scholarly journals Rape embryogenesis. II. Development of embryo proper

2015 ◽  
Vol 48 (3) ◽  
pp. 391-421 ◽  
Author(s):  
Teresa Tykarska
Keyword(s):  
Cell Walls ◽  
Apical Meristem ◽  
Root Cap ◽  
Globular Embryo ◽  
Segmentation Boundary ◽  
Mother Cells ◽  
Upper Boundary

It was found in the continued studies on rape embryogenesis, started by the description of the proembryo (Tykarska, 1976) that the development of embryo is extremely regular and based on differentiating divisions. It appeared that the transverse segmentation boundary and cell walls separating the mother cells of the histogens in the proembryo can be distinguished in all the later stages of the embryo. The border between the cytoledons and epicotyl part of the embryonal axis, and the hypocotyl corresponds to the segmentation boundary between layer l and layer l' at the octant stage. As border between the hypocotyl and radicle was assumed the upper boundary of the root cap reaching usually to the level of the boundary between segments II and III of dermatogen and periblem. The apical meristem of the shoot forms from dermatogen and the periaxial cells of the globular embryo subepidermis. The promeristem of the radicle constists of 3 layers of initial cells surrounding on all sides the inactive layer of central binding cells.

scholarly journals DNA synthesis in the nuclei of Pinus silvestris embryos during

2015 ◽  
Vol 43 (4) ◽  
pp. 459-464
Author(s):  
P. Brodzki
Keyword(s):  
Dna Synthesis ◽  
Apical Meristem ◽  
Pinus Silvestris ◽  
Vascular Elements ◽  
Mother Cells

DNA synthesis starts earliest in the apical meristem of the shoot, and latest in the cotyledons. Mitoses appear simultaneously in the apical meristem and in the hypocotyl cortex. Synthesis continues in the mother cells of vascular elements and cotyledon parenchyma when mitosis ceases. In the cotyledons DNA synthesis is rather synchronous and leads to the elimination of 2 C nuclei.

scholarly journals Key events during the transition from rapid growth to quiescence in budding yeast require posttranscriptional regulators

2013 ◽  
Vol 24 (23) ◽  
pp. 3697-3709 ◽  
Author(s):  
Lihong Li ◽  
Shawna Miles ◽  
Zephan Melville ◽  
Amalthiya Prasad ◽  
Graham Bradley ◽  
...  
Keyword(s):  
Cell Walls ◽  
Posttranscriptional Regulation ◽  
Cell Formation ◽  
Cell Types ◽  
G1 Arrest ◽  
Quiescent State ◽  
Diauxic Shift ◽  
Cell Wall Assembly ◽  
Daughter Cells ◽  
Mother Cells

Yeast that naturally exhaust the glucose from their environment differentiate into three distinct cell types distinguishable by flow cytometry. Among these is a quiescent (Q) population, which is so named because of its uniform but readily reversed G1 arrest, its fortified cell walls, heat tolerance, and longevity. Daughter cells predominate in Q-cell populations and are the longest lived. The events that differentiate Q cells from nonquiescent (nonQ) cells are initiated within hours of the diauxic shift, when cells have scavenged all the glucose from the media. These include highly asymmetric cell divisions, which give rise to very small daughter cells. These daughters modify their cell walls by Sed1- and Ecm33-dependent and dithiothreitol-sensitive mechanisms that enhance Q-cell thermotolerance. Ssd1 speeds Q-cell wall assembly and enables mother cells to enter this state. Ssd1 and the related mRNA-binding protein Mpt5 play critical overlapping roles in Q-cell formation and longevity. These proteins deliver mRNAs to P-bodies, and at least one P-body component, Lsm1, also plays a unique role in Q-cell longevity. Cells lacking Lsm1 and Ssd1 or Mpt5 lose viability under these conditions and fail to enter the quiescent state. We conclude that posttranscriptional regulation of mRNAs plays a crucial role in the transition in and out of quiescence.

scholarly journals Domain-specific and cell type-specific localization of two types of cell wall matrix polysaccharides in the clover root tip.

