Skip to main content
Genetics logoLink to Genetics
. 1999 May;152(1):441–450. doi: 10.1093/genetics/152.1.441

Impacts of seed and pollen flow on population genetic structure for plant genomes with three contrasting modes of inheritance.

X S Hu 1, R A Ennos 1
PMCID: PMC1460592  PMID: 10224273

Abstract

The classical island and one-dimensional stepping-stone models of population genetic structure developed for animal populations are extended to hermaphrodite plant populations to study the behavior of biparentally inherited nuclear genes and organelle genes with paternal and maternal inheritance. By substituting appropriate values for effective population sizes and migration rates of the genes concerned into the classical models, expressions for genetic differentiation and correlation in gene frequency between populations can be derived. For both models, differentiation for maternally inherited genes at migration-drift equilibrium is greater than that for paternally inherited genes, which in turn is greater than that for biparentally inherited nuclear genes. In the stepping-stone model, the change of genetic correlation with distance is influenced by the mode of inheritance of the gene and the relative values of long- and short-distance migration by seed and pollen. In situations where it is possible to measure simultaneously Fst for genes with all three types of inheritance, estimates of the relative rates of pollen to seed flow can be made for both the short- and long-distance components of migration in the stepping-stone model.

Full Text

The Full Text of this article is available as a PDF (177.0 KB).

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. 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]
  2. Doligez A., Baril C., Joly H. I. Fine-scale spatial genetic structure with nonuniform distribution of individuals. Genetics. 1998 Feb;148(2):905–919. doi: 10.1093/genetics/148.2.905. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Dong J., Wagner D. B. Paternally inherited chloroplast polymorphism in Pinus: estimation of diversity and population subdivision, and tests of disequilibrium with a maternally inherited mitochondrial polymorphism. Genetics. 1994 Mar;136(3):1187–1194. doi: 10.1093/genetics/136.3.1187. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Epperson B. K., Li T. Measurement of genetic structure within populations using Moran's spatial autocorrelation statistics. Proc Natl Acad Sci U S A. 1996 Sep 17;93(19):10528–10532. doi: 10.1073/pnas.93.19.10528. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Latta R. G., Mitton J. B. A comparison of population differentiation across four classes of gene marker in limber pine (Pinus flexilis James). Genetics. 1997 Jul;146(3):1153–1163. doi: 10.1093/genetics/146.3.1153. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Nagylaki T. The island model with stochastic migration. Genetics. 1979 Jan;91(1):163–176. doi: 10.1093/genetics/91.1.163. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Powell W., Morgante M., McDevitt R., Vendramin G. G., Rafalski J. A. Polymorphic simple sequence repeat regions in chloroplast genomes: applications to the population genetics of pines. Proc Natl Acad Sci U S A. 1995 Aug 15;92(17):7759–7763. doi: 10.1073/pnas.92.17.7759. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Takahata N., Palumbi S. R. Extranuclear differentiation and gene flow in the finite island model. Genetics. 1985 Feb;109(2):441–457. doi: 10.1093/genetics/109.2.441. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Weiss M. O. [Israel nursing as I saw it]. Ahot Beyisrael. 1965 Sep;11(55):28–29. [PubMed] [Google Scholar]
  10. Wright S. Isolation by Distance. Genetics. 1943 Mar;28(2):114–138. doi: 10.1093/genetics/28.2.114. [DOI] [PMC free article] [PubMed] [Google Scholar]

Articles from Genetics are provided here courtesy of Oxford University Press

RESOURCES