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. 1994 Mar;136(3):1187–1194. doi: 10.1093/genetics/136.3.1187

Paternally Inherited Chloroplast Polymorphism in Pinus: Estimation of Diversity and Population Subdivision, and Tests of Disequilibrium with a Maternally Inherited Mitochondrial Polymorphism

J Dong 1, D B Wagner 1
PMCID: PMC1205873  PMID: 8005423

Abstract

We have surveyed a chloroplast DNA restriction fragment length polymorphism in 745 individuals, distributed rangewide in eight allopatric natural populations of jack pine (Pinus banksiana Lamb.) and eight allopatric natural populations of lodgepole pine (Pinus contorta Dougl.). The polymorphic region of the chloroplast genome is located near duplicated psbA genes. Fourteen length variants were found in the survey, and these variants distinguished the two species qualitatively. Variant diversities were high in both species (h(es) = 0.43 in jack pine; h(es) = 0.44 in lodgepole pine). Population subdivision was weak within and among lodgepole pine subspecies and in jack pine (i.e., θvalues were less than 0.05). This weak subdivision is compatible with theoretical predictions for paternally inherited markers in wind-pollinated outcrossers, as well as for polymorphisms with high length mutation rates. If these populations are at a drift-migration equilibrium, the chloroplast DNA restriction fragment data and previous mitochondrial frequency data from the same individuals are consistent with gene flow that is differential through seeds and pollen. The new data have permitted the first empirical tests of disequilibrium between maternally and paternally inherited factors. As expected, these tests failed to detect convincing evidence of non-random association between chloroplast and mitochondrial variants.

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Selected References

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  1. Aldrich J., Cherney B. W., Merlin E., Christopherson L. The role of insertions/deletions in the evolution of the intergenic region between psbA and trnH in the chloroplast genome. Curr Genet. 1988 Aug;14(2):137–146. doi: 10.1007/BF00569337. [DOI] [PubMed] [Google Scholar]
  2. Asmussen M. A., Arnold J., Avise J. C. Definition and properties of disequilibrium statistics for associations between nuclear and cytoplasmic genotypes. Genetics. 1987 Apr;115(4):755–768. doi: 10.1093/genetics/115.4.755. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Birky C. W., Jr, Fuerst P., Maruyama T. Organelle gene diversity under migration, mutation, and drift: equilibrium expectations, approach to equilibrium, effects of heteroplasmic cells, and comparison to nuclear genes. Genetics. 1989 Mar;121(3):613–627. doi: 10.1093/genetics/121.3.613. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Blasko K., Kaplan S. A., Higgins K. G., Wolfson R., Sears B. B. Variation in copy number of a 24-base pair tandem repeat in the chloroplast DNA of Oenothera hookeri strain Johansen. Curr Genet. 1988 Sep;14(3):287–292. doi: 10.1007/BF00376749. [DOI] [PubMed] [Google Scholar]
  5. Brown A. H. Sample sizes required to detect linkage disequilibrium between two or three loci. Theor Popul Biol. 1975 Oct;8(2):184–201. doi: 10.1016/0040-5809(75)90031-3. [DOI] [PubMed] [Google Scholar]
  6. Hong Y. P., Hipkins V. D., Strauss S. H. Chloroplast DNA diversity among trees, populations and species in the California closed-cone pines (Pinus radiata, Pinus muricata and Pinus attenuata). Genetics. 1993 Dec;135(4):1187–1196. doi: 10.1093/genetics/135.4.1187. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Lidholm J., Gustafsson P. The chloroplast genome of the gymnosperm Pinus contorta: a physical map and a complete collection of overlapping clones. Curr Genet. 1991 Jul;20(1-2):161–166. doi: 10.1007/BF00312780. [DOI] [PubMed] [Google Scholar]
  8. Lidholm J., Szmidt A., Gustafsson P. Duplication of the psbA gene in the chloroplast genome of two Pinus species. Mol Gen Genet. 1991 May;226(3):345–352. doi: 10.1007/BF00260645. [DOI] [PubMed] [Google Scholar]
  9. Maroof M. A., Zhang Q., Neale D. B., Allard R. W. Associations between nuclear loci and chloroplast DNA genotypes in wild barley. Genetics. 1992 May;131(1):225–231. doi: 10.1093/genetics/131.1.225. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Nei M. Estimation of average heterozygosity and genetic distance from a small number of individuals. Genetics. 1978 Jul;89(3):583–590. doi: 10.1093/genetics/89.3.583. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Ogihara Y., Terachi T., Sasakuma T. Intramolecular recombination of chloroplast genome mediated by short direct-repeat sequences in wheat species. Proc Natl Acad Sci U S A. 1988 Nov;85(22):8573–8577. doi: 10.1073/pnas.85.22.8573. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Palmer J. D., Nugent J. M., Herbon L. A. Unusual structure of geranium chloroplast DNA: A triple-sized inverted repeat, extensive gene duplications, multiple inversions, and two repeat families. Proc Natl Acad Sci U S A. 1987 Feb;84(3):769–773. doi: 10.1073/pnas.84.3.769. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Schnabel A., Asmussen M. A. Definition and properties of disequilibria within nuclear-mitochondrial-chloroplast and other nuclear-dicytoplasmic systems. Genetics. 1989 Sep;123(1):199–215. doi: 10.1093/genetics/123.1.199. [DOI] [PMC free article] [PubMed] [Google Scholar]

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