Differentiation and positioning of nuclei in eggs of the cecidomyid Heteropeza pygmaea

1976 ◽  
Vol 22 (1) ◽  
pp. 99-113
Author(s):  
M. Meats ◽  
J.B. Tucker
Keyword(s):  
Structural Changes ◽  
Early Stage ◽  
Cell Formation ◽  
Longitudinal Axis ◽  
Posterior Pole ◽  
Spindle Orientation ◽  
Specific Sequence ◽  
Pole Cell ◽  
Polar Granules ◽  
Egg Chamber

During the first three cleavage divisions of the egg nuclei a precise sequence of spindle orientation and elongation parallel to the longitudinal axis of the egg is apparently involved in positioning one nucleus among the polar granules at the posterior pole of the egg. The size of this nucleus, and the position at which the egg cleaves when pole cell formation occurs, appear to constitute part of the mechanism which ensures that only one nucleus is included in the first pole cell. Blastoderm formation occurs without a well-defined migration of nuclei to the egg surface. Nuclei are so large in relation to the size of the egg that uniform spacing and distribution of nuclei ensures that a large proportion are situated near the egg surface. Those nuclei which are near the egg surface divide synchronously to form a layer of blastoderm nuclei, while membranous cleavage furrows invaginate from the egg surface between them. Nuclei in the central region of the egg chamber condense to form yolk nuclei before blastoderm nuclei have been separated from the rest of the egg by the completion of the cleavage membranes. Polar granules provide the only evidence of fine-structural differences in different regions of the egg chamber cytoplasm. They are found near the posterior pole of the egg from an early stage of oogenesis. They undergo a specific sequence of structural changes and increase in size as the egg grows. No microtubular or microfibrillar arrays have been found in the egg chamber which might form a cytoskeletal basis for spindle orientation or for the spatial differences which develop during differentiation of the uncleaved egg cytoplasm.

scholarly journals Identification of a component of Drosophila polar granules

Development ◽  
1988 ◽  
Vol 103 (4) ◽  
pp. 625-640 ◽  
Author(s):  
B. Hay ◽  
L. Ackerman ◽  
S. Barbel ◽  
L.Y. Jan ◽  
Y.N. Jan
Keyword(s):  
Germ Line ◽  
Posterior Pole ◽  
Nuclear Bodies ◽  
Maternal Origin ◽  
Pole Cell ◽  
Polar Granules ◽  
Early Embryos ◽  
Biochemical Studies ◽  
Males And Females ◽  
Pole Cells

Information necessary for the formation of pole cells, precursors of the germ line, is provided maternally and localized to the posterior pole of the Drosophila egg. The maternal origin and posterior localization of polar granules suggest that they may be associated with pole cell determinants. We have generated an antibody (Mab46F11) against polar granules. In oocytes and early embryos, the Mab46F11 antigen is sharply localized to the posterior embryonic pole. In pole cells, it becomes associated with nuclear bodies within, and nuage around, the nucleus. Immunoreactivity remains associated with cells of the germ line throughout the life cycle of both males and females. This antibody recognizes a 72–74 × 10(3) Mr protein and is useful both as a pole lineage marker and in biochemical studies of polar granules.

Oskar anchoring restricts pole plasm formation to the posterior of the Drosophila oocyte

Development ◽  
2002 ◽  
Vol 129 (15) ◽  
pp. 3705-3714 ◽  
Author(s):  
Nathalie F. Vanzo ◽  
Anne Ephrussi
Keyword(s):  
Drosophila Melanogaster ◽  
Translational Control ◽  
Cell Formation ◽  
Positional Information ◽  
Mrna Localization ◽  
Posterior Pole ◽  
Tight Coupling ◽  
Anteroposterior Patterning ◽  
Pole Cell ◽  
Pole Plasm

Localization of the maternal determinant Oskar at the posterior pole of Drosophila melanogaster oocyte provides the positional information for pole plasm formation. Spatial control of Oskar expression is achieved through the tight coupling of mRNA localization to translational control, such that only posterior-localized oskar mRNA is translated, producing the two Oskar isoforms Long Osk and Short Osk. We present evidence that this coupling is not sufficient to restrict Oskar to the posterior pole of the oocyte. We show that Long Osk anchors both oskar mRNA and Short Osk, the isoform active in pole plasm assembly, at the posterior pole. In the absence of anchoring by Long Osk, Short Osk disperses into the bulk cytoplasm during late oogenesis, impairing pole cell formation in the embryo. In addition, the pool of untethered Short Osk causes anteroposterior patterning defects, owing to the dispersion of pole plasm and its abdomen-inducing activity throughout the oocyte. We show that the N-terminal extension of Long Osk is necessary but not sufficient for posterior anchoring, arguing for multiple docking elements in Oskar. This study reveals cortical anchoring of the posterior determinant Oskar as a crucial step in pole plasm assembly and restriction, required for proper development of Drosophila melanogaster.

