Tryon Liam D, Crilly Matthew J, Hood David A
Muscle Health Research Centre, York University, Toronto, Ontario, Canada; and School of Kinesiology and Health Science, York University, Toronto, Ontario, Canada.
Muscle Health Research Centre, York University, Toronto, Ontario, Canada; and School of Kinesiology and Health Science, York University, Toronto, Ontario, Canada
Am J Physiol Cell Physiol. 2015 Aug 15;309(4):C228-38. doi: 10.1152/ajpcell.00266.2014. Epub 2015 Jun 10.
The purpose of this study was to determine how the expression of mitochondrial transcription factor A (Tfam), a protein that governs mitochondrial DNA (mtDNA) transcription and replication, is regulated during a state of reduced organelle content imposed by muscle disuse. We measured Tfam expression at 8 h, 16 h, 24 h, 3 days, or 7 days following denervation and hypothesized that decreases in Tfam expression would precede mitochondrial loss. Muscle mass was lowered by 13% and 38% at 3 and 7 days postdenervation, while cytochrome c oxidase activity fell by 33% and 39% at the same time points. Tfam promoter activation in vivo was reduced by 30-65% between 8 h and 3 days of denervation, while Tfam transcript half-life was increased following 8-24 h of denervation. Protein expression of RNA-binding proteins that promote mRNA degradation (CUG repeat-binding protein and K homology splicing regulator protein) was elevated at 3 and 7 days of denervation. Tfam localization within subsarcolemmal mitochondria was reduced after 3 and 7 days of denervation and was associated with suppression of the cytochrome c oxidase type I transcript at 3 days, indicating that denervation impairs both mitochondrial Tfam import and mtDNA transcription during an early period following denervation. These data suggest that putative signals downregulate Tfam transcription during the earliest stages following denervation but are counteracted by increases in Tfam mRNA stability. Import of Tfam into the mitochondrion seems to be the most critical point of regulation of this protein during the early onset of denervation, an impairment of which is coincident with the loss of mitochondria during muscle disuse.
本研究的目的是确定线粒体转录因子A(Tfam)的表达是如何在肌肉废用导致细胞器含量减少的状态下受到调控的。Tfam是一种控制线粒体DNA(mtDNA)转录和复制的蛋白质。我们在去神经支配后的8小时、16小时、24小时、3天或7天测量了Tfam的表达,并假设Tfam表达的降低会先于线粒体的丢失。去神经支配后3天和7天,肌肉质量分别降低了13%和38%,而细胞色素c氧化酶活性在相同时间点分别下降了33%和39%。去神经支配8小时至3天期间,体内Tfam启动子激活降低了30%-65%,而去神经支配8-24小时后,Tfam转录本半衰期延长。促进mRNA降解的RNA结合蛋白(CUG重复结合蛋白和K同源剪接调节蛋白)的蛋白表达在去神经支配3天和7天时升高。去神经支配3天和7天后,肌膜下线粒体中Tfam的定位减少,且在3天时与细胞色素c氧化酶I型转录本的抑制相关,这表明去神经支配在去神经支配后的早期阶段损害了线粒体Tfam的导入和mtDNA转录。这些数据表明,假定的信号在去神经支配后的最早阶段下调Tfam转录,但被Tfam mRNA稳定性的增加所抵消。在去神经支配早期,Tfam导入线粒体似乎是该蛋白调控的最关键点,这一过程受损与肌肉废用期间线粒体的丢失同时发生。