Is the wild oat embryo monocotylous?

The embryogeny of the wild oat (Avena fatua L.) was studied in detail. The pattern of embryo development was observed to be similar to the other investigated grass taxa, conforming to thePoa variation of the Asterad type. The embryogeny and anatomy of young seedlings showed that the embryo of the wild oat was not monocotylous, but dicotylous. The scutellum of the embryo, as reported for other grasses, was regarded as the first cotyledon, and the first leaf primordium, which developed later into a photosynthesizing leaf and situated opposite the scutellum, was interpreted as the second cotyledon. Observations indicated that the cotyledons of the embryo were placed lateral to the shoot apical meristem, which was terminal in position. The cotyledons were found to be dimorphic in structure and function. The scutellum, a modified cotyledon, functioned as a suctorial organ, transporting nutrients from the endosperm to the embryo axis. The second cotyledon or the first true leaf supplied nutrients directly to the embryo axis through the process of photosynthesis.     

花生ABI3同源基因的定位分析

ABSC ISIC AC ID-INSITIVE3(AB I3)、LEAFY COTYLEDON2(LEC2)和FUSCA3(FUS3)转录因子在种子发育过程中发挥着重要的调控作用。采用Northern杂交技术,用拟南芥AB I3保守的B3结构域部分序列作为探针分别与花生根、茎、叶、子叶RNA进行了杂交,同时也对花生根、茎、叶、子叶(含胚)组织切片进行了原位杂交,结果均显示只有在花生的子叶和胚中有杂交信号出现,表明花生中可能存在AB I3、FUS3和LEC2的同源基因,且它们只分布在花生的子叶和胚中。     

Localization of arabinogalactan-proteins in different stages of embryos and their role in cotyledon formation of <Emphasis Type="Italic">Nicotiana tabacum</Emphasis> L.

Arabinogalactan proteins (AGPs) have been implicated in plant development including sexual plant reproduction. In this paper, the expression of AGPs and the effects of β-glucosyl Yariv reagent (βGlcY, which binds arabinogalactan proteins) in embryo development and cotyledon formation were investigated. Immunofluorescence assay displayed that the expression of AGPs labeled with antibody JIM13 was developmentally regulated. In early stages, AGPs were evenly distributed in the whole embryo, except for a short polar expression in the basal suspensor cell. In the globular stage of embryo, AGPs were condensed in the embryo proper (EP), apex of the EP, and at the juncture of the EP and suspensor. In heart-shaped embryo, APGs were only present at the juncture of the EP and suspensor. Immunogold labeling assay showed that the strong expression of AGPs at the juncture of the EP and suspensor was localized in the cell wall. Provision of βGlcY to the in vitro ovule culture medium caused delayed growth of embryos, cotyledon defect and abnormal venation pattern. Consequently, βGlcY induced the death of defective seedlings with the characteristics of deformed or irregular single cotyledon. Our results suggested that AGPs play functional roles in embryo development, cotyledon formation and seedling morphology establishment in Nicotiana tabacum L.     

Roles of arabinogalactan proteins in cotyledon formation and cell wall deposition during embryo development of <Emphasis Type="Italic">Arabidopsis</Emphasis>

Arabinogalactan proteins (AGPs) are a class of highly glycosylated, widely distributed proteins in higher plants. In the previous study, we found that the green fluorescence from JIM13-labeled AGPs was mainly distributed in embryo proper and the basal part of suspensor but gradually disappeared after the torpedo-stage embryos in Arabidopsis. And (β-d-Glc)₃ Yariv phenylglycoside (βGlcY), a synthetic reagent that specifically binds to AGPs, could inhibit embryo development. In this study, as a continuous work, we investigated the AGP functions in embryo germination, cotyledon formation, and cell wall deposition in Arabidopsis embryos by using immunofluorescent, immunoenzyme, transmission electron microscopy (TEM), and Fourier transform infrared spectroscopy (FTIR) techniques. The results showed that 50 μM βGlcY caused inhibition of embryo germination, formation of abnormal cotyledon embryos, and disorder of cotyledon vasculature. Compared with the normal embryos in vitro and in vivo, the AGPs and pectin signals were quite weaker in the whole abnormal embryos, whereas the cellulose signal was stronger in the shoot apical meristem (SAM) of abnormal embryo by calcofluor white staining. The FTIR assay demonstrated that the cell wall of abnormal embryos was relatively poorer in pectins and richer in cellulose than those of normal embryos. By TEM observation, the SAM cells of the abnormal embryos had less cytoplasm, more plastid and starch grains, and larger vacuole than that of normal embryos. These results indicated that AGPs may play roles in embryo germination, cotyledon formation, cell wall cellulose and pectin deposition, and cell division potentiality during embryo development of Arabidopsis.     

