AI Article Synopsis

  • A gene expression program is crucial for developing mature fat cells (adipocytes), but the role of posttranscriptional factors like the RNA-binding protein PSPC1 isn't well understood.
  • PSPC1 promotes the formation of fat cells in lab conditions and is essential for their proper function in living organisms, as it binds to important RNA sequences involved in adipocyte development.
  • Mice without PSPC1 show less fat storage and higher energy use, which helps prevent obesity and insulin resistance, highlighting the protein’s key role in regulating fat cell development post-transcriptionally.

Article Abstract

A highly orchestrated gene expression program establishes the properties that define mature adipocytes, but the contribution of posttranscriptional factors to the adipocyte phenotype is poorly understood. Here we have shown that the RNA-binding protein PSPC1, a component of the paraspeckle complex, promotes adipogenesis in vitro and is important for mature adipocyte function in vivo. Cross-linking and immunoprecipitation followed by RNA sequencing revealed that PSPC1 binds to intronic and 3'-untranslated regions of a number of adipocyte RNAs, including the RNA encoding the transcriptional regulator EBF1. Purification of the paraspeckle complex from adipocytes further showed that PSPC1 associates with the RNA export factor DDX3X in a differentiation-dependent manner. Remarkably, PSPC1 relocates from the nucleus to the cytoplasm during differentiation, coinciding with enhanced export of adipogenic RNAs. Mice lacking PSPC1 in fat displayed reduced lipid storage and adipose tissue mass and were resistant to diet-induced obesity and insulin resistance due to a compensatory increase in energy expenditure. These findings highlight a role for PSPC1-dependent RNA maturation in the posttranscriptional control of adipose development and function.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5330726PMC
http://dx.doi.org/10.1172/JCI89484DOI Listing

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