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首页> 外文期刊>Cellular Signalling >Parkin ubiquitinates mTOR to regulate mTORC1 activity under mitochondrial stress
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Parkin ubiquitinates mTOR to regulate mTORC1 activity under mitochondrial stress

机译:线粒体应激下帕金泛素使mTOR调节mTORC1活性

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摘要

mTORC1, a kinase complex that is considered a master regulator of cellular growth and proliferation, is regulated by many extra- and intracellular signals. Among these signals, mitochondrial status is known to have an impact on the effects of mTORC1 on cell growth and survival. However, how mitochondrial status affects mTORC1 activity, notably the molecular link, is not fully elucidated. Here, we found that Parkin can interact with and ubiquitinate mTOR. We also identified K2066 and K2306 as Parkin-dependent and mitochondrial stress-induced mTOR ubiquitination residues. This ubiquitination by Parkin is required for maintenance of mTORC1 activity under mitochondrial stress.With regard to the physiological meaning of mTORC1 activity under mitochondrial stress, we suggest that mTORC1 plays a pro-survival role.
机译:mTORC1是一种激酶复合物,被认为是细胞生长和增殖的主要调节剂,它受许多细胞外和细胞内信号的调节。在这些信号中,线粒体状态已知会影响mTORC1对细胞生长和存活的影响。但是,线粒体状态如何影响mTORC1活性,特别是分子连接,尚不完全清楚。在这里,我们发现帕金可以与mTOR相互作用并使其泛素化。我们还将K2066和K2306确定为帕金依赖性和线粒体应激诱导的mTOR泛素化残基。在线粒体应激下维持mTORC1活性需要帕金酸泛素化。关于线粒体应激下mTORC1活性的生理意义,我们建议mTORC1发挥促存活作用。

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