A PARTHENOGENESIS allele from apomictic dandelion can induce egg cell division without fertilization in lettuce

2022 ◽  
Author(s):  
Charles J. Underwood ◽  
Kitty Vijverberg ◽  
Diana Rigola ◽  
Shunsuke Okamoto ◽  
Carla Oplaat ◽  
...  
Keyword(s):  
Cell Division ◽  
Egg Cell

scholarly journals EMBRYO DEVELOPMENT AND ENDOGENOUS NUTRIENT ABSORBTION OF SEA SILVER POMPANO FISH LARVAE FROM NATURAL SPAWN OF BROODSTSOCK, Trachinotus blocii, (LACEPEDE)

2015 ◽  
Vol 7 (1) ◽  
Author(s):  
Tony Setia Dharma
Keyword(s):  
Cell Division ◽  
Embryo Development ◽  
Normal Development ◽  
Fish Larvae ◽  
Yolk Sac ◽  
Egg Cell ◽  
Total Length ◽  
Absorption Pattern ◽  
Newly Hatched Larvae ◽  
Fertilized Egg

<p><em>Silver pompano is a prospective high value commodity to be developed in mariculture. The aims of this research were to understand the development of embryo and absorption pattern of endogenous nutrient at the time of changing from using endogenous to exogenous nutrient. This research was conducted in Institute for Mariculture Research and Development, Gondol, Singaraja, Bali using fertilized eggs which were stocked in concrete tanks 3 m<sup>3</sup>, filled with 2 m<sup>3 </sup>of seawater, in a density of 25 eggs/l. Temperature at the time of hatching was 28-30<sup>o</sup>C. The observation of embryo development and its morphology was performed after hatching by collecting larvae as many as 10. Parameters measured were total length of larvae (TL), yolk sac volume (VK), oil globule volume (VM) and larvae development. The results showed that embryo of silver pompano had a normal development, consisted of several phases i.e., fertilized egg, cell division, neurola, gastrula, complete embryo and hatching as larvae. Newly hatched larvae had endogenous nutrient as yolk sac and oil globule with volume of 2.27.10<sup>-1</sup> mm<sup>3</sup> ± 0.06 and 5.57.10<sup>-1</sup> mm<sup>3</sup> ± 0.02, respectively. Yolk sac was completely absorbed after 35:30 to 46:30 hours and oil globule after 52:30 to 64:30 hours. Initial feeding was given when yolk sac was completely absorbed but before oil globule was completely absorbed. The average total length of larvae was 2.40 ± 0.10 mm.</em></p> <p><em> </em></p> <strong><em>Keywords:</em></strong><em> embryo, larvae, absorption, yolk sac, silver pampano</em>

EMBRYO DEVELOPMENT AND ENDOGENOUS NUTRIENT ABSORBTION OF SEA SILVER POMPANO FISH LARVAE FROM NATURAL SPAWN OF BROODSTSOCK, Trachinotus blocii, (LACEPEDE)

2015 ◽  
Vol 7 (1) ◽  
Author(s):  
Tony Setia Dharma
Keyword(s):  
Cell Division ◽  
Embryo Development ◽  
Normal Development ◽  
Fish Larvae ◽  
Yolk Sac ◽  
Egg Cell ◽  
Total Length ◽  
Absorption Pattern ◽  
Newly Hatched Larvae ◽  
Fertilized Egg

Silver pompano is a prospective high value commodity to be developed in mariculture. The aims of this research were to understand the development of embryo and absorption pattern of endogenous nutrient at the time of changing from using endogenous to exogenous nutrient. This research was conducted in Institute for Mariculture Research and Development, Gondol, Singaraja, Bali using fertilized eggs which were stocked in concrete tanks 3 m3, filled with 2 m3 of seawater, in a density of 25 eggs/l. Temperature at the time of hatching was 28-30oC. The observation of embryo development and its morphology was performed after hatching by collecting larvae as many as 10. Parameters measured were total length of larvae (TL), yolk sac volume (VK), oil globule volume (VM) and larvae development. The results showed that embryo of silver pompano had a normal development, consisted of several phases i.e., fertilized egg, cell division, neurola, gastrula, complete embryo and hatching as larvae. Newly hatched larvae had endogenous nutrient as yolk sac and oil globule with volume of 2.27.10-1 mm3 ± 0.06 and 5.57.10-1 mm3 ± 0.02, respectively. Yolk sac was completely absorbed after 35:30 to 46:30 hours and oil globule after 52:30 to 64:30 hours. Initial feeding was given when yolk sac was completely absorbed but before oil globule was completely absorbed. The average total length of larvae was 2.40 ± 0.10 mm. Keywords: embryo, larvae, absorption, yolk sac, silver pampano

scholarly journals Cytoskeleton dynamics control the first asymmetric cell division in Arabidopsis zygote

