Actin During Pollen Germination

1986 ◽  
Vol 86 (1) ◽  
pp. 1-8
Author(s):  
J. HESLOP-HARRISON ◽  
Y. HESLOP-HARRISON ◽  
M. CRESTI ◽  
A. TIEZZI ◽  
F. CIAMPOLINI
Keyword(s):  
Medium Release ◽  
Pollen Tube ◽  
Vegetative Cell ◽  
Pollen Germination ◽  
Pollen Grain ◽  
Actin Microfilaments ◽  
Vegetative Cells ◽  
Stage Of Development ◽  
Angiosperm Species

The cytoplasm of the vegetative cell of the ungerminated pollen grain of Endymton non-scriplus and other angiosperm species contains numerous fusiform bodies sometimes exceeding 15μm in length and 2.5 μm in width, which bind fluorescent-labelled phalloidin and are likely therefore to constitute a storage form of actin. The bodies are dispersed during the activation of the pollen, being replaced by aggregates of slender phalloidin-binding fibrils, which converge towards the germination apertures and are present in the emerging pollen tube. The storage bodies appear to be homologous with crystalline-fibrillar structures, shown in an earlier paper to be abundantly present in the vegetative cells of Nicotiana pollen. These are composed of massive aggregates of linearly disposed units with individual widths of 4–7 nm, probably to be interpreted as actin microfilaments. Vegetative-cell protoplasts from mature but ungerminated pollen disrupted in osmotically balancing medium release extended phalloidin-binding fibrils of a kind not observed in the intact grain. It is suggested that these are derived by the rapid dissociation of the compact actin storage bodies present in the vegetative cell at this stage of development.

scholarly journals In vitro germination and viability of pea pollen grains after application of organic nano-fertilizers

2017 ◽  
Vol 32 (1) ◽  
pp. 61-65 ◽  
Author(s):  
Natalia Georgieva ◽  
Ivelina Nikolova ◽  
Valentin Kosev ◽  
Yordanka Naydenova
Keyword(s):  
Pollen Tube ◽  
Pollen Germination ◽  
Culture Media ◽  
Pollen Viability ◽  
Pollen Grains ◽  
Pollen Grain ◽  
In Vitro Germination ◽  
Pisum Sativum L ◽  
Pollen Tube Elongation

The objective of this study was to evaluate the influence of two organic nanofertilizers, Lithovit and Nagro, on in vitro germination, pollen tube elongation and pollen grain viability of Pisum sativum L cv. Pleven 4. The effect of their application was high and exceeded data for the untreated control (44.2 and 47.23 % regarding pollen germination and pollen tube elongation, respectively), as well as the effect of the control organic algal fertilizer Biofa (17.5 and 27.9 %, respectively). Pollen grains were inoculated in four culture media. A medium containing 15% sucrose and 1% agar had the most stimulating impact on pea pollen grains. Pollen viability, evaluated by staining with 1% carmine, was within limits of 74.72-87.97%. The highest viability of pollen grains was demonstrated after the application of Nagro organic nano-fertlizer.

scholarly journals Intercellular communication in Arabidopsis thaliana pollen discovered via AHG3 transcript movement from the vegetative cell to sperm

2015 ◽  
Vol 112 (43) ◽  
pp. 13378-13383 ◽  
Author(s):  
Hua Jiang ◽  
Jun Yi ◽  
Leonor C. Boavida ◽  
Yuan Chen ◽  
Jörg D. Becker ◽  
...  
Keyword(s):  
Arabidopsis Thaliana ◽  
Pollen Tube ◽  
Intercellular Communication ◽  
Protein Phosphatase ◽  
Pollen Tube Growth ◽  
Vegetative Cell ◽  
Male Gametophyte ◽  
Pollen Grain ◽  
Sperm Cells ◽  
Coding Region

