Transcriptional regulation of the human acetoacetyl-CoA synthetase gene by PPARγ

被引:15
作者
Aguilo, Francesca
Camarero, Nuria
Relat, Joana
Marrero, Pedro F.
Haro, Diego [1 ]
机构
[1] Univ Barcelona, Sch Pharm, Dept Biochem & Mol Biol, Barcelona, Spain
关键词
acetoacetyl-CoA synthetase (AACS); adipogenesis; gene expression; ketone body utilization; peroxisome-proliferator-activated receptor gamma (PPAR gamma); stimulating protein-1 (Sp1); PROLIFERATOR-ACTIVATED-RECEPTOR; BODY-UTILIZING ENZYME; FUNCTIONAL INTERACTIONS; KETONE-BODIES; C/EBP-BETA; RAT-LIVER; SP1; EXPRESSION; PROMOTER; CELLS;
D O I
10.1042/BJ20090851
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 cytosol of lipogenic tissue, ketone bodies are activated by AACS (acetoacetyl-CoA synthetase) and incorporated into cholesterol and fatty acids. AACS gene expression is particularly abundant in white adipose tissue, as it is induced during adipocyte differentiation. In order to elucidate the mechanism controlling the gene expression of human AACS and to clarify its physiological role, we isolated the human promoter, characterized the elements required to initiate transcription and analysed the expression of the gene in response to PPAR gamma (peroxisome-proliferator-activated receptor gamma), an inducer of adipogenesis. We show that the human AACS promoter is a PPAR gamma target gene and that this nuclear receptor is recruited to the AACS promoter by direct interaction with Sp1 (stimulating protein-1).
引用
收藏
页码:255 / 264
页数:10
相关论文
共 34 条
[1]   SF-1 (steroidogenic factor-1), C/EBPβ (CCAAT/enhancer binding protein), and ubiquitous transcription factors NF1 (nuclear factor 1) and Sp1 (selective promoter factor 1) are required for regulation of the mouse aldose reductase-like gene (AKR1B7) expression in adrenocortical cells [J].
Aigueperse, C ;
Val, P ;
Pacot, C ;
Darne, C ;
Lalli, E ;
Sassone-Corsi, P ;
Veyssiere, G ;
Jean, C ;
Martinez, A .
MOLECULAR ENDOCRINOLOGY, 2001, 15 (01) :93-111
[2]   ACETOACETYL-COENZYME A SYNTHETASE-ACTIVITY IN RAT-LIVER CYTOSOL - A REGULATED ENZYME IN LIPOGENESIS [J].
BERGSTROM, JD ;
ROBBINS, KA ;
EDMOND, J .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1982, 106 (03) :856-862
[3]  
BERGSTROM JD, 1984, J BIOL CHEM, V259, P4548
[4]   ACETOACETYL-COA SYNTHETASE - LIPOGENIC ENZYME IN RAT TISSUES [J].
BUCKLEY, BM ;
WILLIAMSON, DH .
FEBS LETTERS, 1975, 60 (01) :7-10
[5]   Histone deacetylase inhibitors stimulate mitochondrial HMG-CoA synthase gene expression via a promoter proximal Sp1 site [J].
Camarero, N ;
Nadal, A ;
Barrero, MJ ;
Haro, D ;
Marrero, PF .
NUCLEIC ACIDS RESEARCH, 2003, 31 (06) :1693-1703
[6]   Ketogenic HMGCS2 is a c-Myc target gene expressed in differentiated cells of human colonic epithelium and down-regulated in colon cancer [J].
Camarero, Nuria ;
Mascaro, Cristina ;
Mayordomo, Cristina ;
Vilardell, Felip ;
Haro, Diego ;
Marrero, Pedro F. .
MOLECULAR CANCER RESEARCH, 2006, 4 (09) :645-653
[7]   Direct interaction of C/EBPδ and Sp1 at the GC-enriched promoter region synergizes the IL-10 gene transcription in mouse macrophage [J].
Chiang, Ben-Tzu ;
Liu, Yi-Wen ;
Chen, Ben-Kuen ;
Wang, Ju-Ming ;
Chang, Wen-Chang .
JOURNAL OF BIOMEDICAL SCIENCE, 2006, 13 (05) :621-635
[8]   PPARγ regulates adipocyte cholesterol metabolism via oxidized LDL receptor 1 [J].
Chui, PC ;
Guan, HP ;
Lehrke, M ;
Lazar, MA .
JOURNAL OF CLINICAL INVESTIGATION, 2005, 115 (08) :2244-2256
[9]   Peroxisome proliferator-activated receptor-γ transcriptionally up-regulates hormone-sensitive lipase via the involvement of specificity protein-1 [J].
Deng, T ;
Shan, S ;
Li, PP ;
Shen, ZF ;
Lu, XP ;
Cheng, J ;
Ning, ZQ .
ENDOCRINOLOGY, 2006, 147 (02) :875-884
[10]  
ENDEMANN G, 1982, J BIOL CHEM, V257, P3434