BRCA1-Associated ATM Activator-1 (BRAT1)在mTOR调控中的潜在作用

Journal of cancer biology & research Pub Date : 2013-07-01
Eui Young So, Toru Ouchi
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引用次数: 0

摘要

BRCA1-associated ATM activator-1 (BRAT1)是一种DNA损伤反应(DDR)蛋白,可与多种DDR蛋白结合,调控其DNA损伤后的功能。然而,先前的研究也表明BRAT1是细胞生长和凋亡的调节因子。在本研究中,靶向基因缺失表明BRAT1对mTOR及下游蛋白的稳定性和血清诱导表达至关重要。小鼠胚胎成纤维细胞BRAT1的条件缺失抑制血清诱导的细胞周期进程。我们的研究结果表明BRAT1是PIKK信号级联的重要因子。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The Potential Role of BRCA1-Associated ATM Activator-1 (BRAT1) in Regulation of mTOR.

BRCA1-associated ATM activator-1 (BRAT1) was identified by our group as a DNA damage response (DDR) protein, which can bind with many DDR proteins and regulates their functions after DNA damage. However, previous study has also implicated BRAT1 as a regulator of cell growth and apoptosis. In this study, targeted gene deletion showed that BRAT1 is critical in stability and serum-induced expression of mTOR and downstream protein. Conditional deletion of BRAT1 of mouse embryonic fibroblasts suppressed serum-induced cell cycling progress. Our results suggest that BRAT1 is essential factor for PIKK signaling cascades.

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