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LAMPRECHT (1945) reported similar results in interspecific hybrids of Phaseolous species. He obtained sterile plants when Hyp (hypogeal cotyledons) and Ext (exterior stigma) genes of P. multifluorous were transferred to the nuclear genome of P. vulgaris in P. vulgaris cytoplasm. All other genes examined were reciprocally transferred from one species to the other by backcross and selection procedures. He suggested that Hyp and Ext genes were plasma-specific, and produced male sterile P. vulgaris plants in P. vulgaris cytoplasm, Also, Hyp and Ext were unstable in P. vulgaris cytoplasm and frequently mutated to Epi and Int alleles, respectively. These alleles normally occur in P. vulgaris. Similarly, KIHARA (1951) reported that the gene controlling black glume color was preferentially transmitted and frequently mutated to an allele for yellow glume in T. aestivum cytoplasm (and produced mosaics) when transferred from an Ae. caudata chromosome to a T. aestivum chromosome. In these instances species-specific nuclear genes could not be transferred from one diploid species to another, because of incompatable nucleo-cytoplasmic interactions. However, species-specific nuclear genes of the diploid species can be transferred to the nuclear genome of the related polyploid species. The resulting alloplasmic plants with critical nuclear genes from different diploid species can be crossed with one another or with critical diploids to determine the specificity of the nucleo-cytoplasmic interactions. For example, MAAN and LUCKEN (1972) reported that wheat R-lines derived from crosses involving T. boeoticum-Ae. squarrosa amphidiploid did not restore fertility to alloplasmic T. aestivum with Ae. speltoides or T. araraticum cytoplasms, where as wheat R-lines derived from crosses involving Ae. speltoides or T. araraticum did restore fertility to wheat with cytoplasms of these species. These results indicated that Ae. speltoides and T. boeoticum have different cytoplasms and Ae. speltoides and T. araraticum have similar cytoplasms. Therefore, T. aestivum lines with cytoplasm and critical nuclear genes from diploids can be used to study nucleo-cytoplasmic interactions in the genetic background of hexaploid T. aestivum. Also, alloplasmic wheats having cytoplasm of diploid species and with or without the critical nuclear genes may be crossed with other related diploids (which are cross-incompatable at the diploid level) and their interactions may be examined in F1hybrids .


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