1992 ◽  
Vol 118 (2) ◽  
pp. 467-479 ◽  
Author(s):  
M A Lynch ◽  
L A Staehelin
Keyword(s):  
Cell Wall ◽  
Cell Walls ◽  
Cellular Differentiation ◽  
Cortical Cell ◽  
Middle Lamella ◽  
Root Cap ◽  
Root Tip ◽  
Cortical Cells ◽  
Peripheral Cell ◽  
Clover Root

Using immunocytochemical techniques and antibodies that specifically recognize xyloglucan (anti-XG), polygalacturonic acid/rhamnogalacturonan I (anti-PGA/RG-I), and methylesterified pectins (JIM 7), we have shown that these polysaccharides are differentially synthesized and localized during cell development and differentiation in the clover root tip. In cortical cells XG epitopes are present at a threefold greater density in the newly formed cross walls than in the older longitudinal walls, and PGA/RG-I epitopes are detected solely in the expanded middle lamella of cortical cell corners, even after pretreatment of sections with pectinmethylesterase to uncover masked epitopes. These results suggest that in cortical cells XG and PGA/RG-I are differentially localized not only to particular wall domains, but also to particular cell walls. In contrast to their nonoverlapping distribution in cortical cells, XG epitopes and PGA/RG-I epitopes largely colocalize in the epidermal cell walls. The results also demonstrate that the middle lamella of the longitudinal walls shared by epidermal cells and by epidermal and cortical cells constitutes a barrier to the diffusion of cell wall and mucilage molecules. Synthesis of XG and PGA/RG-I epitope-containing polysaccharides also varies during cellular differentiation in the root cap. The differentiation of gravitropic columella cells into mucilage-secreting peripheral cells is marked by a dramatic increase in the synthesis and secretion of molecules containing XG and PGA/RG-I epitopes. In contrast, JIM 7 epitopes are present at abundant levels in columella cell walls, but are not detectable in peripheral cell walls or in secreted mucilage. There were also changes in the cisternal labeling of the Golgi stacks during cellular differentiation in the root tip. Whereas PGA/RG-I epitopes are detected primarily in cis- and medial Golgi cisternae in cortical cells (Moore, P. J., K. M. M. Swords, M. A. Lynch, and L. A. Staehelin. 1991. J. Cell Biol. 112:589-602), they are localized predominantly in the trans-Golgi cisternae and the trans-Golgi network in epidermal and peripheral root cap cells. These observations suggest that during cellular differentiation the plant Golgi apparatus can be both structurally and functionally reorganized.

Light and transmission electron microscopy of English oak ectomycorrhizal short roots

1984 ◽  
Vol 62 (7) ◽  
pp. 1327-1335 ◽  
Author(s):  
H. H. Edwards ◽  
R. V. Gessner
Keyword(s):  
Electron Microscopy ◽  
Cell Walls ◽  
Quercus Robur ◽  
Lipid Droplets ◽  
Apical Meristem ◽  
Fungal Symbiont ◽  
Host Root ◽  
Transmission Electron ◽  
Cell Layers ◽  
English Oak

The incorporation of caffeine in standard transmission electron microscope fixation procedures has allowed good preservation and embedment of ectomycorrhizal short roots of English oak (Quercus robur L.). In the mantle the most conspicuous structures are cystidia which radiate outwards from the surface. These conically shaped cells have knobs at their tips and thickened cell walls. The cystidia and other outer mantle cells contain many cytoplasmic constituents, whereas the inner mantle cells are nearly devoid of cytoplasm. The mantle cells are held together by an intercellular slime network. The Hartig net cells are filled with cytoplasm and contain numerous lipid droplets. Typical dolipore septa separate the cells; however, these cells have irregularly branched shapes. The host root tissue appears little altered by the presence of the fungal symbiont. However, the root cap consists of only a few cell layers. The apical meristem is functional as evidenced by the presence of newly divided cells and microtubules lining enlarging cells.

