亮氨酸
转移RNA
氨基酸
线粒体
生物
蛋白质生物合成
生物化学
信使核糖核酸
细胞生物学
核糖核酸
基因
作者
Christof Schild,Dagmar Hahn,André Schaller,Christopher B. Jackson,Barbara Rothen‐Rutishauser,Jelena Mirkovitch,Jean‐Marc Nuoffer
出处
期刊:Amino Acids
[Springer Nature]
日期:2014-04-07
卷期号:46 (7): 1775-1783
被引量:9
标识
DOI:10.1007/s00726-014-1730-2
摘要
Pentatricopeptide repeat domain protein 1 (PTCD1) is a novel human protein that was recently shown to decrease the levels of mitochondrial leucine tRNAs. The physiological role of this regulation, however, remains unclear. Here we show that amino acid starvation by leucine deprivation significantly increased the mRNA steady-state levels of PTCD1 in human hepatocarcinoma (HepG2) cells. Amino acid starvation also increased the mitochondrially encoded leucine tRNA (tRNALeu(CUN)) and the mRNA for the mitochondrial leucyl-tRNA synthetase (LARS2). Despite increased PTCD1 mRNA steady-state levels, amino acid starvation decreased PTCD1 on the protein level. Decreasing PTCD1 protein concentration increases the stability of the mitochondrial leucine tRNAs, tRNALeu(CUN) and tRNALeu(UUR) as could be shown by RNAi experiments against PTCD1. Therefore, it is likely that decreased PTCD1 protein contributes to the increased tRNALeu(CUN) levels in amino acid-starved cells. The stabilisation of the mitochondrial leucine tRNAs and the upregulation of the mitochondrial leucyl-tRNA synthetase LARS2 might play a role in adaptation of mitochondria to amino acid starvation.
科研通智能强力驱动
Strongly Powered by AbleSci AI