Ma X-F, Gustafson J P
Department of Agronomy, University of Missouri-Columbia, MO 65211, USA.
Cytogenet Genome Res. 2005;109(1-3):236-49. doi: 10.1159/000082406.
Allopolyploidy is a prominent mode of speciation in higher plants. Due to the coexistence of closely related genomes, a successful allopolyploid must have the ability to invoke and maintain diploid-like behavior, both cytologically and genetically. Recent studies on natural and synthetic allopolyploids have raised many discrepancies. Most species have displayed non-Mendelian behavior in the allopolyploids, but others have not. Some species have demonstrated rapid genome changes following allopolyploid formation, while others have conserved progenitor genomes. Some have displayed directed, non-random genome changes, whereas others have shown random changes. Some of the genomic changes have appeared in the F1 hybrids, which have been attributed to the union of gametes from different progenitors, while other changes have occurred during or after genome doubling. Although these observations provide significant novel insights into the evolution of allopolyploids, the overall mechanisms of the event are still elusive. It appears that both genetic and epigenetic operations are involved in the diploidization process of allopolyploids. Overall, genetic and epigenetic variations are often associated with the activities of repetitive sequences and transposon elements. Specifically, genomic sequence elimination and chromosome rearrangement are probably the major forces guiding cytological diploidization. Gene non-functionalization, sub-functionalization, neo-functionalization, as well as other kinds of epigenetic modifications, are likely the leading factors promoting genetic diploidization.
异源多倍体是高等植物中一种重要的物种形成模式。由于密切相关的基因组共存,一个成功的异源多倍体必须具备在细胞学和遗传学上引发并维持类似二倍体行为的能力。最近对天然和人工合成异源多倍体的研究引发了许多差异。大多数物种在异源多倍体中表现出非孟德尔行为,但其他物种则没有。一些物种在异源多倍体形成后显示出快速的基因组变化,而其他物种则保留了祖先基因组。一些表现出定向的、非随机的基因组变化,而其他的则显示出随机变化。一些基因组变化出现在F1杂种中,这归因于来自不同祖先的配子结合,而其他变化则发生在基因组加倍期间或之后。尽管这些观察为异源多倍体的进化提供了重要的新见解,但该事件的总体机制仍然难以捉摸。似乎遗传和表观遗传操作都参与了异源多倍体的二倍体化过程。总体而言,遗传和表观遗传变异通常与重复序列和转座子元件的活动有关。具体来说,基因组序列消除和染色体重排可能是引导细胞学二倍体化的主要力量。基因的非功能化、亚功能化、新功能化以及其他类型的表观遗传修饰,可能是促进遗传二倍体化的主要因素。