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首页> 外文期刊>Breeding science >Modes of inheritance of two apomixis components, diplospory and parthenogenesis, in Chinese chive (Allium ramosum) revealed by analysis of the segregating population generated by back-crossing between amphimictic and apomictic diploids
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Modes of inheritance of two apomixis components, diplospory and parthenogenesis, in Chinese chive (Allium ramosum) revealed by analysis of the segregating population generated by back-crossing between amphimictic and apomictic diploids

机译:通过分析两栖和无融合二倍体之间回交产生的隔离种群,揭示了韭菜(韭葱)中两个无融合生殖成分的遗传模式,即双孢子虫和孤雌生殖。

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摘要

To investigate the mode of inheritance of apomixis in Chinese chive, the degrees of diplospory and parthenogenesis were evaluated in F1 and BC1 progenies derived from crosses between amphimictic and apomictic diploids (2n = 16, 2x). The F1 population was generated by crossing three amphimictic diploids 94Mo13, 94Mo49 and 94Mo50 with an apomictic diploid KaD2 and comprised 110 diploids and 773 triploids. All the diploid F1 plants examined were completely or highly eusporous and completely syngamic. All the triploid F1 plants examined were highly diplosporous and highly parthenogenetic. KaD2 could not transmit its high level of apomixis via monoploid pollen grains. The BC1 population, generated by crossing 94Mo49 with apomictic triploids found in the F1 offspring, exhibited heteroploidy; it comprised haploid, diploid, triploid, tetraploid and various aneuploid individuals. In this generation, clear segregation was observed between diplospory and parthenogenesis. Analysis of the BC1 population suggests that diplospory and parthenogenesis are each controlled by single dominant genes, D and P , respectively. However, all the BC1 plants characterized as parthenogenetic were diplosporous. The absence of phenotypically eusporous parthenogenetic plants can be explained by assuming that the presence of diplospory gene is a prerequisite for the parthenogenesis gene expression in Chinese chive.
机译:为了研究韭菜无融合生殖的遗传模式,在两亲和无融合二倍体之间杂交的F 1 和BC 1 后代中评估了二倍体孢子的形成和孤雌生殖的程度( 2n = 16,2x)。 F 1 群体是通过将两个两性的二倍体94Mo13、94Mo49和94Mo50与无融合性二倍体KaD2杂交而产生的,其中包括110个二倍体和773个三倍体。所检查的所有二倍体F 1 植物均完全或高度疏松并且完全同系。所检查的所有三倍体F 1 植物均为高度二孔性和高度孤雌生殖。 KaD2不能通过单倍体花粉粒传播高水平的无融合生殖。 94Mo49与在F 1 后代中发现的无融合生殖三倍体杂交产生的BC 1 群体表现出异源性。它包括单倍体,二倍体,三倍体,四倍体和各种非整倍体个体。在这一代中,观察到双孢子虫和孤雌生殖之间明显的隔离。对BC 1 种群的分析表明,双孢菌和孤雌生殖分别受单个显性基因D和P控制。然而,所有表现为孤雌生殖的BC 1 植物都是双孔的。假定双孢菌基因的存在是中国韭菜单性生殖基因表达的前提,可以解释为缺乏表型性的单性生殖植物。

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