Fertilization in Plumbago zeylanica: entry and discharge of the pollen tube in the embryo sac

1982 ◽  
Vol 60 (11) ◽  
pp. 2219-2230 ◽  
Author(s):  
Scott D. Russell
Keyword(s):  
Cell Wall ◽  
Pollen Tube ◽  
Female Gametophyte ◽  
Embryo Sac ◽  
Central Cell ◽  
Vegetative Nucleus ◽  
Egg Cell ◽  
Ultrastructural Organization ◽  
Plumbago Zeylanica ◽  
Male Gametes

The ultrastructural organization of the megagametophyte of Plumbago zeylanica, which lacks synergids, was examined in chemically and physically fixed ovules after entry of the pollen tube. Similar to angiosperms with conventionally organized megagametophytes, the pollen tube enters the ovule through a micropyle, formed by the inner integument, and approaches the female gametophyte by growing between nucellar cells. Unlike other described female gametophytes, however, continued pollen tube growth results in direct penetration of the base of the egg through cell wall projections forming a filiform apparatus and is completed between the egg and central cell without disrupting either of these cells' plasma membranes. A terminal pollen tube aperture forms when the pollen tube reaches an area of strong curvature near the summit of the egg; this results in the release of two sperm cells, the vegetative nucleus, and a limited amount of pollen cytoplasm. The formerly continuous chalazal egg cell wall is locally disrupted near the tip of the pollen tube and apparently is thus modified for reception of male gametes. Discharged pollen cytoplasm rapidly degenerates between the egg and central cell, but unlike pollen tube discharge in conventionally organized megagametophytes, it is unassociated with the degeneraton of any receptor cell within the female gametophyte. Sperm nuclei are transmitted, one to the egg and the other to the central cell, to effect double fertilization by nuclear fusion with their respective female reproductive nuclei. The vegetative nucleus and discharged pollen cytoplasm degenerate between the developing embryo and endosperm during early embryogenesis. The emerging concept that the egg of Plumbago possesses combined egg and synergid functions is supported by the present study and suggests that the megagametophyte of this plant displays a highly specialized egg apparatus composed exclusively of a single, modified egg cell.

Cytoskeletal organisation and modification during pollen tube arrival, gamete delivery and fertilisation in Plumbago zeylanica

Zygote ◽  
1993 ◽  
Vol 1 (2) ◽  
pp. 143-154 ◽  
Author(s):  
Bing-Quan Huang ◽  
Elisabeth S. Pierson ◽  
Scott D. Russell ◽  
Antonio Tiezzi ◽  
Mauro Cresti
Keyword(s):  
Pollen Tube ◽  
Embryo Sac ◽  
Central Cell ◽  
Egg Cell ◽  
Target Cells ◽  
Sperm Cells ◽  
Plumbago Zeylanica ◽  
Rhodamine Phalloidin ◽  
Male Gametes ◽  
Pollen Tube Penetration

The cytoskeletal organisation of the isolated embryo sac and egg cells of Plumbago zeylanica was examined before, during and after pollen tube penetration into the embryo sac to determine the potential involvement of microtubules and actin filaments in fertilisation. Material was singly and triply stained using Hoechst 33258 to localise DNA, fluorescein isothiocyanate (FITC)-labelled anti- α-tubulin to detect microtubules and rhodamine-phalloidin to visualise F-actin. Microtubules in the unfertilised egg cell are longitudinally aligned in the micropylar and mid-lateral areas, aggregating into bundles near the filiform apparatus. In the perinuclear cytoplasm of the egg cell, microtubules become more or less randomly aligned. F-actin bundles form a longitudinally aligned mesh in the chalazal cytoplasm of the egg cell. In the central cell, microtubules and F-actin are distributed along transvacuolar strands and are also evident in the perinuclear region and at the periphery of the cell. During pollen tube penetration, sparse microtubule bundles near the pathway of the pollen tube may form an apparent microtubular ‘conduit’ surrounding the male gametes at the delivery site. Actin aggregates become organised near the pathway of the pollen tube and at the delivery site of the sperm cells. Subsequently, actin aggregates form a ‘corona’ structure in the intercellular region between the egg and central cell where gametic fusion occurs. The corona may have a role in maintaining the close proximity of the egg and central cell and helping the two sperm cells move and bind to their target cells. The cytoskeleton may also be involved in causing the two nuclei of the egg and central cell to approach one another at the site of gametic fusion and transporting the two sperm nuclei into alignment with their respective female nucleus. The cytoskeleton is reorganised during early embryogenesis.

