ORIGIN AND ONTOGENESIS OF SOMATIC EMBRYOS IN HEYEA BRASILIENSIS (EUPHORBIACEAE)

In Hevea, currently described culture conditions allow the induction of two modes of embryogenesis in callus formed on excised portions of the internal integument of immature seeds. One mode is of unicellular origin and is transitory, only resulting in the production of globular proembryos. The other is of multicellular origin and produces embryos. Specific culture conditions appear to favor one or the other mode of development in a given genotype. The ontogenesis of embryos of multicellular origin bypasses the classical stages of zygotic embryogenesis. The structural abnormalities observed in most somatic embryos are probably responsible for the low germination rates obtained.     

Morphohistological analysis of the origin and development of somatic embryos from leaves of mature Quercus robur

Summary In oak species, there is paucity of information on the anatomical changes underlying differentiation of somatic embryos from explants of mature trees. A histological study was undertaken to ascertain the cellular origin and ontogenesis of somatic embryos in leaf cultures from a 100-yr-old Quercus robur tree. Somatic embryogenesis was induced in expanding leaves excised from shoots forced from branch segments, following culture on three successive media containing different concentrations of α-naphthaleneacetic acid and 6-benzylaminopurine. The somatic embryogenesis followed an indirect pathway from a callus tissue formed in the leaf lamina. After 4–6 wk of culture, meristematic cells originated in superficial layers of callus protuberances, but these cells evolved into differentiated vacuolated cells rather than embryos. A subsequent dedifferentiation into embryogenic cells occurred later (9–12 wk of culture) within a dissociating callus. Embryogenic cells exhibited dense protein-rich protoplasm, high nucleoplasmic ratio, and contained small starch grains. Successive divisions of these cells led to the formation of a few-celled proembryos and embryogenic cell clumps within a thick common cell wall, which seemed to have originated unicellularly. However, a multicellular origin of larger embryogenic clumps could not be dismissed; these gave rise to embryonic nodular structures that developed somatic embryos of both uni- and multicellular origin. Somatic embryos at successive stages of development, including cotyledonary-stage embryos with shoot and root meristems, were apparent.     

In vitro culture of ovules ofTriticum aestivum at early stages of embryogenesis

Because most of the intergenericGramineae embryos abort before they can be isolated and cultured, our object was to grow ovules at an early stage of embryogenesis. Ovules were at size 1 to 7 mm. The youngest stages represented ovules containing several-celled proembryos; the oldest stage consisted of embryos at the level of differentiation of the organs. 1357 ovules were jointly inoculated in 12 different media of which only 3 appeared to be most suitable for the growth and differentiation of globular proembryos. From several-celled proembryos (ovules at the size of 1.5 – 2.5 mm) only compact calluses developed. The capability of proembryos to differentiate and to form fully developed embryos and consequently plants started when the ovules were inoculated at the size of 2.5 – 3.0 mm. Since the medium plays an important role in the process of differentiation of proembryos, the application of similar culture conditions is suggested for the in vitro culture of haploid or hybrid proembryos obtained among wide crosses inGramineae.List of abbreviations COC Coconut milk - BAP 6-benzylaminopurine - YE Yeast extract - CH Casein hydrolysate - KT Kinetin - ZT Zeatin     

Genotypic and media factors affecting stabilization of polyembryogenic cultures in norway spruce (Picea abies (L.) Karst.)

Embryonal-suspensor mass lines (ESM lines) from mature embryos of three open-pollinated families of Norway spruce [Picea abies (L.) Karst.] were stabilized on several culture media varying in nutrient composition. A pattern of relationship between parameters of polyembryogenic culture performance and medium composition was genetically determined. Stabilized ESM lines could be classified into two phenovariants: (i) lines of homogenous ESM composed entirely of somatic proembryos, and (ii) lines of heterogeneous ESM composed of a mixture of nonembryogenic callus and aggregates of somatic proembryos. The formation of one or the other phenovariant was independent of genotype, but strongly determined by the medium composition.Abbreviations ABA abscisic acid - BA 6-benzyladenine - ESM embryonal-suspensor mass - N nitrogen - NAA -naphthyl-1-acetic acid     

Proembryo culture: in vitro development of early globular-stage zygotic embryos from Brassica juncea

