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1.
An overview of a set of our previous papers titled "Dynamics of microtubular cytoskeleton in higher plant meiosis" is presented, in addition to some data on subcellular mechanisms underlying cytoskeleton reorganization during meiotic division in pollen mother cells. An illustrated scheme of cytoskeleton rearrangements during plant meiosis, both with successive and simultaneous cytokinesis, is given. 相似文献
2.
By means of morphological analyses of meiotic abnormalities in pollen mother cells of cereal distant hybrids, processes of cytoskeleton cycle at the middle prometaphase (chaotic stage) were studied. It was shown that elements of the bipolar spindle (central and opposite kinetochore fibres) are formed at the chaotic stage of meiotic prometaphase. 相似文献
3.
Rearrangements of microtubular cytoskeleton during telophase in pollen mother cells of some dicotyledon plants with the simultaneous cytokinesis during normal and abnormal meiosis were studied. At telophase I, a potentially functional phragmoplast forms between daughter nuclei, but no cell plate is present. During interkinesis, the phragmoplast plays the role of an interphase cytoskeleton array. Dynamics of microtubule reorganization in polar regions of the telophase spindle is discussed in addition to the role played by microtubule convergence centers in cytoskeleton rearrangements during meiosis. 相似文献
4.
Intracellular morphological processes of successive cytokinesis in cereal pollen mother cells during normal and abnormal meiosis were studied. It was shown that the central spindle fiber system transforms into a phragmoplast at telophase. A model of centrifugal movement of the phragmoplast as a modification of B-anaphase has been proposed. 相似文献
5.
By means of morphological analyses of meiotic abnormalities in pollen mother cells (PMCs) of cereal wide hybrids, haploids and meiotic mutants, the processes involved in cytoskeleton cycle at late prometaphase (a sub-stage of transition from chaotic figure to bipolar spindle) were studied. A significance of the four processes of late prometaphase--axial orientation, lateral association, consolidation and convergance of spindle fibers--is discussed. 相似文献
6.
The early prometaphase and initial stages of meiotic spindle formation in higher plant PMCs were studied by means of a new approach worked out by the authors: a morphological dissection that consists in the analysis of various abnormalities of the process under study. Wide cereal hybrids F1 were used as a source of such abnormalities: phenotypes with C-, S-shaped and combined spindle, with spindles surrounded by microtubule (MT) ring and phenotypes with chaotic circular MT system in M1. Three stages of early prometaphase not described before (disintegration of perinuclear MT band, straightening of its bundles, and their translocation throughout the cytoplasm) were revealed. 相似文献
7.
The abnormal cytoskeleton cycle in meiosis in pollen mother cells of cereal wide hybrids F reveals the role of polar microtubules in phragmoplast formation during successive cytokinesis. The cytoskeletal rearrangements during successive and simultaneous cytokinesis in higher plant meiosis are compared. 相似文献
8.
Analyses of correspondent meiotic abnormalities is a good tool for studying cytoskeletal rearrangements during plant cell division. The paper reports on the wheat x wheatgrass F1 hybrids, showing various abnormalities during organization of the prophase perinuclear band of microtubules (PNB) in male meiosis. Based on these data, it may be concluded that the perinuclear system of microtubules (MT) in higher plant meiosis is formed from fibrils of the radial system as a result of their translocation in the cell cytoplasm space. According to our data, at this stage the radial MT arrays pass through the following consequence of events: separating from the nuclear envelope, 2) approaching, 3) tangential orientation to the nuclear surface, 4) bending, 5) co-orientation, lateral interaction. As a result, a flat ring of well organized concentric bent MT bundles encircling the nucleus meridionally is organized. 相似文献
9.
Shamina NV 《Tsitologiia》2003,45(7):650-654
A planar meridional perinuclear band of microtubules was observed at the late meiotic prophase I in a range of higher plant species. A distinct high-organized structure and a long time of existence allow to consider it as a new class of MTs dependent on the cell cycle in plant meiosis. MTs of the perinuclear band convert into meiotic spindle through a complex process of spatial rearrangements. 相似文献
10.
Five major mictotubule arrays characteristic of cell cycle in the higher plants were noticed: cortical coils, preprophase band, radial array, division spindle, and phragmoplast. The organization of mocrotubules into ordered arrays; their dynamics and function during plant cell division are discussed in this review. 相似文献
11.
The process of formation of multiple spindles in mononucleate pollen mother cells during meiosis in general wide hybrids F1 and haploids is described. It is assumed that the abnormality may be caused by aberration of a special process at late prometaphase providing for the spindle consolidation. 相似文献
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13.
Summary One of the intriguing aspects of development in plants is the precise control of division plane and subsequent placement of walls resulting in the specific architecture of tissues and organs. The placement of walls can be directed by either of two microtubule cycles. The better known microtubule cycle is associated with control of the future division plane in meristematic growth where new cells become part of tissues. The future daughter domains are determined before the nucleus enters prophase and the future site of cytokinesis is marked by a preprophase band (PPB) of cortical microtubules. The spindle axis is then organized in accordance with the PPB and, following chromosome movement, a phragmoplast is initiated in the interzone and expands to join with parental walls at the site previously occupied by the PPB. The alternative microtubule cycle lacks both the hooplike cortical microtubules of interphase and the PPB. Wall placement is determined by a radial microtubule system that defines a domain of cytoplasm either containing a nucleus or destined to contain a nucleus (the nuclear cytoplasmic domain) and controls wall placement at its perimeter. This more flexible system allows for cytoplasmic polarization and migration of nuclei in coenocytes prior to cellularization. The uncoupling of cytokinesis from karyokinesis is a regular feature of the reproductive phase in plants and results in specific, often unusual, patterns of cells which reflect the position of nuclei at the time of cellularization (e.g., the arrangement of spores in a tetrad, cells of the male and female gametophytes of angiosperms, and the distinctive cellularization of endosperm). Thus, both microtubule cycles are required for completion of plant life cycles from bryophytes to angiosperms. In angiosperm seed development, the two methods of determining the boundaries of domains where walls will be deposited are operative side by side. Whereas the PPB cycle drives embryo development, the radial-microtubule-system cycle drives the common nuclear type of endosperm development from the syncytial stage through cellularization. However, a switch to the PPB cycle can occur in endosperm, as it does in barley, when peripheral cells divide to produce a multilayered aleurone. The triggers for the switch between microtubule cycles, which are currently unknown, are key to understanding plant development.Dedicated to Professor Brian E. S. Gunning on the occasion of his 65th birthday 相似文献
14.