EMBRYO STRUCTURE AND STORAGE RESERVE HISTOCHEMISTRY IN THE PALM WASHINGTONIA FILIFERA

The seed of Washingtonia filifera (Lindl.) Wendl. is hemispherical and has a smooth testa. The embryo is located on the rounded side of the seed near the raphe. The embryo consists of a prominent single cotyledon, an epicotyl, and a small root apex. The shoot apex is oriented at a right angle to the long axis of the embryo and possesses 2 to 3 leaf primordia. The cotyledon functions as a storage organ and is composed of three cell types with similar ultrastructure. These three types—the parenchyma, protoderm, and procambium—can be distinguished on the basis of position, size, and shape. The procambial strands in the cotyledon consist of a ring of bundles grouped into two distinct sympodia and extend from beneath the shoot apical meristem to the tip of the cotyledon where they are situated very close to the surface. The most prominent organelles within all cell types are protein bodies, lipid bodies, and crystalline protein fibers. The protein bodies contain small crystalline inclusions which are presumed to be phytin. Protein bodies in the protoderm were smaller, denser-staining, and contained fewer crystalline inclusions than those in the parenchyma or procambium. On a volume basis, the parenchyma was shown to be 43% protein bodies, 25% lipid bodies, 15% cytoplasm, 7% cell wall, 4% intercellular space, 2% nuclei, and 4% other organelles (mitochondria and plastids).     

Roles of extensins in cotyledon primordium formation and shoot apical meristem activity in Nicotiana tabacum

Extensins are cell wall basic glycoproteins with a polypeptide backbone that is extremely rich in hydroxyproline. In this paper, the function of extensins in embryo development was studied in Nicotiana tabacum. By using Western blot and immunohistochemistry, the extensin JIM20 epitopes were found to express in different developmental stages of embryos, and specifically in the top of the embryo proper (EP) and the suspensor of the late globular embryos. In order to clarify the functions of extensins, a potent hydroxyproline synthesis inhibitor, 3,4-dehydro-L-proline (3,4-DHP), was used in ovule and embryo culture. The results showed that the addition of 3,4-DHP caused abnormal embryos with single, asymmetry and supernumerary cotyledon primordia, and continuous culture led to cotyledon defects in the germinated seedlings. Histological sections showed that the shoot apical meristem (SAM) of the abnormal seedlings was dissimilar from the controls, especially in the seedlings with cup-shaped cotyledons. Furthermore, the vasculature of the abnormal cotyledons was in an out-of-order format and contained at least two main veins. Finally, both the hydroxyproline assay and fluorescent immunolocalization confirmed that 3,4-DHP treatment reduced the level of extensins in the cultured ovules and embryos. These results indicate that extensins may play important roles in the cotyledon primordium formation, SAM activity, and vasculature differentiation during embryo development.     

fusca3: A Heterochronic Mutation Affecting Late Embryo Development in Arabidopsis

Molecular studies of late embryogenesis and seed development have emphasized differential gene expression as a means of identifying discrete stages of embryogenesis. Little has been done to identify factors that regulate the length of a given developmental stage or the degree of overlap between adjacent developmental programs. We designed a genetic screen to identify mutations that disrupt late embryo development in Arabidopsis without loss of hormonal responses. One such mutation, fusca3 (fus3), alters late embryo functions, such as the establishment of dormancy and desiccation tolerance, and reduces storage protein levels. fus3 cotyledons bear trichomes, and their ultrastructure is similar to that of leaf primordia. Immature fus3 embryos enter germinative development, and the shoot apical meristems develop leaf primordia before seed desiccation begins. The cotyledons resemble leaf primordia, yet retain some cotyledon characteristics; thus, cotyledon- and leaf-specific functions are expressed simultaneously. Together, these observations are consistent with a heterochronic interpretation of the fus3 mutation.     

