2009
DOI: 10.1155/2009/209303
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snRNP: Rich Nuclear Bodies inHyacinthus orientalisL. Microspores and Developing Pollen Cells

Abstract: The aim of the present work was the characterization of nuclear bodies in the microspore and developing pollen cells of Hyacinthus orientalis L.. 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 a… Show more

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Cited by 5 publications
(3 citation statements)
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“…Initially, we used modified AgNOR staining to visualize nuclear bodies and Cajal bodies in particular (Zienkiewicz & Bednarska ) since REN1 protein co‐localized there as well. Unfortunately, we were not able to observe these structures in Arabidopsis pollen probably due to smaller size of pollen grains and their rougher surface than in Hyacinthus for which this protocol was originally developed.…”
Section: Discussionmentioning
confidence: 99%
See 1 more Smart Citation
“…Initially, we used modified AgNOR staining to visualize nuclear bodies and Cajal bodies in particular (Zienkiewicz & Bednarska ) since REN1 protein co‐localized there as well. Unfortunately, we were not able to observe these structures in Arabidopsis pollen probably due to smaller size of pollen grains and their rougher surface than in Hyacinthus for which this protocol was originally developed.…”
Section: Discussionmentioning
confidence: 99%
“…After maceration, flowers were impregnated by 50% AgNO 3 in water, 55 °C, 20 min; then incubated in 1:1 mixture of 2% gelatin in 1% formic acid and 50% AgNO 3 for 20 min in dark. The plant material was then washed with distilled water for 10 min and then treated with 5% sodium thiosulfate for 10 min (Zienkiewicz & Bednarska ; modified). Individual anthers of sequential developmental series were prepared on glass slide, covered with water, squashed and observed under the microscope (Nicon Eclipse TE2000‐E).…”
Section: Methodsmentioning
confidence: 99%
“…Visualization of CBs in living plant cells revealed also that plant CBs exhibit dynamic movement, fusing together and splitting apart within the nucleus (Boudonck et al 1999 ). Moreover, the number of CBs in plant cells was observed to change during the cell cycle and differentiation (Boudonck et al 1998 ; Straatman and Schel 2001 ; Seguí-Simarro et al 2006 ; Zienkiewicz and Bednarska 2009 ). Recently, plant CBs were shown to contain also Atcoilin (Collier et al 2006 ; Koroleva et al 2009 ), which is a homolog of the mammalian protein coilin, a marker of CB in animal cells.…”
Section: Introductionmentioning
confidence: 99%