单子叶植物无融合生殖的研究进展

植物的无融合生殖是指不经过雌雄配子融合而产生种子的一种特殊生殖方式。由于利用无融合生殖途径可以固定杂种优势,从而改良现有植物的育种策略,因此对无融合生殖的研究已成为生物学科的新生长点。本文主要从无融合生殖的概念和类型,无融合生殖在单子叶植物中的分布,无融合生殖的胚胎学,分子生物学和遗传学机制及创造新的无融合生殖种质资源的方法等6方面对单子叶植物的无融合生殖的研究进展进行了综述,并提出了今后开展无融合生殖研究的思路和设想。     

高粱SSA-1无融合生殖胚胎学研究

经常规石蜡切片法,在光学水平观察了高粱（Ｓｏｒｇｈｕｍ ｂｉｃｏｌｏｒ （Ｌ．） Ｍｏｅｎｃｈ） ＳＳＡ－１ 无融合生殖的胚胎发生。高粱ＳＳＡ－１ 的无融合生殖为无孢子生殖和二倍体孢子生殖两种类型。两种生殖类型的单核胚囊经３ 次有丝分裂形成７ 细胞（８ 核）的成熟胚囊,由卵细胞、２ 个助细胞、２ 个极核和３ 个反足细胞组成。反足细胞迅速分裂增殖,形成由２０—３０ 个细胞组成的细胞团。此外,还具有一定频率的无孢子生殖多孢原和多胚囊现象。在未授粉情况下,卵细胞自发分裂形成典型的禾本科类型单子叶胚。经切片统计表明,ＳＳＡ－１ 的无融合生殖频率为４２％ ,证明该系为一兼性无融合生殖系。文中还讨论了ＳＳＡ－１ 无融合生殖过程的特点。     

高梁SSA—1无融合生殖胚胎学研究

经常规石蜡切片法,在光学水平观察了高染（Ｓｏｒｇｈｕｍｂｉｃｏｌｏｒｂｉｃｏｌｏｒ．）Ｍｏｅｎｃｈ）ＳＳＡ－１无融合生殖的胚胎发生。高染ＳＳＡ－１的无融合生殖为无孢子生殖和二倍体孢子生殖两种类型。两种生殖类型的单核胚囊经３次有丝分裂成７细胞（８核）的成熟胚囊,由卵细胞、２个助细胞、２个极核和３个足细胞组成,反足细胞迅速分裂增殖,形成由２０－３０个细胞组成的细胞团。此外,还具有一定频率的无孢子生殖多     

植物无融合生殖研究的新进展

植物无融合生殖是指不经过雌雄配子融合而产生种子的一种特殊生殖方式,能使基因型的杂合性得以保持,从而可固定杂种优势。对近几年来植物无融合生殖的研究进展及发展动态作一综述,列举了新发现的具有无融合生殖特性的植物种类：总结了控制无融合生殖的遗传机理：指出该研究领域中存在的问题：展望了该领域的发展前景。     

濒危植物焕镛木的兼性无融合生殖

2001—2002年连续两年在广西环江木论和广西罗城大黄泥的2个焕镛木(Woonyoungia septentrionalis (Dandy) Law)自然种群中,对单性异株的濒危植物焕镛木进行繁育系统测定,对即将开花的雌花花蕾分别进行套袋、套网、人工授粉处理,并用自然授粉雌花作对照,其座果率和结实率统计结果表明：自然授粉、人工授粉、套袋和套网处理的花均能结实,但它们的座果率和结实率存在较大的差异。在两个种群中,人工授粉和自然授粉的总结实率(PERS)均比套袋和套网处理的高,其中人工授粉的最高,套网处理的最低。由此可见,焕镛木既能通过有性生殖方式结实,又能通过无融合生殖方式结实,而且这两种生殖方式获得的种子均能萌发成幼苗,由此断定,焕镛木的繁育系统为兼性无融合生殖。这是首次报道木兰科植物存在无融合生殖现象。     

植物的无融合生殖

植物的无融合生殖肖辅珍,王景林（首都师范大学生物系,北京１０００３７）１无融合生殖及其类型无融合生殖（Ａｐｏｍｉｘｉｓ）是被子植物不经过精卵结合而产生种子的特殊生殖方式［１］。它广泛存在于自然界的多种植物中,或代替有性生殖（专性的）,或与有性生殖共存...     

