Identification of a differentially-expressed gene in fatty liver of overfeeding geese

Acta Biochim Biophys Sin (Shanghai). 2007 Sep;39(9):649-56. doi: 10.1111/j.1745-7270.2007.00329.x.

Abstract

In response to overfeeding, geese develop fatty liver. To understand the fattening mechanism, mRNA differential display reverse transcription PCR was used to study the gene expression differences between French Landes grey geese and Xupu white geese in conditions of overfeeding and normal feeding. One gene was found to be up-regulated in the fatty liver in both breeds, and it has a 1797 bp cDNA with 83% identity to chicken SELENBP1. The sequence analysis revealed that its open reading frame of 1413 bp encodes a protein of 471 amino acids, which contains a putative conserved domain of 56 kDa selenium binding protein with high homology to its homologues of chicken (95%), rat (86%), mouse (84%), human (86%), monkey (86%), dog (86%), and cattle (86%). The function of this protein has been briefly reviewed based on published information. In tissue expression analysis, the expression of geese SELENBP1 mRNA was found to be higher in liver or kidney than in other tested tissues. The results showed that overfeeding could increase the mRNA expression level of geese SELENBP1.

Publication types

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

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Avian Proteins / biosynthesis
  • Avian Proteins / genetics
  • Base Sequence
  • Cattle
  • Dogs
  • Eating / genetics*
  • Fatty Liver / genetics*
  • Fatty Liver / metabolism
  • Female
  • Geese / genetics*
  • Geese / physiology
  • Gene Expression Regulation
  • Humans
  • Hyperphagia / genetics*
  • Male
  • Mice
  • Molecular Sequence Data
  • Rats
  • Selenium-Binding Proteins / biosynthesis*
  • Selenium-Binding Proteins / genetics*

Substances

  • Avian Proteins
  • Selenium-Binding Proteins