Nrac, a novel nutritionally-regulated adipose and cardiac-enriched gene

PLoS One. 2012;7(9):e46254. doi: 10.1371/journal.pone.0046254. Epub 2012 Sep 27.

Abstract

Obesity increases the risk of multiple diseases, such as type 2 diabetes and coronary heart diseases, and therefore the current obesity epidemic poses a major public health issue. Therapeutic approaches are urgently needed to treat obesity as well as its complications. Plasma-membrane proteins with restricted tissue distributions are attractive drug targets, because of their accessibility to various drug delivery mechanisms and potentially alleviated side effects. To identify genes involved in metabolism, we performed RNA-Seq on fat in mice treated with a high-fat diet or fasting. Here we show that the gene A530016L24Rik (human ortholog C14orf180), named Nrac, is a novel nutritionally-regulated adipose and cardiac-enriched gene. Nrac is expressed specifically and abundantly in fat and the heart. Both fasting and obesity reduced Nrac expression in white adipose tissue, and fasting reduced its expression in brown fat. Nrac is localized to the plasma membrane, and highly induced during adipocyte differentiation. Nrac is therefore a novel adipocyte marker and has potential functions in metabolism.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adipocytes / metabolism*
  • Adipocytes / pathology
  • Adipogenesis / genetics*
  • Adipose Tissue, Brown / metabolism*
  • Adipose Tissue, Brown / pathology
  • Adipose Tissue, White / metabolism*
  • Adipose Tissue, White / pathology
  • Amino Acid Sequence
  • Animals
  • Cell Differentiation
  • Diet, High-Fat
  • Disease Models, Animal
  • Fasting
  • Gene Expression
  • Humans
  • Male
  • Membrane Proteins / chemistry
  • Membrane Proteins / genetics*
  • Membrane Proteins / metabolism
  • Mice
  • Mice, Inbred C57BL
  • Molecular Sequence Data
  • Myocardium / metabolism
  • Obesity / genetics*
  • Obesity / pathology
  • Organ Specificity
  • Protein Structure, Tertiary
  • Sequence Homology, Amino Acid

Substances

  • Membrane Proteins
  • Nrac protein, mouse

Grants and funding

The present work was supported in part by a fund (176412) from Wayne State University to R.Z. and by the National Natural Science Foundation of China (Grant Nos. 90408028, 31171238, 30800642 and 10747150) to F.G. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.