Cited by 60Peroxisome Proliferator-Activated ReceptorsAdipose Tissue and MetabolismGenomics and Chromatin Dynamics

Identification of novel PPARγ target genes by integrated analysis of ChIP-on-chip and microarray expression data during adipocyte differentiation

Nakachi, Yutaka, Yagi, Ken, Nikaido, Itoshi, Bono, Hidemasa, Tonouchi, Mio, Schönbach, Christian, Okazaki, Yasushi·2008·Biochemical and Biophysical Research Communications

Abstract

PPARgamma (peroxisome proliferator-activated receptor gamma) acts as a key molecule of adipocyte differentiation, and transactivates multiple target genes involved in lipid metabolic pathways. Identification of PPARgamma target genes will facilitate to predict the extent to which the drugs can affect and also to understand the molecular basis of lipid metabolism. Here, we have identified five target genes regulated directly by PPARgamma during adipocyte differentiation in 3T3-L1 cells using integrated analyses of ChIP-on-chip and expression microarray. We have confirmed the direct PPARgamma regulation of five genes by luciferase reporter assay in NIH-3T3 cells. Of these five genes Hp, Tmem143 and 1100001G20Rik are novel PPARgamma targets. We have also detected PPREs (PPAR response elements) sequences in the promoter region of the five genes computationally. Unexpectedly, most of the PPREs detected proved to be atypical, suggesting the existence of more atypical PPREs than previously thought in the promoter region of PPARgamma regulated genes.

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Crossref · 10.1016/j.bbrc.2008.05.037

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  • PPAR isomers are master regulators of hundreds of target genes involved in fatty acid oxidation, cholesterol and lipoprotein metabolism, lipid droplet formation, and inflammation.

    “PPAR isomers are master regulators of hundreds of target genes involved in FAO, cholesterol and lipoprotein metabolism, LD formation, and inflammation [75,76].”

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Authors
Nakachi, Y., Yagi, K., Nikaido, I., Bono, H., Tonouchi, M., Schönbach, C., & Okazaki, Y.
Affiliations
  • Saitama Medical University (JP)
  • Agilent Technologies (Japan) (JP)
  • Nanyang Technological University (SG)
Corresponding author
Okazaki, Yasushi
Venue
Biochemical and Biophysical Research Communications
Publisher
Elsevier BV
Published
2008-07
Volume
372
Issue
2
Pages
362-366
ISSN
0006-291X (ISSN-L)
OpenAlex
W2054670962
Cited by
60
References
0
Citations by year
2026: 1 · 2025: 1 · 2024: 3 · 2023: 2 · 2022: 3 · 2021: 4 · 2020: 2 · 2019: 3 · 2018: 1 · 2017: 5 · 2016: 3 · 2014: 5 · 2013: 5 · 2012: 5
FWCI
2.33
Type
journal article
Language
en
Open access
closed
Locations
  • Biochemical and Biophysical Research Communications (publishedVersion)
  • PubMed (publishedVersion)
Funders
  • Promotion and Mutual Aid Corporation for Private Schools of Japan
  • Nanyang Technological University
  • Ministry of Education, Culture, Sports, Science and Technology
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Peroxisome Proliferator-Activated Receptors
  • Health Sciences › Medicine › Physiology › Adipose Tissue and Metabolism
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Genomics and Chromatin Dynamics
Keywords
PPARγ, target genes, adipogenesis, 3T3-L1 cells, ChIP-chip, gene expression microarrays, PPAR response element, lipid metabolism, transcriptional regulation
MeSH terms
Animals, Antibodies, Luciferases, Adipocytes, Genes, Reporter, Gene Expression Regulation, Developmental, Oligonucleotide Array Sequence Analysis, 3T3-L1 Cells, Chromatin Immunoprecipitation, PPAR gamma, Adipogenesis, Mice

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