无融合生殖

自1745年博内(Bonnet)在研究蚜虫中发现孤雌生殖以来,世界各地的植物学家,也在众多的植物中发现了这种奇特的生殖现象,迄今为止,已记录到36科300余种植株的孤雌生殖。为同有性生殖和无性生殖相区分,植物学家把它定名为无融合生殖。 由于无融合生殖生理机制十分复杂,长期以来,对其概念的界定,植物学界一直没有统一。我国学者蔡得田和陈冬玲,在1993年提出:无融合生殖是指发生在植物胚珠中,不经过精卵融合形成胚,以种子进行繁殖的生殖方式。此界定包括三部分内容,一是它与无性生殖明显的区别是发生在性器官中;二是没有性融合过程而区别于有性生殖;三是以种子繁殖     

水蔗草兼性无融合生殖胚胎学研究

对水蔗草 (ApludamuticaL .)的生殖方式进行研究 ,结果表明水蔗草进行兼性无融合生殖。胚囊发育分为两种类型 ,即有性生殖的蓼型和无孢子生殖的大黍型。无融合生殖胚囊频率为 6 0 .74%。在大孢子母细胞发育至四分体后 ,珠孔端的 3个大孢子解体。合点端的大孢子未解体时 ,邻近大孢子的 1个珠心细胞开始特化 ,形成无融合生殖的原始细胞 ,由该原始细胞发育形成有 1个卵细胞、1个助细胞和 2个极核的四核胚囊。     

水蔗草兼性无融合生殖胚胎学研究

对水蔗草(Apluda mutica L.)的生殖方式进行研究,结果表明水蔗草进行兼性无融合生殖.胚囊发育分为两种类型,即有性生殖的蓼型和无孢子生殖的大黍型.无融合生殖胚囊频率为60.74%.在大孢子母细胞发育至四分体后,珠孔端的3个大孢子解体.合点端的大孢子未解体时,邻近大孢子的1个珠心细胞开始特化,形成无融合生殖的原始细胞,由该原始细胞发育形成有1个卵细胞、1个助细胞和2个极核的四核胚囊.     

无融合生殖与柑橘多胚现象的研究进展

植物无融合生殖是指植物的胚珠组织不经历正常的减数分裂和受精作用,而直接进行胚发育形成种子的无性生殖方式。无融合生殖植物完全继承了母体的全部基因型,因而具有独特研究与育种意义。芸香科柑橘属植物具有独特的多胚现象,其珠心组织能够发育成不定胚(称为珠心胚)进行无融合生殖。文中介绍了柑橘类植物的珠心胚生殖现象、细胞学和遗传学研究进展。珠心胚现象虽然对柑橘杂交后代获得有较大影响,但在生产上可产生性状整齐一致的后代,可以培育无病毒苗木。     

植物无融合生殖研究新进展

无融合生殖是指不经过雌雄配子融合而产生种子的一种特殊生殖方式,能使基因型的杂合性得以保持,从而可以固定杂种优势,对作物育种具有极其重要的意义。目前大量的研究都在设法将无融合生殖作为一种重要的植物育种手段。本文对近几年来无融合生殖新种质资源的发现、主要研究方法、遗传机制和相关基因等方面的最新进展作了介绍,并对无融合生殖研究中存在的问题和发展前景作了讨论。     

A current perspective on apomixis in ferns

This review provides a synopsis of apogamous reproduction in ferns and highlights important progress made in recent studies of fern apomixis. First, a summary of the apomictic fern life cycle is provided, distinguishing between two pathways to diploid spore production that have been documented in apomictic ferns (premeiotic endomitosis and meiotic first division restitution) and briefly discussing the evolutionary implications of each. Next, recent trends in fern apomixis research are discussed, exposing a shift in focus from the observation and characterization of apomixis in ferns to more integrated studies of the evolutionary and ecological implications of this reproductive mode. Peer-reviewed contributions from the past decade are then summarized, spanning the identification of new apomictic lineages through to the developmental, phylogenetic, and population genetic insights that have been made in studies of fern apomixis during that time. Gaps in our understanding are also discussed, including the extent and implications of recombinant apomixis in ferns, the possible reversibility of reproductive mode (from apomictic to sexual) in ferns, and the genomic causes and consequences of apomixis in seed free vascular plants. To conclude, future directions for fern apomixis research are proposed in the context of modern technological advances and recent insights from studies of apomixis in other groups.     

MIME--有丝分裂替代减数分裂及其在作物无融合生殖中的应用

无融合生殖因其在杂种优势固定中的巨大潜力而受到广泛关注,人工创制无融合生殖是当前无融合生殖研究的重要方向,有丝分裂替代减数分裂(Mitosis instead of Meiosis,MIME)能产生与母本遗传组成完全一致的二倍体配子,是人工创制无融合生殖的关键步骤。文中对MIME的发生及其在作物无融合生殖中的应用以及MIME应用中的问题进行综述,以期为扩大MIME在作物无融合生殖中的应用提供参考。     

Apomixis technology and the paradox of sex

Most plant species produce genetically variable seeds by the fusion of meiotically reduced egg cells and pollen grains. However, a small proportion of seed plants produces clonal, asexual seeds by the process of apomixis. The fixation of heterosis by apomixis is of great interest for plant breeding. The prospect of changing sexual crop species into apomictic crop species by genetic engineering--apomixis technology--has recently caused a boom in apomixis research. According to evolutionary biological theories, a dominant apomixis gene will rapidly become fixed in an outcrossing sexual population. Therefore, in theory, apomixis transgenes could have unconditional advantages that could result in the uncontrollable spread of the transgenes. By contrast, 'classic' transgenes might only have conditional advantages. Paradoxically, sexual reproduction and not apomixis is common in nature. However, this is no guarantee that apomixis transgenes will be ecologically safe because there could be essential differences between natural and transgenic apomicts.     

