Identification of GATA2 and AP-1 Activator elements within the enhancer VNTR occurring in intron 5 of the human SIRT3 gene

被引:24
作者
Bellizzi, Dina [1 ]
Covello, Giuseppina [1 ]
Di Cianni, Fausta [1 ]
Tong, Qiang [2 ]
De Benedictis, Giovanna [1 ]
机构
[1] Univ Calabria, Dept Cell Biol, I-87036 Arcavacata Di Rende, Italy
[2] Baylor Coll Med, USDA ARS, Childrens Nutr Res Ctr, Dept Pediat, Houston, TX 77030 USA
关键词
AP-1; site; enhancer VNTR; GATA2; SIRT3; gene; TRANSCRIPTION FACTOR GATA-2; IN-SITU HYBRIDIZATION; CHROMOSOMAL ORGANIZATION; HISTONE DEACETYLASE; REGULATORY ELEMENTS; LYSINE ACETYLATION; ENDOTHELIN-1; GENE; CELL FORMATION; HUMAN GENOME; MITOCHONDRIAL;
D O I
10.1007/s10059-009-0110-3
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
Human SIRT3 gene contains an intronic VNTR enhancer. A T > C transition occurring in the second repeat of each VNTR allele implies the presence/absence of a putative GATA binding motif. A partially overlapping AP-1 site, not affected by the transition, was also identified. Aims of the present study were: 1) to verify if GATA and AP-1 sites could bind GATA2 and c-Jun/c-Fos factors, respectively; 2) to investigate whether such sites modulate the enhancer activity of the SIRT3-VNTR alleles. DAPA assay proved that GATA2 and c-Jun/c-Fos factors are able to bind the corresponding sites. Moreover, co-transfection experiments showed that the over-expression of GATA2 and c-Jun/c-Fos factors boosts the VNTR enhancer activity in an allelic-specific way. Furthermore, we established that GATA2 and c-Jun/c-Fos act additively in modulating the SIRT3-VNTR enhancer function. Therefore, GATA2 and AP-1 are functional sites and the T S > C transition of the second VNTR repeat affects their activity.
引用
收藏
页码:87 / 92
页数:6
相关论文
共 37 条
[1]   A role for the mitochondrial deacetylase Sirt3 in regulating energy homeostasis [J].
Ahn, Bong-Hyun ;
Kim, Hyun-Seok ;
Song, Shiwei ;
Lee, In Hye ;
Liu, Jie ;
Vassilopoulos, Athanassios ;
Deng, Chu-Xia ;
Finkel, Toren .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2008, 105 (38) :14447-14452
[2]   SIRT3 is pro-apoptotic and participates in distinct basal apoptotic pathways [J].
Allison, Simon J. ;
Milner, Jo .
CELL CYCLE, 2007, 6 (21) :2669-2677
[3]   A novel VNTR enhancer within the SIRT3 gene, a human homologue of SIR2, is associated with survival at oldest ages [J].
Bellizzi, D ;
Rose, G ;
Cavalcante, P ;
Covello, G ;
Dato, S ;
De Rango, F ;
Greco, V ;
Maggiolini, M ;
Feraco, E ;
Mari, V ;
Franceschi, C ;
Passarino, G ;
De Benedictis, G .
GENOMICS, 2005, 85 (02) :258-263
[4]   Characterization of a bidirectional promoter shared between two human genes related to aging:: SIRT3 and PSMD13 [J].
Bellizzi, D. ;
Dato, S. ;
Cavalcante, P. ;
Covello, G. ;
Di Cianni, F. ;
Passarino, G. ;
Rose, G. ;
De Benedictis, G. .
GENOMICS, 2007, 89 (01) :143-150
[5]   THE C-FOS PROTEIN INTERACTS WITH C-JUN/AP-1 TO STIMULATE TRANSCRIPTION OF AP-1 RESPONSIVE GENES [J].
CHIU, R ;
BOYLE, WJ ;
MEEK, J ;
SMEAL, T ;
HUNTER, T ;
KARIN, M .
CELL, 1988, 54 (04) :541-552
[6]   The human SIRT3 protein deacetylase is exclusively mitochondrial [J].
Cooper, Helen M. ;
Spelbrink, Johannes N. .
BIOCHEMICAL JOURNAL, 2008, 411 :279-285
[7]   GATA-2 and HNF-3β regulate the human alcohol dehydrogenase 1A (ADH1A) gene [J].
Dannenberg, LO ;
Chen, HJ ;
Edenberg, HJ .
DNA AND CELL BIOLOGY, 2005, 24 (09) :543-552
[8]  
DORFMAN DM, 1992, J BIOL CHEM, V267, P1279
[9]   Mammalian sirtuins - emerging roles in physiology, aging, and calorie restriction [J].
Haigis, Marcia C. ;
Guarente, Leonard P. .
GENES & DEVELOPMENT, 2006, 20 (21) :2913-2921
[10]   Sirtuins deacetylate and activate mammalian acetyl-CoA synthetases [J].
Hallows, William C. ;
Lee, Susan ;
Denu, John M. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2006, 103 (27) :10230-10235