scholarly journals Ultrastructure of fertilization in Plumbago zeylanica

2014 ◽  
Vol 50 (1-2) ◽  
pp. 185-189 ◽  
Author(s):  
Scott D. Russell ◽  
David D. Cass
Keyword(s):  
Cell Wall ◽  
Pollen Tube ◽  
Female Gametophyte ◽  
Tube Growth ◽  
Vegetative Nucleus ◽  
Plumbago Zeylanica ◽  
Specialized Cell ◽  
Wall Ingrowths ◽  
Male Gametes ◽  
Cell Wall Ingrowths

The synergidless female gametophyte of <em>Plumbago zeylanica</em> receives the pollen tube through specialized cell wall ingrowths at the base of the egg; tube growth continues between egg and central cells. Pollen tube discharge occurs between egg and central cell and results in release of two male gametes, vegetative nucleus, and some pollen cytoplasm. Except for the location of gamete discharge, details of transmission and fusion of gametic nuclei appear to conform to reports of these processes in taxa possessing conventional embryo sacs.

scholarly journals Recent advances in understanding female gametophyte development

F1000Research ◽  
2018 ◽  
Vol 7 ◽  
pp. 804 ◽  
Author(s):  
Debra J Skinner ◽  
Venkatesan Sundaresan
Keyword(s):  
Cell Fate ◽  
Female Gametophyte ◽  
Cell Communication ◽  
Embryo Sac ◽  
Cell Types ◽  
Egg Cell ◽  
Male Gametes ◽  
Reproductive Unit ◽  
Genetic Mechanisms ◽  
Female Gametophyte Development

The haploid female gametophyte (embryo sac) is an essential reproductive unit of flowering plants, usually comprising four specialized cell types, including the female gametes (egg cell and central cell). The differentiation of these cells relies on spatial signals which pattern the gametophyte along a proximal-distal axis, but the molecular and genetic mechanisms by which cell identities are determined in the embryo sac have long been a mystery. Recent identification of key genes for cell fate specification and their relationship to hormonal signaling pathways that act on positional cues has provided new insights into these processes. A model for differentiation can be devised with egg cell fate as a default state of the female gametophyte and with other cell types specified by the action of spatially regulated factors. Cell-to-cell communication within the gametophyte is also important for maintaining cell identity as well as facilitating fertilization of the female gametes by the male gametes (sperm cells).

scholarly journals Spatio-Temporal Distribution of Cell Wall Components in the Placentas, Ovules and Female Gametophytes of Utricularia during Pollination

2021 ◽  
Vol 22 (11) ◽  
pp. 5622
Author(s):  
Bartosz Jan Płachno ◽  
Małgorzata Kapusta ◽  
Piotr Świątek ◽  
Krzysztof Banaś ◽  
Vitor F. O. Miranda ◽  
...  
Keyword(s):  
Pollen Tube ◽  
Female Gametophyte ◽  
Embryo Sac ◽  
Temporal Distribution ◽  
Arabinogalactan Proteins ◽  
Central Cell ◽  
Nutritive Tissue ◽  
Pollen Tube Guidance ◽  
Micropylar Canal

In most angiosperms, the female gametophyte is hidden in the mother tissues and the pollen tube enters the ovule via a micropylar canal. The mother tissues play an essential role in the pollen tube guidance. However, in Utricularia, the female gametophyte surpasses the entire micropylar canal and extends beyond the limit of the integument. The female gametophyte then invades the placenta and a part of the central cell has direct contact with the ovary chamber. To date, information about the role of the placenta and integument in pollen tube guidance in Utricularia, which have extra-ovular female gametophytes, has been lacking. The aim of this study was to evaluate the role of the placenta, central cell and integument in pollen tube pollen tube guidance in Utricularia nelumbifolia Gardner and Utricularia humboldtii R.H. Schomb. by studying the production of arabinogalactan proteins. It was also determined whether the production of the arabinogalactan proteins is dependent on pollination in Utricularia. In both of the examined species, arabinogalactan proteins (AGPs) were observed in the placenta (epidermis and nutritive tissue), ovule (integument, chalaza), and female gametophyte of both pollinated and unpollinated flowers, which means that the production of AGPs is independent of pollination; however, the production of some AGPs was lower after fertilization. There were some differences in the production of AGPs between the examined species. The occurrence of AGPs in the placental epidermis and nutritive tissue suggests that they function as an obturator. The production of some AGPs in the ovular tissues (nucellus, integument) was independent of the presence of a mature embryo sac.

scholarly journals Cytochemical study of the embryo sac of Nicotiana tabacum L.