The question of cotyledon homology in angiosperms

The flowering plants (Magnoliophyta) are separated into two large classes distinguished by the morphology of their embryos. The embryos of monocots (class Liliopsida) have a single terminal cotyledon, while the embryos of dicots (class Magnoliopsida) usually have two lateral cotyledons. The cotyledons of monocots and dicots also differ in form, and there are no true intermediates. In addition, the third leaf of Nymphaealean seedlings appears to be identical to the single cotyledon of monocots. From this it is concluded that the cotyledons of monocots and dicots are not homologous. In addition, dissimilarity of cotyledons and succeeding leaves in dicots, together with recent genetic studies, suggests that the two cotyledons of dicots are not homologous with the succeeding leaves of the same plant. This interpretation is consistent with the view that the Nymphaealean embryo’s third leaf is homologous to the first leaf (cotyledon) of monocots. Because dicotyledonous embryos are common among seed plants and are present in the Gnetopsids, the most likely scenario is that the dicots share a widespread seed plant symplesiomorphy and that the monocots have lost this character state. A less parsimonious hypothesis of monocotyledonous embryos as plesiomorphic for angiosperms is also discussed. Genetic analysis of early embryo development in a variety of vascular plants may be the only way to conclusively determine the evolutionary origin of the distinctive difference between monocot and dicot embryos.     

Structure of the zygotic embryos and seedlings of Butia capitata (Arecaceae)

Butia capitata, an endemic palm of the Brazilian savanna threatened by deforestation, demonstrates low germinability due to seed dormancy. The present study characterizes the structure of the zygotic embryo and describes germination and seedling development. Pyrenes were sown into sandy soil substrates to germinate, and their embryos were also cultivated in vitro in MS medium; structural evaluations were made during their development. Seedling growth through the endocarp germ pore culminates in the protrusion of the cotyledonary petiole, with the root and leaf sheaths subsequently being emitted laterally from its extremity. The embryos are composed of the cotyledon (whose proximal third has a haustorial function) and a diminutive embryo axis that is contained within the cotyledonary petiole. The protoderm, ground meristem, and procambium can be observed in their typical positions in the embryo axis and cotyledon. The development of the vegetative axis could be observed on the second day of in vitro cultivation, with elongation of the embryo axis and the beginning of the differentiation of the first eophyll. Elongation of the cotyledonary petiole and the differentiation of the parenchyma and tracheary elements were observed during the second to fifth day. Although the hypocotyl–radicle axis is less differentiated than the plumule, root protrusion occurs on the eighth day, and the leaf sheaths are only emitted between the twelfth and the sixteenth days; the haustorium atrophied during this stage. The embryonic structure of B. capitata does not impose limitations on seed germination as dormancy is of the non-profound physiological type, and the 50 % elongation of the cotyledonary petiole serves as a morphological indicator of germination.     

Endophyte transmission and activity in the Anabaena-Azolla association

Summary The survival of Azolla was studied in an artificial system which simulated the soil/water interface and the desiccation of soil during a fallow period in lowland rice culture. Tests with non-sporulating and sporulating Azolla fronds showed that Azolla only survives with sporulated fronds. At their reappearance the Azolla fronds already harboured the Anabaena endophyte. A detailed light microscopic and transmission electron microscopic study of macro- and micros-porocarp formation and development revealed that the endophyte is transmitted by the macrosporocarps and not by the microsporocarps. The Anabaena cells within the macrosporocarps are found just below the indusium cap. These cells are not nitrogen-fixing akinetes. The free-living Anabaena cells at the stem apex and below the overarching developing leaves do not bear heterocysts and accordingly are non nitrogen-fixing. During the development of the leaf the Anabaena enters the leaf cavity, but later the pore of this, cavity closes and the imprisoned cyanobacteria are lysed before the leaf decays. As the Azolla leaves age a nitrogen-fixing capability is successively built up concomittantly with the production of heterocysts. Heterocyst frequencies of 40–50% can be found inAnabaena azollae. Usually a gradient of nitrogen-fixing capacity occurs along the Azolla rhizome with two distinct peaks at leaf number 7/8 and at leaf number 13/14 from the apex.     

