Polarization of Subsidiary Cell Division in Maize Stomatal Complexes

Rice (Oryza sativa) is a water-intensive crop, and like other plants uses stomata to balance CO2 uptake with water-loss. To identify agronomic traits related to rice stomatal complexes, an anatomical screen of 64 Thai and 100 global rice cultivars was undertaken. Epidermal outgrowths called papillae were identified on the stomatal subsidiary cells of all cultivars. These were also detected on eight other species of the Oryza genus but not on the stomata of any other plant species we surveyed. Our rice screen identified two cultivars that had “mega-papillae” that were so large or abundant that their stomatal pores were partially occluded; Kalubala Vee had extra-large papillae, and Dharia had approximately twice the normal number of papillae. These were most accentuated on the flag leaves, but mega-papillae were also detectable on earlier forming leaves. Energy dispersive X-Ray spectrometry revealed that silicon is the major component of stomatal papillae. We studied the potential function(s) of mega-papillae by assessing gas exchange and pathogen infection rates. Under saturating light conditions, mega-papillae bearing cultivars had reduced stomatal conductance and their stomata were slower to close and re-open, but photosynthetic assimilation was not significantly affected. Assessment of an F3 hybrid population treated with Xanthomonas oryzae pv. oryzicola indicated that subsidiary cell mega-papillae may aid in preventing bacterial leaf streak infection. Our results highlight stomatal mega-papillae as a novel rice trait that influences gas exchange, stomatal dynamics, and defense against stomatal pathogens which we propose could benefit the performance of future rice crops.

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Development of the Stomatal Complexes During Ontogeny in Eucalyptus and Angophora (Myrtaceae)

Australian Journal of Botany ◽

10.1071/bt9910043 ◽

1991 ◽

Vol 39 (1) ◽

pp. 43 ◽

Cited By ~ 1

Author(s):

DJ Carr ◽

SGM Carr

Keyword(s):

Mother Cell ◽

Subsidiary Cell ◽

Epidermal Cells ◽

Stomatal Development ◽

Simple Pattern ◽

Sister Cell ◽

Stomatal Complexes ◽

Guard Mother Cell ◽

Subsidiary Cells ◽

Seedling Leaf

The mode of stomatal development is studied in cotyledons, seedling and adult leaves of species of eucalypts and three species of Angophora. In the cotyledons of all species examined the early stomatal initials are unilabrate or dolabrate. The stomatal initials in seedling leaves of species of the Corymbosae and Clavigerae are anisocytic. In the 4th seedling leaf in species of a group we have previously called Monocalyptus the stomatal initials are also anisocytic. All other eucalypts retain the early cotyledonary mode of origin of stomata throughout life. These two modes of origin, whether anisocytic or by unilabrate and dolabrate initials, are set in all eucalypts from the 4th seedling leaf onward. Secondary characteristics of the adult stomata, e.g. number of subsidiary cells, are more complex than those of the seedling leaves; rarely, the relatively simple pattern of the seedling leaves may persist in the adult leaves of a given species. In species in which the initials in adult leaves are unilabrate or dolabrate, groups of stomata may share one or more subsidiary cells or be juxtaposed without an intervening subsidiary cell. The sister cell(s) of the guard mother cell may precociously develop a thicker cuticle than ordinary epidermal cells, and this may be apparent at maturity. The abaxial stomata of the cotyledons (but not of seedling or adult leaves) are regularly aligned parallel to the main venation. The existence of three main types of origin of stomata characteristic of three large non-interbreeding groups of eucalypts is of interest in the taxonomy of the genus.

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Organelle distribution and cell differentiation in the formation of stomatal complexes in barley

Canadian Journal of Botany ◽

10.1139/b71-228 ◽

1971 ◽

Vol 49 (9) ◽

pp. 1623-1625 ◽

Cited By ~ 3

Author(s):

Eduardo Zeiger

Keyword(s):

Cell Division ◽

Cell Differentiation ◽

Phase Contrast ◽

Leaf Epidermis ◽

Organelle Movement ◽

Stomatal Complexes ◽

Subsidiary Cells ◽

Highly Correlated ◽

Asymmetrical Divisions ◽

Interference Phase

Interference – phase contrast observations of leaf epidermis in barley revealed the arrangement of organelles in cells that form stomatal complexes. Organelle movement and alignment were highly correlated with the process of cell division and differentiation that leads to mature stomata. Organelle rearrangement was most marked at the asymmetrical divisions that formed subsidiary cells of stomatal complexes.

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

Proceedings, annual meeting, Electron Microscopy Society of America ◽

10.1017/s0424820100051396 ◽

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.

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Stimulated Virus Production in Vinblastine and Cytochalasin-Induced Multinucleate Cells

Proceedings, annual meeting, Electron Microscopy Society of America ◽

10.1017/s0424820100067923 ◽

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.

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

Proceedings, annual meeting, Electron Microscopy Society of America ◽

10.1017/s0424820100146497 ◽

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.

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

Proceedings, annual meeting, Electron Microscopy Society of America ◽

10.1017/s0424820100158200 ◽

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.

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

Essays in Biochemistry ◽

10.1042/ebc20190066 ◽

2020 ◽

Vol 64 (2) ◽

pp. 223-232 ◽

Cited By ~ 1

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.

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