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Possibly, nuclear genomes of the polyploid species (i.e. T. aestivum) have substantial inter-genomic variability because of the heterogeneity (or multiplicity) of the homoeoalleles derived from the diploid parental progenitor species. Therefore, polyploid species genomes may be less species-specific in their interactions with certain alien cytoplasms than the genomes of the diploid progenitors. Interactions between polyploid nuclear genomes and the cytoplasms of two or more of the related species may result in apparently similar plant phenotypes, or different genotypes of a polyploid species may produce apparently different phenotypes in their interactions with the same cytoplasm. For example, T. aestivum plants with the cytoplasms of T. boeoticum (MAAN and LUCKEN 1970) or S. cereale (MAAN and LUCKEN, 1971) had male sterility, greatly reduced vigor and reduced seed viability ; the similar phenotype indicated similar interactions between Triticum genomes and T. boeoticum or S. cereale cytoplasms. Also, the difference in the extent of male sterility and delayed maturity of alloplasmic T. aestivum cvs. Chris, Selkirk, and Chinese Spring lines with Ae. ovata cytoplasms indicated that these nuclear genotypes give different interactions with Ae. ovata cytoplasm (MAAN, unpublished). These examples of apparent nonspecificity of nucleo-cytoplasmic interactions between hexaploid T. aestivum genomes and T. boeoticum, S. cereale or Ae. ovata cytoplasms can be explained as follows : The Ae. ovata cytoplasm has similar effects on the expression of various T. aestivum genotypes ; alloplasmic plants have reduced male fertility and delayed maturity. The magnitude of the cytoplasmic effects is modified by the nuclear genes in the three T. aestivum cultivars. Similarly, alloplasmic T. aestivum with the cytoplasms of T. boeoticum or S. cereale can be distinguished by a closer examination of anther size and spore development. Alloplasmic plants with T. boeoticum cytoplasm have smaller anthers with 0% stainable pollen grains and plants with S. cereale cytoplasm have fairly well developed anthers with some stainable pollen grains. Therefore, apparent non-specificity of the interactions between T. aestivum genomes and the cytoplasms of T. boeoticum, S. cereale, Ae. ovata or certain other species does not distract from the other evidence for the specificity of interspecific nucleo-cytoplasmic interactions.

Even though certain interactions between T. aestivum genomes and the alien cytoplasma may appear to be less species-specific, the use of the T. aestivum genome as a tester allows greater flexibility in the choice of cytogenetic techniques that can be used, because aneuploid stocks allow study of chromosomal location of nuclear genes controlling cytoplasmic effects and relatively easy transfer of alien genes to wheat chromosomes. Also, inherent heterogeniety of the parental genomes and the homoeoalleles makes 6x T. aestivum more compatable with alien cytoplasms than 4x T. durum. For example, T. aestivum with cytoplasms of Ae. squarrosa, Ae. cylindrica, Ae. ventricosa, Ae. crassa, Ae. juvenalis or Ae. uniaristata is fertile and of near-normal vigor. T. durum is not viable in the cytoplasms of Ae. squarrosa, Ae. cylindrica, or Ae. ventricosa. Plants of T. durum in Ae. crassa, Ae. juvenalis or Ae. uniaristata cytoplasms have greatly reduced vigor. Interactions with T. durum genomes and the cytoplasms of these 6 Aegilops species indicate cytoplasmic similarity between diploid Ae. squarrosa and tetraploid Ae. cylindrica or Ae. ventricosa, and between diploid Ae. uniaristata and polyploids Ae. crassa or Ae. juvenalis. Obviously, T. durum is more species-specific than T. aestivum in its interactions with alien cytoplasms (MAAN, 1978).


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