Mitochondrial DNA

Molecular barcoding of venomous snakes and species-specific multiplex PCR assay to identify snake groups for which antivenom is available in Thailand

A. Supikamolseni, Ngaoburanawit, N., Sumontha, M., Chanhome, L., Suntrarachun, S., Peyachoknagul, S., and Srikulnath, K., Molecular barcoding of venomous snakes and species-specific multiplex PCR assay to identify snake groups for which antivenom is available in Thailand, vol. 14, pp. 13981-13997, 2015.

DNA barcodes of mitochondrial COI and Cytb genes were constructed from 54 specimens of 16 species for species identification. Intra- and interspecific sequence divergence of the COI gene (10 times) was greater than that of the Cytb gene (4 times), which suggests that the former gene may be a better marker than the latter for species delimitation in snakes. The COI barcode cut-off scores differed by more than 3% between most species, and the minimum interspecific divergence was greater than the maximum intraspecific divergence.

Molecular identification of Echinococcus granulosus on the Tibetan Plateau using mitochondrial DNA markers

D. Hu, Song, X., Wang, N., Zhong, X., Wang, J., Liu, T., Jiang, Z., Dawa, T., Gu, X., Peng, X., and Yang, G., Molecular identification of Echinococcus granulosus on the Tibetan Plateau using mitochondrial DNA markers, vol. 14, pp. 13915-13923, 2015.

Cystic echinococcosis (CE) is an important worldwide zoonotic disease that causes large economic losses and human suffering. Echinococcus granulosus, the causative agent of CE, exhibits different genotypes in different locations. In order to identify its genotypes and analyze its genetic structure on the Tibetan Plateau, we collected 72 hydatid cysts from different intermediate hosts and amplified and sequenced their mitochondrial cytochrome c oxidase subunit 2 (cox2) genes. Seventy isolates were identified as the E.

Respiratory chain complex III deficiency in patients with tRNA-leu mutation

J. Jiang, Wang, X. L., and Ma, Y. Y., Respiratory chain complex III deficiency in patients with tRNA-leu mutation, vol. 14, pp. 18629-18636, 2015.

The aim of this study was to investigate the clinical and genetic profiles of mitochondrial disease resulting from deficiencies in the respiratory chain complex III. Three patients, aged between 8 months and 12 years, were recruited for this study. The activities of mitochondrial respiratory chain complexes in the peripheral leucocytes were spectrophotometrically measured. The entire mitochondrial DNA (mtDNA) sequence was analyzed. Samples obtained from the three patients and their families were subjected to restriction fragment length polymorphism and gene sequencing analyses.

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