We have systematically investigated the nutritional requirements for in vitro culture of zygotic proembryos of Brassica juncea. Normal embryo development in vitro was achieved in a new embryo culture medium (ECM) which contains mineral salts, sugars, amino acids, organic acids and coconut water. The culture system is comprised of two agar layers, with the top layer containing a higher osmolality than the bottom layer. Proembryos were embedded in the top layer in which the osmotic pressure decreased gradually during culture because of the diffusion of osmotically active compounds into the bottom layer. Using such a double-layer culture system and the ECM, proembryos as small as 35 μm (8–36 cells) could be cultured and developed into normal, mature embryos with an efficiency of at least 75%. In contrast to previous findings, we found that the removal of the suspensor had only a small effect on the development of embryos 55 μm or smaller, but no effect on larger proembryos. We expect this system to be very useful for investigations of the mechanism of plant embryogenesis.     

Origin and development of secondary somatic embryos in transformed embryogenic cultures of <Emphasis Type="Italic">Medicago sativa</Emphasis>

Non-transformed and transformed embryogenic cultures of alfalfa (Medicago sativa L. cv. Zaječarska 83), long-term maintained on growth regulator-free medium, were histologically analyzed. In all examined cultures, somatic embryos at various stages of development were observed and secondary embryos were formed in the cotyledonary, hypocotylary and radicular region of the primary embryos. Detailed histological analysis of the torpedo shape somatic embryo revealed that secondary somatic embryos arose directly from single epidermal cells of hypocotylary axis after an unequal periclinal division. Bipolar proembryos were composed of one smaller cytoplasm rich cell and one larger more vacuolated cell. Further cell division pattern was similar for both non-transformed and transformed embryos. However, multicellular origin of secondary embryos in a direct process and even from callus can not be excluded.     

In Vitro Embryogenesis in Unfertilized Embryo Sacs of Oryza sativa L.

Haploid rice plantlets were induced from cultured ovaries in our previously reported experiment. The present paper is an embryological study on this subject. Young flowers of two japonica cultivars were excised and cultured just in the same manner as before. Liquid medium used for float culture was N6+3% sucrose+0.125 ppm MCPA. The inoculated materials were checked to be at late uninuclcate pollen stage which corresponded mainly to the uuinuelcate embryo sac stage, but as well as some 2- or 4-nucleate embryo sacs. Samples were fixed at 23 days intervals in acetomethanol (1:3), stained in toto with diluted Ehrlich's hematoxylin and sectioned by paraffin method for microscopical observation. 4 days after inoculation most of the embryo sacs developed up to 8-nucleate stage with polarized differentiation of the egg apparatus, central cell and antipodals. From 7th day on, proembryos of various sizes and shapes appeared in the micropylar region of some embryo sacs; some consisted of meristcmatic ceils, others were highly vacuo]ated. One-celled as well as linear multicellular suspensors atypical of in vivo zygote proembryos were observed, ttowever, it was uncertain whether the proembryos originated from the egg cell, the synergids, or the differentiating egg apparatus as a whole. Another peculiar event occured during culture was the formation of endosperm-like free nuclei from the unfertilized polar nuclei in some embryo sacs. Sometimes the free nuclei were numerous and showed a tendency of cell formation in localized areas. 12–15 days after inoculation, the proembryos developed into mieroseopieal ealli with globular or pearlike shape, wbieh continued enlarging to visible size with naked eyes at about 18–24 th day. Further growth eventually led the ealli protruding out the ovary wall beyond 32–35 the day. These observations indicate that the embryo sue, similarly as the pollen, can be induced to embryogenesis in vitro. This may open a new way to study the mechanism controlling gametophytie and sporophytie developmental pathways of embryo sac and provide means for large-scale production of "embryo sac plants" in future.     

Histological study of somatic embryogenesis induction on zygotic embryos of macaw palm (<Emphasis Type="Italic">Acrocomia aculeata</Emphasis> (Jacq.) Lodd. ex Martius)

The aim of this paper was to describe the histological events that led to somatic embryogenesis in macaw palm (Acrocomia aculeata (Jacq.) Lodd. ex Martius). Zygotic embryos were inoculated on Y₃ medium containing 9 μM 4-amino-3,5,6-trichloropicolonic acid (picloram). Somatic embryos regenerated from nodular callus on induction medium with activated charcoal under photoperiod or without activated charcoal under dark. Many proembryos originated from the fundamental meristem after 10–20 days of culture. When transferred to medium containing activated charcoal, under photoperiod, calli regenerated into somatic embryos of unicellular origin. These embryos had protoderm, plumule and procambial strands and some of them could germinate. After 30–40 days of culture, meristematic masses grew from procambial cells. The masses generated nodular callus, and after transfer to medium without activated charcoal, under dark, they generated somatic embryos of multicellular origin. Those embryos did not regenerate into plants.     

