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Evaluation of cytochrome b mtDNA sequences in genetic diversity studies of Channa marulius (Channidae: Perciformes)

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Abstract

Channa marulius (Hamilton, 1822) is a commercially important freshwater fish and a potential candidate species for aquaculture. The present study evaluated partial Cytochrome b gene sequence of mtDNA for determining the genetic variation in wild populations of C. marulius. Genomic DNA extracted from C. marulius samples (n = 23) belonging to 3 distant rivers; Mahanadi, Teesta and Yamuna was analyzed. Sequencing of 307 bp Cytochrome b mtDNA fragment revealed the presence of 5 haplotypes with haplotype diversity value of 0.763 and nucleotide diversity value of 0.0128. Single population specific haplotype was observed in Mahanadi and Yamuna samples and 3 haplotypes in Teesta samples. The analysis of data demonstrated the suitability of partial Cytochrome b sequence in determining the genetic diversity in C. marulius population.

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References

  1. Munro ISR (1955) The marine and freshwater fishes of Ceylon. Dept. Ext. Affairs, Canberra, 348 pp, 56 pls

  2. Bardach JE, Ryther JH, McLarney W (1972) Aquaculture: the farming and husbandry of freshwater and marine organisms. Wiley, New York, 867p

    Google Scholar 

  3. Talwar PK, Jhingran AG (1992) Inland fishes of India. Rec Ind J 3:19–24

    Google Scholar 

  4. CAMP (1998) Report of the workshop conservation assessment and management plan (CAMP) for freshwater fishes of India. Organized by Zoo Outreach Activity and National Bureau of Fish Genetic Resources, Lucknow

  5. Lecomte F, Grant WS, Dodson JJ, Rodriguez-Sanchez R, Bowen BW (2004) Living with uncertainty: genetic imprints of climate shifts in east Pacific anchovy (Engraulis mordax) and sardine (Sardinops sagax). Mol Ecol 13:2169–2182

    Article  CAS  PubMed  Google Scholar 

  6. Fontana F, Conterio F, Gandolfi G, Tagliavini J, Rosenthal H, Bronzi P, McKenzie DJ (2007) Mitochondrial DNA sequences of 6 sturgeon species and phylogenetic relationships within Acipenseridae. J Appl Ichthyol 15(4–5):17–22

    Google Scholar 

  7. Pages M, Desse-Berset N, Tongard C, Brosse L, Hänni C, Berrebi P (2009) Historical presence of the sturgeon Acipenser sturio in the Rhone Basin determined by the analysis of ancient DNA cytochrome b sequences. Conserv Genet 10:217–224

    Article  CAS  Google Scholar 

  8. Murray WB, Wang JY, Yang SC, Stevens JD, Fisk A, Svavarsson J (2008) Mitochondrial cytochrome b variation in sleeper sharks (Squaliformes: Somniosidae). Mar Biol 153:1015–1022

    Article  CAS  Google Scholar 

  9. Oleinik AG, Skurikhina LA, Brykov VA (2007) Divergence of Salvelinus sp from north eastern Asia based on mitochondrial DNA. Ecol Freshw 16:87–98

    Article  Google Scholar 

  10. Bouza C, Vilas R, Castro J (2008) Mitochondrial haplotype variability of brown trout populations from north-western Iberian Peninsula, a secondary contact area between lineages. Conserv Genet 9:917–920

    Article  Google Scholar 

  11. Daemen E, Cross T, Ollevier F, Volckaert FAM (2001) Analysis of genetic structure of European eel (Anguilla anguilla) using microsatellite DNA and mtDNA markers. Mar Biol 139:755–764

    Article  CAS  Google Scholar 

  12. Fayazi J, Moradi M, Rahimi G, Ashtyani R, Galledari H (2006) Genetic differentiation and phylogenetic relationships among Barbus xanthopterus (Cyprinidae) populations in south west of Iran using mitochondrial DNA markers. Pak J Biol Sci 9(12):2249–2254

