交易激励
神经生长因子IB
神经元源性孤儿受体1
核受体
细胞生物学
转录因子
线粒体
小异二聚体伴侣
生物
细胞凋亡
细胞色素c
癌症研究
化学
遗传学
基因
作者
Hui Li,Siva K. Kolluri,Jian Gu,Marcia I. Dawson,Xihua Cao,Peter D. Hobbs,Bingzhen Lin,Guo-quen Chen,Jiang-song Lu,Feng Lin,Zhihua Xie,Joseph A. Fontana,John C. Reed,Xiao-kun Zhang
出处
期刊:Science
[American Association for the Advancement of Science]
日期:2000-08-18
卷期号:289 (5482): 1159-1164
被引量:657
标识
DOI:10.1126/science.289.5482.1159
摘要
TR3, an immediate-early response gene and an orphan member of the steroid-thyroid hormone-retinoid receptor superfamily of transcription factors, regulates apoptosis through an unknown mechanism. In response to apoptotic stimuli, TR3 translocates from the nucleus to mitochondria to induce cytochrome c release and apoptosis. Mitochondrial targeting of TR3, but not its DNA binding and transactivation, is essential for its proapoptotic effect. Our results reveal a mechanism by which a nuclear transcription factor translocates to mitochondria to initiate apoptosis.
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