Characteristics of microsporogenesis in the Siberian larch growing under the conditions of technogenic load

Studies of microsporogenesis in the Siberian larch growing in Krasnoyarsk and its suburbs have shown that meiosis starts in October. Microsporocytes winter at prophase I (leptoneme, diploneme). Reduction divisions in male generative buds are resumed and terminated in spring, in March. However, in the case of thaws during the autumn-winter period, meiotic division proceeds in the larch buds and this leads to the formation of degrading tetrads and pollen. Hence, the organic quiescence is absent in the larch in winter. It was shown that in the larch growing in the city, meiosis proceed more asynchronously than in the background tree stands. An increase of chromosomal aberrations during the reduction division was noted under the conditions of technogenic pollution.     

Specific features of microsporogenesis in the Siberian larch growing under the conditions of technogenic load

Studies of microsporogenesis in the Siberian larch growing in Krasnoyarsk and its suburbs have shown that meiosis starts in October. Microsporocytes winter at prophase I (leptoneme, diploneme). Reduction divisions in male generative buds are resumed and terminated in spring, in March. However, in the case of thaws during the autumn-winter period, meiotic division proceeds in the larch buds and this leads to the formation of degrading tetrads and pollen. Hence, the organic quiescence is absent in the larch in winter. It was shown that in the larch growing in the city, meiosis proceed more asynchronously than in the background tree stands. An increase of chromosomal aberrations during the reduction division was noted under the conditions of technogenic pollution.__________Translated from Ontogenez, Vol. 36, No. 2, 2005, pp. 128–134.Original Russian Text Copyright © 2005 by Romanova, Tretyakova.     

Meiosis during Microsporogenesis in Siberian Spruce (Picea obovata Ledeb.) in the South of Central Siberia

Russian Journal of Developmental Biology - The results of meiosis studies during microsporogenesis in Siberian spruce (Picea obovata Ledeb.) in the forest ecosystems of the south of Central Siberia...     

Selective cell elimination during microsporogenesis in sedges

The underlying mechanisms responsible for elimination of three of the four meiotic products during microsporogenesis in sedges have remained obscure. Although programmed cell death (PCD) is known to be an integral part of plant development, several aspects, such as the enormous size difference between functional and eliminated cells, nuclear viability of the smaller cells targetted for elimination and the possible dangers of employing PCD-like mechanisms during gametophyte development point to a novel way of selective cell elimination associated with asymmetric division. This paper throws some light on the possible roles of cell plate dynamics and cell fate determinants in pseudomonad development. The rarity and significance of asymmetric division with morphogenetic consequences associated with meiosis are discussed in the context of generally prevalent, mitosis- associated asymmetric divisions during development. Received: 16 December 1999 / Revision accepted: 28 March 2000     

Distribution of cellulosic wall in the anthers of Arabidopsis during microsporogenesis

Key message

Cellulose-specific staining revealed that tapetal cells and microsporocytes lose cellulosic walls before the onset of meiosis. Cellulosic wall degradation in microsporocytes might be independent of tapetal cells (or TPD1).

Abstract

Some cell types in a variety of angiosperms have been reported to lack cell walls. Here, we report that the tapetal cells of the anther of Arabidopsis thaliana did not appear to have a cellulosic wall based on staining with Calcofluor and Renaissance 2200. During sporogenous cell formation, cellulosic wall was present in all anther tissues. However, before meiosis it was almost absent on the tapetal cells and on the microsporocytes. In a sporocyteless/nozzle (spl/nzz) mutant, which lacks several components (microsporocytes, tapetum, middle layer and endothecium), cellulosic wall was detected in all anther cells. In another mutant, tapetum determinant1 (tpd1), which lacks tapetum and has more microsporocytes, cellulosic wall was almost absent on the microsporocytes before meiosis, similar to the wild type. These results suggest that the tapetum cells and microsporocytes lose cellulosic walls during microsporocyte formation, and that cell wall degradation occurs downstream of SPL/NZZ and is independent of TPD1.     

Spindle Dynamics during Meiosis in Drosophila Oocytes

Mature oocytes of Drosophila are arrested in metaphase of meiosis I. Upon activation by ovulation or fertilization, oocytes undergo a series of rapid changes that have not been directly visualized previously. We report here the use of the Nonclaret disjunctional (Ncd) microtubule motor protein fused to the green fluorescent protein (GFP) to monitor changes in the meiotic spindle of live oocytes after activation in vitro. Meiotic spindles of metaphase-arrested oocytes are relatively stable, however, meiotic spindles of in vitro–activated oocytes are highly dynamic: the spindles elongate, rotate around their long axis, and undergo an acute pivoting movement to reorient perpendicular to the oocyte surface. Many oocytes spontaneously complete the meiotic divisions, permitting visualization of progression from meiosis I to II. The movements of the spindle after oocyte activation provide new information about the dynamic changes in the spindle that occur upon re-entry into meiosis and completion of the meiotic divisions. Spindles in live oocytes mutant for a lossof-function ncd allele fused to gfp were also imaged. The genesis of spindle defects in the live mutant oocytes provides new insights into the mechanism of Ncd function in the spindle during the meiotic divisions.     

