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Species identification of Malayan Gaur, Kedah-Kelantan and Bali cattle using polymerase chain reaction-restricted fragment length polymorphism.
Romaino, S M N; Fazly-Ann, Z A; Loo, S S; Hafiz, M M; Hafiz, M D; Iswadi, M I; Kashiani, P; Rosli, M K A; Syed-Shabthar, S M F; Md-Zain, B M; Abas-Mazni, O.
Affiliation
  • Romaino SM; Agro-Biotechnology Institute, Malaysia (ABI), Serdang, Selangor, Malaysia.
  • Fazly-Ann ZA; Agro-Biotechnology Institute, Malaysia (ABI), Serdang, Selangor, Malaysia.
  • Loo SS; Agro-Biotechnology Institute, Malaysia (ABI), Serdang, Selangor, Malaysia.
  • Hafiz MM; Agro-Biotechnology Institute, Malaysia (ABI), Serdang, Selangor, Malaysia.
  • Hafiz MD; Agro-Biotechnology Institute, Malaysia (ABI), Serdang, Selangor, Malaysia.
  • Iswadi MI; Agro-Biotechnology Institute, Malaysia (ABI), Serdang, Selangor, Malaysia.
  • Kashiani P; Agro-Biotechnology Institute, Malaysia (ABI), Serdang, Selangor, Malaysia.
  • Rosli MK; School of Environmental and Natural Resource Sciences, Faculty of Science and Technology, Universiti Kebangsaan Malaysia, Bangi, Selangor, Malaysia.
  • Syed-Shabthar SM; School of Environmental and Natural Resource Sciences, Faculty of Science and Technology, Universiti Kebangsaan Malaysia, Bangi, Selangor, Malaysia.
  • Md-Zain BM; School of Environmental and Natural Resource Sciences, Faculty of Science and Technology, Universiti Kebangsaan Malaysia, Bangi, Selangor, Malaysia abgbadd1966@yahoo.com.
  • Abas-Mazni O; Agro-Biotechnology Institute, Malaysia (ABI), Serdang, Selangor, Malaysia.
Genet Mol Res ; 13(1): 406-14, 2014 Jan 21.
Article in En | MEDLINE | ID: mdl-24535867
ABSTRACT
Mitochondrial DNA (mtDNA) is a useful genetic marker that can be used for species identification. The cytochrome b (Cyt b) gene is a suitable mtDNA candidate gene for use in phylogenetic analyses due to its sequence variability, which makes it appropriate for comparisons at the subspecies, species, and genus levels. This study was conducted to develop a rapid molecular method for species identification of Malayan gaur (Bos gaurus hubbacki), Kedah-Kelantan (KK) (Bos indicus), and Bali (Bos javanicus) cattle in Malaysia. DNA was extracted from blood samples of 8 Malayan gaurs, 30 KK, and 28 Bali cattle. A set of both specific and universal primers for the Cyt b gene were used in PCR amplification. DNA sequences obtained were then analyzed using BioEdit and Restriction Mapper softwares. The PCR products obtained from Cyt b gene amplification were then subjected to restriction enzyme digestion. The amplification, using both specific and universal primers, produced a 154- and a 603-bp fragment, respectively, in all three species. Two restriction enzymes, NlaIV and SspI, were used to obtain specific restriction profiles that allowed direct identification of Malayan gaur, KK, and Bali cattle. Our findings indicate that all three species can be identified separately using a combination of universal primers and the restriction enzyme SspI.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Polymorphism, Restriction Fragment Length / Cattle Type of study: Diagnostic_studies / Prognostic_studies Limits: Animals Country/Region as subject: Asia Language: En Journal: Genet Mol Res Journal subject: BIOLOGIA MOLECULAR / GENETICA Year: 2014 Document type: Article Affiliation country: Malaysia

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Polymorphism, Restriction Fragment Length / Cattle Type of study: Diagnostic_studies / Prognostic_studies Limits: Animals Country/Region as subject: Asia Language: En Journal: Genet Mol Res Journal subject: BIOLOGIA MOLECULAR / GENETICA Year: 2014 Document type: Article Affiliation country: Malaysia