2016 ◽  
Vol 113 (49) ◽  
pp. 14157-14162 ◽  
Author(s):  
Yusuke Kimata ◽  
Takumi Higaki ◽  
Tomokazu Kawashima ◽  
Daisuke Kurihara ◽  
Yoshikatsu Sato ◽  
...  
Keyword(s):  
Cell Division ◽  
Asymmetric Cell Division ◽  
Imaging System ◽  
Major Elements ◽  
Flowering Plants ◽  
Egg Cell ◽  
Apical Region ◽  
Apical Direction ◽  
Multicellular Organisms ◽  
Cytoskeleton Dynamics

The asymmetric cell division of the zygote is the initial and crucial developmental step in most multicellular organisms. In flowering plants, whether zygote polarity is inherited from the preexisting organization in the egg cell or reestablished after fertilization has remained elusive. How dynamically the intracellular organization is generated during zygote polarization is also unknown. Here, we used a live-cell imaging system with Arabidopsis zygotes to visualize the dynamics of the major elements of the cytoskeleton, microtubules (MTs), and actin filaments (F-actins), during the entire process of zygote polarization. By combining image analysis and pharmacological experiments using specific inhibitors of the cytoskeleton, we found features related to zygote polarization. The preexisting alignment of MTs and F-actin in the egg cell is lost on fertilization. Then, MTs organize into a transverse ring defining the zygote subapical region and driving cell outgrowth in the apical direction. F-actin forms an apical cap and longitudinal arrays and is required to position the nucleus to the apical region of the zygote, setting the plane of the first asymmetrical division. Our findings show that, in flowering plants, the preexisting cytoskeletal patterns in the egg cell are lost on fertilization and that the zygote reorients the cytoskeletons to perform directional cell elongation and polar nuclear migration.

The Ultrastructure of the Nuclear Events of Binary Fission in Paramecium bursaria and the Effects of Colchicine on Cell Division

1974 ◽  
Vol 32 ◽  
pp. 276-277
Author(s):  
L. M. Lewis
Keyword(s):  
Cell Division ◽  
Nuclear Envelope ◽  
Condensed Chromatin ◽  
Binary Fission ◽  
Paramecium Bursaria ◽  
Nuclear Events ◽  
Division Axis

The effects of colchicine on extranuclear microtubules associated with the macronucleus of Paramecium bursaria were studied to determine the possible role that these microtubules play in controlling the shape of the macronucleus. In the course of this study, the ultrastructure of the nuclear events of binary fission in control cells was also studied.During interphase in control cells, the micronucleus contains randomly distributed clumps of condensed chromatin and microtubular fragments. Throughout mitosis the nuclear envelope remains intact. During micronuclear prophase, cup-shaped microfilamentous structures appear that are filled with condensing chromatin. Microtubules are also present and are parallel to the division axis.

Stimulated Virus Production in Vinblastine and Cytochalasin-Induced Multinucleate Cells

1970 ◽  
Vol 28 ◽  
pp. 186-187
Author(s):  
Krishan Awtar
Keyword(s):  
Cell Division ◽  
Normal Cell ◽  
Virus Production ◽  
Multinucleate Cells ◽  
Daughter Cells ◽  
Cell Divisions ◽  
Nuclear Membranes ◽  
Division 2 ◽  
Vinblastine Sulfate

Exposure of cells to low sublethal but mitosis-arresting doses of vinblastine sulfate (Velban) results in the initial arrest of cells in mitosis followed by their subsequent return to an “interphase“-like stage. A large number of these cells reform their nuclear membranes and form large multimicronucleated cells, some containing as many as 25 or more micronuclei (1). Formation of large multinucleate cells is also caused by cytochalasin, by causing the fusion of daughter cells at the end of an otherwise .normal cell division (2). By the repetition of this process through subsequent cell divisions, large cells with 6 or more nuclei are formed.

Immunogold and immunoblot studies on a cell surface protein found in primary mesenchyme cells and in the cortical secretory vesicles of the sea urchin egg

1987 ◽  
Vol 45 ◽  
pp. 832-833
Author(s):  
G.L. Decker ◽  
M.C. Valdizan
Keyword(s):  
Cell Surface ◽  
Sea Urchin ◽  
Surface Protein ◽  
Egg Cell ◽  
Secretory Vesicles ◽  
Cell Surface Protein ◽  
Surface Complexes ◽  
Mesenchyme Cells ◽  
Lowicryl K4m ◽  
Primary Mesenchyme Cells

A monoclonal antibody designated MAb 1223 has been used to show that primary mesenchyme cells of the sea urchin embryo express a 130-kDa cell surface protein that may be directly involved in Ca2+ uptake required for growth of skeletal spicules. Other studies from this laboratory have shown that the 1223 antigen, although in relatively low abundance, is also expressed on the cell surfaces of unfertilized eggs and on the majority of blastomeres formed prior to differentiation of the primary mesenchyme cells.We have studied the distribution of 1223 antigen in S. purpuratus eggs and embryos and in isolated egg cell surface complexes that contain the cortical secretory vesicles. Specimens were fixed in 1.0% paraformaldehyde and 1.0% glutaraldehyde and embedded in Lowicryl K4M as previously reported. Colloidal gold (8nm diameter) was prepared by the method of Mulpfordt.

