摘要
与急性早幼粒细胞性白血病蛋白 (promyelocyticleukemiaprotein ,PML)在体内相互作用共定位于细胞核PML致癌结构域 (PMLoncogenicdomains,PODs)的人Daxx(humanDaxx ,hDaxx) ,能结合Fas死亡结构域诱导细胞凋亡。细胞肿瘤抑制子p5 3抑制细胞及病毒转录 ,提高细胞内Fas的表达并调节细胞凋亡。为了探索hDaxx与 p5 3在诱导细胞凋亡中有无相互作用及其作用效果 ,利用酵母双杂交体系测定发现p5 3通过C端与hDaxx结合 ,共免疫沉淀反应及Westernblot结果显示hDaxx与 p5 3能在体内外直接结合。hDaxx与 p5
Human Daxx (hDaxx), a novel transcriptional repression protein, interacts and colocalizes with promyelocytic leukemia protein (PML) in PML oncogenetic domains (PODs). The hDaxx binding the death domains (DD) of Fas induces apopotosis. Cellular tumor suppressors p53 inhibits the transcription of cells and virus. The p53 enhances the expression of Fas and mediates apopotosis. In order to probe the interaction and effect of hDaxx with p53, hDaxx was interacts with p53 by its C terminus 62 amino acids using yeast two hybrid assay. Western blot showed that hDaxx binds to p53 in vivo and in vitro by co immuno precipitation reaction. Combination and interaction of hDaxx with p53 may mediate cellular cycles.
出处
《微生物学杂志》
CAS
CSCD
2001年第4期32-34,共3页
Journal of Microbiology
基金
国家教育部高等学校骨干教师资助计划 ( 2 0 0 0 6 5 )