The reaper-binding protein scythe modulates apoptosis and proliferation during mammalian development

被引:78
作者
Desmots, F
Russell, HR
Lee, YS
Boyd, K
McKinnon, PJ
机构
[1] St Jude Childrens Res Hosp, Dept Genet & Tumor Cell Biol, Memphis, TN 38105 USA
[2] St Jude Childrens Res Hosp, Anim Resource Ctr, Memphis, TN 38105 USA
关键词
D O I
10.1128/MCB.25.23.10329-10337.2005
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Scythe (BAT3 [HLA-B-associated transcript 3]) is a nuclear protein that has been implicated in apoptosis, as it can modulate Reaper, a central apoptotic regulator in Drosophila melanogaster. While Scythe can markedly affect Reaper-dependent apoptosis in Xenopus laevis cell extracts, the function of Scythe in mammals is unknown. Here, we report that inactivation of Scythe in the mouse results in lethality associated with pronounced developmental defects in the lung, kidney, and brain. In all cases, these developmental defects were associated with dysregulation of apoptosis and cellular proliferation. Seythe(-/-) cells were also more resistant to apoptosis induced by menadione and thapsigargin. These data show that Scythe is critical for viability and normal development, probably via regulation of programmed cell death and cellular proliferation.
引用
收藏
页码:10329 / 10337
页数:9
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