Differential display of expressed genes reveals a novel function of SFRS18 in regulation of intramuscular fat deposition

Int J Biol Sci. 2009;5(1):28-33. doi: 10.7150/ijbs.5.28. Epub 2008 Dec 17.

Abstract

Intramuscular fat (IMF) content plays a key role in establishing pork quality. In the present study, differential-display reverse transcription-polymerase chain reaction (DDRT-PCR) was used to identify differentially expressed (DE) genes between longissimus dorsi (LD) muscles with extremely different IMF content. A major DE gene associated with IMF content was identified as splicing factor serine-arginine rich protein (SFRS18) gene, also known as SRrp130. The gene exhibited relatively higher expression levels in LD muscles with higher IMF content. A full-length cDNA sequence of pig SFRS18 gene was obtained by in silico comparative cloning coupled with PCR target sequencing, while the current EST (expressed sequence tag) database supported two transcript variants of the pig gene. Differential expression of the SFRS18 gene was further confirmed using quantitative PCR. The mRNA levels of SFRS18 gene showed significant and positive correlation with IMF content in LD muscle (r = 0.54, P < 0.01). Collectively, these results suggest that the SFRS18 gene is involved in the regulation of IMF deposition in pig and that it may be a useful tool in selecting animals for desired amounts of fatness for high quality pork.

Keywords: IMF; SFRS18; differential display; expression level; muscle.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adipose Tissue / metabolism
  • Adipose Tissue / physiology*
  • Adiposity / genetics*
  • Animals
  • Base Sequence
  • Cloning, Molecular
  • DNA, Complementary / genetics
  • Expressed Sequence Tags
  • Gene Expression Regulation / physiology*
  • Meat*
  • Molecular Sequence Data
  • Muscle, Skeletal / metabolism
  • Muscle, Skeletal / physiology*
  • Nuclear Proteins / genetics
  • Nuclear Proteins / metabolism*
  • RNA-Binding Proteins / genetics
  • RNA-Binding Proteins / metabolism*
  • Reverse Transcriptase Polymerase Chain Reaction
  • Sequence Analysis, DNA
  • Serine-Arginine Splicing Factors
  • Sus scrofa / genetics
  • Sus scrofa / metabolism*

Substances

  • DNA, Complementary
  • Nuclear Proteins
  • RNA-Binding Proteins
  • Serine-Arginine Splicing Factors