    Article  Google Scholar 

  13. So N, VanHoudt JKJ, Volckaert FAM (2006) Genetic diversity and population history of the migratory catfishes Pangasianodon hypophthalmus and Pangasius bocourti in the Cambodian Mekong River. Fish Sci 72:469–476

    Article  CAS  Google Scholar 

  14. Hsu KC, Shih NT, Ni HI, Tsao Shao K (2007) Genetic variation in Trichiurus lepturus (Perciformes: Trichiuridae) in water of Taiwan: several species or cohort distribution? Raffles Bull Zool 14:215–220

    Google Scholar 

  15. Brown J, Stapien CA (2008) Ancient divisions, recent expansions: phylogeography and population genetics of the round Gobi Appolonia melanostoma. Mol Ecol 17:2598–2615

    Article  CAS  PubMed  Google Scholar 

  16. Abol-Munafi AB, Ambok MA, Ismail P, MinhTam B (2007) Molecular data from the cytochrome b for the phylogeny of Channidae (Channa sp) in Malaysia. Biotechnology 6(1):22–27

    Article  CAS  Google Scholar 

  17. Li X, Musikasinthorn P, Kumazawa Y (2006) Molecular phylogenetic analysis of snakeheads (Perciformes: Channidae) using mitochondrial DNA sequences. Ichthyol Res 53:148–159

    Article  Google Scholar 

  18. Haniffa MA, Nagarajan M, Gopalakrishnan A, Basheer VS, Muneer A (2006) Genetic variability of Channa punctatus populations using randomly amplified polymorphic DNA. Aquac Res 37:1151–1155

    Article  Google Scholar 

  19. Hanniffa MA, Nagarajan M, Gopalakrishnan A, Musammilu KK (2007) Allozyme variation in threatened freshwater fish spotted Murrel (Channa punctatus) in south Indian river system. Biochem Genet 45(3/4):363–373

    Article  Google Scholar 

  20. Ponniah AG, Sarkar UK (2000) Fish biodiversity of north east India. NBFGR-NATP Publ 2:24–25

    Google Scholar 

  21. Abdul Muneer PM, Gopalakrishnan A, Musammilu KK, Mohindra V, Lal KK, Basheer VS, Lakra WS (2009) Genetic variation and population structure of endemic yellow catfish, Horabagrus brachysoma (Bagridae) among three populations of Western Ghat region using RAPD and microsatellite markers. Mol Biol Rep 36:1779–1791

    Article  CAS  PubMed  Google Scholar 

  22. Ruzzante DE, Taggart CT, Cook D (1996) Spatial and temporal variation in the genetic composition of a larval cod (Gadus morhua) aggregation: cohort contribution and genetic stability. Can J Fish Aquat Sci 53:2695–2705

    Article  Google Scholar 

  23. Kocher TD, Thomas WK, Meyer A, Edwards SV, Pabo S, Villablanca FX, Wilson AC (1989) Dynamics of mitochondrial DNA evolution in animals: amplification and sequencing with conserved primers. Proc Natl Acad Sci USA 86:6196–6200

    Article  CAS  PubMed  Google Scholar 

  24. Thompson JD, Higgins DG, Gibson TJ (1994) CLUSTAL W: improving the sensitivity of progressive multiple sequence alignment through sequence weighting, position-specific gap penalties and weight matrix choice. Nucleic acids research advance access. Nucleic Acids Res 22:4673–4680

    Article  CAS  PubMed  Google Scholar 

  25. Tamura K, Dudley J, Nei M, Kumar S (2007) MEGA 4: molecular evolutionary genetics analysis (MEGA) software version 4.0. Mol Biol Evol 24:1596–1599

    Article  CAS  PubMed  Google Scholar 

  26. Excoffier LG, Schneider LS (2005) Arlequin ver. 3.0: an integrated software package for population genetics data analysis. Evol Bioinformatics Online 1:47–50