Sexual and apomictic plant reproduction in the genomics era: exploring the mechanisms potentially useful in crop plants

Arabidopsis, Mimulus and tomato have emerged as model plants in researching genetic and molecular basis of differences in mating systems. Variations in floral traits and loss of self-incompatibility have been associated with mating system differences in crops. Genomics research has advanced considerably, both in model and crop plants, which may provide opportunities to modify breeding systems as evidenced in Arabidopsis and tomato. Mating system, however, not recombination per se, has greater effect on the level of polymorphism. Generating targeted recombination remains one of the most important factors for crop genetic enhancement. Asexual reproduction through seeds or apomixis, by producing maternal clones, presents a tremendous potential for agriculture. Although believed to be under simple genetic control, recent research has revealed that apomixis results as a consequence of the deregulation of the timing of sexual events rather than being the product of specific apomixis genes. Further, forward genetic studies in Arabidopsis have permitted the isolation of novel genes reported to control meiosis I and II entry. Mutations in these genes trigger the production of unreduced or apomeiotic megagametes and are an important step toward understanding and engineering apomixis.     

Problems of apomictic reproduction in the FamiliesCompositae andRosaceae

For many years several taxa belonging to the familiesCompositae andRosaceae have been subjected to an intensive research on apomixis. These two families, together with theGramineae have headed the list of the most thoroughly examined taxonomic groups in this field. At present, new methods are being elaborated and new problems solved within the following genera known to be apomictic, viz.Antennaria, Hieracium, Taraxacum, Alchemilla, Potentilla andRubus. Many general problems still require more attention in future studies. Seven of them are considered in the present article: 1. frequency of apomixis; 2. occurrence of apospory and diplospory within one taxon; 3. nonfunctional apospory; 4. facultativeness of autonomous apomixis; 5. origin of endosperm; 6. timing of embryo and endosperm development in apomicts; 7. instability of the endosperm type. BothCompositae andRosaceae produce suitable material for such research projects.     

On the origin and evolution of apomixis in Boechera

The genetic mechanisms causing seed development by gametophytic apomixis in plants are predominantly unknown. As apomixis is consistently associated with hybridity and polyploidy, these confounding factors may either (a) be the underlying mechanism for the expression of apomixis, or (b) obscure the genetic factors which cause apomixis. To distinguish between these hypotheses, we analyzed the population genetic patterns of diploid and triploid apomictic lineages and their sexual progenitors in the genus Boechera (Brassicaceae). We find that while triploid apomixis is associated with hybridization, the majority of diploid apomictic lineages are likely the product of intra-specific crosses. We then show that these diploid apomicts are more likely to sire triploid apomictic lineages than conspecific sexuals. Combined with flow cytometric seed screen phenotyping for male and female components of apomixis, our analyses demonstrate that hybridization is an indirect correlate of apomixis in Boechera.     

The evolution of apomixis in angiosperms: A reappraisal

Abstract

Apomixis, the asexual reproduction via seed, has long been regarded a blind alley of evolution. This hypothesis was based on the assumption that apomixis is an irreversible, phylogenetically derived trait that would rapidly lead to extinction of the respective lineages. However, recent updates of the taxonomic distribution of apomixis in angiosperms suggest an alternative evolutionary scenario. Apomixis is taxonomically scattered and occurs in both early and late branching lineages, with several reversals from apomixis to obligate sex along phylogeny. Genetic control of apomixis is based on altered expression patterns of the same genes that control sexual development; epigenetic changes following polyploidization and/or hybridization may trigger shifts from sexuality to apomixis. Mendelian inheritance confirms the facultative nature and possible reversibility of apomixis to sexual reproduction. Apomixis, therefore, could represent a transition period in the evolution of polyploid complexes, with polyspory in paleopolyploids being a remnant of lost apomixis. In neopolyploids, apomixis helps to overcome sterility and allows for geographical range expansions of agamic polyploid complexes. The facultative nature of apomixis allows for reversal to sexuality and further speciation of paleopolyploid lineages. Thus, apomixis may facilitate diversification of polyploid complexes and evolution in angiosperms.