枣树体细胞胚发生和组织学研究

以临泽小枣子叶切块为外植体,在附加０．２mg/L IBA 1．0mg/L 6-BA的ＭＳ培养基上１周后切块边缘可诱导出白色胚愈伤组织,继续培养１个月后愈伤组织中产生体细胞胚。体细胞胚发生不同步,经历球形胚、心形胚、子叶胚等阶段,与合子胚发育途径相似。组织切片表面胚性愈伤组织细胞体积小,细胞核大、细胞质浓,细胞排列紧密;而非胚性愈伤组织细胞体积大、细胞核小、细胞质稀薄,子叶胚时期体细胞胚内部出现维管束,并观察到螺纹导管。     

In Vitro Seed Germination and Developmental Morphology of Seedling in Cymbidium ensifolium

The process of in vitro seed germination of Cymbidium ensifoliumcultivar Si-ji-lan could be divided into the following five stages: (1) Proembryos wereswollen, outer layer cells became irregular in shape. The tangential wall of outer layer cells of proembryos was thickened. The terminal cells were much smaller than basiccells. (2) Seeds germinated and differentiated into protocorms with terminal or lateralmeristem. (3) On one flank of the terminal meristem a single cotyledon was differen-tiated. (4) After the first foliage leaf was formed in the opposite side of the cotyledon,the protocorms developed into rhizomes. (5) As the third or forth leaf was formed, young roots were initiated. The results stained by Suden IV shot that the possiblecause for quite slow seed germination rate of Cymbidium ensifolium in vitro is due tothe thickened layers of seed coat, reducing its penetrability on the surface of proem-bryo. During seed germination the lipid and starch in the embryo cells were reduced.The reduction of starches may be closely correlated to the meristem formation.     

枣合子胚和体细胞胚发育过程的观察与比较

本实验对临猗梨枣、壶瓶枣、晋矮1号等13个品种的枣胚的发育过程进行了观察,并诱导晋矮1号成熟胚的愈伤组织通过体细胞胚发生途径形成再生植株。结果表明:体细胞胚产生于愈伤组织的表层细胞或内部细胞。在鱼雷胚期已有导管的分化,子叶期的维管组织呈“Y”形。枣合子胚及体细胞胚的发育均经历了原胚、球形胚、心形胚、鱼雷胚和子叶胚五个时期。大多数品种的枣胚从球形胚期或心形胚期即开始败育,只有极少数品种可发育到成熟胚,而且合子胚形成的能力、胚败育时发育的程度等均存在着大的品种间差异,同一品种甚至同一子房内胚的发育进程也不同步。     

Embryo and Endosperm Development in Isatis Tinctoria L. and the Histochemical Study of Its Storage Reserve

The ovule is anatropous and bitegmic. The nuceIlar cells have disorganized except the chalazal proliferating tissue. The curved embryo sac comprises an egg apparatus and a central cell with two palar nuclei and wall ingrowths on its micropylar lateral wall. The antipodal cells disappear. Embryo development is of the Onagrad type. The filament suspensor grows to a length of 785 μm and degenerats at tarpedo embryo stage. The basal cell produces wall ingrowths on the micropylar end wall and lateral wall. The cells of mature embryo contain many globular protein bodies, 2.5–7.5 μm in diameter, composed of high concentration of protein and phytin, insoluble polysaccharide and lipid. The cells, except procambium, also contain many small starch grains. Some secretory cavities scattered in the ground tissue have liquidlike granules composed of protein, ploysacchaide and lipid. Endosperm development follows the nuclear pattern. At the late heart embryo stage, the endosperm around the embryo and the upper suspensor and the peripheral endosperm of the basal region of the U-shaped embryo sac becomes cellular. The endosperm at micropylar and chalazal ends remains free nuclear phase until the late bended cotyledon stage. Wall ingrowths at both micropylar and chalazal end wall and lateral wall of the embryo sac become more massive during endosperm development. Wall ingrowths also occur on the outer walls of the outer layer endosperm cells at both ends and lateral region of the embryo sac. When the embryo matures, many layers of chalazal endosperm ceils including 2–4 layers of transfer cells, a few of micropylar endosperm cells and 1–5 layers of peripheral endosperm cells are present. The nutrients of the embryo and endosperm at different stages of development are also discussed.     