An Arabidopsis pollen grain (male gametophyte) consists of three cells: the vegetative cell, which forms the pollen tube, and two sperm cells enclosed within the vegetative cell. It is still unclear if there is intercellular communication between the vegetative cell and the sperm cells. Here we show that ABA-hypersensitive germination3 (AHG3), encoding a protein phosphatase, is specifically transcribed in the vegetative cell but predominantly translated in sperm cells. We used a series of deletion constructs and promoter exchanges to document transport of AHG3 transcripts from the vegetative cell to sperm and showed that their transport requires sequences in both the 5′ UTR and the coding region. Thus, in addition its known role in transporting sperm during pollen tube growth, the vegetative cell also contributes transcripts to the sperm cells.

scholarly journals Messenger RNas : their utilization and degradation during pollen germination and tube growth

2014 ◽  
Vol 50 (1-2) ◽  
pp. 13-20 ◽  
Author(s):  
Joseph P. Mascarenhas ◽  
Joann Mermelstein
Keyword(s):  
Protein Synthesis ◽  
Pollen Tube ◽  
Pollen Tube Growth ◽  
Pollen Germination ◽  
Actinomycin D ◽  
Electrophoretic Analysis ◽  
Pollen Grain ◽  
Tube Growth ◽  
Messenger Rnas ◽  
Pollen Maturation

During pollen germination and tube growth at least 230 new proteins are synthesized, as determined by <sup>35</sup>S-methionime labeling and two dimensional gel electrophoretic analysis of the labeled proteins. The same number and pattern of protein spots is seen whether or not actinomycin D is included in the, medium, indicating that the mRNAs present in the unger-minated pollen grain and those newly synthesized code for the same proteins. The genetic program during at least the latter part of pollen maturation prior to anthesis and that during pollen germination and tube growth thus appears to be similar if not identical. During the first hour of pollen tube growth about 500/0 of the protein synthesis that occurs utilizes previously synthesized mRNAs. The remaining 50% occurs on newly made mRNAs. The ungerminated mature pollen grain contains 196 pg of RNA and approximately 6 X 10<sup>6</sup> molecules of poly(A)+ RNA, i.e. mRNAs. The rate of protein synthesis corrected for internal pool changes in the labeled amino acid used (<sup>3</sup>H-leucine) is highest during the first 15 min of pollen tube growth. The rate decreases rapidly thereafter for the next 45 min. Concurrent with the reduction in rate of protein synthesis there is a reduction in the poly(A) content of the pollen RNA and in the amount of poly(A) per pollen, grain. The total RNA per pollen grain, however, appears not to change during this period.

scholarly journals Formation and development of sperms in angiosperms

2014 ◽  
Vol 50 (1-2) ◽  
pp. 99-101 ◽  
Author(s):  
S. Tatintseva
Keyword(s):  
Pollen Tube ◽  
Delivery System ◽  
Pollen Grain ◽  
Female Gamete ◽  
Sperm Cells ◽  
Angiosperm Species ◽  
Different Levels ◽  
Full Maturity

Spermiogelnesis has been studied in a large number of Angiosperm species characterizing different levels of phylogenetic system. The formation and development of male gamets can be described as formation of sperm cells that undergo ontogenesis which stimulates changes up to full maturity of the pollen grain. The process of ontogenesis is aimed at creating a suitable delivery system by the pollen tube to a female gamete.

Stigma, pollen tube transmitting tract, and epidermal micromorphology of the style of Sarracenia purpurea (Sarraceniaceae)

Botany ◽  
2020 ◽  
Vol 98 (4) ◽  
pp. 209-229
Author(s):  
Jinyan Guo ◽  
Chad T. Halson
Keyword(s):  
Pollen Tube ◽  
Pollen Germination ◽  
Visual Cues ◽  
Pollen Grain ◽  
Sarracenia Purpurea ◽  
Transmitting Tract ◽  
Conducting Tissue ◽  
Secretory Glands ◽  
Semi Solid ◽  
Photosynthetic Activities

