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The Rise of Apomixis in Natural Plant Populations

机译:自然植物种群中无融合生殖的兴起

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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.
机译:通过种子无性繁殖的无融合生殖通过保持理想的基因型世代相传,在植物育种中具有许多潜在的应用。由于大多数主要农作物都不表达天然无融合生殖,因此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,我们回顾了自然无融合生殖的起源,建立和维持的知识状态。许多研究表明,在二倍体或多倍体细胞类型上的杂交是形成未减少雌配子体的主要诱因,这代表着向无融合生殖迈出的第一步,必须与孤雌生殖结合,即未受精卵细胞的发育。尽管如此,大多数无融合生殖植物仍需要对胚乳施肥。这三个步骤的耦合似乎是向自然无融合生殖转变的主要限制。不定胚是通向无融合生殖的另一种发育途径。多倍体的副作用通常促进建立新的无融合生殖世系。多倍体对二倍体亲代和祖细胞产生直接的生殖屏障;它可能导致基因自交不亲和(SI)系统崩溃,这是建立假配偶无融合生殖世系的自育能力所必需的;最后,多倍体可以通过增加植物的适应性潜力间接帮助在新的生态位中建立无融合生殖细胞型。此步骤之后可能是一个多元化和范围扩大的阶段,通常被描述为地理孤雌生殖。在农作物中利用无融合生殖必须考虑花粉转移和渗入性作物田中的潜在风险,可以通过使用不育的花粉或习性变种来克服。另一个风险是逃逸到自然植被中以及无融合生殖植物的潜在入侵,这需要仔细管理和考虑生态条件。

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