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Genetic divergence in wild population of Labeo rohita (Hamilton, 1822) from nine Indian rivers, analyzed through MtDNA cytochrome b region

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Abstract

The present study examined partial cytochrome b gene sequence of mitochondrial DNA for polymorphism and its suitability to determine the genetic differentiation in wild Labeo rohita. The 146 samples of L. rohita were collected from nine distant rivers; Satluj, Brahmaputra, Son, Chambal Mahanadi, Rapti, Chauka, Bhagirathi and Tons were analyzed. Sequencing of 307 bp of Cyto b gene revealed 35 haplotypes with haplotype diversity 0.751 and nucleotide diversity (π) 0.005. The within population variation accounted for 84.21% of total variation and 15.79% was found to among population. The total Fst value, 0.158 (P < 0.05) was found to be significant. The results concluded that the partial cyto b is polymorphic and can be a potential marker to determining genetic stock structure of L. rohita wild population.

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References

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

    Google Scholar 

  2. Reddy PVGK (1999) Genetic resources of Indian major carps. FAO fisheries technical paper. No. 387. FAO, Rome, p 76

    Google Scholar 

  3. Lu G, Li S, Bernatchez L (1997) Mitochondrial DNA diversity, population structure, and conservation genetics of four native carps within Yangtze river, China. Can J Fish Aquat Sci 58:47–58

    Article  Google Scholar 

  4. FAO (2006) Fishstat plus—universal software for fish statistics time series, version 2.3 2000. FAO; Fisheries department, Fisheries information, data and satistical unit. http://www.fao.org/fi/statist/FISOFT/FISHPLUS.asp

  5. Reddy PVGK (2005) Carp genetic resources of India, carp genetic resources for aquaculture in Asia. World Fish Center publishing Inc., Malaysia, pp 39–53

    Google Scholar 

  6. Ferguson A, Taggart JB, Prodohl PA, McMeel O, Thompson C, Stone C, McGinnity P, Hynes RA (1995) The application of molecular markers to the study and conservation of fish populations with special reference to Salmo. J Fish Biol 47:103–126

    Article  CAS  Google Scholar 

  7. Chaturvedi A, Mohindra V, Singh RK, Lal KK, Punia P, Bhaskar R, Mandal A, Narain L, Lakra WS (2011) Population genetic structure and phylogeography of cyprinid fish, Labeo dero (Hamilton, 1822) inferred from allozyme and microsatellite DNA marker analysis. Mol Biol Rep 38(5):3513–3529. doi:10.1007/s11033-010-0462-y

    Article  PubMed  CAS  Google Scholar 

  8. Mandal A, Mohindra V, Singh RK, Punia P, Singh AK, Lal KK (2011) Mitochondrial DNA variation in natural populations of endangered Indian feather-back fish, Chitala chitala. Mol Biol Rep :10.1007/s11033-011-0917-9

  9. He A, Luo Y, Yang H, Liu L, Li S, Wang C (2011) Complete mitochondrial DNA sequences of the Nile tilapia (Oreochromis niloticus) and blue tilapia (Oreochromis aureus): genome characterization and phylogeny applications. Mol Biol Rep 38(3):2815–2821. doi:10.1007/s11033-010-0324-7

    Google Scholar 

  10. 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 15:17–22

    Google Scholar 

  11. 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 

  12. 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 

  13. 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 

  14. Li GY, Wang XZ, Zhao YH, Zhang J, Zhang CG, He SP (2009) Speciation and phylogeography of Opsariichthys bidens (Pisces: Cypriniformes: Cyprinidae) in China: analysis of the cytochrome b gene of mtDNA from diverse populations. Zool Stud 48:569–583

    Google Scholar 

  15. Watanabe K, Kanagawa N, Kakioka R, Itai T, Mori S (2009) Genetic diversity and conservation units in wild and captive populations of endangered freshwater fishes: a case of Hemigrammocypris rasborella in Shizuoka, Japan. Ichthyol Res 56:411–416

    Article  Google Scholar 

  16. 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 

  17. 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  PubMed  CAS  Google Scholar 

  18. 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  PubMed  CAS  Google Scholar 

  19. 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  PubMed  CAS  Google Scholar 

  20. Excoffier LG, Schneider S (2005) Arlequin (version 3.0): an integrated software package for population genetics data analysis. Evol Bioinform Online 1:47–50

    CAS  Google Scholar 

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

    Article  PubMed  CAS  Google Scholar 

  22. Johns GC, Avise JC (1998) A comparative summary of genetic distances in the vertebrates from the mitochondrial cytochrome b gene. Mol Biol Evol 15:1481–1490

    PubMed  CAS  Google Scholar 

  23. Perdices A, Cunha C, Coelho MM (2004) Phylogenetic structure of Zacco platypus (Teleostei, Cyprinidae) populations on the upper and middle Chang Jiang (=Yangtze) drainage inferred from cytochrome b sequences. Mol Phyl Evol 31:192–203

    Article  CAS  Google Scholar 

  24. Grant WS, Bowen BW (1998) Shallow population histories in deep evolutionary lineages of marine fishes: insights from sardines and anchovies and lessons for conservation. J Heredity 89:415–426

    Article  Google Scholar 

  25. Daniel W.McShea (1995) Complexity and Homoplasy. Santa Fe Institute, Santa Fe

  26. Ward RD, Woodwark M, Skinbinski DOF (1994) A comparison of genetic diversity levels in marine, freshwater and anadromous fishes. J Fish Biol 44:213–232

    Article  Google Scholar 

  27. Habib M, Lakra WS, Mohindra V, Khare P, Barman AS, Singh A, Lal KK, Punia P, Khan AA (2010) Evaluation of cytochrome b mtDNA sequences in genetic diversity studies of Channa marulius (Channidae:Perciformes). Mol Biol Rep 38(2):841–846. doi:10.1007/s11033-010-0175-2

    Article  PubMed  Google Scholar 

  28. Chauhan T, Lal KK, Mohindra V, Singh RK, Punia P, Gopalakrishnan A, Sharma PC, Lakra WS (2007) Evaluating genetic differentiation in wild populations of the Indian major carp, Cirrhinus mrigala (Hamilton–Buchanan, 1882): evidence from allozyme and microsatellite markers. Aquaculture 269:135–149

    Article  CAS  Google Scholar 

Download references

Acknowledgments

The authors are thankful to Dr. S. Ayyappan, Secretary DARE and Director General, ICAR, New Delhi for his encouragement and guidance. The work presented here is part of the ongoing programme entitled. “Outreach Activity on Fish Genetic Stocks” with financial support from Indian Council of Agricultural research, New Delhi. Excellent technical co-operation from Sh. Rajesh Kumar and Sh. R. S. Sah is duly acknowledged.

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Correspondence to Kuldeep K. Lal.

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Luhariya, R.K., Lal, K.K., Singh, R.K. et al. Genetic divergence in wild population of Labeo rohita (Hamilton, 1822) from nine Indian rivers, analyzed through MtDNA cytochrome b region. Mol Biol Rep 39, 3659–3665 (2012). https://doi.org/10.1007/s11033-011-1140-4

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