclear/physiology, Transcription Factors/physiology
Pubmed
Web of science
Open Access
Yes
Create date
24/01/2008 15:27
Last modification date
20/08/2019 13:59