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Heredity
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Evolutionary divergence between sympatric species of southern African Hakes, Merluccius capensis and M. paradoxus. II. restriction enzyme analysis of mitochondrial DNA
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  • Original Article
  • Published: 01 August 1988

Evolutionary divergence between sympatric species of southern African Hakes, Merluccius capensis and M. paradoxus. II. restriction enzyme analysis of mitochondrial DNA

  • Inga I Becker1,
  • W Stewart Grant1 nAff2,
  • Ralph Kirby1 &
  • …
  • Frank T Robb1 

Heredity volume 61, pages 21–30 (1988)Cite this article

  • 744 Accesses

  • 26 Citations

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Abstract

We used 11 restriction endonucleases to measure nucleotide sequence variation in mitochondrial DNA (mtDNA) within and between two species of hake from the coastal waters of South Africa. A total of 14 different composite genotypes were observed among 26 individuals of Merluccius capensis, but only 6 composite genotypes were observed for 24 individuals of M. paradoxus. A parsimony network connecting the composite genotypes for these species did not correspond with the geographies of either set of samples. In M. capensis, the restriction patterns of three enzymes (Ava I, Xba I, Xho I) and the network of composite genotypes indicate that an addition of about 400 nucleotides in length and a deletion of 200 nucleotides have occurred in pathways leading from the most common genotype. The amount of nucleotide site polymorphism for M. capensis was 0·022 and was significantly greater than the level of polymorphism in M. paradoxus, which was 0·009. These results suggest that M. paradoxus may have experienced a population bottleneck in the past. The amount of sequence divergence between these species was 11·6 per cent (±0·036) and is typical for well differentiated species. Using the assumptions of the molecular clock, this represents a divergence time of 5·8 (±1·8) million years.

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References

  • Aquadro, C F, and Greenberg, B D. 1983. Human mitochondrial DNA variation and evolution: analysis of nucleotide sequences from seven individuals. Genetics, 103, 287–312.

    CAS  PubMed  PubMed Central  Google Scholar 

  • Avise, J C, and Saunders, N C. 1984. Hybridization and introgression among species of sunfish (Lepomis): analysis by mitochondrial DNA and allozyme markers. Genetics, 108, 237–255.

    CAS  PubMed  PubMed Central  Google Scholar 

  • Avise, J C, Lansman, R A, and Shade, R O. 1979. The use of restriction endonucleases to measure mitochondrial DNA sequence relatedness in natural populations. I. Population structure and evolution in the genus Permyscus. Genetics, 92, 279–295.

    CAS  PubMed  PubMed Central  Google Scholar 

  • Avise, J C, Shapira, J F, Daniel, S W, Aquadro, C F, and Lansman, R A. 1983. Mitochondrial DNA differentiation during the speciation process in Peromyscus. Mol Biol Evol. 1, 38–56.

    CAS  PubMed  Google Scholar 

  • Avise, J C, Helfman, G S, Saunders, N C, and Hales, L S. 1986. Mitochondrial DNA differentiation in North Atlantic eels: population genetic consequences of an unusual life history pattern. Proc Natl Acad Sci USA, 83, 4350–4354.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Bermingham, E, and Avise, J C. 1986. Molecular zoogeography of freshwater fishes in the southeastern United States. Genetics, 113, 939–965.

    CAS  PubMed  PubMed Central  Google Scholar 

  • Bermingham, E, Lamb, T, and Avise, J C. 1986. Size polymorphism and heteroplasmy in the mitochondrial DNA of lower vertebrates. J Heredity, 77, 249–252.

    Article  CAS  Google Scholar 

  • Brown, G G, and Simpson, M V. 1981. Intra- and interspecific variation of the mitochondrial genome in Rattus norvegicus and Rattus rattus: restriction enzyme analysis of variant mitochondrial DNA molecules and their evolutionary relationships. Genetics, 97, 125–143.

