Paternal expression of a novel imprinted gene, Peg12/Frat3, in the mouse 7C region homologous to the Prader-Willi syndrome region

Biochem Biophys Res Commun. 2002 Jan 11;290(1):403-8. doi: 10.1006/bbrc.2001.6160.

Abstract

Paternally expressed imprinted genes (Pegs) were systematically screened by comparing gene expression profiles of parthenogenetic and normal fertilized embryos using an oligonucleotide array. A novel imprinted gene, Peg12/Frat3, was identified along with 10 previously known Pegs. Peg12/Frat3 is expressed primarily in embryonic stages and might be a positive regulator of the Wnt signaling pathway. It locates next to the Zfp127 imprinted gene in the mouse 7C region, which has syntenic homology to the human Prader-Willi syndrome region on chromosome 15q11-q13, indicating that this imprinted region extends to the telomeric side in the mouse.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Carrier Proteins
  • Chromosomes, Human, Pair 15
  • Crosses, Genetic
  • Fathers*
  • Female
  • Genomic Imprinting*
  • Humans
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Mice, Inbred DBA
  • Mice, Inbred ICR
  • Models, Genetic
  • Neoplasm Proteins
  • Nerve Tissue Proteins / biosynthesis*
  • Nerve Tissue Proteins / genetics*
  • Neurons / metabolism
  • Oligonucleotide Array Sequence Analysis
  • Polymerase Chain Reaction
  • Polymorphism, Genetic
  • Prader-Willi Syndrome / genetics*
  • Reverse Transcriptase Polymerase Chain Reaction
  • Signal Transduction

Substances

  • Carrier Proteins
  • Neoplasm Proteins
  • Nerve Tissue Proteins
  • Peg12 protein, mouse