2014 ◽  
Vol 50 (1-2) ◽  
pp. 121-125
Author(s):  
V. P. Babbikova ◽  
O. A. Khvendynich ◽  
L. S. Serdyuk
Keyword(s):  
Cell Nucleus ◽  
Mitotic Cycle ◽  
Cell Formation ◽  
Embryo Sac ◽  
Central Cell ◽  
Egg Cell ◽  
Cell Nuclei ◽  
Cytochemical Study ◽  
Male Gametes ◽  
S Period

The mitotic cycle in the egg cell and physico-chemical state of chromatin in the egg cell and central cell of the tobacco embryo sac were studied. It was revealed that during egg cell formation a change in the mitotic cycle kinetics takes place, it consists in prolongation of the S-period as compared with that of somatic cells and G1 - period as compared with that of male gametes. Egg cell and central cell nuclei differ in chromatin structure. Condensed chromatin dominates in the egg cell nucleus, diffuse chromatin in the central cell nucleus, but both show only weak metabolic activity.

scholarly journals The ultrastructure of the mature embryo sac in the natural tetraploid of red clover (Trifolium pratense L.): that has a very low rate of seed formation

2014 ◽  
Vol 66 (1) ◽  
pp. 13-20 ◽  
Author(s):  
Gönül Algan ◽  
H. Nurhan Bakar
Keyword(s):  
Endoplasmic Reticulum ◽  
Trifolium Pratense ◽  
Embryo Sac ◽  
Red Clover ◽  
Mature Embryo ◽  
Polar Nucleus ◽  
Central Cell ◽  
Egg Cell ◽  
Ultrastructural Organization ◽  
Seed Formation

In this study, ultrastructural organization of cells in the mature embryo sac of natural tetraploid <em>Trifolium pratense</em> L. was investigated. The mature embryo sac of this plant contains an egg cell with two synergids at the micropylar end, and a central cell with two polar nuclei. The ultrastructure of these cells agrees with what is known for most angiosperms studied with the electron microscope. The egg cell is a large and highly vacuolate cell, partially surrounded by a wall. Much of the cytoplasm is located around the nucleus at the chalazal end and there are few numbers of channel-shaped endoplasmic reticulum, mitochondria, plastids and numerous ribosomes distributed throughout the cytoplasm. Unlike the egg cell, much of the cytoplasm in synergid cells is located at micropylar part of the cell and the synergid cytoplasm contains especially, large numbers of rough endoplasmic reticulum, free ribosomes, mitochondria and plastids. The central cell of <em>T. pratense</em> L. contains two large polar nuclei which lie close to the egg apparatus. Each polar nucleus has a single, large, dense nucleolus that contains several nucleolar vacuoles. Much of the central cell cytoplasm consisting of granular and agranular endoplasmic reticulum, mitochondria, plastids, ribosomes, dictyosomes and lipid bodies are placed around polar nuclei.

Calcium Distribution and Accumulation in Ovules of Plumbago Zeylanica

2000 ◽  
Vol 6 (S2) ◽  
pp. 696-697
Author(s):  
Hua Zhu ◽  
Scott D. Russell
Keyword(s):  
Pollen Tube ◽  
Apoptotic Cell ◽  
Embryo Sac ◽  
Flowering Plants ◽  
Cell Type ◽  
Mobile Form ◽  
Plumbago Zeylanica ◽  
Male Gametes ◽  
High Concentrations ◽  
Potassium Pyroantimonate

The embryo sac (ES) of Plumbago zeylanica, unlike most other flowering plants, lacks synergidsthe cell type that usually receives the pollen tube and the male gametes. Normally, synergids store copious amounts of calcium, estimated to exceed 15% by weight; this is believed to attract pollen tubes, which penetrate the ES, and may trigger the release of the sperm cells within one of the two synergids. If high concentrations of calcium are truly required for fertilization, the ES of Plumbago should also contain significant quantities. Synergids in normal flowering plants are preprogrammed for cell death, receiving the contents of the pollen tube directly in their cells, whereas synergid-lacking angiosperms apparently do not have such an apoptotic cell in the ES. Potassium pyroantimonate labeling was used to localize principally loosely-bound calcium, because it is a relatively mobile form of the Ca2+ ion that is available for redistribution during fertilization events.

Embryology of Brassica campestris: the entrance and discharge of the pollen tube in the synergid and the formation of the zygote

1992 ◽  
Vol 70 (8) ◽  
pp. 1577-1590 ◽  
Author(s):  
M. J. Sumner
Keyword(s):  
Endoplasmic Reticulum ◽  
Cell Wall ◽  
Plasma Membrane ◽  
Pollen Tube ◽  
Brassica Campestris ◽  
Periodic Acid ◽  
Outer Integument ◽  
Central Cell ◽  
Egg Cell ◽  
Intense Staining

