Fiucci Giusy, Beaucourt Séverine, Duflaut Dominique, Lespagnol Alexandra, Stumptner-Cuvelette Pamela, Géant Anne, Buchwalter Gilles, Tuynder Marcel, Susini Laurent, Lassalle Jean-Michel, Wasylyk Christine, Wasylyk Bohdan, Oren Moshe, Amson Robert, Telerman Adam
Molecular Engines Laboratories, 20 Rue Bouvier, 75011 Paris, France.
Proc Natl Acad Sci U S A. 2004 Mar 9;101(10):3510-5. doi: 10.1073/pnas.0400177101. Epub 2004 Feb 25.
Siah proteins are E3 ubiquitin ligases. They are homologues of the Drosophila seven in absentia (Sina), a protein required for the R7 photoreceptor development. We have previously found that the expression of human siah-1 and its mouse homologue siah-1b are induced by p53 during apoptosis and tumor reversion. So far, no evidence that the siah-1b gene is a direct transcriptional target of p53 has been provided. In the present study we investigate this issue. Northern blot analysis with a specific probe demonstrates an increase in siah-1b transcription on activation of endogenous and inducible exogenous p53. To explore whether this effect is directly mediated by p53 we analyzed 20 kb of chromosome X DNA, containing the siah-1b locus. A p53-binding site was identified in the siah-1b promoter, located at nucleotides -2155/-2103 relative to the translational start site. This site is composed of two half-sites, conforming to the p53-binding consensus sequence but separated by a nonclassical 33-bp spacer. In luciferase assays, p53 induces a substantial increase in siah-1b promoter activity. Gel shift and DNase-I-footprinting studies, combined with mutational analysis and chromatin immunoprecipitation, indicate that p53 effectively binds the siah-1b promoter in vitro and in vivo. Thus, the siah-1b gene is a direct transcriptional target of p53.
Siah蛋白是E3泛素连接酶。它们是果蝇中无七(Sina)蛋白的同源物,Sina是R7光感受器发育所必需的一种蛋白质。我们之前发现,在细胞凋亡和肿瘤逆转过程中,人类siah-1及其小鼠同源物siah-1b的表达由p53诱导。到目前为止,尚未有证据表明siah-1b基因是p53的直接转录靶点。在本研究中,我们对这一问题进行了调查。用特异性探针进行的Northern印迹分析表明,内源性和可诱导的外源性p53激活后,siah-1b转录增加。为了探究这种效应是否直接由p53介导,我们分析了包含siah-1b基因座的20 kb X染色体DNA。在siah-1b启动子中鉴定出一个p53结合位点,相对于翻译起始位点位于核苷酸-2155/-2103处。该位点由两个半位点组成,符合p53结合共有序列,但被一个非经典的33 bp间隔区隔开。在荧光素酶测定中,p53可使siah-1b启动子活性大幅增加。凝胶迁移和DNase-I足迹研究,结合突变分析和染色质免疫沉淀,表明p53在体外和体内均能有效结合siah-1b启动子。因此,siah-1b基因是p53的直接转录靶点。