S M Wick 《Cell biology international reports》1985,9(4):357-371
Immunofluorescence microscopy of flowering plant root cells indicates that the earliest interphase microtubules appear during cytokinesis, radiating from the former spindle poles and subsequently from the nuclear envelope. They form networks that have microtubule focal points in the cortex underlying cell faces and in the cytoplasm between the nucleus and cortex. Cortical networks are rapidly replaced by the highly aligned array normally associated with interphase. An antibody that in animal cells identifies the location of pericentriolar material, the site of microtubule initiation, is also localized around the plant cell nuclear envelope at the time that putative early interphase microtubule networks are seen. 相似文献
15.
Trompier D Alibert M Davanture S Hamon Y Pierres M Chimini G 《The Journal of biological chemistry》2006,281(29):20283-20290
Fluorescence resonance energy transfer and native PAGE analytical techniques were employed to assess the quaternary structure of ABCA1, an ATP binding cassette transporter playing a crucial role in cellular lipid handling. These experimental approaches support the conclusion that ABCA1 is associated in dimeric structures that undergo transition into higher order structures, i.e. tetramers, during the ATP catalytic cycle. Our data hence underline molecular assembly as a crucial parameter in ABCA1 function and the advantage of native PAGE as analytical tool for intractable membrane proteins. 相似文献
16.
Summary The microtubule and F-actin cytoskeleton of nondifferentiated germlings ofUromyces phaseoli was studied using immunofluorescence methodologies. The microtubules were oriented mostly parallel to the longitudinal axis of the hypha. Microtubule depolymerizing agents, such as cold, demecolcine, griseofulvin and nocodazole, were effective in destroying the microtubule network, but not the F-actin system. Repolymerization of microtubules, following release from these agents, occurred first in the hyphal apices and not near the nuclei or spindle pole bodies. It was concluded that the microtubule nucleating region in such fungal cells is located in the apical regions. Enhanced microtubule arrays were visualized following incubation of the cells in taxol, an agent known to favor microtubule polymerization. 相似文献
17.
Localization of small heat shock proteins to the higher plant endomembrane system. 总被引:1,自引:0,他引:1
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K W Helm P R LaFayette R T Nagao J L Key E Vierling 《Molecular and cellular biology》1993,13(1):238-247
Three related gene families of low-molecular-weight (LMW) heat shock proteins (HSPs) have been characterized in plants. We describe a fourth LMW HSP family, represented by PsHSP22.7 from Pisum sativum and GmHSP22.0 from Glycine max, and demonstrate that this family of proteins is endomembrane localized. PsHSP22.7 and GmHSP22.0 are 76.7% identical at the amino acid level. Both proteins have amino-terminal signal peptides and carboxyl-terminal sequences characteristic of endoplasmic reticulum (ER) retention signals. The two proteins closely resemble class I cytoplasmic LMW HSPs, suggesting that they evolved from the cytoplasmic proteins through the addition of the signal peptide and ER retention motif. The endomembrane localization of these proteins was confirmed by cell fractionation. The polypeptide product of PsHSP22.7 mRNA was processed to a smaller-M(r) form by canine pancreatic microsomes; in vivo, GmHSP22.0 polysomal mRNA was found to be predominantly membrane bound. In vitro-processed PsHSP22.7 corresponded in mass and pI to one of two proteins detected in ER fractions from heat-stressed plants by using anti-PsHSP22.7 antibodies. Like other LMW HSPs, PsHSP22.7 was observed in higher-molecular-weight structures with apparent masses of between 80 and 240 kDa. The results reported here indicate that members of this new class of LMW HSPs are most likely resident ER proteins and may be similar in function to related LMW HSPs in the cytoplasm. Along with the HSP90 and HSP70 classes of HSPs, this is the third category of HSPs localized to the ER. 相似文献
18.
The interphase microtubule cytoskeleton of five different microvessel endothelial cell cultures, recently established from bovine corpus luteum, was analysed using anti-tubulin immunofluorescence. An antibody against acetylated microtubules detected four cell types each of which possessed a single cilia. The length of the cilia were up to 10 microns for cell types 1 and 2. Ciliary stubs had a length of up to 0.37 microns in cell types 4 and 5. Cilia were missing in cell type 3. Long and short cilia were located in the perinuclear region from where cytoplasmic microtubules radiated. Cell type 3 displayed straight microtubules rather than the wavy path seen in the other cell types. The amount of tyrosinated microtubules visualized by a specific antibody was consistently higher than that of posttranslationally acetylated microtubules. The latter were more apparent in cell types 4 and 5 than in the other cell types. We conclude: Differences in the cytoplasmic microtubule inventory of each microvessel endothelial cell type points at individual functions maintained in culture. 相似文献
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