scholarly journals snRNP: Rich Nuclear Bodies inHyacinthus orientalisL. Microspores and Developing Pollen Cells

2009 ◽  
Vol 2009 ◽  
pp. 1-12 ◽  
Author(s):  
K. Zienkiewicz ◽  
E. Bednarska
Keyword(s):  
Pollen Development ◽  
Rna Synthesis ◽  
Generative Cell ◽  
Pollen Grains ◽  
Strong Relationship ◽  
Nuclear Bodies ◽  
Cajal Body ◽  
Sm Proteins ◽  
Hyacinthus Orientalis

The aim of the present work was the characterization of nuclear bodies in the microspore and developing pollen cells ofHyacinthus orientalisL.. The combination of Ag-NOR, immunofluorescence and immunogold techniques was used in this study. The obtained results showed the presence of highly agyrophylic extranucleolar bodies in microspore and developing pollen cells, which were finally identified as Cajal bodies. In all cases, a strong accumulation of snRNP-indicating molecules including TMG cap, Sm proteins and U2 snRNA, was observed in the examined nuclear bodies. In contrast to their number the size of the identified structures did not change significantly during pollen development. In the microspore and the vegetative cell of pollen grains CBs were more numerous than in the generative cell. At later stages of pollen development, a drastic decrease in CB number was observed and, just before anthesis, a complete lack of these structures was indicated in both pollen nuclei. On the basis of these results, as well as our previous studies, we postulate a strong relationship between Cajal body numbers and the levels of RNA synthesis and splicing machinery elements in microspore and developing pollen cells.

scholarly journals snRNP protein expression enhances the formation of Cajal bodies containing p80-coilin and SMN

2001 ◽  
Vol 114 (24) ◽  
pp. 4407-4419 ◽  
Author(s):  
Judith E. Sleeman ◽  
Paul Ajuh ◽  
Angus I. Lamond
Keyword(s):  
Protein Expression ◽  
Cell Lines ◽  
Nuclear Bodies ◽  
Cajal Body ◽  
Cajal Bodies ◽  
Primary Cells ◽  
Sm Proteins ◽  
Body Formation ◽  
Stable Cell Lines ◽  
Snrnp Protein

Splicing snRNPs (small nuclear ribonucleoproteins) are essential sub-units of the spliceosome. Here we report the establishment of stable cell lines expressing fluorescently tagged SmB, a core snRNP protein. Analysis of these stable cell lines has allowed us to characterize the nuclear pathway that leads to snRNP accumulation in nuclear speckles and has identified a limiting nucleolar step in the pathway that can be saturated by overexpression of Sm proteins. After nuclear import, newly assembled snRNPs accumulate first in a subset of Cajal bodies that contain both p80-coilin and the survival of motor neurons protein (SMN) and not in bodies that contain p80-coilin but lack SMN. Treatment of cells with leptomycin B (LMB) inhibits both the accumulation of snRNPs in nuclear bodies and their subsequent accumulation in speckles. The formation of Cajal bodies is enhanced by Sm protein expression and the assembly of new snRNPs. Formation of heterokaryons between HeLa cell lines expressing Sm proteins and primary cells that usually lack Cajal bodies results in the detection of Cajal bodies in primary cell nuclei. Transient over-expression of exogenous SmB alone is sufficient to induce correspondingly transient Cajal body formation in primary cells. These data indicate that the level of snRNP protein expression and snRNP assembly, rather than the expression levels of p80-coilin or SMN, may be a key trigger for Cajal body formation.

scholarly journals Ultrastructural and metabolic transformations of differentiating Hyacinthus orientalis L, pollen grain cells. I. RNA and protein synthesis

2014 ◽  
Vol 53 (2) ◽  
pp. 145-158 ◽  
Author(s):  
Elżbieta Bednarska
Keyword(s):  
Protein Synthesis ◽  
Vegetative Cell ◽  
Generative Cell ◽  
Growth Dynamics ◽  
Pollen Grains ◽  
Pollen Grain ◽  
Cell Protein ◽  
Replication Process ◽  
Rna And Protein Synthesis ◽  
Hyacinthus Orientalis

