Supplementary Figure 1. Compararison of the expression of the genes within the 10q23 locus using either Troglitazone or Rosiglitazone as the PPAR  agonist.

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Supplementary Figure 1. Compararison of the expression of the genes within the 10q23 locus using either Troglitazone or Rosiglitazone as the PPAR  agonist during adipogenesis in SGBS cells. mRNA was extracted from SGBS cells at the given time points following introduction of the differentiation medium. Real-time PCRs were carried out to measure mRNA levels of the genes of interest. Relative Fold Change

Supplementary Figure 2. Western blot data for the three genes within the 10q23 locus during SGBS cell adipogenesis using Troglitazone as the PPAR  agonist. Protein was extracted from SGBS cells at the given time points following introduction of the differentiation medium supplemented with Troglitazone. Western blots were carried out to examine the protein levels of the genes of interest. A representative Western blot result is presented. Day 5Day 0 Day 10 Day 20Day 31Day 40Day 49 36B4 HHEX IDE KIF11 RAN Differentiation with Troglitazone

Relative Fold Change HHEX 36B4 KIF11 Day 03 hours6 hours Day 2Day 3Day 4Day 5 A. B. 3 hours and Day 5 compared with Time 0: ** P<0.01; *** P<10 -4 ** *** ** *** Supplementary Figure 3. Expression time course of the three genes within the 10q23 locus during early adipogenesis in SGBS cell. mRNA and protein were extracted from SGBS cells at given time points (Day 0, 3hrs, 6hrs, Day 2, Day 3, Day 4 and Day 5) following introduction of the differentiation medium supplemented with Rosiglitazone. Real- time PCR normalized for 36B4 mRNA expression (A) and Western blots (B) were carried out to measure either mRNA or protein levels of the gene of interest, respectively. Standard deviation was calculated based on three independent mRNA replicates. A representative Western blot result is presented.

Supplementary Figure 4. Consistency of HHEX real-time PCR result utilizing two primer sets. mRNA were extracted from SGBS cells at given time points following introduction of the differentiation medium supplemented with Troglitazone. Real-time PCRs were carried out to measure mRNA levels of HHEX utilizing two separate primer pairs. Two primer pairs on HHEX (Differentiation with Troglitazone) Relative Fold Change