Activation of the human pregnancy-specific glycoprotein PSG-5 promoter by KLF4 and Sp1

被引:25
作者
Blanchon, L
Nores, R
Gallot, D
Marceau, G
Borel, V
Yang, VW
Bocco, JL
Lémery, D
Panzetta-Dutari, G
Sapin, V [1 ]
机构
[1] INSERM, U384, Biochim Lab, Fac Med, F-63000 Clermont Ferrand, France
[2] Univ Auvergne, ARDEMO, F-63000 Clermont Ferrand, France
[3] Univ Nacl Cordoba, Fac Ciencias Quim, CONICET, CIBICI,Dept Bioquim Clin, RA-5000 Cordoba, Argentina
[4] CHU Clermont Ferrand, Hotel Dieu, F-63000 Clermont Ferrand, France
[5] Emory Univ, Sch Med, Dept Med, Div Digest Dis, Atlanta, GA 30322 USA
关键词
placenta; JEG-3; transcription factors; GKLF; KLF4; PSG development; Sp1;
D O I
10.1016/j.bbrc.2006.03.032
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
Pregnancy-specific glycoproteins (PSGs) are major placental proteins thought to be essential for the maintenance of gestation. Little is known about the regulation of expression of the 11 genes encoding these proteins. It was previously demonstrated that Kruppel-like factor 6 (KLF6) and specific-protein 1 (Sp1) bind to conserved sequence within the PSG-5 gene promoter. Informatics analysis revealed the presence of one potential binding site for Kruppel-like factor 4 (KLF4), in the PSG-5 promoter, suggesting a potential transcriptional regulator role for KLF4. Using gene promoter-reporter transfections and X-ChIP assays, we demonstrated that KLF4 is ail activator of the PSG-5 promoter by binding to a KLF consensus like binding which includes the Core Promoter Element region (-147/-140). Furthermore, we used previous data showing the binding of Sp1 transcription factor to a GT-box (-443/-437) and co-transfection assays with KLF4 and Sp1 to demonstrate the strong synergic activity of these two factors on the PSG-5 promoter. (c) 2006 Elsevier Inc. All rights reserved.
引用
收藏
页码:745 / 753
页数:9
相关论文
共 47 条
[1]   Positive- and negative-acting Kruppel-like transcription factors bind a transforming growth factor β control element required for expression of the smooth muscle cell differentiation marker SM22α in vivo [J].
Adam, PJ ;
Regan, CP ;
Hautmann, MB ;
Owens, GK .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (48) :37798-37806
[2]   Kruppel-like factor 4 (KLF4) represses histidine decarboxylase gene expression through an upstream Sp1 site and downstream gastrin responsive elements [J].
Ai, WD ;
Liu, Y ;
Langlois, M ;
Wang, TC .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (10) :8684-8693
[3]   PPARγ is required for placental, cardiac, and adipose tissue development [J].
Barak, Y ;
Nelson, MC ;
Ong, ES ;
Jones, YZ ;
Ruiz-Lozano, P ;
Chien, KR ;
Koder, A ;
Evans, RM .
MOLECULAR CELL, 1999, 4 (04) :585-595
[4]   MATERNAL LEVELS OF PREGNANCY-SPECIFIC BETA-1-GLYCOPROTEIN (SP-1) ARE ELEVATED IN PREGNANCIES AFFECTED BY DOWNS-SYNDROME [J].
BARTELS, I ;
LINDEMANN, A .
HUMAN GENETICS, 1988, 80 (01) :46-48
[5]   Co-localization of KLF6 and KLF4 with pregnancy-specific glycoproteins during human placenta development [J].
Blanchon, L ;
Bocco, JL ;
Gallot, D ;
Gachon, AM ;
Lémery, D ;
Déchelotte, P ;
Dastugue, B ;
Sapin, V .
MECHANISMS OF DEVELOPMENT, 2001, 105 (1-2) :185-189
[6]  
BOCCO JL, 1989, BIOCHEM INT, V18, P999
[7]  
Brembeck FH, 2000, J BIOL CHEM, V275, P28230
[8]   Kruppel-like factor 6 (KLF6) affects the promoter activity of the α1-proteinase inhibitor gene [J].
Chiambaretta, F ;
Nakamura, H ;
De Graeve, F ;
Sakai, H ;
Marceau, G ;
Maruyama, Y ;
Rigal, D ;
Dastugue, B ;
Sugar, J ;
Yue, BYJT ;
Sapin, V .
INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 2006, 47 (02) :582-590
[9]   The biology of the mammalian Kruppel-like family of transcription factors [J].
Dang, DT ;
Pevsner, J ;
Yang, VW .
INTERNATIONAL JOURNAL OF BIOCHEMISTRY & CELL BIOLOGY, 2000, 32 (11-12) :1103-1121
[10]   Opposing effects of Kruppel-like factor 4 (gut-enriched Kruppel-like factor) and Kruppel-like factor 5 (intestinal-enriched Kruppel-like factor) on the promoter of the Kruppel-like factor 4 gene [J].
Dang, DT ;
Zhao, WD ;
Mahatan, CS ;
Geiman, DE ;
Yang, VW .
NUCLEIC ACIDS RESEARCH, 2002, 30 (13) :2736-2741