RNA and protein synthesis were investigated in generative and vegetative cells during maturation of pollen grains. The rate of RNA and protein synthesis was analysed in reference to the successive interphase periods of the life cycle of pollen cells as well as against the background of the growth dynamics of the cell volume. The results of studies demonstrated that the pollen grain increases in size owing to the growth of the vegetative cell. The generative one does not grow. RNA synthesis and that of proteins in differentiating pollen cells has a different course. In the growing vegetative cell it lasts longer and is more intensive than in the generative cell which does not grow. RNA and protein synthesis in the vegetative cell take place in the period from the callose stage to the stage of lemon-shaped generative cell, that is in the period of phases G<sub>1</sub>, S and G<sub>2</sub>. This synthesis is positively correlated with the growth of the pollen grain. RNA and protein synthesis in the generative cell comprises the period from the callose-less lenticular stage to the stage of spherical generative cell, that is the phases S and early phase G<sub>2</sub>. These results suggest that in the vegetative cell RNA and protein synthesis is utilised above all to increase of its cell, instead in non growing generative cell protein synthese is probably limited mostly to a histones and enzymatic proteins serving for the DNA replication process.

Resolution of Channels in the Exine by Translocation of Colloidal Iron

1971 ◽  
Vol 29 ◽  
pp. 352-353
Author(s):  
John R. Rowley
Keyword(s):  
Phosphate Buffer ◽  
Pollen Development ◽  
Osmium Tetroxide ◽  
Pollen Grains ◽  
Deionized Water ◽  
Colloidal Iron ◽  
Fixed Material ◽  
Epilobium Angustifolium ◽  
Untreated Material ◽  
Microspore Mitosis

The morphology of the exine of many pollen grains, at the time of flowering, is such that one can suppose that transport of substances through the exine occurred during pollen development. Holes or channels, microscopic to submicroscopic, are described for a large number of grains. An inner part of the exine of Epilobium angustifolium L. and E. montanum L., which may be referred to as the endexine, has irregularly shaped channels early in pollen development although by microspore mitosis there is no indication of such channeling in chemically fixed material. The nucleus in microspores used in the experiment reported here was in prophase of microspore mitosis and the endexine, while lamellated in untreated grains, did not contain irregularly shaped channels. Untreated material from the same part of the inflorescence as iron treated stamens was examined following fixation with 0.1M glutaraldehyde in cacodylate-HCl buffer at pH 6.9 (315 milliosmoles) for 24 hrs, 4% formaldehyde in phosphate buffer at pH 7.2 (1,300 milliosmoles) for 12 hrs, 1% glutaraldehyde mixed with 0.1% osmium tetroxide for 20 min, osmium tetroxide in deionized water for 2 hrs and 1% glutaraldehyde mixed with 4% formaldehyde in 0.1M cacodylate-HCl buffer at pH 6.9 for two hrs.

Nuclear coiled bodies and the nucleolus

1994 ◽  
Vol 52 ◽  
pp. 20-21
Author(s):  
K. Brasch ◽  
J. Williams ◽  
D. Gallo ◽  
T. Lee ◽  
R. L. Ochs
Keyword(s):  
Mouse Liver ◽  
Nuclear Body ◽  
Nuclear Bodies ◽  
Model Systems ◽  
Coiled Body ◽  
Rrna Processing ◽  
Malignant Cells ◽  
Sm Proteins ◽  
Coiled Bodies ◽  
Unique Protein

Though first described in 1903 by Ramon-y-Cajal as silver-staining “accessory bodies” to nucleoli, nuclear bodies were subsequently rediscovered by electron microscopy about 30 years ago. Nuclear bodies are ubiquitous, but seem most abundant in hyperactive and malignant cells. The best studied type of nuclear body is the coiled body (CB), so termed due to characteristic morphology and content of a unique protein, p80-coilin (Fig.1). While no specific functions have as yet been assigned to CBs, they contain spliceosome snRNAs and proteins, and also the nucleolar protein fibrillarin. In addition, there is mounting evidence that CBs arise from or are generated near the nucleolus and then migrate into the nucleoplasm. This suggests that as yet undefined links may exist, between nucleolar pre-rRNA processing events and the spliceosome-associated Sm proteins in CBs.We are examining CB and nucleolar changes in three diverse model systems: (1) estrogen stimulated chick liver, (2) normal and neoplastic cells, and (3) polyploid mouse liver.

