Autor: |
Hassan S; Bahauddin Zakariya University, Institute of Zoology, Multan, Punjab, Pakistan., Naeem M; Bahauddin Zakariya University, Institute of Zoology, Multan, Punjab, Pakistan., Nasir MF; University of Education, Department of Zoology, Division of Science & Technology, Lahore, Punjab, Pakistan., Riaz P; Bahauddin Zakariya University, Institute of Zoology, Multan, Punjab, Pakistan., Khan MN; University of Jhang, Department of Zoology, Jhang, Punjab, Pakistan., Atiq I; Ghazi University Dera Ghazi Khan, Department of Zoology, Punjab, Pakistan. |
Abstrakt: |
Molecular appraoch for identification of unknown species by using Cytochrome b gene is an effective and reliable as compared with morphological based identification. For DNA barcoding universal molecular genes were used to identify the species. Cytochrome b is a specific gene used for identification purpose. DNA barcoding is a reliable and effective method compared to the different traditional morphological methods of specie identification. So,in the present study which was conducted to identify the species, a total of 50 fish samples were collected from five different sites. DNA was extracted by using the Phenol Chloroform method from muscle tissue. Five sequences were sequenced (one from each site), analyzed, and identified specific species as Pangasius pangasius. Identified sequences were variable in length from 369 bp (Site 1), 364 bp (Site 2), 364 bp (Site 3), 352 bp (Site 4), and 334 bp (Site 5). Identity matches on the NCBI database confirmed the specific specie as P. pangasius. A distancing tree was drawn to show maximum likelihood among the same and different species. Yet, in many cases fishes on diverse development stages are difficult to identify by morphological characters. DNA-based identification methods offer an analytically powerful addition or even an alternative tool for species identification and phylogenetic study. This work intends to provide an updated and extensive overview on the DNA based methods for fish species identification by using Cytochrome b gene as targeted markers for identification purpose. |