Sexual reproduction in grand fir (Abies grandis)

1982 ◽  
Vol 60 (11) ◽  
pp. 2197-2214 ◽  
Author(s):  
Hardev Singh ◽  
John N. Owens
Keyword(s):  
Pollen Germination ◽  
Apical Meristem ◽  
Pollen Grains ◽  
Root Apical Meristem ◽  
Proximal Pole ◽  
Abies Grandis ◽  
Young Embryo ◽  
Suspensor Differentiation ◽  
Mother Cells ◽  
Embryonal Mass

Phenology and anatomy of the postdormancy reproductive phase of Abies grandis Lindl, were studied. The dormant microsporangia contained compactly arranged pollen mother cells (PMC). The pollen cones broke dormancy in the 3rd week of February and soon afterwards the PMC entered meiosis. Microspore tetrads formed by the 2nd week of March. Pollen grains were shed at the five-celled stage in the 3rd week of April. The pollen grains were bisaccate and showed a triradiate mark on the proximal pole. The dormant ovulate-cone buds bore rudimentary ovuliferous scales, each with two ovular areas. Ovulate cones broke dormancy at the end of January. Megaspore mother cells differentiated by the end of February and the integument was initiated soon afterwards. A megaspore triad formed in the 2nd week of April. By the 3rd week of April, at the time of pollination, the ovule contained a free-nuclear gametophyte, and the integument had developed a stigmatic micropylar funnel. Numerous microdroplets were observed on the surface of the funnel to which pollen adhered. After pollination the funnel became infolded, enclosing the pollen grains. Pollen germination, pollen tube growth through the nucellus, and syngamy took only 3–4 days and occurred in the 3rd week of June. The female gametophyte was long and bore two or three archegonia. The proembryo consisted of four tiers of four cells each. The suspensors developed from the subterminal tier of cells. The four terminal cells formed the embryonal mass, whose proximal cells elongated and developed into a secondary suspensor. Differentiation of the root apical meristem and the cotyledons in the young embryo occurred in the 1st week of July and the embryo matured in the 3rd week of August.

scholarly journals Histological and biochemical changes in Pinus spp. seeds during germination and post-germinative growth: triacylglycerol distribution and catalase activity

2000 ◽  
Vol 27 (12) ◽  
pp. 1109
Author(s):  
Marie-Noëlle Jordy ◽  
Susanna Danti ◽  
Jean-Michel Favre ◽  
Milvia Luisa Raccchi
Keyword(s):  
Apical Meristem ◽  
Temporal Evolution ◽  
Peripheral Zone ◽  
Pinus Pinaster Ait ◽  
Storage Area ◽  
Spatio Temporal ◽  
Mother Cells ◽  
Pinus Spp ◽  
Specific Lipid

The spatio-temporal evolution of catalase (CAT) activity and triacylglycerol distribution was investigated in seeds and seedlings from Pinus pinaster Ait., P. pinea L. and P. radiata D. Don during germination and post-germination. The high amount of triacylglycerols contained in the whole dehydrated embryo from the three species was progressively depleted, first, in the radicle and then in hypocotyl and cotyledons during post-germinative growth. In parallel, histological localisation of CAT activity and the quantitative analysis confirmed the involvement of this enzyme in cell detoxification from peroxide released during the intense lipid breakdown. Two isozymes, CAT-1 and CAT-2, were identified during post-germinative growth. Both were particularly active in the hypocotyl and radicle, while CAT-2 was specifically active in the photosynthetic tissues. These results emphasise that CAT activity is also independent from lipid metabolism in certain tissues. The role of each isoenzyme is discussed in connection with the metabolic changes occurring during seed germination and seedling growth. Special attention is given to the role of the shoot apex in triacylglycerol storage and breakdown. Central mother cells have been shown as a specific lipid storage area of the shoot apical meristem, in contrast with the peripheral zone in which lipid reserves were always reduced.

Sexual reproduction of mountain hemlock (Tsuga mertensiana)

1975 ◽  
Vol 53 (17) ◽  
pp. 1811-1826 ◽  
Author(s):  
John N. Owens ◽  
Marje Molder
Keyword(s):  
Cell Walls ◽  
Pollen Tubes ◽  
Linear Tetrad ◽  
Form Complex ◽  
Male Gametes ◽  
Canal Cell ◽  
Micropylar Canal ◽  
Tsuga Mertensiana ◽  
Mother Cells ◽  
Ventral Canal

