Gnipová Anna, Šubrtová Karolína, Panicucci Brian, Horváth Anton, Lukeš Julius, Zíková Alena
Biology Center, Institute of Parasitology, Czech Academy of Sciences, České Budějovice, Czech Republic Department of Biochemistry, Faculty of Natural Sciences, Comenius University, Bratislava, Slovakia.
Biology Center, Institute of Parasitology, Czech Academy of Sciences, České Budějovice, Czech Republic Faculty of Science, University of South Bohemia, České Budějovice, Czech Republic.
Eukaryot Cell. 2015 Mar;14(3):297-310. doi: 10.1128/EC.00238-14. Epub 2015 Jan 23.
The highly conserved ADP/ATP carrier (AAC) is a key energetic link between the mitochondrial (mt) and cytosolic compartments of all aerobic eukaryotic cells, as it exchanges the ATP generated inside the organelle for the cytosolic ADP. Trypanosoma brucei, a parasitic protist of medical and veterinary importance, possesses a single functional AAC protein (TbAAC) that is related to the human and yeast ADP/ATP carriers. However, unlike previous studies performed with these model organisms, this study showed that TbAAC is most likely not a stable component of either the respiratory supercomplex III+IV or the ATP synthasome but rather functions as a physically separate entity in this highly diverged eukaryote. Therefore, TbAAC RNA interference (RNAi) ablation in the insect stage of T. brucei does not impair the activity or arrangement of the respiratory chain complexes. Nevertheless, RNAi silencing of TbAAC caused a severe growth defect that coincides with a significant reduction of mt ATP synthesis by both substrate and oxidative phosphorylation. Furthermore, TbAAC downregulation resulted in a decreased level of cytosolic ATP, a higher mt membrane potential, an elevated amount of reactive oxygen species, and a reduced consumption of oxygen in the mitochondria. Interestingly, while TbAAC has previously been demonstrated to serve as the sole ADP/ATP carrier for ADP influx into the mitochondria, our data suggest that a second carrier for ATP influx may be present and active in the T. brucei mitochondrion. Overall, this study provides more insight into the delicate balance of the functional relationship between TbAAC and the oxidative phosphorylation (OXPHOS) pathway in an early diverged eukaryote.
高度保守的ADP/ATP载体(AAC)是所有需氧真核细胞线粒体(mt)和胞质区室之间关键的能量连接,因为它将细胞器内产生的ATP与胞质ADP进行交换。布氏锥虫是一种具有医学和兽医学重要性的寄生原生生物,拥有一种与人类和酵母ADP/ATP载体相关的单一功能性AAC蛋白(TbAAC)。然而,与此前对这些模式生物进行的研究不同,本研究表明TbAAC很可能不是呼吸超复合物III+IV或ATP合酶体的稳定组分,而是在这种高度分化的真核生物中作为一个物理上独立的实体发挥作用。因此,在布氏锥虫的昆虫阶段进行TbAAC RNA干扰(RNAi)消除并不会损害呼吸链复合物的活性或排列。尽管如此,TbAAC的RNAi沉默导致了严重的生长缺陷,这与底物和氧化磷酸化导致的mt ATP合成显著减少相吻合。此外,TbAAC下调导致胞质ATP水平降低、mt膜电位升高、活性氧含量增加以及线粒体中氧气消耗减少。有趣的是,虽然此前已证明TbAAC是ADP流入线粒体的唯一ADP/ATP载体,但我们的数据表明,可能存在第二种ATP流入载体并在布氏锥虫线粒体中发挥作用。总体而言,本研究为早期分化的真核生物中TbAAC与氧化磷酸化(OXPHOS)途径之间功能关系的微妙平衡提供了更多见解。