Hojsgaard Diego, Hörandl Elvira
Department of Systematics, Biodiversity and Evolution of Plants (with Herbarium), Albrecht-von-Haller Institute for Plant Sciences, University of Göttingen, Göttingen, Germany.
Front Plant Sci. 2019 Apr 2;10:358. doi: 10.3389/fpls.2019.00358. eCollection 2019.
Apomixis, the asexual reproduction via seed, has many potential applications for plant breeding by maintaining desirable genotypes over generations. Since most major crops do not express natural apomixis, it is useful to understand the origin and maintenance of apomixis in natural plant systems. Here, we review the state of knowledge on origin, establishment and maintenance of natural apomixis. Many studies suggest that hybridization, either on diploid or polyploid cytotypes, is a major trigger for the formation of unreduced female gametophytes, which represents the first step toward apomixis, and must be combined to parthenogenesis, the development of an unfertilized egg cell. Nevertheless, fertilization of endosperm is still needed for most apomictic plants. Coupling of these three steps appears to be a major constraint for shifts to natural apomixis. Adventitious embryony is another developmental pathway toward apomixis. Establishment of a newly arisen apomictic lineage is often fostered by side-effects of polyploidy. Polyploidy creates an immediate reproductive barrier against the diploid parental and progenitor populations; it can cause a breakdown of genetic self-incompatibility (SI) systems which is needed to establish self-fertility of pseudogamous apomictic lineages; and finally, polyploidy could indirectly help to establish an apomictic cytotype in a novel ecological niche by increasing adaptive potentials of the plants. This step may be followed by a phase of diversification and range expansion, mostly described as geographical parthenogenesis. The utilization of apomixis in crops must consider the potential risks of pollen transfer and introgression into sexual crop fields, which might be overcome by using pollen-sterile or cleistogamous variants. Another risk is the escape into natural vegetation and potential invasiveness of apomictic plants which needs careful management and consideration of ecological conditions.
无融合生殖是通过种子进行的无性繁殖,通过在多代中保持理想的基因型,在植物育种中有许多潜在应用。由于大多数主要作物不表现出天然的无融合生殖,了解天然植物系统中无融合生殖的起源和维持是很有用的。在这里,我们综述了关于天然无融合生殖的起源、建立和维持的知识现状。许多研究表明,二倍体或多倍体细胞型上的杂交是形成未减数雌配子体的主要触发因素,这是迈向无融合生殖的第一步,并且必须与孤雌生殖(未受精卵细胞的发育)相结合。然而,大多数无融合生殖植物仍然需要胚乳受精。这三个步骤的耦合似乎是向天然无融合生殖转变的主要限制因素。不定胚是通向无融合生殖的另一条发育途径。新出现的无融合生殖谱系的建立通常受到多倍体副作用的促进。多倍体对二倍体亲本和祖先种群立即产生生殖障碍;它可能导致遗传自交不亲和(SI)系统的崩溃,而这是建立假受精无融合生殖谱系自交育性所必需的;最后,多倍体可以通过增加植物的适应潜力,间接地帮助在新的生态位中建立无融合生殖细胞型。这一步骤之后可能是一个多样化和范围扩展的阶段,大多被描述为地理孤雌生殖。在作物中利用无融合生殖必须考虑花粉转移和渗入有性作物田的潜在风险,这可以通过使用花粉不育或闭花受精变种来克服。另一个风险是无融合生殖植物逃逸到自然植被中以及潜在的入侵性,这需要仔细管理并考虑生态条件。