TRIM2:防止细胞凋亡的双刃剑。

Thomas Hollemann
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引用次数: 0

摘要

TRIM2属于TRIM-NHL类泛素e3连接酶,具有抑制细胞凋亡的双重功能。Liao等人在近期发表的文章中报道,在谷氨酰胺剥夺的情况下,TRIM2转录被ATF4激活,增加长链脂肪酸进入线粒体的摄取。在这里,TRIM2作为CPT1的直接激活剂,独立于其E3泛素连接酶活性,并防止由饥饿引发的细胞凋亡。相反,TRIM e3 -泛素连接酶被描述为泛素化,从而靶向促凋亡BIM在蛋白酶体中的降解。因此,TRIM2通过其连接酶活性抑制细胞凋亡,但也不依赖于这种刺激的能量代谢。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
TRIM2: a double-edged sword preventing apoptosis

TRIM2 belongs to the TRIM-NHL class of ubiquitin E3-ligases and inhibits apoptosis by a dual function. Liao et al. reported in the recent issue that under glutamine deprivation, TRIM2 transcription is activated by ATF4 to increase the uptake of long fatty acids into mitochondria. Here, TRIM2 acts as a direct activator of CPT1 independent of its E3 ubiquitin ligase activity and prevents apoptosis otherwise triggered by starvation. On the contrary, TRIM E3-ubiquitin ligase has been described to ubiquitinate and thus target proapoptotic BIM for its degradation in the proteasome. Thus, TRIM2 inhibits apoptosis classically via its ligase activity but also independent of this stimulating energy metabolism.

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