Characterization and systematic implications of the diversity in timing of programmed cell death of the suspensors in Leguminosae

? Premise of the study: In angiosperm seeds, the developing embryo acquires nutrients via a suspensor that typically undergoes programmed cell death (PCD) at the early cotyledon stage. However, in Leguminosae (the third largest angiosperm family), the suspensors can disappear at the heart-shaped stage (i.e., prior to the cotyledon stage) or still persist at the cotyledon stage. Here, in a comprehensive survey of legume suspensors and embryos, the variation and the evolutionary direction of timing of suspensor PCD in Leguminosae were characterized, and systematic implications were evaluated. ? Methods: Suspensor development and morphology for 66 leguminous species from 49 genera, 21 tribes, and 3 subfamilies were comparatively studied using standard paraffin sectioning and light microscopy. ? Key results: Three patterns of suspensor PCD were observed at the early cotyledon stage. (A) The suspensor persisted. (B) The suspensor separated from the wall of the embryo sac and persisted as a vestige at the radicle apex. (C) The suspensor disappeared completely, and the absorption of nutrients by embryo was carried out via a "contact zone" between the embryo and the endosperm. Pattern C of early suspensor PCD was found only in the tribe Fabeae. An ancestral character reconstruction revealed that the long-lived suspensors of pattern A represented a plesiomorphic condition in Leguminosae and that the suspensors of pattern C evolved only once in the common ancestor of Fabeae. ? Conclusions: In Leguminosae, short-lived suspensors have thus evolved multiple times from long-lived suspensors. It remains largely unknown, however, how the embryo acquires nutrients after the early suspensor PCD.     

Bud induction inSesamum indicum by splitting shoot apices followed by treatment with Amo-1618

Couples of buds were induced at the eccentric sites in the axial of the cotyledon inSesamum indicum by treating the embryo with a growth retardant Amo-1618 after the embyro shoot apex was split in the intercotyledonary plane, or incised between the primordia of the first opposite leaves. They appeared at first to have been transformed from the primordia of the first leaves. Developmental studies of the buds, however, revealed that they did not arise from the primordia, but from their adjacent area which is the presumptive stem tissue situated between the primordia and the cotyledon. Buds could occur only when the original shoot apex of the embryo as well as the first leaf primordia were degenerated. From experimental and circumstantial evidences, they were interpreted as axially buds induced at an unusual site.     

Differential DNA Endoreduplication and Protein Profile during Cotyledon Ontogeny of Vigna radiata

Differential regeneration response of the two cotyledon types. ‘Cot E’ (attached to the embryo) and ‘Cot’, of Vigna radiata have been reported earlier. The present preliminary study addresses V. radiata cotyledon development with respect to patterns of endoreduplication and protein accumulation. In this communication two distinct types of cotyledon (in relation to their attachment with the embryonal axis), differing in regeneration responses, were characterized in terms of polyploidy levels and profiles, and extent of protein synthesis/accumulation. The embryo development was studied histologically from the first day after fertilization till seed coat formation and divided into 8 different stages to determine stages of cotyledon development. Early cotyledonary stage of embryo was recorded on the 6 DAF, at this stage ‘Cot’ and ‘Cot E’ were inseparable and referred to as stage VI. ‘Cot’ and ‘Cot E’ could be distinguished from 9 DAF onwards. Two major events, endoreduplication of DNA and protein synthesis/accumulation that occur during the cotyledon development of grain-legumes, were analysed to probe the differential status, if any, in these two cotyledon types. The cell division phase of cotyledon development continues upto stage VII, while cell expansion phase starts at the stage VIII. The cotyledonary cells began to undergo the endoreduplicating cell cycle (ECC) from stage VII and continue until seed maturity. During the cell division phase the mitotic cycle and ECC occur simultaneously; whereas, only ECC continues in the cell expansion phase. Analysis of protein content indicated that ‘Cot E’ always contained comparatively higher amount during in vivo development than that of ‘Cot’. Similarity indices between ‘Cot’/’Cot E’ were 46.15%,82.35% and 90.9% at stage VII, stage VIII and at maturity, respectively, as computed from the presence oftotal polypeptides. The differential temporal pattern of DNA-endoreduplication and storage protein accumulation clearly dictates the influence of differential gene expression and regulation control in the developmental- type determination of the two cotyledons.     

海金沙胚胎发育的研究

利用石蜡切片法研究了海金沙胚胎发育过程。合子的第一次分裂面垂直于颈卵器的长轴,产生两个相等的子细胞,靠近颈卵器颈部的营养器官原始细胞和远离颈部的基足原始细胞。前者发育成子代孢子体的营养器官,后者发育成基足。胚胎在32细胞阶段后,第一叶顶端细胞与第一根顶端细胞几乎同时发生。第一叶突出帽状体之后,由第一叶基部保留下来的茎干顶端细胞产生第二叶。据营养器官的形态结构判断,在海金沙胚胎发育中最早出现的营养器官是叶和根。