The complete mitochondrial genome of red grouper Plectropomus leopardus and its applications in identification of grouper species

• Published in: Aquaculture 2008-04, Vol.276 (1-4), p.44-49
• Main Authors: Zhu, Ze Yuan, Yue, Gen Hua
• Format: Article
• Language: English
• Subjects: Agnatha. Pisces; Animal aquaculture; Animal productions; Aquaculture; Biological and medical sciences; Diversity; evolution; Fish; fish culture; Fundamental and applied biological sciences. Psychology; General aspects; genetic variation; Genomics; Genotype & phenotype; Grouper; Marine; Mitochondrial DNA; Mitochondrial genome; molecular systematics; Perciformes; phylogeny; Plectropomus leopardus; Plectropomus maculatus; Plectropomus sp; Ribonucleic acid; RNA; sequence analysis; Serranidae; Species identification; Vertebrates: general zoology, morphology, phylogeny, systematics, cytogenetics, geographical distribution
• ISSN: 0044-8486; 1873-5622
• DOI: 10.1016/j.aquaculture.2008.02.008

Aquaculture of high-value finfish species, such as groupers, is an industry of increasing importance world wide. Groupers are represented by 15 genera and 159 species. Phenotypical classification of grouper species is difficult. Mitochondrial DNA (mtDNA) sequences can be used in differentiating species. We report the first complete mitochondrial genome sequence among grouper species, the complete mtDNA of Leopard coral grouper (Plectropomus leopardus). The complete mtDNA of P. leopardus was 16,714 bp long including a 1077 bp control region, 13 protein-coding genes, two rRNA and 22 tRNA. Phylogenetic analyses using concatenated amino acid sequences of 12 protein-coding genes of 29 fish species representing 12 suborders indicated that P. leopardus was located in the cluster of fish species from the order Perciformes, supporting the traditional taxonomic classification of fish. Using nucleotide sequences of the NADH2 genes of 49 grouper species from eight genera, we constructed phylogenetic trees showing most of these species could be differentiated with sequences of the NADH2 gene, and the P. leopardus was closely related to P. maculatus, in agreement their phenotypic similarity. We developed one duplex PCR which could differentiate the two species P. leopardus and P. maculatus based on the D-loop DNA sequences of these two species. The complete mtDNA sequence of P. leopardus and duplex PCR provide useful tools for genetic studies and aquaculture of P. leopardus.