TitleGatm, a creatine synthesis enzyme, is imprinted in mouse placenta.
Publication TypeJournal Article
Year of Publication2003
AuthorsSandell, LL, Guan, X-J, Ingram, R, Tilghman, SM
JournalProc Natl Acad Sci U S A
Volume100
Issue8
Pagination4622-7
Date Published2003 Apr 15
KeywordsAmidinotransferases, Animals, Base Sequence, CpG Islands, DNA Methylation, DNA, Complementary, Female, Gene Expression Regulation, Developmental, Gene Expression Regulation, Enzymologic, Genomic Imprinting, Mice, Mice, Inbred C57BL, Peromyscus, Placenta, Pregnancy
Abstract

To increase our understanding of imprinting and epigenetic gene regulation, we undertook a search for new imprinted genes. We identified Gatm, a gene that encodes l-arginine:glycine amidinotransferase, which catalyzes the rate-limiting step in the synthesis of creatine. In mouse, Gatm is expressed during development and is imprinted in the placenta and yolk sac, but not in embryonic tissues. The Gatm gene maps to mouse chromosome 2 in a region not previously shown to contain imprinted genes. To determine whether Gatm is located in a cluster of imprinted genes, we investigated the expression pattern of genes located near Gatm: Duox1-2, Slc28a2, Slc30a4 and a transcript corresponding to LOC214616. We found no evidence that any of these genes is imprinted in placenta. We show that a CpG island associated with Gatm is unmethylated, as is a large CpG island associated with a neighboring gene. This genomic screen for novel imprinted genes has elucidated a new connection between imprinting and creatine metabolism during embryonic development in mammals.

Alternate JournalProc. Natl. Acad. Sci. U.S.A.