Bermejo-Nogales Azucena, Calduch-Giner Josep Alvar, Pérez-Sánchez Jaume
Nutrigenomics and Fish Growth Endocrinology Group, Institute of Aquaculture Torre de la Sal (CSIC-IATS), Ribera de Cabanes, Castellón, Spain.
PLoS One. 2015 Apr 15;10(4):e0122889. doi: 10.1371/journal.pone.0122889. eCollection 2015.
Mitochondrial oxidative phosphorylation provides over 90% of the energy produced by aerobic organisms, therefore the regulation of mitochondrial activity is a major issue for coping with the changing environment and energy needs. In fish, there is a large body of evidence of adaptive changes in enzymatic activities of the OXPHOS pathway, but less is known at the transcriptional level and the first aim of the present study was to define the molecular identity of the actively transcribed subunits of the mitochondrial respiratory chain of a livestock animal, using gilthead sea bream as a model of farmed fish with a high added value for European aquaculture. Extensive BLAST searches in our transcriptomic database (www.nutrigroup-iats.org/seabreamdb) yielded 97 new sequences with a high coverage of catalytic, regulatory and assembly factors of Complex I to V. This was the basis for the development of a PCR array for the simultaneous profiling of 88 selected genes. This new genomic resource allowed the differential gene expression of liver and muscle tissues in a model of 10 fasting days. A consistent down-regulated response involving 72 genes was made by the liver, whereas an up-regulated response with 29 and 10 differentially expressed genes was found in white skeletal muscle and heart, respectively. This differential regulation was mostly mediated by nuclear-encoded genes (skeletal muscle) or both mitochondrial- and nuclear-encoded genes (liver, heart), which is indicative of a complex and differential regulation of mitochondrial and nuclear genomes, according to the changes in the lipogenic activity of liver and the oxidative capacity of glycolytic and highly oxidative muscle tissues. These insights contribute to the identification of the most responsive elements of OXPHOS in each tissue, which is of relevance for the appropriate gene targeting of nutritional and/or environmental metabolic disturbances in livestock animals.
线粒体氧化磷酸化提供了需氧生物产生的90%以上的能量,因此线粒体活性的调节是应对不断变化的环境和能量需求的一个主要问题。在鱼类中,有大量证据表明氧化磷酸化途径的酶活性存在适应性变化,但在转录水平上了解较少。本研究的首要目的是利用金头鲷作为欧洲水产养殖中有高附加值的养殖鱼类模型,确定一种家畜动物线粒体呼吸链中活跃转录亚基的分子身份。在我们的转录组数据库(www.nutrigroup-iats.org/seabreamdb)中进行广泛的BLAST搜索,得到了97个新序列,这些序列高度覆盖了复合体I至V的催化、调节和组装因子。这是开发用于同时分析88个选定基因的PCR阵列的基础。这种新的基因组资源使得在禁食10天的模型中能够对肝脏和肌肉组织进行差异基因表达分析。肝脏做出了涉及72个基因的一致下调反应,而在白色骨骼肌和心脏中分别发现了29个和10个差异表达基因的上调反应。这种差异调节主要由核编码基因(骨骼肌)或线粒体和核编码基因(肝脏、心脏)介导,这表明根据肝脏的生脂活性以及糖酵解和高氧化肌肉组织的氧化能力的变化,线粒体和核基因组存在复杂的差异调节。这些见解有助于确定每个组织中氧化磷酸化最敏感的元件,这对于家畜动物营养和/或环境代谢紊乱的适当基因靶向具有重要意义。