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

被引:25
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
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