Organization and Evolution of Plant Genomes, Unité de Recherche en Génomique Végétale, 91057 Evry Cedex, France.
New Phytol. 2010 Apr;186(1):86-101. doi: 10.1111/j.1469-8137.2010.03186.x. Epub 2010 Feb 10.
To understand key mechanisms leading to stabilized allopolyploid species, we characterized the meiotic behaviour of wheat allohexaploids in relation to structural and genetic changes. For that purpose, we analysed first generations of synthetic allohexaploids obtained through interspecific hybridization, followed by spontaneous chromosome doubling, between several genotypes of Triticum turgidum and Aegilops tauschii wheat species, donors of AB and D genomes, respectively. As expected for these Ph1 (Pairing homoeologous 1) gene-carrying allopolyploids, chromosome pairing at metaphase I of meiosis essentially occurs between homologous chromosomes. However, the different synthetic allohexaploids exhibited progenitor-dependent meiotic irregularities, such as incomplete homologous pairing, resulting in univalent formation and leading to aneuploidy in the subsequent generation. Stability of the synthetic allohexaploids was shown to depend on the considered genotypes of both AB and D genome progenitors, where few combinations compare to the natural wheat allohexaploid in terms of regularity of meiosis and euploidy. Aneuploidy represents the only structural change observed in these synthetic allohexaploids, as no apparent DNA sequence elimination or rearrangement was observed when analysing euploid plants with molecular markers, developed from expressed sequence tags (ESTs) as well as simple sequence repeat (SSR) and transposable element sequences.
为了了解导致稳定异源六倍体物种的关键机制,我们研究了小麦异源六倍体的减数分裂行为与结构和遗传变化的关系。为此,我们分析了通过种间杂交获得的第一代人工合成异源六倍体,然后通过自发染色体加倍,这些人工合成异源六倍体是小麦物种 Triticum turgidum 和 Aegilops tauschii 的 AB 和 D 基因组的供体。正如这些携带 Ph1(配对同源 1 基因)的异源多倍体所预期的那样,减数分裂中期 I 的染色体配对主要发生在同源染色体之间。然而,不同的人工合成异源六倍体表现出与亲本有关的减数分裂不规则性,例如不完全的同源配对,导致单价体的形成,并导致随后的后代出现非整倍体。人工合成异源六倍体的稳定性取决于 AB 和 D 基因组亲本的考虑基因型,其中少数组合在减数分裂和整倍体的规律性方面与天然小麦异源六倍体相似。非整倍体是这些人工合成异源六倍体中观察到的唯一结构变化,因为在用从表达序列标签 (EST) 以及简单重复序列 (SSR) 和转座元件序列开发的分子标记分析整倍体植物时,没有观察到明显的 DNA 序列缺失或重排。