Interaction of Maf transcription factors with Pax-6 results in synergistic activation of the glucagon promoter

被引:59
作者
Planque, N [1 ]
Leconte, L [1 ]
Coquelle, FM [1 ]
Benkhelifa, S [1 ]
Martin, P [1 ]
Felder-Schmittbuhl, MP [1 ]
Saule, S [1 ]
机构
[1] Ctr Univ Orsay, CNRS, UMR 146, Inst Curie,Sect Rech, F-91405 Orsay, France
关键词
D O I
10.1074/jbc.M104523200
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
In the endocrine pancreas, a-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 GI 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.
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页码:35751 / 35760
页数:10
相关论文
共 56 条
[1]   The Ets transcription factors interact with each other and with the c-Fos/c-Jun complex via distinct protein domains in a DNA-dependent and -independent manner [J].
Basuyaux, JP ;
Ferreira, E ;
Stehelin, D ;
Buttice, G .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (42) :26188-26195
[2]   mafA, a novel member of the maf proto-oncogene family, displays developmental regulation and mitogenic capacity in avian neuroretina cells [J].
Benkhelifa, S ;
Provot, S ;
Lecoq, O ;
Pouponnot, C ;
Calothy, G ;
Felder-Schmittbuhl, MP .
ONCOGENE, 1998, 17 (02) :247-254
[3]   The Maf transcription factors: regulators of differentiation [J].
Blank, V ;
Andrews, NC .
TRENDS IN BIOCHEMICAL SCIENCES, 1997, 22 (11) :437-441
[4]   Pax-6 in development and evolution [J].
Callaerts, P ;
Halder, G ;
Gehring, WJ .
ANNUAL REVIEW OF NEUROSCIENCE, 1997, 20 :483-532
[5]  
CARRIERE C, 1995, CELL GROWTH DIFFER, V6, P1531
[6]   CHARACTERIZATION OF QUAIL PAX-6 (PAX-QNR) PROTEINS EXPRESSED IN THE NEURORETINA [J].
CARRIERE, C ;
PLAZA, S ;
MARTIN, P ;
QUATANNENS, B ;
BAILLY, M ;
STEHELIN, D ;
SAULE, S .
MOLECULAR AND CELLULAR BIOLOGY, 1993, 13 (12) :7257-7266
[7]   Functional domains of the cone-rod homeobox (CRX) transcription factor [J].
Chau, KY ;
Chen, SM ;
Zack, DJ ;
Ono, SJ .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (47) :37264-37270
[8]   Crx, a novel Otx-like paired-homeodomain protein, binds to and transactivates photoreceptor cell-specific genes [J].
Chen, SM ;
Wang, QL ;
Nie, ZQ ;
Sun, H ;
Lennon, G ;
Copeland, NG ;
Gilbert, DJ ;
Jenkins, NA ;
Zack, DJ .
NEURON, 1997, 19 (05) :1017-1030
[9]  
Chow RL, 1999, DEVELOPMENT, V126, P4213
[10]   THE MOUSE SEGMENTATION GENE KR ENCODES A NOVEL BASIC DOMAIN LEUCINE-ZIPPER TRANSCRIPTION FACTOR [J].
CORDES, SP ;
BARSH, GS .
CELL, 1994, 79 (06) :1025-1034