Study of the differential transcription in liver of growth hormone receptor (GHR), insulin-like growth factors (IGF1, IGF2) and insulin-like growth factor receptor (IGF1R) genes at different postnatal developmental ages in pig breeds

Mol Biol Rep. 2012 Mar;39(3):3055-66. doi: 10.1007/s11033-011-1068-8. Epub 2011 Jun 22.

Abstract

The objective of this study was to determine hepatic expression levels of GHR, IGF1R, IGF1 and IGF2 genes in young growing gilts at different developmental ages (60-210 days) in five pig breeds: Polish Large White (PLW), Polish Landrace (PL), Pulawska (Pul), Duroc (Dur) and Pietrain (Pie). We studied the differences among pig breeds as well as within each breed for pigs in different developmental ages. Obtained results revealed major differences among breeds in hepatic gene expression of porcine GHR, IGF1R, IGF1 and IGF2 genes in different developmental ages. The differences among breeds of GHR expression were significantly higher in PLW, PL at the age of 60, 90, 120 days as compared to Pul, Dur and Pie. In turn, the highest level of IGF1R expression was observed in PL at age of 150, 180 and 210 days, whereas in case of IGF1 the highest level was recorded in Pie gilts at the age of 60 and 90 days. Moreover trait associated study revealed highly significant correlations between hepatic expressions of IGF1R and IGF2 genes and carcass composition traits (P < 0.01) The results of study suggest that porcine GHR, IGF1R, IGF1 and IGF2 genes may be potential candidate genes for postnatal growth and carcass composition traits. Therefore, the implementation of the hepatic expression of GH/IGF genes into the pig breeding and gene assisted selection program in different pig breeds should be considered. However, further population wide study is needed to clarify the hepatic expression association with economic traits, such as body growth, meat quality and carcass composition traits.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Age Factors
  • Animals
  • Body Composition / genetics
  • Breeding / methods*
  • DNA Primers / genetics
  • Female
  • Linear Models
  • Liver / metabolism*
  • Meat
  • Receptors, Somatomedin / metabolism*
  • Receptors, Somatotropin / metabolism*
  • Reverse Transcriptase Polymerase Chain Reaction
  • Somatomedins / metabolism*
  • Species Specificity
  • Sus scrofa / genetics*
  • Sus scrofa / growth & development*
  • Sus scrofa / metabolism

Substances

  • DNA Primers
  • Receptors, Somatomedin
  • Receptors, Somatotropin
  • Somatomedins