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1.
Mol Genet Metab ; 85(4): 301-7, 2005 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-15905112

RESUMO

In human cells, biotin is essential to maintain metabolic homeostasis and as regulator of gene expression. The enzyme holocarboxylase synthetase (HCS) transforms biotin into its active form 5'-biotinyl-AMP and this compound is used to biotinylate five biotin-dependent carboxylases or to activate a soluble guanylate cyclase (sGC) and a cGMP-dependent protein kinase (PKG). The HCS-sGC-PKG pathway is responsible for maintaining the mRNA levels of enzymes involved in biotin utilization including HCS, carboxylases, and a biotin carrier known as sodium-dependent multivitamin transporter (SMVT). To understand the role of SMVT in the control of biotin utilization, we have studied the effect of biotin availability on SMVT protein and mRNA expression levels in HepG2 cells by Western blot analysis and rtPCR, respectively; and their functional impact on the rate of [3H]biotin uptake in human cells. Our results showed that human HepG2 cells grown in a biotin-deficient medium have a lower rate of biotin uptake than normal cells. The impairment in biotin uptake is associated with a reduction in the amount of both SMVT protein mass and mRNA levels. Transfection of HepG2 cells with a vector containing a luciferase reporter gene under the control of the rat SMVT promoter demonstrated that its transcriptional activity is regulated by biotin availability through activation of the HCS-sGC-PKG pathway. Our results support the proposed role of SMVT in the altruistic regulation of biotin utilization in liver cells that has been associated with sparing biotin depletion of the brain.


Assuntos
Biotina/metabolismo , Proteínas Quinases Dependentes de GMP Cíclico/metabolismo , Fígado/metabolismo , Proteínas de Transporte de Monossacarídeos/metabolismo , Simportadores/metabolismo , Ativação Transcricional , Animais , Biotina/deficiência , Biotina/genética , Biotinilação , Western Blotting , Técnicas de Cultura de Células , Proteínas Quinases Dependentes de GMP Cíclico/genética , Transportador de Glucose Tipo 1 , Humanos , Proteínas de Membrana Transportadoras , Proteínas de Transporte de Monossacarídeos/genética , RNA Mensageiro , Ratos , Reação em Cadeia da Polimerase Via Transcriptase Reversa , Simportadores/genética
2.
Arch Med Res ; 33(5): 439-47, 2002.
Artigo em Inglês | MEDLINE | ID: mdl-12459313

RESUMO

Biotin, a water-soluble vitamin, is used as cofactor of enzymes involved in carboxylation reactions. In humans, there are five biotin-dependent carboxylases: propionyl-CoA carboxylase; methylcrotonyl-CoA carboxylase; pyruvate carboxylase, and two forms of acetyl-CoA carboxylase. These enzymes catalyze key reactions in gluconeogenesis, fatty acid metabolism, and amino acid catabolism; thus, biotin plays an essential role in maintaining metabolic homeostasis. In recent years, biotin has been associated with several diseases in humans. Some are related to enzyme deficiencies involved in biotin metabolism. However, not all biotin-responsive disorders can be explained based on the classical role of the vitamin in cell metabolism. Several groups have suggested that biotin may be involved in regulating transcription or protein expression of different proteins. Biotinylation of histones and triggering of transduction signaling cascades have been suggested as underlying mechanisms behind these non-classical biotin-deficiency manifestation in humans.


Assuntos
Biotina/metabolismo , Biotina/fisiologia , Sequência de Aminoácidos , Carbono-Nitrogênio Ligases/metabolismo , Catálise , Feminino , Regulação Enzimológica da Expressão Gênica , Histonas/metabolismo , Humanos , Masculino , Modelos Biológicos , Modelos Químicos , Dados de Sequência Molecular , Deficiência Múltipla de Carboxilase/genética , Gravidez , Transdução de Sinais , Transcrição Gênica
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