Abstract
The Argentine stem weevil is a serious pest of pasture and other graminaceous crops in New Zealand. Fifteen populations from South America, New Zealand and Australia were examined in an effort to determine the geographical origin of the species in New Zealand. Our previously reported RAPD analysis of these populations (Williams et al., 1994) revealed that the source of the pest was the Rio de la Plata on the east coast of South America. As a second approach to examining genetic variation, RFLP analysis of the mitochondrial genome, using the digoxigenin-labelled boll weevil mitochondrial genome as a probe, was also performed. The mitochondrial analysis revealed that the species possesses an unusually large mitochondrial genome of 32 kb, which exhibits extremely low levels of polymorphism both in the introduced and native populations. This low variation is in contrast with the informative level of inter- and intrapopulation variation revealed by RAPD.
Similar content being viewed by others
Article PDF
References
Aagaard, J E, Vollmer, S S, Sorenson, F C, and Strauss, S H. 1995. Mitochondrial DNA products among RAPD profiles are frequent and strongly differentiated between races of Douglas-fir. Mol Ecol, 4, 441–447.
Avise, J C, Arnold, J, Ball, R M, Bermingham, E, Lamb, T, Neigel, J E. et al. 1987. Intraspecific phylogeography: the mitochondrial DNA bridge between population genetics and systematics. Ann Rev Ecol Syst, 18, 489–522.
Baba-Aïssa, F, Solignac, M, Dennebouy, N, and David, J R. 1988. Mitochondrial DNA variability in Drosophila simulans: quasi absence of polymorphism within each of three cytoplasmic races. Heredity, 61, 419–426.
Boehringer-Mannheim. 1993. The DIG System User's Guide for Filter Hybridization. Boehringer Mannheim GmbH Biochemica, Mannheim.
Boyce, T M, Zwick, M E, and Aquadro, C F. 1989. Mitochondrial DNA in the bark weevils: size, structure and heteroplasmy. Genetics, 123, 825–836.
Brown, J R, Beckenbach, A T, and Smith, M J. 1992. Mitochondrial DNA length variation and heteroplasmy in populations of white sturgeon (Acipenser transmontanus). Genetics, 132, 221–228.
Chapco, W, Kelln, R A, and Mcfadyen, D A. 1992. Intraspecific mitochondrial DNA variation in the migratory grasshopper, Melanoplus sanguinipes. Heredity, 69, 547–557.
Clary, D O, and Wolstenholme, D R. 1985. The mitochondrial DNA molecule of Drosophila yakuba: Nucleotide sequence, gene organization, and genetic code. J Mol Evol, 22, 252–271.
Goldson, S L, and Emberson, R M. 1980. Relict diapause in an introduced weevil in New Zealand. Nature, 286, 489–490.
Grant, W S, and Leslie, R W. 1993. Effect of meta-population structure on nuclear and organellar DNA variability in semi-arid environments of southern Africa. S Af J Sci, 89, 287–293.
Gyllensten, U, Wharton, D, Josefsson, A, and Wilson, A C. 1991. Paternal inheritance of mitochondrial DNA in mice. Nature, 352, 255–257.
Hoeh, W R, Blakley, K H, and Brown, W M. 1991. Heteroplasmy suggests limited biparental inheritance of Mytilus mitochondrial DNA. Science, 251, 1488–1490.
Kambhampati, S, and Rai, K. 1991. Mitochondrial DNA variation within and among populations of the mosquito Aedes albopictus. Genome, 34, 288–292.
Kondo, R, Satta, Y, Matsuura, E T, Ishiwa, H, Taka-Hata, N, and Chigusa, S I. 1990. Incomplete maternal transmission of mitochondrial DNA in Drosophila. Genetics, 126, 657–663.
Lansman, R A, Avise, J C, Aquardo, 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.
Latorre, A, Hernández, C, MartÃnez, D, Castro, J A, Ramón, M, and Moya, A. 1992. Population structure and mitochondrial DNA gene flow in Old World populations of Drosophila subobscura. Heredity, 68, 15–24.
Lorenz, M, Weihe, A, and Börner, T. 1994. DNA fragments of organellar origin in random amplified polymorphic DNA (RAPD) patterns of sugar beet (Beta vulgaris L.). Theor Appl Genet, 88, 775–779.
Moritz, C, Dowling, T E, and Brown, W M. 1987. Evolution of animal mitochondrial DNA: relevance for population biology and systematics. Ann Rev Ecol Syst, 18, 269–292.
Nigro, L. 1988. Natural populations of Drosophila simulans show great uniformity of the mitochondrial DNA restriction map. Genetica, 77, 133–136.