In vitro development of early proembryos and plant regeneration via microculture in Oryza sativa

Two convenient and efficient microculture techniques (liquid droplet and shallow-layered culture) were used to rear 2-day-old and 3 to 4 day-old proembryos in rice. Among four cultivars, growth rate and frequency of embryogenesis were higher in the japonica cultivars than in the indica cultivars during proembryo culture. Two-day-old proembryos could grow and form callus only in Km8p and N6 among four kinds of tested media, and plantlets regenerated via organogenesis. Plant regeneration from callus initiated from three- and four-day-old proembryos occurred through somatic embryogenesis and organogenesis. For in vitro embryogenesis it was essential to supplement the medium with 14 amino acids and coconut milk. The highest frequency of embryogenesis and the frequency of total induction after 14 days of culture were approximately 42% and 95% for 3-day-old proembryos, and 45% and 100% for 4-day-old proembryos, respectively. This revised version was published online in June 2006 with corrections to the Cover Date.     

韭菜胚囊发育与胚胎发生

韭菜胚囊发育为葱型,胚胎发生属柳叶菜型。成熟胚囊中,三个反足细胞形态上常类似卵器,其中二个呈助细胞状,一个呈卵细胞状。卵状反足细胞可分裂成多细胞原胚,但随着胚乳的发育而退化。在未受精胚囊中,卵细胞和卵状反足细胞均可分裂,它们的发生过程与合子胚相似,但因无胚乳哺育,均不能继续发育。论证了反足细胞胚的性质,初步探讨了胚乳与反足细胞无配子生殖的关系。     

An electron microscope study on in vitro parthenogenesis in sunflower

Summary Electron microscope studies have been conducted on the parthenogenesis induced by in vitro culture of unfertilized ovules of sunflower (Helianthus annuus). In comparison with the state of the egg prior to inoculation, some eggs 5 days after culture show striking ultrastructural changes, which include, among others, nuclear migration, an increase in the number and activity of the organelles, a loss of polarity and wall formation at the chalazal end of the cell. Most of these changes are similar to those that occur normally in the zygote, indicating that parthenogenic development has been triggered in these eggs. Such eggs have been termed activated and are presumed to be capable of undergoing parthenogenesis. The parthenogenic proembryos which result share some features in common with zygotic proembryos. In addition, some parthenogenic proembryos exhibit unique properties not found in zygotic proembryos. These include embryos that consist of two parts differing markedly in density, an inversion of polarity, the frequent occurrence of autophagic vacuoles, the thickening of cell walls, a centripetal growth mode of wall formation, the appearance of an incomplete cell wall, free nuclear division, amitosis and degeneration. We believe that these ultrastructural peculiarities are the effects of in vitro culture.     

甘蓝型油菜小孢子胚状体发生的细胞学观察

应用甘蓝型油菜ＤＨ系保６０４为材料研究小孢子胚发生过程,结果表明,在小孢子离体培养１～５ｄ内,随培养天数增加,小孢子的存活率迅速下降,部分小孢子培养后出现细胞膨大和分裂,并沿２－细胞。“ｆ”形３细胞,多细胞原体,胚柄球形胚,心形胚最终发育成鱼雷形胚,一般在心形胚阶段,胚柄脱离胚主体部分游离到培养基中,大多数膨大的细胞不能分裂或分裂后停止发育或发育异常。     

First stages of microspore reprogramming to embryogenesis through anther culture in Prunus armeniaca L.

