The complete mitochondrial genome sequence and gene organization of the mud crab (Scylla paramamosain) with phylogenetic consideration

Gene. 2013 Apr 25;519(1):120-7. doi: 10.1016/j.gene.2013.01.028. Epub 2013 Feb 4.

Abstract

The complete mitochondrial genome is of great importance for better understanding the genome-level characteristics and phylogenetic relationships among related species. In the present study, we determined the complete mitochondrial genome DNA sequence of the mud crab (Scylla paramamosain) by 454 deep sequencing and Sanger sequencing approaches. The complete genome DNA was 15,824 bp in length and contained a typical set of 13 protein-coding genes, 22 transfer RNA (tRNA) genes, two ribosomal RNA (rRNA) genes and a putative control region (CR). Of 37 genes, twenty-three were encoded by the heavy strand (H-strand), while the other ones were encoded by light strand (L-strand). The gene order in the mitochondrial genome was largely identical to those obtained in most arthropods, although the relative position of gene tRNA(His) differed from other arthropods. Among 13 protein-coding genes, three (ATPase subunit 6 (ATP6), NADH dehydrogenase subunits 1 (ND1) and ND3) started with a rare start codon ATT, whereas, one gene cytochrome c oxidase subunit I (COI) ended with the incomplete stop codon TA. All 22 tRNAs could fold into a typical clover-leaf secondary structure, with the gene sizes ranging from 63 to 73 bp. The phylogenetic analysis based on 12 concatenated protein-coding genes showed that the molecular genetic relationship of 19 species of 11 genera was identical to the traditional taxonomy.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Brachyura / classification*
  • Brachyura / genetics*
  • DNA Primers
  • DNA, Mitochondrial / genetics
  • Gene Order
  • Genes, rRNA
  • Genome, Mitochondrial*
  • Nucleic Acid Conformation
  • Phylogeny*
  • Polymerase Chain Reaction
  • RNA, Ribosomal / genetics
  • RNA, Transfer / genetics
  • RNA, Transfer / isolation & purification
  • Sequence Analysis, DNA

Substances

  • DNA Primers
  • DNA, Mitochondrial
  • RNA, Ribosomal
  • RNA, Transfer