    CAS  Google Scholar 

  27. Rozas J, Sánchez-Delbarrio JC, Messeguer X, Rozas R (2003) DnaSP, DNA polymorphism analyses by the coalescent and other methods. Bioinformatics 19:2496–2497

    Article  CAS  PubMed  Google Scholar 

  28. Kocher TD, Conroy JA, McKaye KR, Stauffer JR (1993) Similar morphologies of cichlid fish in Lakes Tanganyika and evolution, edited by M. H. A. Keenleyside. Chapman and Hall, Malawi are due to convergence. Mol Phylogenet Evol 2:158–165

  29. Song CB, Near TJ, Page LM (1998) Phylogenetic relationships among Percid fishes as inferred from mitochondrial cytochrome b DNA sequence data. Mol Phylogenet Evol 10:343–353

    Article  CAS  PubMed  Google Scholar 

  30. Abol-Munafi AB, Ambok MA, Ismail P, MinhTam B (2007) Molecular data from the cytochrome b for the phylogeny of Channidae (Channa sp) in Malaysia. Biotechnology 6(1):22–27

    Article  CAS  Google Scholar 

  31. Apostolidis AP, Triantaphyllidis C, Kouvatsi A, Economidis PS (1997) Mitochondrial DNA sequence variation and phylogeography among Salmo trutta L (Greek brown trout) populations. Mol Ecol 6(6):531–542

    Article  CAS  PubMed  Google Scholar 

  32. Finne KL (2001) Phylogeographic structure of the Atlantic pupfish, Cyprinodon variegatus (Cyprinodontidae), along the eastern coast of North America. Unpublished M.S. Thesis, Virginia Polytechnic Institute and State University, Blacksburg, Virginia

  33. Tinti F, di Nunno C, Guarniero I, Talenti M, Tommasini S, Fabbri E, Piccinetti C (2002) Mitochondrial DNA sequence variation suggests the lack of genetic heterogeneity in the adriatic and ionian stocks of Sardina pilchardus. Mar Biotechnol 4:163–172

    Article  CAS  PubMed  Google Scholar 

  34. Marshall CRE (2005) Evolutionary genetics of barramundi (Lates calcarifer) in the Australian region. Unpublished Ph.D Thesis, School of Biological Sciences and Biotechnology, Murdoch University, Perth, Western Australia

  35. Vrijenhoek RC (1998) Conservation genetics of freshwater fish. J Fish Biol 53(Suppl A):394–412

    Article  Google Scholar 

  36. Chondar SL (1999) Biology of fin fishes and shellfishes. SCSC Publishers, Howrah, India

    Google Scholar 

  37. Avise JC (1994) Molecular markers, natural history, and evolution. Chapman and Hall, New York

    Google Scholar 

  38. Lakra WS, Goswami M, Gopalakrishnan A (2009) Molecular identification and phylogenetic relationships of seven Indian Sciaenids (Pisces: Perciformes, Sciaenidae) based on 16S rRNA and cytochrome c oxidase subunit I mitochondrial genes. Mol Biol Rep 36:831–839

    Article  CAS  PubMed  Google Scholar 

  39. Bowen BW, Meylan AB, Perran R (1992) Global population structure and natural history of Green Turtle (Chelonia mydas) in terms of matriarchal phylogeny. Evolution 46:865–881

    Article  Google Scholar 

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Acknowledgments

The authors thank Sh. A.K. Pathak (Scientist and OIC ARIS Cell, NBFGR) for providing the locality map. Excellent technical cooperation from Sh. Akhilesh Mishra, Sh. Rajesh Kumar and Sh. R.S Sah is duly acknowledged.

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Correspondence to W. S. Lakra.

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Habib, M., Lakra, W.S., Mohindra, V. et al. Evaluation of cytochrome b mtDNA sequences in genetic diversity studies of Channa marulius (Channidae: Perciformes). Mol Biol Rep 38, 841–846 (2011). https://doi.org/10.1007/s11033-010-0175-2

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  • DOI: https://doi.org/10.1007/s11033-010-0175-2

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