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首页> 外文期刊>Proceedings of the National Academy of Sciences of the United States of America >Inhibition of Reaper-induced apoptosis by interaction with inhibitor of apoptosis proteins (IAPs)
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Inhibition of Reaper-induced apoptosis by interaction with inhibitor of apoptosis proteins (IAPs)

机译:通过与凋亡蛋白抑制剂(IAPs)相互作用抑制收割者诱导的凋亡

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摘要

IAPs comprise a family of inhibitors of apo- ptosis found in viruses and animals. In vivo binding studies demonstrated that both baculovirus and Drosophila IAPs physically interact with an apoptosis-inducing protein of Drosophila, Reaper (RPR), through their baculovirus IAP repeat (BIR) region. Expression of IAPs blocked RPR-induced apoptosis and resulted in the accumulation of RPR in punc- tate perinuclear locations which coincided with IAP localiza- tion. When expressed alone, RPR rapidly disappeared from the cells undergoing RPR-induced apoptosis. Expression of P35, a caspase inhibitor, also blocked RPR-induced apoptosis and delayed RPR decline, but RPR remained cytoplasmic in its location.
机译:IAP包含一类在病毒和动物中发现的细胞凋亡抑制剂。体内结合研究表明,杆状病毒和果蝇IAPs都通过杆状病毒IAP重复(BIR)区与果蝇的死细胞(RPR)诱导凋亡。 IAP的表达阻断了RPR诱导的凋亡,并导致RPR在点状核周位置积聚,这与IAP定位相吻合。当单独表达时,RPR迅速从经历RPR诱导的细胞凋亡的细胞中消失。 Caspase抑制剂P35的表达也阻断RPR诱导的凋亡并延迟RPR下降,但RPR仍在其位置呈细胞质。

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