    CAS  PubMed  PubMed Central  Google Scholar 

  • Brown, W M. 1983. Evolution of animal mitochondrial DNA. Chapter 4. In Nei, M. and Koehn, R. K. (eds.) Evolution of Genes and Proteins. Sinauer Assoc., Sunderland, Mass USA, pp. 62–88.

    Google Scholar 

  • Brown, W M, George, M, Jr, and Wilson, A C. 1979. Rapid evolution of animal mitochondrial DNA. Proc Natl Acad Sci USA, 76, 1967–1971.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Cann, R L, and Wilson, A C. 1983. Length mutations in human mitochondrial DNA. Genetics, 104, 699–711.

    CAS  PubMed  PubMed Central  Google Scholar 

  • Cann, R L, Stoneking, M, and Wilson, A C. 1987. Mitochondrial DNA and human evolution. Nature 325, 31–36.

    Article  CAS  PubMed  Google Scholar 

  • Chapman, R W, and Powers, D A. 1984. A method for the rapid isolation of mitochondrial DNA from fishes. Tech. Rep. Maryland Sea Grant Prog. No. UM-SG-TS-84-05, 11p.

  • Densmore, L D, Wright, J W, and Brown, W M. 1985. Length variation and heteroplasmy are frequent in mitochondrial DNA from parthenogenetic and bisexual lizards (genus Chemidorphorus). Genetics, 110, 689–707.

    CAS  PubMed  PubMed Central  Google Scholar 

  • Engels, W R. 1981. Estimating genetic divergence and genetic variability with restriction endonucleases. Proc Natl Acad Sci USA, 78, 6329–6333.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Fauron, C M-R, and Wolsten-Holme, D R. 1976. Structural heterogeneity of mitochondrial DNA molecules within the genus Drosophila. Proc Natl Acad Sci USA, 73, 3623–3627.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Ferris, S D, Brown, W M, Davidson, W S, and Wilson, A C. 1981. Extensive polymorphism in the mitochondrial DNA of apes. Proc Natl Acad Sci USA. 78, 6319–6323.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Ferris, S D, Sage, R D, Prager, E M, Ritte, V, and Wilson, A C. 1983. Mitochondrial DNA evolution in mice. Genetics, 105, 681–721.

    CAS  PubMed  PubMed Central  Google Scholar 

  • Giles, R E, Blanc, H, Cann, H M, and Wallace, D C. 1980. Maternal inheritance of human mitochondrial DNA. Proc Acad Sci USA, 77, 6715–6719.

    Article  CAS  Google Scholar 

  • Grant, W S, Leslie, R W, and Becker, I I. 1988a. Genetic stock structure of the southern African hakes. Merluccius capensis and M. paradoxus. Mar Ecol Prog Sci, (In press).

  • Grant, W S, Becker, I I, and Leslie, R W. 1988b. Evolutionary divergence between sympatric species of southern African hakes, Merluccius capensis and M. paradoxus. I. Electrophoretic analysis of proteins. Heredity, 61, 13–20.

    Article  CAS  Google Scholar 

  • Graves, J E, Ferris, S D, and Dizon, A E. 1984. Close genetic similarity of Atlantic and Pacific skipjack tuna (Katsuwonus pelamis) demonstrated with restriction endonuclease analysis of mitochondrial DNA. Mar Biol, 79, 315–319.

    Article  CAS  Google Scholar 

  • Gyllensten, U, and Wilsonn, A C. 1987. Mitochondrial DNA of salmonids: inter- and intraspecific variability detected with restriction enzymes. In Ryman, N., and Utter, F. M. (eds.) Population Genetics and Fishery Management, Washington Sea Grant Prog., Univ. Washington Press, Seattle, Washington, pp. 301–317.

    Google Scholar 

  • Hudson, R R. 1982. Estimating genetic variability with restriction endonucleases. Genetics, 100, 711–719.

    CAS  PubMed  PubMed Central  Google Scholar 

  • Kornfield, I, and Bogdanowicz, S M. 1987. Differentiation of mitochondrial DNA in Atlantic herring. Fish Bull USA, (in press).

