Evidence for paternal transmission and heteroplasmy in the mitochondrial genome of Silene vulgaris, a gynodioecious plant

• Published in: Heredity 2005-07, Vol.95 (1), p.50-58
• Main Authors: McCauley, D.E, Bailey, M.F, Sherman, N.A, Darnell, M.Z
• Format: Article
• Language: English
• Subjects: adenosinetriphosphatase; atpA gene; Biomedical and Life Sciences; Biomedicine; coxI gene; cytochrome-c oxidase; Cytogenetics; cytoplasmic inheritance; Disorders of Sex Development; DNA, Mitochondrial; Ecology; Evolutionary Biology; genes; genetic recombination; Genome; Genotype; Genotypes; gynodioecy; Haplotypes; heteroplasmy; Human Genetics; Inheritance Patterns; maternal effect; mitochondrial DNA; original-article; paternal effect; Plant Genetics and Genomics; Salmonidae; Silene - genetics; Silene vulgaris
• ISSN: 0018-067X; 1365-2540
• DOI: 10.1038/sj.hdy.6800676

Gynodioecy refers to the co-occurrence of females and hermaphrodites in the same population. In many gynodioecious plants, sex is determined by an epistatic interaction between mitochondrial and nuclear genes, resulting in intragenomic evolutionary conflict, should the mitochondrial genome be maternally inherited. While maternal inheritance of the mitochondrial genome is common in angiosperms, few gynodioecious species have been studied. Here, the inheritance of the mitochondrial genes atpA and coxI was studied in 318 Silene vulgaris individuals distributed among 23 crosses. While maternal inheritance was indicated in 96% of the individuals studied, one or more individuals from each of four sib groups displayed a genotype that was identical to the father, or that did not match either parent. Given evidence that inheritance is not strictly maternal, it was hypothesized that some individuals could carry a mixture of maternally and paternally derived copies of the mitochondrial genome, a condition known as heteroplasmy. Since heteroplasmy might be difficult to detect should multiple versions of the mitochondrial genome co-occur in highly unequal copy number, a method was devised to amplify low-copy number forms of atpA differentially. Evidence for heteroplasmy was found in 23 of the 99 individuals studied, including cases in which the otherwise cryptic form of atpA matched the paternal genotype. The distribution of shared nucleotide sequence polymorphism among atpA haplotypes and the results of a population survey of the joint distribution of atpA and coxI haplotypes across individuals supports the hypothesis that heteroplasmy facilitates formation of novel mitochondrial genotypes by recombination.