作者: Elena R. GarcÍa-Trevijano , M. Ujue Latasa , M. Victoria Carretero , Carmen Berasain , José M. Mato
关键词: Methylation 、 Regulation of gene expression 、 Liver cytology 、 Hepatocyte 、 Cellular differentiation 、 Cell biology 、 Gene expression 、 Biochemistry 、 Biology 、 Methionine 、 Methionine Adenosyltransferase
摘要: Methionine metabolism starts with the formation of S-adenosylmethionine (AdoMet), most important biological methyl donor. This reaction is catalyzed by methionine adenosyltransferase (MAT). MAT product two different genes: MAT1A, which expressed only in adult liver, and MAT2A, widely distributed, fetal replaces MAT1A hepatocarcinoma. In preservation high expression low MAT2A critical for maintenance a functional differentiated organ. Here we describe that cultured rat hepatocytes progressively decreased, as described other liver-specific genes, was induced. We find this switch gene prevented adding AdoMet to culture medium. also show decreased addition markedly increased transcription dose-dependent fashion. effect mimicked methionine, blocked 3-deazaadenosine L-ethionine, but not D-ethionine, indicating specific mediated probably methylation reaction. These findings identify key molecule differentially regulates helps maintain status hepatocyte.