화학공학소재연구정보센터
Biochemical and Biophysical Research Communications, Vol.290, No.1, 403-408, 2002
Paternal expression of a novel imprinted gene, peg12/frat3, in the mouse 7C region homologous to the Prader-Willi syndrome region
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. (C) 2002 Elsevier Science.