  • Lansman, R A, Shade, R O, Shapira, J F, and Avise, J C. 1981. The use of restriction endonucleases to measure mtDNA sequence relatedness in natural populations. III. Techniques and potential applications. J Mol Evol 17, 214–226.

    Article  CAS  PubMed  Google Scholar 

  • Lansman, R A, Avise, J C, Aquadro, C F, Shapira, J F, and Daniel, S W. 1983. Extensive genetic variation in mitochondrial DNAs among geographic populations of the deer mouse. Peromyscus maniculatus Evolution, 37, 1–16.

    CAS  Google Scholar 

  • Lamb, T, and Avise, J C. 1986. Directional introgression of mitochondrial DNA in a hybrid population of tree frogs: the influence of mating behavior. Proc Natl Acad Sci USA, 83, 2526–2530.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Mack, A L, Gill, F B, Colburn, R, and Spolsky, C. 1986. Mitochondrial DNA: a source of genetic markers for studies of similar passerine bird species. Auk, 203, 676–681.

    Google Scholar 

  • Maniatis, T, Fritsch, E F, and Sambrook, J. 1982. Molecular Cloning. Cold Spring Harbor Lab., New York.

    Google Scholar 

  • Nei, M, and Li, W H. 1979. Mathematical model for studying genetic variation in terms of restriction endonucleases. Proc Natl Acad Sci USA, 76, 5269–5273.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Saunders, N C, Kessler, L G, and Avise, J C. 1986. Genetic variation and geographic differentiation in mitochondrial DNA of the horseshoe crab, Limulus polyphemus. Genetics, 112, 613–627.

    CAS  PubMed  PubMed Central  Google Scholar 

  • Skibinski, D O F. 1985. Mitochondrial DNA variation in Mytilus edulis L. and the Padstow mussel. J Mar Biol Ecol, 92, 251–258.

    Article  Google Scholar 

  • Solignac, M, Monnerot, M, and Mounolou, J-C. 1986. Mitochondrial DNA evolution in the melanogaster species subgroup of Drosophila. J Mol Evol, 23, 31–40.

    Article  CAS  PubMed  Google Scholar 

  • Spolsky, C, and Uzzell, T. 1984. Natural interspecies transfer of mitochondrial DNA in amphibians. Proc Natl Acad Sci USA, 81, 5802–5805.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Upholt, W B. 1977. Estimation of DNA sequence divergence from comparison of restriction endonuclease digests. Nucl Acid Res, 4, 1257–1267.

    Article  CAS  Google Scholar 

  • Upholt, W B, and Dawid, I B. 1977. Mapping of mitochondrial DNA of individual sheep and goats: rapid evolution in the D-loop region. Cell, 11, 571–583.

    Article  CAS  PubMed  Google Scholar 

  • Wilson, A C, Cann, R L, Carr, S M, George, M, Gyllensten, U B, Helm-Bychowski, K M, Higuchi, R G, Palumbi, S R, Prager, E M, Sage, R D, and Stonek-Ing, M. 1985. Mitochondrial DNA and two perspectives on evolutionary genetics. Biol J Linn Soc, 26, 375–400.

    Article  Google Scholar 

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Author information

Author notes
  1. W Stewart Grant

    Present address: Department of Genetics, University of the Witwatersrand, Johannesburg, 2050, South Africa

Authors and Affiliations

  1. Department of Microbiology, University of Cape Town, Rondebosch, 7700, South Africa

    Inga I Becker, W Stewart Grant, Ralph Kirby & Frank T Robb

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  1. Inga I Becker
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Becker, I., Grant, W., Kirby, R. et al. Evolutionary divergence between sympatric species of southern African Hakes, Merluccius capensis and M. paradoxus. II. restriction enzyme analysis of mitochondrial DNA. Heredity 61, 21–30 (1988). https://doi.org/10.1038/hdy.1988.87

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  • Received: 17 September 1987

  • Issue date: 01 August 1988

  • DOI: https://doi.org/10.1038/hdy.1988.87

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