Pollen characterization of ornamental species of Mammillaria Haw. (Cactaceae/Cactoideae)

2019 ◽  
Vol 6 (1) ◽  
pp. 13 ◽  
Author(s):  
Denise M. D. S. Mouga ◽  
Gabriel R. Schroeder ◽  
Nilton P. Vieira Junior ◽  
Enderlei Dec
Keyword(s):  
Pollen Morphology ◽  
Pollen Grains ◽  
Radial Symmetry ◽  
Morphological Data ◽  
Medium Size ◽  
Ornamental Species

The pollen morphology of thirteen species of Cactaceae was studied: M. backebergiana F.G. Buchenau, M. decipiens Scheidw, M. elongata DC, M. gracilis Pfeiff., M. hahniana Werderm., M. marksiana Krainz, M. matudae Bravo, M. nejapensis R.T. Craig & E.Y. Dawson, M. nivosa Link ex Pfeiff., M. plumosa F.A.C. Weber, M. prolifera (Mill.) Haw, M. spinosissima var. “A Peak” Lem. and M. voburnensis Scheer. All analysed pollen grains are monads, with radial symmetry, medium size (M. gracilis, M. marksiana, M. prolifera, large), tricolpates (dimorphs in M. plumosa [3-6 colpus] and M. prolifera [3-6 colpus]), with circular-subcircular amb (quadrangular in M. prolifera and M. plumosa with six colpus). The pollen grains presented differences in relation to the shape and exine thickness. The exine was microechinate and microperforated. The pollen morphological data are unpublished and will aid in studies that use pollen samples. These pollen grains indicate ornamental cacti.

Pollen development in maize plants subjected to molybdenum deficiency

1979 ◽  
Vol 57 (18) ◽  
pp. 1946-1950 ◽  
Author(s):  
S. C. Agarwala ◽  
C. Chatterjee ◽  
P. N. Sharma ◽  
C. P. Sharma ◽  
N. Nautiyal
Keyword(s):  
Acid Phosphatase ◽  
Pollen Development ◽  
Pollen Grains ◽  
Starch Phosphorylase ◽  
Maize Plants ◽  
Male Flowers

A reduction in the size of tassels, male flowers, and anthers resulted from molybdenum deficiency in maize. In molybdenum-deficient plants, anthesis was suppressed or delayed and the anthers had fewer and smaller pollen grains that lacked dense cytoplasmic contents, appeared shrivelled, and had poor viability. Because of molybdenum deficiency, there was a decrease in the activity of starch phosphorylase in mature and freshly shed pollen grains and decreases in the activities of invertase and acid phosphatase at all the five stages at which pollen grains were assayed for the enzymes. The activities of catalase and peroxidase were increased by molybdenum deficiency at all five stages and that of ribonuclease at four out of the five stages of pollen development.

scholarly journals Prunus necrotic ringspot virus Early Invasion and Its Effects on Apricot Pollen Grain Performance

2007 ◽  
Vol 97 (8) ◽  
pp. 892-899 ◽  
Author(s):  
Khalid Amari ◽  
Lorenzo Burgos ◽  
Vicente Pallas ◽  
María Amelia Sanchez-Pina
Keyword(s):  
Developmental Stages ◽  
Generative Cell ◽  
Pollen Grains ◽  
Growth Zone ◽  
Pollen Tubes ◽  
Climatic Conditions ◽  
Pollen Grain ◽  
Ringspot Virus ◽  
Prunus Necrotic Ringspot Virus

The route of infection and the pattern of distribution of Prunus necrotic ringspot virus (PNRSV) in apricot pollen were studied. PNRSV was detected both within and on the surface of infected pollen grains. The virus invaded pollen during its early developmental stages, being detected in pollen mother cells. It was distributed uniformly within the cytoplasm of uni- and bicellular pollen grains and infected the generative cell. In mature pollen grains, characterized by their triangular shape, the virus was located mainly at the apertures, suggesting that PNRSV distribution follows the same pattern as the cellular components required for pollen tube germination and cell wall tube synthesis. PNRSV also was localized inside pollen tubes, especially in the growth zone. In vitro experiments demonstrated that infection with PNRSV decreases the germination percentage of pollen grains by more than half and delays the growth of pollen tubes by ≈24 h. However, although PNRSV infection affected apricot pollen grain performance during germination, the presence of the virus did not completely prevent fertilization, because the infected apricot pollen tubes, once germinated, were able to reach the apricot embryo sacs, which, in the climatic conditions of southeastern Spain, mature later than in other climates. Thus, infected pollen still could play an important role in the vertical transmission of PNRSV in apricot.