Entomophilous flowers of the genus Sarracenia have a unique umbrella-shaped style, which consists of a broadened and flattened umbrella canopy and a thin cylindrical umbrella stalk. Anatomical and micromorphological features of the style of Sarracenia purpurea L. were studied using light microscopy and scanning electron microscopy. This study found that the pollen tube transmitting tracts (PTTTs) start as a semi-solid canal filled with endotrophic conducting tissue, and run from the peripheral to the center of the canopy where the PTTT becomes a hollow canal supported by ectotrophic conducting tissue. The presence of stomata on the epidermis of the canopy and chloroplasts in its ground parenchyma indicate photosynthetic activities. Convex epidermal cells with intense cuticular striations on the canopy that are similar yet different from those on various regions of the sepals and petals indicate that it may provide contrasting visual cues for pollinators. Multicellular secretory glands and trichomes, which may provide olfactory cues and tactical cues respectively, are also found on the canopy. Thus, the stylar umbrella not only serves as a region for pollen grain capture, pollen germination, and pollen tube transmission but may also play an important role during pollinator–flower interactions.

scholarly journals Hyperoside promotes pollen tube growth by regulating the depolymerization effect of actin-depolymerizing factor 1 on microfilaments in okra

2021 ◽  
Vol 8 (1) ◽  
Author(s):  
Biying Dong ◽  
Qing Yang ◽  
Zhihua Song ◽  
Lili Niu ◽  
Hongyan Cao ◽  
...  
Keyword(s):  
Pollen Tube ◽  
Pollen Tube Growth ◽  
Pollen Germination ◽  
Pollen Tubes ◽  
Tube Growth ◽  
Actin Depolymerizing Factor ◽  
Specific Mechanism ◽  
Promoting Effect ◽  
New Research

AbstractMature pollen germinates rapidly on the stigma, extending its pollen tube to deliver sperm cells to the ovule for fertilization. The success of this process is an important factor that limits output. The flavonoid content increased significantly during pollen germination and pollen tube growth, which suggests it may play an important role in these processes. However, the specific mechanism of this involvement has been little researched. Our previous research found that hyperoside can prolong the flowering period of Abelmoschus esculentus (okra), but its specific mechanism is still unclear. Therefore, in this study, we focused on the effect of hyperoside in regulating the actin-depolymerizing factor (ADF), which further affects the germination and growth of pollen. We found that hyperoside can prolong the effective pollination period of okra by 2–3-fold and promote the growth of pollen tubes in the style. Then, we used Nicotiana benthamiana cells as a research system and found that hyperoside accelerates the depolymerization of intercellular microfilaments. Hyperoside can promote pollen germination and pollen tube elongation in vitro. Moreover, AeADF1 was identified out of all AeADF genes as being highly expressed in pollen tubes in response to hyperoside. In addition, hyperoside promoted AeADF1-mediated microfilament dissipation according to microfilament severing experiments in vitro. In the pollen tube, the gene expression of AeADF1 was reduced to 1/5 by oligonucleotide transfection. The decrease in the expression level of AeADF1 partially reduced the promoting effect of hyperoside on pollen germination and pollen tube growth. This research provides new research directions for flavonoids in reproductive development.

The growth of the pollen tube wall in Oenothera organensis

1975 ◽  
Vol 18 (3) ◽  
pp. 519-532
Author(s):  
H.G. Dickinson ◽  
J. Lawson
Keyword(s):  
Pollen Tube ◽  
Tube Wall ◽  
Wall Material ◽  
Fibrillar Material ◽  
Stage Of Development ◽  
Large Numbers ◽  
Membrane Bound ◽  
Pollen Tube Wall ◽  
Different Sources ◽  
Dictyosome Vesicles