The postanthesis synergids and zygote of Brassica campestris cv. Candle were examined using techniques of light, fluorescence, and electron microscopy. The pollen tube enters the degenerate synergid by way of the filiform apparatus. A degeneration of one of the two synergids occurs after anthesis and is independent of pollination. The first sign of synergid degeneration is a more intense staining of one of the synergids, followed by a loss of organelle membrane integrity. There is a disappearance of the plasma membrane and dictyosome cisternae; however, profiles of degenerate synergid mitochondria, plastids, and dilated endoplasmic reticulum remain along with dictyosome vesicles that contain periodic acid – thiocarbo-hydrazide – silver proteinate positive substances. The zygote, shortly after fertilization, is reduced in size and lacks the large micropylar vacuole characteristic of the mature unfertilized egg cell. Plastids and mitochondria are concentrated around the centrally located nucleus of the zygote, and dictyosomes, active in vesicle production, are located in the lateral and chalazal regions of the cell, adjacent to the cell wall. The lateral cell walls are periodic acid – Schiff's and Calcofluor positive, while the ampulliform chalazal tip of the cell is weakly periodic acid – Schiff s positive and Calcofluor negative. Microtubules, with the long axis perpendicular to the long axis of the zygote, are abundant in the ampulliform chalazal tip of the cell. Following fertilization the central cell becomes highly vacuolate. There is continuity between the zygote – central cell plasma membrane, the central cell vacuole tonoplast, and membranes of the central cell endoplasmic reticulum. Central cell wall projections, of the transfer cell type, are located in the lateral regions of the megagametophyte adjacent to the developing zygote cell and are positioned adjacent to the region of inner and outer integument starch. Key words: Brassica, ultrastructure, synergid, megagametophyte, pollen tube, zygote.

Ultrastructural observations of the mature megagametophyte and the fertilization in wheat (Triticum aestivum)

1985 ◽  
Vol 63 (2) ◽  
pp. 163-178 ◽  
Author(s):  
Ruilin You ◽  
William A. Jensen
Keyword(s):  
Triticum Aestivum ◽  
Pollen Tube ◽  
Cell Walls ◽  
Embryo Sac ◽  
Mature Embryo ◽  
Central Cell ◽  
The Other ◽  
Egg Cell ◽  
Filiform Apparatus ◽  
Egg Apparatus

The mature embryo sac of wheat contains an egg apparatus composed of an egg cell and two synergids at the micropylar end, a central cell with two large polar nuclei in the middle, and a mass of 20 to 30 antipodals at the chalazal end. A comparison was made of the ultrastructural features of the various cells of the embryo sac. The features included the position of the nucleus and vacuoles, the number, structure, and distribution of organelles, and the extent of the cell walls surrounding each cell. The pollen tube enters one synergid through the filiform apparatus from the micropyle. The penetration and discharge of the pollen tube causes the further degeneration of that synergid, which had already undergone changes before pollination. The second synergid does not change further in appearance following the penetration of the first by the pollen-altered tube. Half an hour after pollination at 20–25 °C, two male nuclei are seen in the cytoplasm of the egg and the central cell. At about 1 h after pollination, one sperm has made contact with the egg nucleus, while the other sperm is fusing with one of the polar nuclei.

scholarly journals Transcriptional repression specifies the central cell for double fertilization

2020 ◽  
Vol 117 (11) ◽  
pp. 6231-6236 ◽  
Author(s):  
Meng-Xia Zhang ◽  
Shan-Shan Zhu ◽  
Yong-Chao Xu ◽  
Ya-Long Guo ◽  
Wei-Cai Yang ◽  
...  
Keyword(s):  
Cell Fate ◽  
Transcriptional Repression ◽  
Female Gametophyte ◽  
Embryo Sac ◽  
Central Cell ◽  
Egg Cell ◽  
Accessory Cell ◽  
Double Fertilization ◽  
Genetic Rescue ◽  
Key Innovation

Double fertilization is a key innovation for the evolutionary success of angiosperms by which the two fertilized female gametes, the egg cell and central cell, generate the embryo and endosperm, respectively. The female gametophyte (embryo sac) enclosed in the sporophyte is derived from a one-celled haploid cell lineage. It undergoes successive events of mitotic divisions, cellularization, and cell specification to give rise to the mature embryo sac, which contains the two female gametes accompanied by two types of accessory cells, namely synergids and antipodals. How the cell fate of the central cell is specified has long been equivocal and is further complicated by the structural diversity of female gametophyte across plant taxa. Here, MADS-box protein AGL80 was verified as a transcriptional repressor that directly suppresses the expression of accessory cell-specific genes to specify the central cell. Further genetic rescue and phylogenetic assay of the AGL80 orthologs revealed a possible conserved mechanism in the Brassicaceae family. Results from this study provide insight into the molecular determination of the second female gamete cell in Brassicaceae.

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