Regulation of Separase in Meiosis: Separase is Activated at the Metaphase I-II Transition in Xenopus Oocytes during Meiosis

Separase is a cysteine protease conserved in all eukaryotes and functions to remove the sisterchromatid cohesion in anaphase by cleaving the SCC1 subunit of the cohesin complex. Theregulation of separase activity as the degradation of its inhibitor, securin, and the downregulationof the inhibitory phosphorylation has never been directly investigated in themeiotic cell cycle of vertebrates. In this study, we cloned the full-length gene encodingXenopus separase from an oocyte cDNA library. Purified xSeparase can cleave the human ?-kleisin subunit of cohesin in vitro but cannot bind with hSecurin when these two proteins areco-expressed in 293T cells. Similar to its human counterpart, xSeparase cleaves itself uponactivation but at a single site. The cleavage site is conserved with one of the three selfcleavagesites in hSeparase. Using self-cleavage as a reporter for its activation, wedemonstrated that xSeparase was transiently activated between the two meioses and may beinvolved in the homologous chromosome separation, as observed in other organisms. Takingthe advantage of the inability of xSecurin to interact with hSeparase, we demonstrated that theCSF extract re-inhibit both full-length and auto-cleaved hSeparase, indicating thatphosphorylation inhibition of separase does occur under the physiological condition. Inaddition, we found that the endogenous xSecurin was accumulated in response toprogesterone-induced oocyte maturation, and was degraded at both the anaphase I and II in anAPC/C-dependent manner.     

Genetic variability of Siberian fir (Abies sibirica Ledeb.) inferred from AFLP markers

Genetic variability of AFLP markers was studied in 20 populations of Siberian fir (Abies sibirica (Pinaceae) and in two populations of Far-Eastern Manchurian fir A. nephrolepis and Sakhalin fir A. sachalinensis each. Four pairs of selective primers were used. In total, 168 samples from three fir species were genotyped for 117 polymorphic loci. According to the AMOVA results, the variability proportion characterizing the differences between three Abies species was several times higher (F(CT) = 0.53) than that accounting for among-population differences within the species (F(SC) = 0.125). Differentiation of the A. sibirica populations based on AFLP markers exceeded 14% (F(ST) = 0.141). Significant correlation between the genetic distances calculated from the AFLP data and the geographic distances between populations was found. The results of AFLP variability analysis supported and supplemented the conclusions inferred previously from allozyme and cpSSR data: several genetically similar geographic groups of Siberian fir were identified. These groups differ both in allele frequencies and in the levels of genetic variation.     

Relationship of strontium and calcium concentrations with the parameters of cell structure in Siberian spruce and fir tree-rings

This study addressed distribution of calcium and strontium in Siberian spruce (Picea obovata Ledeb.) and Siberian fir (Abies sibirica Ledeb.) tree-rings and its dependence on these woody species cell structure. Calcium concentration was found to decrease gradually from earlywood to latewood, whereas strontium showed an opposite trend. However, their trends at the scale of several rings are co-directed in the samples analyzed. A strong linear relationship was identified between the distribution of Sr/Ca concentration ratio and tree-ring density profile for both woody species. Radiographic density of Siberian spruce tree-ring cell walls and Ca and Sr concentrations in them were determined to have negative correlation with cell wall thickness. In earlywood of annual rings of a spruce the radiographic density of cell wall reaches 2.0 g/cm³ and decreases to 1.2 g/cm³ in latewood. The hypothesis put forward in this study to explain these strontium and calcium distributions in the tree-rings is that the concentrations of the element ions change with development of different cell wall layers. The high value of radiographic density of a cellular wall in earlywood and its relationship with cell wall thickness can be explained by the presence of ions of calcium in a cellular wall. Ions of calcium absorb X-ray radiation more strongly in comparison with light chemical elements. It can become the reason of observable relationship between radiographic density of cell wall and cell wall thickness.     