The growth of the pollen tube wall of Oenothera is effected by the expulsion of fibrillar material from the cytoplasm into the developing wall. This material may also be seen in the cytoplasm, contained in membrane-bound vesicles. It is not clear how the content of the vesicles is discharged, but it appears not to involve the participation of microtubules. The source of the cytoplasmic fibrillar bodies depends upon the stage of development of the pollen tube. The earilest growth is derived from the inclusion into the wall of vesicles containing pre-formed materials present in the grain on pollination. During the next stage of growth the wall is derived from the content of double-membraned inclusions also present in the pollen. The content of the former vesicles is not so similar to the wall as the latter, but intermediates between the 2 types of vesicle may be seen in the cytoplasm, indicating that the former are formed from the latter. Most of the tube wall is derived from the products of dictyosomes in the pollen grain or tube. These dicytosomes are few in number and they must be exceedingly active. This, and the observation that dictyosome vesicles are frequently associated with banked complexes of mitochondria, indicates that some steps in the metabolism of the vesicular content, perhaps phosphorylation, take place distant from the dicytosomes. These different sources of fibrillar material presumably permit the rapid starting of tube growth, without any attendant metabolism. However, it would be impossible to include enough pre-formed wall material in the grain to enable the full growth of the tube, so once started, it seems that the tube then relies on the elaboration of simple reserves for the contruction of its wall. These reserves are likely to be held in the pollen, and may be the large numbers of starch grains characteristic of the pollen cytoplasm.

In Vitro Germination of Eucalyptus Pollen: Response to Variation in Boric Acid and Sucrose

1989 ◽  
Vol 37 (5) ◽  
pp. 429 ◽  
Author(s):  
BM Potts ◽  
JB Marsden-Smedley
Keyword(s):  
Pollen Tube ◽  
Boric Acid ◽  
Pollen Tube Growth ◽  
Pollen Germination ◽  
Sucrose Concentration ◽  
Response Surfaces ◽  
Tube Growth ◽  
Pollen Competition

The effect of boric acid (0-450 ppm) and sucrose (0-40%) on pollen germination and pollen tube growth in Eucalyptus globulus, E. morrisbyi, E. ovata and E. tirnigera was examined in vitro. Over the con- centrations tested, sucrose had by far the largest effect upon both pollen germination and tube lengths. The optimum sucrose concentration for pollen germination (30%) and pollen tube growth (20%) differed markedly with very little (<lo%) germination occurring in the absence of sucrose. The interaction of sucrose and boric acid was significant. However, in general both pollen germination and pollen tube growth were increased by the addition of up to 100 ppm boric acid, but above this level the response plateauxed. The four species differed significantly in their pattern of response to both boric acid and sucrose and the predicted optima derived from analysis of response surfaces differed between species. The predicted sucrose concentration for optimal germination and growth of E. urnigera pollen was consistently less than the other species and in terms of the optimal level of boric acid for pollen tube growth species can be ranked in the order E. globulus > E. ovata > E. morrisbyi = E. urnigera. Pollen germination and tube growth of all four species on a medium comprising 20% sucrose and 200 ppm boric acid would not differ significantly from the observed maximum response of each species and this could suffice as a generalised medium. However, if only percentage germination is to be assessed 30% sucrose would be preferable. It is argued that subtle interspecific differences in optimal in vitro con- ditions for pollen germination and pollen tube growth are likely to reflect differences in pollen physiology which in vivo may have important implications for the success of hybridisation where pollen competition occurs.

scholarly journals Pollen tube incompatibility reaction on the stigma in selfpollinated Sinapis alba L.

2014 ◽  
Vol 65 (1-2) ◽  
pp. 101-105 ◽  
Author(s):  
Renata Śnieżko ◽  
Krystyna Winiarczyk
Keyword(s):  
Pollen Tube ◽  
Pollen Tube Growth ◽  
Pollen Grains ◽  
Pollen Tubes ◽  
Sinapis Alba ◽  
Pollen Grain ◽  
Tube Growth ◽  
Sinapis Alba L ◽  
Growth Changes ◽  
Incompatibility Reaction

After selfpollination of <em>Sinapis alba</em> L. pollen tubes growth is inhibited on the stigma. The pollen grains germinate 3-4 hours after pollination. The pollen give rise to one or more pollen tubes. They grow along the papillae. In the place of contact between the papilla and pollen tube the pellicula is digested. Then the direction of pollen tube growth changes completely. Pollen tubes grow back on the exine of their own pollen grain, or turn into the air. The pollen tubes growth was inhibited in 6-8 hours after selfpollination. After crosspollination usually there is no incompatibility reaction.

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