Meiosis of pollen mother cells begins in October of the year in which cones are initiated. They reach pachytene then become dormant until the next March. Meiosis is complete and the winged pollen mature by mid-June. Meiosis of the megaspore mother cell occurs in May, forming a linear tetrad of megaspores. The female gametophyte undergoes free nuclear division at pollination in mid-June. No pollination drop is present; rather, the pollen adheres to the sticky, splayed edge of the micropyle, where it germinates and pollen tubes grow toward the nucellus. The nucellus elongates into the micropylar canal, forming a nucellar beak, which makes contact with the pollen tubes. Several pollen tubes penetrate the nucellus.At the time of fertilization early in August, each ovule contains two to four aichegonia each having two to four neck cells in one tier. Pollen tubes penetrate the neck cells and two male gametes are formed. The ventral canal cell breaks down and fusion occurs in the center of the archegonium. Four free nuclei form and migrate to the base of the archegonium. cell walls form, and a 16-celled proembryo develops. Both simple and cleavage polyembryony occur. Rosette cells divide but do not form complex embryos. The embryo and seed are mature in October and the cones dry and open during October and November. Mature cones averaged 70 seeds, of which 46% were filled.Reproduction in mountain hemlock (Tsuga mertensiana (Bong.) Carr.) is similar to that in other species of Tsuga except for the presence of winged pollen. Any attempt to place the species in the genus Picea or place it as a hybrid midway between Picea and Tsuga is unfounded based on all of the more-conservative reproductive and embryological characteristics.

The Fine Structure of the Stegmata in Calamus Axillaris during Maturation

IAWA Journal ◽  
1995 ◽  
Vol 16 (1) ◽  
pp. 61-68 ◽  
Author(s):  
Uwe Schmitt ◽  
Gudrun Weiner ◽  
Walter Liese
Keyword(s):  
Cell Walls ◽  
Apical Meristem ◽  
Wall Material ◽  
Wall Thickening ◽  
Primary Wall ◽  
Maturation Process ◽  
Silica Body ◽  
The Third ◽  
Dense Cytoplasm ◽  
Rattan Palm

The maturation process of stegmata in the rattan palm Calamus axillaris Becc. was investigated by electron microscopy. Near the apical meristem immature stegmata contain a dense cytoplasm and a centrally located nucleus, but no silica-bodies. Their cell walls, as weIl as those of adjacent fibres, show primary wall-like characteristics. At the third and fourth internode, silica-bodies form within a vacuole of the still immature stegmata; the nucleus becomes displaced towards the parenchyma side of a stegma. Between the fifth and tenth internode, the stegma walls thicken, first at the cell corners adjacent to fibres with subsequent extension to the fibre side. This part of a stegma wall becomes extremely thick and finally envelopes nearly half of the now fully developed silica-body. Its parenchyma side, however, remains free from additional wall material. After completion of wall thickening, the cytoplasm of a stegma degenerates.

scholarly journals Activation of embryo during rape (Brassica napus L.) seed germination II. Transversal organisation of radicle apical meristem

2014 ◽  
Vol 49 (4) ◽  
pp. 387-395 ◽  
Author(s):  
Mieczysław Kuraś
Keyword(s):  
Brassica Napus ◽  
Seed Germination ◽  
Cross Sections ◽  
Apical Meristem ◽  
Mature Embryo ◽  
Root Cap ◽  
Root Apical Meristem ◽  
Quiescent Centre ◽  
Brassica Napus L ◽  
Cell Patterns

Series of microtome cross sections of the root apical meristem were investigated in the mature embryo and young seedling of rape. The cell patterns are described in 3 layers of promeristem. Radial sectors of the root cap and protoderm, formed by common dermatocalyptrogen initials, and radial sectors of the cortex, produced by periblem initials were identified on all cross sections of the root. Between these sectors 4 segmentation boundaries of proembryo quadrants were distinguished, running across the whole root proper. The boundaries between the 4 sectors of connecting cells arising from the upper hypophysis derivative and the boundaries between the 4 sectors of the columella originating from the lower hypophysis derivative do not follow the same course and are not identical with the boundaries of the proembryo quadrants. Therefore during the whole embryogenesis, the central connecting cells, considered generally as cortex initials (iec), take no part in the development of the cortex but they form the quiescent centre of the radicle. Neither do the columella initial cells participate in the development of the lateral parts of the root cap.

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