scholarly journals Pollen grain of barley (Hordeum vulgare L.) - pattern of development

2014 ◽  
Vol 58 (3) ◽  
pp. 313-320 ◽  
Author(s):  
Maria Charzyńska ◽  
Nella Lenart
Keyword(s):  
General Pattern ◽  
Generative Cell ◽  
Cell Plate ◽  
Pollen Grain ◽  
Vegetative Nucleus ◽  
Hordeum Vulgare L ◽  
Cell Stage ◽  
Stage Of Development ◽  
Plate Formation ◽  
Microspore Stage

Pollen development in barley follows the general pattern established for other species of <em>Poaceae</em>: 1) microspore division occurs at the vacuolate microspore stage with polarly located nucleus; 2) microspore mitosis is immediately followed by phragmoplast and cell plate formation; 3) in consequence or unequal microspore division, the generative cell, at first attached to the pollen wall, is separated from the vegetative cell by a callosic wall; 4) during the postmitotic two-cell stage of development, the vegetative nucleus migrates to the aperture pole and is followed by the generative cell that is detached and free of callose wall. In this position the generative cell divides into two sperm cells. These data do not confirm the interpretation of pollen grain development in barley given by Cass and Karas in Can. J. Bot. 53: 1051-1062, 1975.

Development of sperm cells in barley

1975 ◽  
Vol 53 (10) ◽  
pp. 1051-1062 ◽  
Author(s):  
David D. Cass ◽  
Ilana Karas
Keyword(s):  
Cell Membrane ◽  
Vegetative Cell ◽  
Generative Cell ◽  
Pollen Grains ◽  
Complete Separation ◽  
Pollen Wall ◽  
Vegetative Nucleus ◽  
Sperm Cells ◽  
Subsequent Stage ◽  
Microspore Stage

Ultrastructural events in barley sperm development were examined from the uninucleate microspore stage to establishment of two mature sperm cells in pollen grains. Microspore mitosis produces a vegetative nucleus and a naked generative cell, both embedded in vegetative cell cytoplasm. The generative cell membrane is enclosed by vegetative cell membrane. The generative cell, at first apparently unattached, becomes attached to the pollen wall and acquires a cell wall by centripetal vesicle accumulation. Wall formation may be complete at the time of generative cell karyokinesis; karyokinesis occurs while the generative cell is attached to the pollen wall. Cytokinesis of the generative cell is delayed. The subsequent stage is a binucleate, attached generative cell with a wall. Generative cell cytokinesis appears to involve formation of a partition between the two sperm nuclei. Eventual complete separation of the sperm cells occurs only after the two-celled derivative of the generative cell detaches from the pollen wall. Final stages in sperm cell separation are considered to result from degradation of the partitioning and surrounding wall, not from furrowing of a naked binucleate generative cell according to previous suggestions. Mature plastids were not observed in the generative cell or the sperms.

The Formation of the Generative Cell in the Pollen Grain of Endymion Non-Scriptus (L)

1968 ◽  
Vol 3 (4) ◽  
pp. 573-578
Author(s):  
R. E. ANGOLD
Keyword(s):  
Cell Wall ◽  
Somatic Cells ◽  
Generative Cell ◽  
Cell Plate ◽  
Pollen Grain ◽  
Generative Nucleus ◽  
A Cell ◽  
Generative Nuclei

The generative cell wall in the pollen grain of Endymion non-scriptus is formed, as in somatic cells, from a cell plate between the vegetative and generative nuclei. This wall curves around the generative nucleus, and fuses with the intine to enclose the generative cell. The generative cell is subsequently freed from the intine by the constriction of the generative cell wall between the generative nucleus and the intine.

scholarly journals Pollen ultrastructure in anther cultures of Datura innoxia. III. Incomplete microspore division

1976 ◽  
Vol 22 (3) ◽  
pp. 493-501
Author(s):  
J.M. Dunwell ◽  
N. Sunderland
Keyword(s):  
Mitotic Spindle ◽  
Generative Cell ◽  
Marked Change ◽  
Pollen Grain ◽  
Wall Material ◽  
Pollen Embryogenesis ◽  
Vegetative Nucleus ◽  
Central Position ◽  
Datura Innoxia ◽  
Anther Cultures