Confocal microscopy of the cytoskeleton in living plant cells following microinjection of fluorescent probes

1993 ◽  
Vol 51 ◽  
pp. 130-131
Author(s):  
Ann Cleary
Keyword(s):  
Cell Division ◽  
Fluorescent Probes ◽  
Actin Filaments ◽  
Intracellular Transport ◽  
Cell Structure ◽  
Plant Cells ◽  
Cell Plate ◽  
Cell Cortex ◽  
Living Plant ◽  
Rhodamine Phalloidin

Microinjection of fluorescent probes into living plant cells reveals new aspects of cell structure and function. Microtubules and actin filaments are dynamic components of the cytoskeleton and are involved in cell growth, division and intracellular transport. To date, cytoskeletal probes used in microinjection studies have included rhodamine-phalloidin for labelling actin filaments and fluorescently labelled animal tubulin for incorporation into microtubules. From a recent study of Tradescantia stamen hair cells it appears that actin may have a role in defining the plane of cell division. Unlike microtubules, actin is present in the cell cortex and delimits the division site throughout mitosis. Herein, I shall describe actin, its arrangement and putative role in cell plate placement, in another material, living cells of Tradescantia leaf epidermis.The epidermis is peeled from the abaxial surface of young leaves usually without disruption to cytoplasmic streaming or cell division. The peel is stuck to the base of a well slide using 0.1% polyethylenimine and bathed in a solution of 1% mannitol +/− 1 mM probenecid.

Electronmicroscopic localization of ribonucleic acids in ciliate Bursaria truncatella during cell division

1990 ◽  
Vol 48 (3) ◽  
pp. 132-133
Author(s):  
Vladimir Popenko ◽  
Natalya Cherny ◽  
Maria Yakovleva
Keyword(s):  
Cell Division ◽  
High Specificity ◽  
Longitudinal Axis ◽  
Gold Complexes ◽  
Somatic Nucleus ◽  
Ribonucleic Acids ◽  
Biological Meaning ◽  
Bivalent Cations ◽  
Lowicryl K4m ◽  
Short Time

Highly polyploid somatic nucleus (macronucleus) of ciliate Bursaria truncatella under goes severe changes in morphology during cell division. At first, macronucleus (Ma) condences, diminishes in size and turns perpendicular to longitudinal axis of the cell. After short time, Ma turns again, elongates and only afterwards the process of division itself occurs. The biological meaning of these phenomena is not clear.Localization of RNA in the cells was performed on sections of ciliates B. truncatella, embedded in “Lowicryl K4M” at various stages: (1) before cell division (Figs. 2,3); (11) at the stage of macronucleus condensation; (111) during elongation of Ma (Fig.4); (1111) in young cells (0-5min. after division). For cytochemical labelling we used RNaseAcolloidal gold complexes (RNase-Au), which are known to bind to RNA containing cell ularstructures with high specificity. The influence of different parameters on the reliability and reproducibility of labelling was studied. In addition to the factors, discussed elsewhere, we found that the balance of mono- and bivalent cations is of great significance.

Centromere assembly and non-random sister chromatid segregation in stem cells

2020 ◽  
Vol 64 (2) ◽  
pp. 223-232 ◽  
Author(s):  
Ben L. Carty ◽  
Elaine M. Dunleavy
Keyword(s):  
Stem Cells ◽  
Cell Division ◽  
Cell Fate ◽  
Sister Chromatid ◽  
Asymmetric Cell Division ◽  
Protein A ◽  
Germline Stem Cells ◽  
Sister Chromatids ◽  
Centromere Protein A ◽  
Oocyte Meiosis

Abstract Asymmetric cell division (ACD) produces daughter cells with separate distinct cell fates and is critical for the development and regulation of multicellular organisms. Epigenetic mechanisms are key players in cell fate determination. Centromeres, epigenetically specified loci defined by the presence of the histone H3-variant, centromere protein A (CENP-A), are essential for chromosome segregation at cell division. ACDs in stem cells and in oocyte meiosis have been proposed to be reliant on centromere integrity for the regulation of the non-random segregation of chromosomes. It has recently been shown that CENP-A is asymmetrically distributed between the centromeres of sister chromatids in male and female Drosophila germline stem cells (GSCs), with more CENP-A on sister chromatids to be segregated to the GSC. This imbalance in centromere strength correlates with the temporal and asymmetric assembly of the mitotic spindle and potentially orientates the cell to allow for biased sister chromatid retention in stem cells. In this essay, we discuss the recent evidence for asymmetric sister centromeres in stem cells. Thereafter, we discuss mechanistic avenues to establish this sister centromere asymmetry and how it ultimately might influence cell fate.

Cell division is required for resolution of dimer chromosomes at the dif locus of Escherichia coli

1998 ◽  
Vol 27 (2) ◽  
pp. 257-268 ◽  
Author(s):  
Walter W. Steiner ◽  
Peter L. Kuempel
Keyword(s):  
Escherichia Coli ◽  
Cell Division
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