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酵母雷帕霉素靶蛋白复合体1氨基酸感应中的新型tRNA功能

Novel tRNA function in amino acid sensing of yeast Tor complex1.

作者信息

Kamada Yoshiaki

机构信息

Laboratory of Biological Diversity, National Institute for Basic Biology, Okazaki, 444-8585, Japan.

Department of Basic Biology, School of Life Science, The Graduate University for Advanced Studies (SOKENDAI), Okazaki, 444-8585, Japan.

出版信息

Genes Cells. 2017 Feb;22(2):135-147. doi: 10.1111/gtc.12462. Epub 2017 Jan 13.

Abstract

TOR complex1 (TORC1), a master regulator of cell growth, is regulated by amino acids. Amino acids are fundamental nutrients, and 20 species of amino acids building proteins are not interchangeable with each other. Therefore, TORC1 should sense each amino acid individually. Mammalian mTORC1 is controlled by Rag GTPases and their regulators. However, Rag factors are dispensable for amino acid sensing by TORC1 in the budding yeast, suggesting an alternative mechanism of TORC1 regulation. Here, genetic investigation discovered the involvement of (aminoacyl-)tRNA ((aa-)tRNA) in TORC1 regulation. Biochemical TORC1 assay also showed that tRNA directly inhibits TORC1 kinase activity. Reducing cellular tRNA molecule desensitizes TORC1 inactivation by nitrogen starvation in vivo. Based on these results, I propose a model of the TORC1 regulatory mechanism in which free tRNA released from protein synthesis under amino acid starvation inhibits TORC1 activity. Therefore, TORC1 uses tRNA-mediated mechanism and Rag factors in parallel to sense intracellular amino acids.

摘要

TOR复合物1(TORC1)是细胞生长的主要调节因子,受氨基酸调控。氨基酸是基本营养物质,构成蛋白质的20种氨基酸彼此不可互换。因此,TORC1应该分别感知每种氨基酸。哺乳动物的mTORC1受Rag GTP酶及其调节因子控制。然而,在芽殖酵母中,Rag因子对于TORC1感知氨基酸并非必需,这表明存在TORC1调节的另一种机制。在此,遗传学研究发现了(氨酰基 - )tRNA((aa - )tRNA)参与TORC1调节。生化TORC1分析还表明,tRNA直接抑制TORC1激酶活性。减少细胞内tRNA分子可使体内氮饥饿导致的TORC1失活不敏感。基于这些结果,我提出了一种TORC1调节机制模型,即在氨基酸饥饿时从蛋白质合成中释放的游离tRNA抑制TORC1活性。因此,TORC1并行使用tRNA介导的机制和Rag因子来感知细胞内氨基酸。

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