共查询到20条相似文献,搜索用时 15 毫秒
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Iso T Sartorelli V Poizat C Iezzi S Wu HY Chung G Kedes L Hamamori Y 《Molecular and cellular biology》2001,21(17):6080-6089
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Sequestration of p53 in the cytoplasm by adenovirus type 12 E1B 55-kilodalton oncoprotein is required for inhibition of p53-mediated apoptosis
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The adenovirus E1B 55-kDa protein is a potent inhibitor of p53-mediated transactivation and apoptosis. The proposed mechanisms include tethering the E1B repression domain to p53-responsive promoters via direct E1B-p53 interaction. Cytoplasmic sequestration of p53 by the 55-kDa protein would impose additional inhibition on p53-mediated effects. To investigate further the role of cytoplasmic sequestration of p53 in its inhibition by the E1B 55-kDa protein we systematically examined domains in both the Ad12 55-kDa protein and p53 that underpin their colocalization in the cytoplasmic body and show that the N-terminal transactivation domain (TAD) of p53 is essential for retaining p53 in the cytoplasmic body. Deletion of amino acids 11 to 27 or even point mutation L22Q/W23S abolished the localization of p53 to the cytoplasmic body, whereas other parts of TAD and the C-terminal domain of p53 are dispensable. This cytoplasmic body is distinct from aggresome associated with overexpression of some proteins, since it neither altered vimentin intermediate filaments nor associated with centrosome or ubiquitin. Formation of this structure is sensitive to mutation of the Ad12 55-kDa protein. Strikingly, mutation S476/477A near the C terminus of the Ad12 55-kDa protein eliminated the formation of the cytoplasmic body. The equivalent residues in the Ad5 55-kDa protein were shown to be critical for its ability to inhibit p53. Indeed, Ad12 55-kDa mutants that cannot form a cytoplasmic body can no longer inhibit p53-mediated effects. Conversely, the Ad12 55-kDa protein does not suppress p53 mutant L22Q/W23S-mediated apoptosis. Finally, we show that E1B can still sequester p53 that contains the mitochondrial import sequence, thereby potentially preventing the localization of p53 to mitochondria. Thus, cytoplasmic sequestration of p53 by the E1B 55-kDa protein plays an important role in restricting p53 activities. 相似文献
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NRSE 与 NRSF 及其对神经元特异性基因表达的调控作用 总被引:3,自引:0,他引:3
神经限制性沉默元件 (NRSE) 是一段长度为 21~23 bp 的保守 DNA 序列,存在于许多神经元特异表达基因的转录调控区中,神经限制性沉默因子 (NRSF) 能特异性结合到 NRSE dsDNA 上,并通过其 N 端和 C 端阻遏结构域分别连接共阻遏蛋白 Sin3A/B 和 CoREST , Sin3A 招募 HDAC 对组蛋白进行去乙酰基化修饰, CoREST 则作为平台蛋白招募特异的“沉默组件”,以此维持基因沉默 . 最近的研究显示, NRSE dsRNA 能在转录水平与 NRSF 蛋白直接作用,而不是作为 siRNA 或 miRNA 在转录后水平启动神经元特异性基因的表达 . 相似文献
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p21/CDKN1A mediates negative regulation of transcription by p53 总被引:11,自引:0,他引:11
Löhr K Möritz C Contente A Dobbelstein M 《The Journal of biological chemistry》2003,278(35):32507-32516