Prunus armeniaca L. is a worldwide known species, very important particularly in the Mediterranean basin. Microspore embryogenesis through in vitro anther culture is a widely used method to obtain haploid and doubled haploid (DHs) plants which are being routinely used in breeding programmes for new superior cultivar development in many crops. Haploid-diploidization through gametic embryogenesis allows single-step development of complete homozygous lines from heterozygous parents. In the case of fruit crops, with long reproductive cycle, a high degree of heterozygosity, large size, and, often, self-incompatibility, there is no way to obtain haploidization through conventional methods. Induction of microspore embryogenesis in vitro is switched by a stress treatment. In many species, heat or cold stress has been reported to trigger pollen embryogenesis, the response being genotype dependent. In the present work we analyzed whether microspore reprogramming could be induced in apricot cultivars by cold stress through anther culture. We report the development of an in vitro anther culture protocol in P. armeniaca L. and analyse the response of several cultivars to stress treatments and culture media for inducing pollen embryogenesis. Results showed the formation of multicellular pollen and proembryos. The effect of two culture media in the embryogenic response was also analyzed, being the responses genotype-dependent. Monitoring of the cellular changes on the microspores was performed by structural and confocal microscopy analyses. Results indicated that the reprogramming of the microspore and the first steps of the embryogenic pathway have been achieved in different varieties of P. armeniaca, which constitutes a crucial step in the design of protocols for the regeneration of microspore-derived embryos and DH plants, for future potential applications in breeding programmes of this economically important fruit tree.     

Direct somatic embryogenesis and plant regeneration from single cell suspension cultures of Elymus giganteus Vahl

Summary A yellowish, nodular callus was induced from mature embryos of Elymus giganteus Vahl on MS medium containing 2.0 mg/l 2,4-dichlorophenoxyacetic acid (2,4-D) and 0.5 mg/l kinetin, from which a cell suspension culture was initiated in liquid MS medium supplemented with 0.5 mg/l 2,4-D, 1.0 mg/l kinetin and 0.2 mg/1 naphthaleneacetic acid (NAA). By filtering through a series of sieves with decreasing mesh sizes and collecting the resultant filtrate, a suspension culture composed mainly of single embryogenic cells was established. In a medium containing 0.3 mg/l 2,4-D, 1.0 mg/l 6-benzylaminopurine (6-BAP) and 500 mg/l casein hydrolysate (CH), the single cells underwent direct somatic embryogenesis resulting in the formation of proembryos. These proembryos developed into mature embryos when placed in a double-layer liquid overlay culture. Intact plants were developed from somatic embryos when they were transferred onto solidified MS medium without added growth regulators.     

Regeneration of fertile green plants from oat isolated microspore culture

Regeneration of fertile green plants from isolated oat microspores is reported for the first time. Factors critical for microspore growth and regeneration include cold pre-treatment, pH of culture medium and the use of conditioned culture medium. It was found that cold pre-treatment at 4°C in the dark for a minimum of 6 weeks was necessary to consistently achieve microspore growth into multicellular structures (MCS). Longer pre-treatments of up to 9 weeks were tested and found to be positively correlated with the number of MCS produced. Microspore culture medium with pH 8.0 produced significantly more MCS larger than eight cells in size than media with pH 5.8. The use of medium conditioned by actively growing barley microspores significantly increased the numbers of MCS larger than eight cells in size compared to non-conditioned media. Plants were regenerated only from cultures using conditioned medium. A total of 2 green plants and 15 albinos were regenerated. Of the green plants, one had the haploid chromosome complement (n = 3x = 21) and the other had the parental hexaploid chromosome complement (2n = 6x = 42) which may be due to spontaneous chromosome doubling. The hexaploid plant set seed naturally and the haploid plant set seed after its chromosome complement was doubled with colchicine.     

On the origin of differentiation

Following the origin of multicellularity in many groups of primitive organisms there evolved more than one cell type. It has been assumed that this early differentiation is related to size — the larger the organism the more cell types. Here two very different kinds of organisms are considered: the volvocine algae that become multicellular by growth, and the cellular slime moulds that become multicellular by aggregation. In both cases there are species that have only one cell type and others that have two. It has been possible to show that there is a perfect correlation with size: the forms with two cell types are significantly larger than those with one. Also in both groups there are forms of intermediate size that will vary from one to two cell types depending on the size of the individuals, suggesting a form of quorum sensing. These observations reinforce the view that size plays a critical role in influencing the degree of differentiation.     

The formation of symplasmic domains by plugging of plasmodesmata: a general event in plant morphogenesis?

