Planque N, Leconte L, Coquelle F M, Benkhelifa S, Martin P, Felder-Schmittbuhl M P, Saule S
CNRS-UMR 146, Institut Curie-Section de Recherche, Bât 110, Centre Universitaire, 91405 Orsay, France.
J Biol Chem. 2001 Sep 21;276(38):35751-60. doi: 10.1074/jbc.M104523200. Epub 2001 Jul 16.
In the endocrine pancreas, alpha-cell-specific expression of the glucagon gene is mediated by DNA-binding proteins that interact with the G1 proximal promoter element. Among these proteins, the paired domain transcription factor Pax-6 has been shown to bind to G1 and to transactivate glucagon gene expression. Close to the Pax-6-binding site, we observed the presence of a binding site for a basic leucine zipper transcription factor of the Maf family. In the present study, we demonstrate the presence of Maf family members in the endocrine pancreas that bind to G1 and transactivate glucagon promoter expression. In transient transfection experiments, we found that the transactivating effect on the glucagon promoter was greatly enhanced by the simultaneous expression of Maf transcription factors and Pax-6. This enhancement on glucagon transactivation could be correlated with the ability of these proteins to interact together but does not require binding of Maf proteins to the G1 element. Furthermore, we found that Maf enhanced the Pax-6 DNA binding capacity. Our data indicate that Maf transcription factors may contribute to glucagon gene expression in the pancreas.
在内分泌胰腺中,胰高血糖素基因的α细胞特异性表达由与G1近端启动子元件相互作用的DNA结合蛋白介导。在这些蛋白质中,配对结构域转录因子Pax-6已被证明可与G1结合并反式激活胰高血糖素基因表达。在靠近Pax-6结合位点处,我们观察到存在Maf家族的碱性亮氨酸拉链转录因子的结合位点。在本研究中,我们证明了在内分泌胰腺中存在与G1结合并反式激活胰高血糖素启动子表达的Maf家族成员。在瞬时转染实验中,我们发现Maf转录因子和Pax-6的同时表达极大地增强了对胰高血糖素启动子的反式激活作用。这种对胰高血糖素反式激活的增强可能与这些蛋白质相互作用的能力相关,但并不需要Maf蛋白与G1元件结合。此外,我们发现Maf增强了Pax-6的DNA结合能力。我们的数据表明,Maf转录因子可能有助于胰腺中胰高血糖素基因的表达。