Roles and regulation of transcription factor MafA in islet β-cells

被引:65
作者
Aramata, Shinsaku [1 ]
Han, Song-Iee [2 ]
Kataoka, Kohsuke [1 ]
机构
[1] Nara Inst Sci & Technol, Grad Sch Biol Sci, Nara 6300192, Japan
[2] Univ Tsukuba, Grad Sch Life & Environm Sci, Tsukuba, Ibaraki 3058572, Japan
关键词
insulin; transcriptional regulation; glucose response; glucotoxicity; diabetes;
D O I
10.1507/endocrj.KR-101
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Insulin is a critical hormone in the regulation of blood glucose levels. It is produced exclusively by pancreatic islet beta-cells. beta-cell-enriched transcription factors, such as Pdx1 and Beta2, have dual roles in the activation of the insulin gene promoter establishing beta-cell-specific insulin expression, and in the regulation of beta-cell differentiation. It was shown that MafA, a beta-cell-specific member of the Maf family of transcription factors, binds to the conserved C1/RIPE3b element of the insulin promoter. The Maf family proteins regulate tissue-specific gene expression and cell differentiation in a wide variety of tissues. MafA acts synergistically with Pdx1 and Beta2 to activate the insulin gene promoter, and mice with a targeted deletion of mafA develop age-dependent diabetes. MafA also regulates genes involved in beta-cell function such as Glucose transporter 2, Glucagons-like peptide 1 receptor, and Prohormone convertase 1/3. The abundance or MafA in beta-cells is regulated at both the transcriptional and post-translational levels by glucose and oxidative stress. This review summarizes recent progress in determining the functions and roles of MafA in the regulation of insulin gene transcription in beta-cells.
引用
收藏
页码:659 / 666
页数:8
相关论文
共 43 条
[1]   β-cell-specific inactivation of the mouse Ipf1/Pdx1 gene results in loss of the β-cell phenotype and maturity onset diabetes [J].
Ahlgren, U ;
Jonsson, J ;
Jonsson, L ;
Simu, K ;
Edlund, H .
GENES & DEVELOPMENT, 1998, 12 (12) :1763-1768
[2]   Synergistic activation of the insulin gene promoter by the β-cell enriched transcription factors MafA, Beta2, and Pdx1 [J].
Aramata, S ;
Han, S ;
Yasuda, K ;
Kataoka, K .
BIOCHIMICA ET BIOPHYSICA ACTA-GENE STRUCTURE AND EXPRESSION, 2005, 1730 (01) :41-46
[3]   Phosphorylation of MafA is essential for its transcriptional and biological properties [J].
Benkhelifa, S ;
Provot, S ;
Nabais, E ;
Eychène, A ;
Calothy, G ;
Felder-Schmittbuhl, MP .
MOLECULAR AND CELLULAR BIOLOGY, 2001, 21 (14) :4441-4452
[4]   A mutation in NRL is associated with autosomal dominant retinitis pigmentosa [J].
Bessant, DAR ;
Payne, AM ;
Mitton, KP ;
Wang, QL ;
Swain, PK ;
Plant, C ;
Bird, AC ;
Zack, DJ ;
Swaroop, A ;
Bhattacharya, SS .
NATURE GENETICS, 1999, 21 (04) :355-356
[5]   Phylogenomic analysis and expression patterns of large Maf genes in Xenopus tropicalis provide new insights into the functional evolution of the gene family in osteichthyans [J].
Coolen, M ;
Sii-Felice, K ;
Bronchain, O ;
Mazabraud, A ;
Bourrat, F ;
Rétaux, S ;
Felder-Schmittbuhl, MP ;
Mazan, S ;
Plouhinec, JL .
DEVELOPMENT GENES AND EVOLUTION, 2005, 215 (07) :327-339
[6]   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
[7]   Relative contribution of PDX-1, MafA and E47/β2 to the regulation of the human insulin promoter [J].
Docherty, HM ;
Hay, CW ;
Ferguson, LA ;
Barrow, J ;
Durward, E ;
Docherty, K .
BIOCHEMICAL JOURNAL, 2005, 389 :813-820
[8]   Palmitate inhibits insulin gene expression by altering PDX-1 nuclear localization and reducing MafA expression in isolated rat islets of Langerhans [J].
Hagman, DK ;
Hays, LB ;
Parazzoli, SD ;
Poitout, V .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2005, 280 (37) :32413-32418
[9]   MafA stability in pancreatic β cells is regulated by glucose and is dependent on its constitutive phosphorylation at multiple sites by glycogen synthase kinase 3 [J].
Han, Song-iee ;
Aramata, Shinsaku ;
Yasuda, Kunio ;
Kataoka, Kohsuke .
MOLECULAR AND CELLULAR BIOLOGY, 2007, 27 (19) :6593-6605
[10]   Oxidative stress-mediated, post-translational loss of MafA protein as a contributing mechanism to loss of insulin gene expression in glucotoxic beta cells [J].
Harmon, JS ;
Stein, R ;
Robertson, RP .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2005, 280 (12) :11107-11113