Ultrastructure of organelles during microsporogenesis inTillandsia pallidoflavens (Bromeliaceae)

InTillandsia pallidoflavens none of the organelles undergoes fundamental de- and redifferentiation during microsporogenesis. The plastids are amoeboid, exhibit complex internal structures and gradually start accumulating polysaccharides from meiotic prophase I onwards. These observations contradict reports for other taxa. The ultrastructure of mitochondria and dictyosomes, respectively, is more or less orthodox. The extensive ER, which is only poorly stained by standard methods was identified by image intensifiying techniques. The ribosomes are not only associated with the ER or occur as polyribosomes free in the cytoplasm, but can also form more or less dense clusters.     

Precocious pollen germination in Arabidopsis plants with altered callose deposition during microsporogenesis

Pollination is essential for seed reproduction and for exchanges of genetic information between individual plants. In angiosperms, mature pollen grains released from dehisced anthers are transferred to the stigma where they become hydrated and begin to germinate. Pollen grains of wild-type Arabidopsis thaliana do not germinate inside the anther under normal growth conditions. We report two Arabidopsis lines that produced pollen grains able to in situ precociously germinate inside the anther. One of them was a callose synthase 9 (cs9) knockout mutant with a T-DNA insertion in the Callose Synthase 9 gene (CalS9). Male gametophytes carrying a cs9 mutant allele were defective and no homozygous progeny could be produced. Heterozygous mutant plants (cs9/+) produced approximately 50% defective pollen grains with an altered male germ unit (MGU) and aberrant callose deposition in bicellular pollen. Bicellular pollen grains germinated precociously inside the anther. Another line, a transgenic plant expressing callose synthase 5 (CalS5) under the CaMV 35S promoter, also contained abnormal callose deposition during microsporogenesis and displaced MGUs in pollen grains. We also observed that precocious pollen germination could be induced in wild-type plants by incubation with medium containing sucrose and calcium ion and by wounding in the anther. These results demonstrate that precocious pollen germination in Arabidopsis could be triggered by a genetic alteration and a physiological condition.     

Genetic variation and population differentiation in Siberian fir Abies sibirica ledeb. inferred from allozyme markers

Genetic variation in 24 populations of Siberian fir Abies sibirica Ledeb. from the Urals, West Siberia, East Siberia, South Siberia, and the Baikal region were examined using allozyme markers. Three out of fifteen allozyme loci proved to be polymorphic. Heterozygosity H _e was 6.6–9.6%, which is substantially lower than that in other widely spread boreal conifers. Our results suggest that the Siberian fir populations are subdivided into four geographic groups: (1) the Baikal Lake group, (2) the Sayan and the Altai group, (3) the Middle and Southern Urals group, and (4) Subpolar and Northern Urals group. This pattern of geographic differentiation may be explained by the preservation of the Siberian fir during the last glacial maximum (18 000–22 000 years B.P.) in isolated refugia with subsequent recolonization of the present area. F _ST in the populations examined was 10.16%, which is comparable to the estimate for Larix sibirica (7.9%), a conifer species having a similar range and pattern of geographic population differentiation.     

Genetic variation and population differentiation in Siberian fir Abies sibirica lebed. Inferred from allozyme markers

Genetic variation in 24 populations of Siberian fir Abies sibirica Lebed. from the Urals, West Siberia, East Siberia, South Siberia, and the Baikal region were examined using allozyme markers. Three out of fifteen allozyme loci proved to be polymorphic. Heterozygosity He was 6.6-9.6%, which is substantially lower than that in other widely spread boreal conifers. Our results suggest that the Siberian fir populations are subdivided into four geographic groups: (1) the Baikal Lake group, (2) the Sayan and the Altai group, (3) the Middle and Southern Urals group, and (4) Subpolar and Northern Urals group. This pattern of geographic differentiation may be explained by the preservation of the Siberian fir during the last glacial maximum (18 000-22000 years B.P.) in isolated refugia with subsequent recolonization of the present area. FST in the populations examined was 10.16%, which is comparable to the estimate for Larix sibirica (7.9%), a conifer species having a similar range and pattern of geographic population differentiation.     

Nucleolar RNA Synthesis during Meiosis of Lily Microsporocytes

SEVERAL authors have reported a decrease in nucleolar incorporation of ³H-uridine into RNA in male gametocytes of maize, locusts and mammals during meiotic prophase^1–4, but the inactive nucleolus often persists. In the microsporocytes of Liliutn henryi the cytoplasmic ribosomes reportedly decrease in number during the extended meiotic prophase as the cellular RNA concentration also decreases⁵. Stern (personal communication) has also observed a decrease in RNA content in meiotic cells of Lilium longiflorum. We have examined the RNA synthetic activities of lily microsporocytes to see if the large nucleolus present is engaged in the synthesis of ribosomal RNA.