Isolation of pig mitochondrial 3-hydroxy-3-methylglutaryl-CoA synthase gene promoter: characterization of a peroxisome proliferator-responsive element

Low expression of the mitochondrial 3-hydroxy-3-methylglutaryl- CoA (HMG-CoA) synthase gene during development correlates with an unusually low hepatic ketogenic capacity and lack of hyperketonaemia in piglets. Here we report the isolation and characterization of the 5« end of the pig mitochondrial...

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Detalhes bibliográficos
Autores: Ortiz, José A., Mallolas, Judith, Nicot, Carine, Bofarull, Josep, Rodríguez Rubio, Joan Carles, García Hegardt, Fausto, Haro Bautista, Diego, Marrero González, Pedro F.
Formato: artículo
Estado:Versión aceptada para publicación
Fecha de publicación:1999
País:España
Recursos:Varias* (Consorci de Biblioteques Universitáries de Catalunya, Centre de Serveis Científics i Acadèmics de Catalunya)
Repositorio:Recercat. Dipósit de la Recerca de Catalunya
OAI Identifier:oai:recercat.cat:2445/182199
Acesso em linha:https://hdl.handle.net/2445/182199
Access Level:acceso abierto
Palavra-chave:Àcids grassos
Expressió gènica
Mitocondris
Fatty acids
Gene expression
Mitochondria
Descrição
Resumo:Low expression of the mitochondrial 3-hydroxy-3-methylglutaryl- CoA (HMG-CoA) synthase gene during development correlates with an unusually low hepatic ketogenic capacity and lack of hyperketonaemia in piglets. Here we report the isolation and characterization of the 5« end of the pig mitochondrial HMG-CoA synthase gene. The 581 bp region proximal to the transcription start site permits transcription of a reporter gene, con®rming the function of the promoter. The pig mitochondrial HMG-CoA synthase promoter is trans-activated by the peroxisomal proliferator-activated receptor (PPAR), and a functional response element for PPAR (PPRE) has been localized in the promoter region. Pig PPRE is constituted by an imperfect direct repeat (DR-1) and a downstream sequence, both of which are needed to confer PPAR-sensitivity to a thymidine kinase promoter and to form complexes with PPAR[retinoid X receptor heterodimers. A role of PPAR trans-activation in starvationassociated induction of gene expression is suggested.