Application of Atom Probe Microanalysis for Understanding Microstructure Evolution in Nickel Base Superalloy Welds

2000 ◽  
Vol 6 (S2) ◽  
pp. 350-351
Author(s):  
S. S. Babu ◽  
S. A. David ◽  
M. K. Miller
Keyword(s):  
Microstructure Evolution ◽  
Predictive Models ◽  
Strong Relationship ◽  
Atom Probe ◽  
Systematic Investigation ◽  
Nickel Base Superalloy ◽  
Cooling Conditions ◽  
Nickel Base ◽  
Base Superalloy

The characterization of the microstructure evolution during welding of nickel base superalloys is required for efficient reuse and reclamation of used and failed components. Previous atom probe analysis of electron-beam and laser-beam welds revealed complex alloying elemental partitioning between the γ and γ phases. Rapid cooling conditions in the weld leads to non-equilibrium partitioning and large amplitude Cr and Co levels in the γ phase. These results indicated that there is a strong relationship between weld cooling rate and the precipitation of γ′ precipitates from the γ phase. To understand and develop predictive models, a systematic investigation of the microstructure evolution in CM247DS alloy under controlled thermomechanical conditions are being performed. This paper describes some recent results on the elemental partitioning between γ and γ′ phases obtained with atom probe microanalysis.

scholarly journals Autoradiographic studies of DNA and histone synthesis in successive differentiation stages of pollen grain in Hyacinthus orientalis L.

2014 ◽  
Vol 50 (3) ◽  
pp. 367-380 ◽  
Author(s):  
Elżbieta Bednarska
Keyword(s):  
Dna Replication ◽  
Dna Synthesis ◽  
Vegetative Cell ◽  
Developmental Stages ◽  
Generative Cell ◽  
Pollen Grain ◽  
Cell Nuclei ◽  
Hyacinthus Orientalis ◽  
Histone Synthesis ◽  
Generative Cells

DNA and histone synthesis in five consecutive morphological stages of <em>Hyacinthus orientalis</em> L. pollen grain differentiation were studied autoradiographically. DNA synthesis was found to occur in both the generative and the vegetative cell. DNA replication in the generative cell took place when the generative cell was still adhered to the pollen grain wall but already devoid of callose wall. DNA synthesis in the generative cell slightly preceded that in the vegetative cell. Histones were synthesized in phase S of the generative and vegetative cell. In the generative cell histone synthesis also continued at a lower level after completion of DNA replication. In the developmental stages under study the nuclei of the generative cells were decidedly richer in lysine histones than vegetative cell nuclei.

scholarly journals Tradescantia bracteata pollen in vitro: pollen tubes development and mitosis

2015 ◽  
Vol 46 (4) ◽  
pp. 587-598 ◽  
Author(s):  
E. Lewandowska ◽  
M. Charzyńska
Keyword(s):  
Pollen Tube ◽  
Generative Cell ◽  
Metaphase Plate ◽  
Pollen Grains ◽  
Neutral Red ◽  
Generative Nucleus ◽  
Mitotic Spindles ◽  
Germinating Pollen ◽  
Vacuolar System

About 90 per cent of <i>Tradescantia bracteata</i> pollen germinates <i>in vitro</i> after 15 min. Mitosis starts in the pollen tube after about 3 h. The mitotic trans-formations of chromosomes within the generative nucleus are not synchronized. They involve succesively the linearly arranged chromosomes in the elongated generative nucleus. In metaphase the chromosomes are arranged tandem-like linearly along the pollen tube. The chromatides translocate in anaphase from various distances to the poles in a plane parallel to the metaphase plate. This suggests that chromosomes have individual mitotic spindles and that coordination of the chromosome transformations in the generative cell is much less strict than in a typical somatic mitosis. Starch is the storage material of pollen grains. In the vegetative cytoplasm of mature pollen grains minute reddish-orange vesicular structures are visible after staining with neutral red. They do not fuse with the vacuoles proper arising in germinating pollen grains to form the vacuolar system of the pollen tube.

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