O'Ryan, C, and Harley, E H. 1993. Comparisons of mitochondrial DNA in black and white rhinoceroses. J Mammal, 74, 343–346.
Prestidge, R A, Barker, G M, and Pottinger, R P. 1991. The economic cost of Argentine stem weevil in pastures in New Zealand. Proc 44th New Zealand Weed and Pest Control Conference, pp. 165–170.
Rand, D M, and Harrison, R G. 1989. Molecular population genetics of mtDNA size variation in crickets. Genetics, 121, 551–569.
Roehrdanz, R L. 1989. Intraspecific genetic variability in mitochondrial DNA of the screwworm fly (Cochliomyia hominivorax). Biochem Genet, 27, 551–569.
Roehrdanz, R L, and Johnson, D A. 1988. Mitochondrial DNA variation among geographical populations of the screwworm fly, Cochliomyia hominivorax. J Med Entomoi, 25, 136–141.
Roehrdanz, R L, and North, D L. 1992. Mitochondrial DNA restriction fragment variation and biosystematics of the boll weevil, Anthonomus grandis. Southwestern Entomologist, 17, 101–108.
Sambrook, J, Fritsch, E F, and Maniatis, T. 1989. Molecular Cloning: A Laboratory Manual, 2nd edn. Cold Spring Harbor Laboratory Press, Cold Spring Harbor, NY.
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.
Schaffer, H E, and Sederoff, R R. 1981. Improved estimation of DNA fragment lengths from agarose gels. Analyt Biochem, 115, 113–122.
Sheppard, W S, Steck, G J, and McPheron, B A. 1992. Geographic populations of the medfly may be differentiated by mitochondrial DNA variation. Experientia, 48, 1010–1013.
Simon, C, McIntosh, C, and Deniega, J. 1993. Standard restriction fragment length analysis of the mitochondrial genome is not sensitive enough for phylogenetic analysis or identification of 17-year periodical cicada broods: the potential for a new technique. Ann Entomoi Soc Am, 86, 228–238.
Simon, C, Frati, F, Beckenbach, A, Crespi, B, Liu, H, and Flook, P. 1994. Evolution, weighting, and phylogenetic utility of mitochondrial gene sequences and a compilation of conserved polymerase chain reaction primers. Ann Entomoi Soc Am, 87, 651–701.
Skibinski, D O F, Gallagher, C, and Beynon, C M. 1994. Sex-limited mitochondrial DNA transmission in the marine mussel Mytilus edulis. Genetics, 138, 801–809.
Torrini, A, Schurr, T G, Yang, C-C, Szathmary, E J E, Williams, R C, Schanfield, M S. et al. 1992. Native American mitochondrial DNA analysis indicates that the Amerind and the Nadene populations were founded by two independent migrations. Genetics, 130, 153–162.
Waldman, J R, and Wirgin, I I. 1994. Origin of the present Delaware River striped bass population as shown by analysis of mitochondrial DNA. Trans Am Fish Soc, 123, 15–21.
Wayne, R K, George, S B, Gilbert, D, Collins, P W, Kovach, S D, Girman, D, and Lehman, N. 1991. A morphologic and genetic study of the island fox, Urcoyon littoralis. Evolution, 45, 1849–1868.
Welsh, J, and McClelland, M. 1990. Fingerprinting genomes using PCR with arbitrary primers. Nucl Acids Res, 18, 7213–7218.
Williams, C L, Goldson, S L, Baird, D B, and Bullock, D W. 1994. Geographical origin of an introduced insect pest, Listronotus bonariensis (Kuschel), determined by RAPD analysis. Heredity, 72, 412–419.
Williams, J G K, Kubelik, A R, Livak, K J, Rafalski, J A, and Tingey, S V. 1990. DNA polymorphisms amplified by arbitrary primers are useful as genetic markers. Nucl Acids Res, 18, 6531–6535.
Wilson, A C, Cann, R L, Carr, S M, George, M, Gyllensten, U B, Helm-Bychowski, K M. et al. 1985. Mitochondrial DNA and two perspectives on evolutionary genetics. Biol J Linn Soc, 26, 375–400.
Author information
Authors and Affiliations
Rights and permissions
About this article
Cite this article
Williams, C., Goldson, S. & Bullock, D. Unusual mitochondrial genome in introduced and native populations of Listronotus bonariensis (Kuschel). Heredity 77, 565–571 (1996). https://doi.org/10.1038/hdy.1996.183
Received:
Issue date:
DOI: https://doi.org/10.1038/hdy.1996.183


