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PLoS One ; 8(4): e61938, 2013.
Artigo em Inglês | MEDLINE | ID: mdl-23613978

RESUMO

κ-Casein (CSN3) is known to play an essential role in controlling the stability of the milk micelles. We found that the expression of Csn3 was induced by all-trans retinoic acid (ATRA) during neural differentiation in P19 embryonal carcinoma cells from our study using DNA microarray. In this paper, we describe the detailed time course of Csn3 expression and the induction mechanism of Csn3 transcription activation in this process. The Csn3 expression was induced rapidly and transiently within 24 h of ATRA treatment. Retinoic acid receptor (RAR)-specific agonists were used in expression analysis to identify the RAR subtype involved upregulation of Csn3; a RARα-specific agonist mimicked the effects of ATRA on induction of Csn3 expression. Therefore, RARα may be the RAR subtype mediating the effects of ATRA on the induction of Csn3 gene transcription in this differentiation-promoting process of P19 cells. We found that the promoter region of Csn3 contained a typical consensus retinoic acid response element (RARE), and this RARE was necessary for ATRA-dependent transcriptional regulation. We confirmed that RARα bound to this RARE sequence in P19 cells. These findings indicated that the Csn3 expression is upregulated via ATRA-bound RARα and binding of this receptor to the RARE in the Csn3 promoter region. This will certainly serve as a first step forward unraveling the mysteries of induction of Csn3 in the process of neural differentiation.


Assuntos
Diferenciação Celular/genética , Regulação da Expressão Gênica/efeitos dos fármacos , Neurônios/citologia , Neurônios/metabolismo , Proteínas Nucleares/genética , Proteínas Quinases/genética , Tretinoína/farmacologia , Animais , Sequência de Bases , Complexo do Signalossomo COP9 , Diferenciação Celular/efeitos dos fármacos , Linhagem Celular , Embrião de Mamíferos/citologia , Embrião de Mamíferos/efeitos dos fármacos , Embrião de Mamíferos/metabolismo , Camundongos , Dados de Sequência Molecular , Neurônios/efeitos dos fármacos , Proteínas Nucleares/metabolismo , Motivos de Nucleotídeos/genética , Ligação Proteica/efeitos dos fármacos , Ligação Proteica/genética , Proteínas Quinases/metabolismo , Proteínas Proto-Oncogênicas , Receptores do Ácido Retinoico/metabolismo , Elementos de Resposta/genética , Receptor alfa de Ácido Retinoico , Transcrição Gênica/efeitos dos fármacos
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