Characterization of cis-elements mediating the stimulation of glucose-6-phosphate transporter promoter activity by glucocorticoids

被引:9
作者
Kaltwellis-Opara, A
Zaho, XS
Zimmermann, U
Unterman, TG
Walther, R
Schmoll, D
机构
[1] Univ Greifswald, Dept Med Biochem & Mol Biol, D-17487 Greifswald, Germany
[2] Vet Affairs Chicago Hlth Care Syst, Med Res Unit, Chicago, IL 60612 USA
[3] Univ Greifswald, Dept Urol, D-17487 Greifswald, Germany
关键词
forkhead transcription factor; glucose-6-phosphatase; diabetes mellitus; gluconeogenesis; phosphoenolpyruvate carboxykinase;
D O I
10.1016/S0378-1119(03)00810-2
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The endoplasmatic glucose-6-phosphate transporter is involved in the control of hepatic glucose production and blood glucose homeostasis. In this study, the expression of a luciferase reporter gene under the control of the glucose-6-phosphate transporter gene promoter was examined in transiently transfected hepatoma cells. The promoter activity was stimulated approximately 2.5-fold by dexamethasone. Mutational analyses demonstrated that the regions nucleotide (nt) -215/-209 and nt -197/-183 relative to the translation start site were critical for this regulation. In gel electrophoretic mobility shift assays the transcription factor Fox 01, also called forkhead in rhabdomyosarcoma (FKHR), overexpressed in 293 cells, bound to a probe with the sequence nt -215/-209. The overexpression of Fox 0 1 stimulated the induction of glucose-6-phosphate transporter promoter activity by dexamethasone via nt -215/-209 in hepatoma cells. Recombinant glucocorticoid receptor DNA binding domain protein bound to a probe with the sequence of nt -197/-183 in gel electrophoretic mobility shift assays and an oligonucleotide with this sequence transferred glucocorticoid responsiveness to a heterologous promoter. The data indicate that the glucose-6-phosphate transporter promoter contains a glucocorticoid response unit consisting of binding sites for Fox O1 and the glucocorticoid receptor. (C) 2003 Elsevier B.V. All rights reserved.
引用
收藏
页码:59 / 66
页数:8
相关论文
共 19 条
[1]   Structure of the gene mutated in glycogen storage disease type Ib [J].
Gerin, I ;
Veiga-da-Cunha, M ;
Noël, C ;
Van Schaftingen, E .
GENE, 1999, 227 (02) :189-195
[2]   FUNCTIONAL DOMAINS OF THE HUMAN GLUCOCORTICOID RECEPTOR [J].
GIGUERE, V ;
HOLLENBERG, SM ;
ROSENFELD, MG ;
EVANS, RM .
CELL, 1986, 46 (05) :645-652
[3]   Glucocorticoids activate transcription of the gene for the glucose-6-phosphate transporter, deficient in glycogen storage disease type 1b [J].
Hiraiwa, H ;
Chou, JY .
DNA AND CELL BIOLOGY, 2001, 20 (08) :447-453
[4]   Novel glucocorticoid receptor coactivator effector mechanisms [J].
Jenkins, BD ;
Pullen, CB ;
Darimont, BD .
TRENDS IN ENDOCRINOLOGY AND METABOLISM, 2001, 12 (03) :122-126
[5]   Forkhead transcription factors: new insights into protein kinase B (c-akt) signaling [J].
Kops, GJPL ;
Burgering, BMT .
JOURNAL OF MOLECULAR MEDICINE-JMM, 1999, 77 (09) :656-665
[6]   Distinct hormone stimulation and counteraction by insulin of the expression of the two components of glucose 6-phosphatase in HepG2 cells [J].
Li, YZ ;
van de Werve, G .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2000, 272 (01) :41-44
[7]   Regulation of insulin action and pancreatic β-cell function by mutated alleles of the gene encoding forkhead transcription factor Foxo1 [J].
Nakai, J ;
Biggs, WH ;
Kitamura, T ;
Cavenee, WK ;
Wright, CVE ;
Arden, KC ;
Accili, D .
NATURE GENETICS, 2002, 32 (02) :245-253
[8]   DAF-16 recruits the CREB-binding protein coactivator complex to the insulin-like growth factor binding protein 1 promoter in HepG2 cells [J].
Nasrin, N ;
Ogg, S ;
Cahill, CM ;
Biggs, W ;
Nui, S ;
Dore, J ;
Calvo, D ;
Shi, Y ;
Ruvkun, G ;
Alexander-Bridges, MC .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (19) :10412-10417
[9]  
OBRIEN RM, 1995, MOL CELL BIOL, V15, P1747
[10]   THE PERMISSIVE ROLE OF GLUCOCORTICOIDS ON INTERLEUKIN-1 STIMULATION OF ANGIOTENSINOGEN GENE-TRANSCRIPTION IS MEDIATED BY AN INTERACTION BETWEEN INDUCIBLE ENHANCERS [J].
RON, D ;
BRASIER, AR ;
WRIGHT, KA ;
HABENER, JF .
MOLECULAR AND CELLULAR BIOLOGY, 1990, 10 (08) :4389-4395