4.2 Article

Evaluation of reference genes for gene expression studies in human brown adipose tissue

Journal

ADIPOCYTE
Volume 4, Issue 4, Pages 280-285

Publisher

TAYLOR & FRANCIS INC
DOI: 10.1080/21623945.2015.1039884

Keywords

brown adipose tissue; human; quantitative PCR; reference genes; white adipose tissue; BAT; Brown adipose tissue; CV; Coefficient of variation; PCR; Polymerase chain reaction; PR-BAT; Perirenal BAT; PT-BAT; Perithyroid BAT; qPCR; Quantitative PCR; RMA; Robust multi-array average; SOS; Swedish Obese Subjects; WAT; White adipose tissue

Funding

  1. Sahlgrenska Academy
  2. Swedish federal government under the LUA/ALF
  3. AstraZeneca RD
  4. Research Foundation of the Swedish Diabetes Association
  5. 7TH Framework program International Research Staff Exchange Scheme (IRSES), FUEGO project

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Human brown adipose tissue (BAT) has during the last 5 year been subjected to an increasing research interest, due to its putative function as a target for future obesity treatments. The most commonly used method for molecular studies of human BAT is the quantitative polymerase chain reaction (qPCR). This method requires normalization to a reference gene (genes with uniform expression under different experimental conditions, e.g. similar expression levels between human BAT and WAT), but so far no evaluation of reference genes for human BAT has been performed. Two different microarray datasets with samples containing human BAT were used to search for genes with low variability in expression levels. Seven genes (FAM96B, GNB1, GNB2, HUWE1, PSMB2, RING1 and TPT1) identified by microarray analysis, and 8 commonly used reference genes (18S, B2M, GAPDH, LRP10, PPIA, RPLP0, UBC, and YWHAZ) were selected and further analyzed by quantitative PCR in both BAT containing perirenal adipose tissue and subcutaneous adipose tissue. Results were analyzed using 2 different algorithms (Normfinder and geNorm). Most of the commonly used reference genes displayed acceptably low variability (geNorm M-values <0.5) in the samples analyzed, but the novel reference genes identified by microarray displayed an even lower variability (M-values <0.25). Our data suggests that PSMB2, GNB2 and GNB1 are suitable novel reference genes for qPCR analysis of human BAT and we recommend that they are included in future gene expression studies of human BAT.

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