During the microspore division in Datura innoxia, the mitotic spindle is oriented in planes both perpendicular (PE) and oblique (OB) to the spore wall against which the nucleus is situated. However, irrespective of polarity, the usual type of hemispherical wall is laid down at cytokinesis and isolates the generative cell from the rest of the pollen grain (type A). In PE spores the vegetative nucleus initially occupies a central position in the pollen grain, whereas in OB spores the vegetative nucleus lies at the periphery of the grain close to the generative cell. In anther cultures initiated just before the microspore division is due to take place, no marked change can be observed in either orientation or symmetry of the mitotic spindle when the spores divide. In some, however, cytokinesis is disrupted and deposition of the hemispherical wall arrested. In the absence of a complete wall, differentiation of the generative cell cannot take place and binucleate pollen grains are formed having 2 vegetative-type nuclei (type B). The 2 nuclei in the B pollens are always situated against the pollen-grain wall, suggesting that the disruption phenomenon is related to the OB spores. The incomplete wall always makes contact with the intine on the intine-side of the spindle. Wall material may be represented merely as short stubs projecting out from the intine into the cytoplasm, in which event the 2 nuclei lie close to each other and are separated by only a narrow zone of cytoplasm. In other grains the wall is partially developed between the nuclei and terminates at varying distances from the tonoplast; in these, the nuclei are separated by a wider zone of cytoplasm. The significance of these binucleate grains in pollen embryogenesis is discussed.

Synchronous Pollen Mitosis and the Formation of the Generative Cell in Massulate Orchids

1968 ◽  
Vol 3 (3) ◽  
pp. 457-466
Author(s):  
J. HESLOP-HARRISON
Keyword(s):  
Generative Cell ◽  
Spherical Shape ◽  
Cell Plate ◽  
Spore Wall ◽  
Mitotic Division ◽  
Vegetative Nucleus ◽  
Pollen Mitosis ◽  
Callose Wall ◽  
Freely Suspended ◽  
Radial Spread

In orchd species forming microspores in aggregates, the pollen mitotic division occurs synchronously in all cells of each massula, as do the earlier meiotic divisions. The synchroneity can be traced to the persistence of cytoplasmic connexions between the cells, from the meiotic prophiase until pollen maturation. The mitosis giving the generative nucleus is asymmetrical, and the spindle is truncated at one side, where the microtubules converge towards an amorphuos polar structure lying against the spore wall. The cell plate formed after pollen mitosis is hemispherical, and its curved growth is related to a radial spread of the microtubules of the phragmoplast after the telophase of the division. The plate itself, and the wall derived from it, is identifiable as callose by its fluorescence properties. In the later development of the gametophyte, growth of the callose wall continues until the originally hemispherical generative cell becomes separated from the spore wall. The cell then assumes a spherical shape and moves to the vicinity of the vegetative nucleus, where it remains freely suspended, bathed in the cytoplasm of the vegetative cell but insulated from it by the completely ensheathing callose wall.

Fine Structure Study of Pollen Development in Haemanthus katherinae Baker

1971 ◽  
Vol 8 (2) ◽  
pp. 289-301
Author(s):  
JEAN M. SANGER ◽  
W. T. JACKSON
Keyword(s):  
Fine Structure ◽  
Vegetative Cell ◽  
Daughter Nucleus ◽  
Generative Cell ◽  
Pollen Grains ◽  
Cell Plate ◽  
Structure Study ◽  
Pollen Grain ◽  
Pollen Wall ◽  
Fibrillar Material

When microspores of the African blood lily divide, they form pollen grains which consist of 2 cells of unequal size. This is accomplished when the microspore nucleus is displaced from the centre of the grain prior to division. The displacement is always towards the side of the grain opposite the furrow, and large vacuoles form in the cytoplasm between the furrow and the nucleus. During cell division the cell plate curves around one daughter nucleus and fuses with the pollen wall to enclose the generative cell. The cell-plate attachment always occurs with the wall that is opposite the furrow of the grain. Most of the microspore's organelles become incorporated in the larger vegetative cell, whereas the generative cell has few, if any, plastids and only a small number of other organelles. The wall around the generative cell is composed of finely fibrillar material enclosed within 2 unit membranes. The generative cell eventually becomes detached from the pollen wall, becomes spheroidal, and moves to a position near the centre of the pollen grain. At the same time, the large vacuoles disappear from the vegetative cell and the number of organelles increases substantially.

