BASE SUBSTITUTION PATTERNS IN PARTIAL OF THE CYTOCHROME C OXIDASE UNIT I (COI) mtDNA GENES IN THE RED JUNGLEFOWL (Gallus sp.) of NORTH SULAWESI AND SOME Gallus sp. ACCESSIONS

Authors

  • Decky Kamagi Universitas Negeri Manado

DOI:

https://doi.org/10.53682/ibj.v4i1.6610

Keywords:

COI gene, Red jungle fowl, North Sulawesi

Abstract

Partial of the cytochrome C oxidase unit I (COI) mtDNA genes of the red jungle fowl (Gallus sp.) were isolated and sequenced to examine the base substitution pattern compared to several accessions taken from GenBank. Samples were collected from several areas in North Sulawesi in the form of muscle tissue and prepared with 95% alcohol, and stored at temperatures below 500 C. Total DNA was isolated using the innuPREP DNA micro kit with a modified protocol. The target gene amplification used the primers BirdR1 and BirdF1, and the amplicons were sequenced at the Singapore FirstBase laboratory. Target gene sequences have been blasted through the nucleotide blast program provided by the National Center for Biotechnology Information (NCBI)—sequence analysis using MEGA5 and DnaSPv5 software. Target gene sequences were aligned using the Clustal-W program on MEGA5. The amplified target gene sequence length was 490 bp. The blast results showed that the target gene sequence was 98% identical to the COI gene sequence from several Gallus-gallus accessions from GenBank. The results of multiple alignments between the sequences of some of the genes examined showed the presence of polymorphic sites (S). The number of polymorphic sites (S) is 11, while the conserved sequence (C) is 386/397 = 0.977. The number of haplotypes (h) is 5, and the diversity of haplotypes (Hd) is 0.703. The overall genetic distance average was 0.008. The polymorphic sites and base substitution events occurred at sites number 145 (A↔G), 241 (G↔C), 268 (C↔A), 295 (C↔A), 348 (T↔C), 381(A) ↔T), 384 (T↔C), 390 (T↔A), 393 (C↔T), 394 (T↔C) and 395 (C↔T). The substitution pattern at these polymorphic sites consists of substitution transitions and transversions. The ratio of transition substitution and transversion events (Ts/Tv) = 1.4056. The substitution events at these sites are located at the bases in the first and third positions of the codon. Substitution events at these polymorphic sites partially cause the exchange of amino acids. The exchange of amino acids occurs at codons 49, 81, 90, 99 and 130.

References

Avise, J. C., R. A., Lansman., & R. O., Shade. (1979). Use endonuclease to Measure Mitochondrial DNA Sequence Relatedness in Natural Population. I. Population Structure and Evolution in Genus Peromyscus. Genetics, 92, 279-295.

Brown, W. M., E.M. Prager, A. Wang, & Wilson, A. C. (1982). Mitochondrial DNA sequences of Primates: Tempo and Mode of Evolution. Journal of Molecular Evolution, 18, 225-239.

Desjardins, P., & R. Morais. (1990). Sequence and gene organization of the chicken mitochondrial genome. Journal of Molecular Biology, 212, 599-634.

Fumihito A, Miyake T, Takada M, Shingu R, Endo T, et al. (1996) Monophyletic origin and unique dispersal patterns of domestic fowls. Proc Natl Acad Sci U S A 93: 6792-6795.

Karanth, K.P., S. Lalji, R. V. Collura., & S.C. Beth. (2008). Molecular phylogeny and biogeography of langurs and leaf monkey of South Asia. Molecular Phylogenetic Evolution, 46, 683-694.

Kornegay,J.R., Kocher,T.D., Williams,L.A., & Wilson,A.C. (1993). Pathways of lysozyme evolution inferred from the sequences of cytochrome b in birds. Journal Molecular Evolution. 37(4), 367-379.

Lim, L. S., K. C. Ang, M.C. Mahani, A.W. Shahrom., & B.M. Md-Zain. (2010). Mitochondrial DNA polymorphism and phylogenetic relationships of proto malays in peninsular Malaysia. Journal of Biology Science, 10, 71-83.

Master, J. C., M. Boniotto, S. Crovella, C. Roos, L. Pozzi., & M. Delpero, (2007). Phylogenetic relationships Among the Lorisoidea As Indicates by Craniodental Morphology and Mitochondrial Sequence data, American Journal of Primatology, 69, 6-15.

Moritz, C., T. E. Dowling., &W. M. Brown. (1987). Evolution of animal mitochondrial DNA. Annual Review of Ecology and Systematics, 18, 269-292.

Nishibori, M., Shimogiri, T., Hayashi, T., & Yasue, H. (2005). Molecular evidence for hybridization of species in the genus Gallus except for Gallus varius. Animal Genetics, 36, 367-375.

Randi, E. (1996). A mitochondrial cytochrome b phylogeny of the Alectoris partridges. Mol. Phylogenet. Evol, 6, 214-227.

Sawai H., Kim H. L., Kuno K., Suzuki S., Gotoh H., Takada M., Takahata N., Satta Y., & Fumihito A. (2010). The Origin and Genetic Variation of Domestic Chickens with Special Reference to Junglefowls Gallus g. gallus and G. varius. PlosOne, 5(5).

Roos, C., T. Nadler, & L. Walter, (2008). Mitochondrial phylogeny, taxonomy and biogeography of silver langur spesies group (Trachypithecus cristatus). Molecular, Phylogenetics Evolution 47, 629-636.

Sorenson, M.D., J.C. Ast, D.E. Dimcheff, T. Yuri & D.P. Mindell. (1999). Primers for a PCR based approach to mitochondrial genome sequencing in birds and other vertebrates. Molecular Phylogenetics and Evolution, 12, 105-114.

West, B., & Zhou, B. (1988) Did chickens go north? New evidence for domestication. Journal of Archaeological Science, 15, 515-533.

Downloads

Published

2023-07-04

How to Cite

Kamagi, D. (2023). BASE SUBSTITUTION PATTERNS IN PARTIAL OF THE CYTOCHROME C OXIDASE UNIT I (COI) mtDNA GENES IN THE RED JUNGLEFOWL (Gallus sp.) of NORTH SULAWESI AND SOME Gallus sp. ACCESSIONS. Indonesian Biodiversity Journal, 4(1), 26–33. https://doi.org/10.53682/ibj.v4i1.6610

Issue

Section

Articles