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NF-Y 转录调控果蝇 p53 基因。

NF-Y transcriptionally regulates the Drosophila p53 gene.

机构信息

Department of Applied Biology, Kyoto Institute of Technology, Sakyo-ku, Kyoto 606-8585, Japan.

出版信息

Gene. 2011 Feb 15;473(1):1-7. doi: 10.1016/j.gene.2010.10.009. Epub 2010 Oct 29.

DOI:10.1016/j.gene.2010.10.009
PMID:21044877
Abstract

The p53 protein is important in multicellular organisms, where it regulates the cell cycle and thus functions as a tumor suppressor that contributes to preventing cancer. However, molecular regulation of p53 gene expression is not fully understood. NF-YA is a subunit of the NF-Y trimeric complex, a transcription factor that binds to CCAAT motifs in the promoter regions of a variety of genes playing key roles in cell cycle regulation. We have identified four potential Drosophila NF-Y (dNF-Y)-binding sites located in the 5'-flanking region of the Drosophila p53 (dmp53) gene. Chromatin immunoprecipitation analyses using anti-dNF-YA antibodies confirmed that dNF-YA binds specifically to the genomic region containing CCAAT boxes in the dmp53 gene promoter in vivo. Furthermore, the thorax disclosed phenotype of dNF-YA knockdown flies can be enhanced by dmp53 mutation. In addition, the level of dmp53 mRNA was found to be decreased in the dNF-YA knockdown cells and transient expression of the luciferase gene revealed that wild-type dmp53 gene promoter activity is much stronger than mutated promoter activity in S2 cells. The requirement of CCAAT boxes for dmp53 promoter activity was further confirmed by expression of EGFP in various tissues from transgenic flies carrying wild-type and CCAAT box-mutated versions of dmp53 promoter-GFP fusion genes. These results taken together indicate that dNF-Y is necessary for dmp53 gene promoter activity.

摘要

p53 蛋白在多细胞生物中很重要,它调节细胞周期,因此作为肿瘤抑制因子发挥作用,有助于预防癌症。然而,p53 基因表达的分子调控还不完全清楚。NF-YA 是 NF-Y 三聚体复合物的一个亚基,是一种转录因子,可与细胞周期调节中发挥关键作用的各种基因启动子区域中的 CCAAT 基序结合。我们已经鉴定出位于果蝇 p53(dmp53)基因 5'-侧翼区的四个潜在的果蝇 NF-Y(dNF-Y)-结合位点。使用抗 dNF-YA 抗体的染色质免疫沉淀分析证实,dNF-YA 特异性结合体内 dmp53 基因启动子中包含 CCAAT 盒的基因组区域。此外,dNF-YA 敲低果蝇的胸节表型可以通过 dmp53 突变增强。此外,在 dNF-YA 敲低细胞中发现 dmp53 mRNA 的水平降低,瞬时表达荧光素酶基因表明野生型 dmp53 基因启动子活性远强于 S2 细胞中突变启动子活性。CCAAT 盒对 dmp53 启动子活性的要求进一步通过携带野生型和 CCAAT 盒突变的 dmp53 启动子-GFP 融合基因的转基因果蝇的各种组织中表达 EGFP 得到证实。这些结果表明,dNF-Y 是 dmp53 基因启动子活性所必需的。

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