Unraveling the Molecular Signatures of Oxidative Phosphorylation to Cope with the Nutritionally Changing Metabolic Capabilities of Liver and Muscle Tissues in Farmed Fish

被引:54
作者
Bermejo-Nogales, Azucena [1 ]
Alvar Calduch-Giner, Josep [1 ]
Perez-Sanchez, Jaume [1 ]
机构
[1] Inst Aquaculture Torre de la Sal CSIC IATS, Nutrigen & Fish Growth Endocrinol Grp, Ribera De Cabanes, Castellon, Spain
关键词
CYTOCHROME-C-OXIDASE; GENE-EXPRESSION PROFILE; SPARUS-AURATA L; MITOCHONDRIAL-FUNCTION; NUTRIENT AVAILABILITY; ASSEMBLY FACTORS; PROTEIN COMPLEX; ATP SYNTHASE; NUCLEAR; EVOLUTION;
D O I
10.1371/journal.pone.0122889
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
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.
引用
收藏
页数:20
相关论文
共 64 条
[21]   Transcriptome profiling of the feeding-to-fasting transition in chicken liver [J].
Desert, Colette ;
Duclos, Michel J. ;
Blavy, Pierre ;
Lecerf, Frederic ;
Moreews, Francois ;
Klopp, Christophe ;
Aubry, Marc ;
Herault, Frederic ;
Le Roy, Pascale ;
Berri, Cecile ;
Douaire, Madeleine ;
Diot, Christian ;
Lagarrigue, Sandrine .
BMC GENOMICS, 2008, 9 (1)
[22]   The effect of short-term hypoxic exposure on metabolic gene expression [J].
Everett, Meredith V. ;
Antal, Corina E. ;
Crawford, Douglas L. .
JOURNAL OF EXPERIMENTAL ZOOLOGY PART A-ECOLOGICAL GENETICS AND PHYSIOLOGY, 2012, 317A (01) :9-23
[23]   Genetic variation in feed consumption, growth, nutrient utilization efficiency and mitochondrial function within a farmed population of channel catfish (Ictalurus punctatus) [J].
Eya, Jonathan C. ;
Ashame, Martha F. ;
Pomeroy, Charles F. ;
Manning, Bruce B. ;
Peterson, Brian C. .
COMPARATIVE BIOCHEMISTRY AND PHYSIOLOGY B-BIOCHEMISTRY & MOLECULAR BIOLOGY, 2012, 163 (02) :211-220
[24]   Association of mitochondrial function with feed efficiency in rainbow trout: Diets and family effects [J].
Eya, Jonathan C. ;
Ashame, Martha F. ;
Pomeroy, Charles F. .
AQUACULTURE, 2011, 321 (1-2) :71-84
[25]   Cytochrome c oxidase is regulated by modulations in protein expression and mitochondrial membrane phospholipid composition in estivating African lungfish [J].
Frick, N. T. ;
Bystriansky, J. S. ;
Ip, Y. K. ;
Chew, S. F. ;
Ballantyne, J. S. .
AMERICAN JOURNAL OF PHYSIOLOGY-REGULATORY INTEGRATIVE AND COMPARATIVE PHYSIOLOGY, 2010, 298 (03) :R608-R616
[26]   Tracing the evolution of a large protein complex in the eukaryotes, NADH:Ubiquinone oxidoreductase (Complex I) [J].
Gabaldón, T ;
Rainey, D ;
Huynen, MA .
JOURNAL OF MOLECULAR BIOLOGY, 2005, 348 (04) :857-870
[27]   Assembly Factors of Human Mitochondrial Respiratory Chain Complexes: Physiology and Pathophysiology [J].
Ghezzi, Daniele ;
Zeviani, Massimo .
MITOCHONDRIAL OXIDATIVE PHOSPHORYLATION: NUCLEAR-ENCODED GENES, ENZYME REGULATION, AND PATHOPHYSIOLOGY, 2012, 748 :65-106
[28]   ATP synthase oligomerization: From the enzyme models to the mitochondrial morphology [J].
Habersetzer, Johan ;
Ziani, Widade ;
Larrieu, Isabelle ;
Stines-Chaumeil, Claire ;
Giraud, Marie-France ;
Brethes, Daniel ;
Dautant, Alain ;
Paumard, Patrick .
INTERNATIONAL JOURNAL OF BIOCHEMISTRY & CELL BIOLOGY, 2013, 45 (01) :99-105
[29]   The nuclear encoded subunits of complex I from bovine heart mitochondria [J].
Hirst, J ;
Carroll, J ;
Fearnley, IM ;
Shannon, RJ ;
Walker, JE .
BIOCHIMICA ET BIOPHYSICA ACTA-BIOENERGETICS, 2003, 1604 (03) :135-150
[30]   Mammalian subunit IV isoforms of cytochrome c oxidase [J].
Hüttemann, M ;
Kadenbach, B ;
Grossman, LI .
GENE, 2001, 267 (01) :111-123