Abstract

Adipose tissue renewal and obesity-driven expansion of fat cell number are dependent on proliferation and differentiation of adipose progenitors that reside in the vasculature that develops in coordination with adipose depots. The transcriptional events that regulate commitment of progenitors to the adipose lineage are poorly understood. Because expression of the nuclear receptor PPARγ defines the adipose lineage, isolation of elements that control PPARγ expression in adipose precursors may lead to discovery of transcriptional regulators of early adipocyte determination. Here, we describe the identification and validation in transgenic mice of 5 highly conserved non-coding sequences from the PPARγ locus that can drive expression of a reporter gene in a manner that recapitulates the tissue-specific pattern of PPARγ expression. Surprisingly, these 5 elements appear to control PPARγ expression in adipocyte precursors that are associated with the vasculature of adipose depots, but not in mature adipocytes. Characterization of these five PPARγ regulatory sequences may enable isolation of the transcription factors that bind these cis elements and provide insight into the molecular regulation of adipose tissue expansion in normal and pathological states.

Highlights

  • Obesity is a risk factor in multiple diseases, including type 2 diabetes, cardiovascular disease, and cancer [1]

  • As a first step to discern the transcription factors that control the initial phases of adipocyte determination, we have carried out a comparative genomic analysis to identify conserved sequence elements in the 59-flanking region of the PPARc locus that may be responsible for its pattern of expression

  • CS1, CS2, and CS3 are located between exon A2 and exon B (211 to 232 Kb from the PPARc2 transcriptional start site (TSS)), while CS4 and CS5 are located upstream of the PPARc1 exon A1 and far from the PPARc2 TSS (,279 Kb)

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Summary

Introduction

Obesity is a risk factor in multiple diseases, including type 2 diabetes, cardiovascular disease, and cancer [1]. As a first step to discern the transcription factors that control the initial phases of adipocyte determination, we have carried out a comparative genomic analysis to identify conserved sequence elements in the 59-flanking region of the PPARc locus that may be responsible for its pattern of expression.

Results
Conclusion
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