Dynamics and roles of phragmoplast microfilaments in cell plate formation during cytokinesis of tobacco BY-2 cells

2009 ◽  
Vol 54 (12) ◽  
pp. 2051-2061 ◽  
Author(s):  
Yan Zhang ◽  
WenJie Zhang ◽  
Frantisek Baluska ◽  
Diedrik Menzel ◽  
HaiYun Ren
Keyword(s):  
Cell Plate ◽  
Cell Plate Formation ◽  
Plate Formation

Effect of GnRH injection timing in the production of pronuclear-stage zygotes used for DNA microinjection

Zygote ◽  
2004 ◽  
Vol 12 (3) ◽  
pp. 257-261 ◽  
Author(s):  
Hernan Baldassarre ◽  
Bin Wang ◽  
Melanie Gauthier ◽  
Nathalie Neveu ◽  
Anthoula Lazaris ◽  
...  
Keyword(s):  
Medroxyprogesterone Acetate ◽  
Treatment Protocol ◽  
Hormonal Treatment ◽  
Injection Timing ◽  
Chi Square ◽  
Cell Stage ◽  
Embryo Recovery ◽  
Stage Of Development ◽  
Production Programme ◽  
Dna Microinjection

This study was aimed at developing a hormonal treatment protocol in order to optimize the proportion of pronuclear-stage embryos to be used for DNA microinjection in a goat transgenic founder production programme. A total of 46 adult BELE® and 47 adult standard goats (1–5 years old) were used as donors and recipients, respectively. They were heat-synchronized using intravaginal sponges containing 60 mg medroxyprogesterone acetate for 10 days with an injection of 125 μg cloprostenol on the morning of the eighth day. Recipients were injected with 400 IU eCG at the time of sponge removal while donors received a total of 133 mg NIH-FSH-P1 (Folltropin-V) given twice daily in decreasing doses over 3 days starting 48 h before sponge removal. Ovulation was induced in donors by injecting 100 μg of GnRH at 24 h (GnRH24) or 36 h (GnRH36) after sponge removal. Embryo recovery was performed by oviduct flushing following a standard mid-ventral laparotomy procedure. The proportion of embryos in the pronuclear stage of development was higher in the GnRH36 group (90% vs 34%, p<0.01). Embryos were microinjected with a DNA expression cassette followed by transfer to the oviduct of synchronized recipients. A higher, yet not statistically significant, pregnancy rate was found in the recipients transferred with pronuclear-stage embryos compared with those transferred with 2-cell-stage embryos (64% vs 37%, chi-square p=0.06). One transgenic female founder was produced from the group of recipients transferred with pronuclear-stage microinjected embryos.

scholarly journals Diversification of sterol methyltransferase enzymes in plants and a role for β-sitosterol in oriented cell plate formation and polarized growth

2015 ◽  
Vol 84 (5) ◽  
pp. 860-874 ◽  
Author(s):  
Masatoshi Nakamoto ◽  
Anne-Catherine Schmit ◽  
Dimitri Heintz ◽  
Hubert Schaller ◽  
Daisaku Ohta
Keyword(s):  
Cell Plate ◽  
Polarized Growth ◽  
Cell Plate Formation ◽  
Plate Formation ◽  
Sterol Methyltransferase

The early development of haploid and aneuploid parthenogenetic embryos

Development ◽  
1975 ◽  
Vol 34 (3) ◽  
pp. 645-655
Author(s):  
Matthew H. Kaufman ◽  
Leo Sachs
Keyword(s):  
Early Development ◽  
Polar Body ◽  
Chromosome Counts ◽  
Cell Stage ◽  
Haploid Chromosome Number ◽  
Stage Of Development ◽  
Morula Stage ◽  
Second Polar Body ◽  
Similar Development ◽  
Parthenogenetic Embryos

The early development of parthenogenetically activated oocytes has been studied in C57BL × CBA-T6T6 (F1T6) translocation heterozygote mice and C57BL × CBA-LAC (F1LAC) mice. All F1T6 oocytes had either a quadrivalent or a univalent-trivalent configuration at meiosis I; no such chromosome configurations were observed in the F1LAC oocytes. At ovulation 36·5 % of the F1T6 oocytes had 19 or 21 chromosomes, whereas 97 % of the F1LAC had the normal haploid chromosome number of 20. After parthenogenetic activation, chromosome counts at metaphase of the first cleavage mitosis were made of the eggs with a single pronucleus following extrusion of the second polar body. These activated eggs had similar frequencies of 19, 20 and 21 chromosomes as had the oocytes at ovulation. The activated 1-cell eggs were transferred to the oviducts of pseudopregnant recipients and the embryos recovered 3 days later. At this stage of development, most of the F1T6 embryos with 19 chromosomes were no longer found, but the frequency of 21-chromosome embryos was similar to the frequency of 21-chromosome oocytes and activated eggs. There was a similar mean number of cells in the embryos with 20 and 21 chromosomes. The results indicate that nearly all the embryos with 19 chromosomes failed to develop, probably beyond the 2-cell stage, whereas oocytes with 21 chromosomes had a similar development to oocytes with 20 chromosomes up to the morula stage.

Sign in / Sign up

Export Citation Format

Share Document