Summary The plasmodesmal network was examined in multicellular protoplast-derived calluses of the dicotyledonSolanum nigrum which had not yet formed any visible adventitious organs and in globular proembryogenic structures developed from scutellar calluses of the monocotyledonMolinia caerulea. Electron microscopical analyses revealed that both calluses and proembryos consisted of small, undifferentiated cells. The interconnecting plasmodesmata at many cell interfaces were structurally inconspicuous in both systems; in particular cell walls, however, all plasmodesmata were occluded with an osmiophilic, dense material. As the blocking material was obviously located in the microchannels of the plasmodesmal cytoplasmic sleeves, the plugged plasmodesmata can be assumed to be nonfunctional. Thus, selective occlusion of all the plasmodesmata in specific cell walls resulted in the symplasmic disconnection of particular adjacent cells. Complex patterns of symplasmic continuity and discontinuity were established within the developing tissues. Some cells or groups of cells were entirely symplasmically disconnected from the surrounding cells by plugged plasmodesmata and might function as independent domains. However, blockage of plasmodesmata was achieved by the surrounding cells rather than by those cells belonging to the isolated domains. The demarcation of symplasmic domains might be a general prerequisite for differential morphogenesis, since they were found to be established very early in the course of morphogenetic processes.     

In-vitro culture of fertilized embryo sacs of maize: Zygotes and two-celled proembryos can develop into plants

Fertilized embryo sacs of Zea mays L. surrounded by a few layers of nucellar cells were cultured in vitro. Primary expiants contained zygotes or twocelled proembryos. Embryos of various sizes and shapes were isolated from 12–48% of explants after two weeks of culture in hormone-free media supplemented with 6–12% of sucrose. Many embryos were at the transition or proembryo stages whilst the rest were either differentiated, with a scutellum, a coleoptile and a shoot apex, or had a deformed apical part. Organogenesis started in 36–89% of embryos cultured on a semisolid medium supplemented with coconut water. Most of the embryos formed only roots but up to 9% of embryos regenerated into plants. This simple method leads the way to plant regeneration from in-vitro-manipulated zygotes or proembryos of maize.Abbreviation NBM medium composed of N6 macronutrients, B5 micronutrients and MS vitamins This research was supported by an I.N.R.A. post-doctoral fellowship. The authors thank R. Blanc for donor plant culture, Dr. M. Cock (Reconnaissance Cellulaire et Amélioration des Plantes, Université Lyon 1) for correction of the English and P. Audenis for micrograph development.     

Origin and Development of Somatic Embryoids Formed Directly on Immature Embryos of Trifolium repens In Vitro

When immature zygotic embryos of Trifolium repens are culturedin vitro in the presence of 0.05 mg 1^–1 BAP, the cellsof the hypocotyl epidermis proliferate to produce somatic embryoidsdirectly without an intervening callus phase. The young epidermalcells show features of proembryogenic cells, and the first signof embyroid induction is a shift from regular equational, anticlinaldivisions to irregular, periclinal and oblique quantal divisions.Multicellular budding and single-cell initiation apparentlyboth occur, with multicellular budding being the more frequentpattern in the present study. Most early proembryoids resembleglobular zygotic proembryos but appear to lack a suspensor.It is suggested that the subtending embryonic tissue fulfilsthe role of a suspensor or proembryonal complex. Secondary proliferationsfrom the young cotyledon and hypocotyl epidermis of primaryembryoids are formed by processes similar to those producingprimary embryoids, and also from structures initially resemblingepidermal hairs. These hair-like structures arise from singlesuperficial cells which show evidence of cutinisation and callosedeposition suggesting some degree of physical separation fromneighbouring cells. Trifolium repens, tissue culture, somatic embryogenesis, embryoid, legume     

Effectiveness of three micropropagation techniques to dissociate cytochimeras in Musa spp

In vitro mutagenesis of multicellular meristems of Musa spp. leads to a high degree of chimerism. Repeated vegetative propagation must be carried out to dissociate chimeras but the minimum number of cycles required is unknown. In general, mutated cells are difficult to monitor but mutations which result in a change in genome number are an exception. We simulated this case by colchicine treatment, followed by flow cytometric analysis. Colchicine treatment induced ploidy chimerism (mixoploidy), and chimera dissociation was assessed using three different propagation systems (shoot-tip culture technique - ST, multi-apexing culture technique - MA and corm slice culture technique - CS). The average percentage of cytochimeras was reduced from 100% to 36% after three subcultures using shoot-tip culture, from 100% to 24% when propagating by the corm slice culture technique and from 100% to 8% after the same number of subcultures using the multi-apexing technique. All propagation systems failed to eliminate chimerism completely. Factors that may influence chimera dissociation in vitro are discussed. This revised version was published online in June 2006 with corrections to the Cover Date.