scholarly journals Transcriptomic and functional analysis of the oosome, a unique form of germ plasm in the waspNasonia vitripennis

2018 ◽  
Author(s):  
Honghu Quan ◽  
Jeremy Lynch
Keyword(s):  
Molecular Basis ◽  
Germ Plasm ◽  
Cell Formation ◽  
Solid Sphere ◽  
The Novel ◽  
Developmental Networks ◽  
Pole Cell ◽  
Polar Granules ◽  
Developmental Role ◽  
Pole Cells

AbstractBackgroundThe oosome is the germline determinant in the waspNasonia vitripennisand is homologous to the polar granules ofDrosophila. Despite a common evolutionary origin and developmental role, the oosome is morphologically quite distinct from polar granules. It is a solid sphere that migrates within the cytoplasm before budding out and forming pole cells.ResultsTo gain an understanding of both the molecular basis of the novel form of the oosome, and the conserved essential features of germ plasm, we quantified and compared transcript levels between embryo fragments that contained the oosome, and those that did not. The identity of the localized transcripts indicated thatNasoniauses different molecules to carry out conserved germ plasm functions. In addition, functional testing of a sample of localized transcripts revealed potentially novel mechanisms of ribonucleoprotein assembly and pole cell cellularization in the wasp.ConclusionsOur results demonstrate that numerous novel and unexpected molecules have been recruited in order produce the unique characteristics of the oosome and pole cell formation inNasonia. This work will serve as the basis for further investigation into the patterns of germline determinant evolution among insects, the molecular basis of extreme morphology of ribonucleoproteins, and the incorporation of novel components into developmental networks.

Restoration of pole-cell-forming ability to u.v.-irradiated Drosophila embryos by injection of mitochondrial lrRNA

Development ◽  
1989 ◽  
Vol 107 (4) ◽  
pp. 733-742 ◽  
Author(s):  
S. Kobayashi ◽  
M. Okada
Keyword(s):  
Dna Sequences ◽  
Nuclear Dna ◽  
Mitochondrial Gene ◽  
Cell Formation ◽  
Nuclear Bodies ◽  
Cdna Insert ◽  
Pole Cell ◽  
Polar Granules ◽  
Pole Cells

Screening a cDNA library generated from poly(A) +RNA of Drosophila cleavage embryos, we selected a cDNA clone (pDE20.6). The cDNA hybridized specifically with a poly(A) +RNA that is capable of restoring embryos from u.v.-caused inability of pole cell formation. The RNA hybrid-selected by pDE20.6 was also able to induce pole cells in the anterior region of embryos, if it was coinjected with u.v.-irradiated polar plasm, although the RNA or irradiated polar plasm alone was not effective. Pole cells thus formed in the anterior or in the u.v.-irradiated posterior region were identified by polar granules and nuclear bodies, morphological markers for normal pole cells. Furthermore, the RNA-induced pole cells were able to migrate into gonadal rudiments. The nucleotide sequence of pDE20.6 cDNA insert was highly homologous with the mitochondrial large rRNA (lrRNA) gene, but not with any nuclear DNA sequences. Using pDE20.6 as a primer, a full-length cDNA of mitochondrial lrRNA was generated and cloned. The RNA transcribed in vitro from the cDNA was able to restore pole cell formation. The cDNA hybridized only with a 1.5 kb poly(A) +RNA on a Northern blot. The 1.5 kb RNA sedimented more with the post-mitochondrial (P3) fraction than with the mitochondrial (P2) fraction, while the majority of transcripts from another mitochondrial gene was detected in the P2 fraction.

Drosophila virilis oskar transgenes direct body patterning but not pole cell formation or maintenance of mRNA localization in D. melanogaster

Development ◽  
1994 ◽  
Vol 120 (7) ◽  
pp. 2027-2037 ◽  
Author(s):  
P.J. Webster ◽  
J. Suen ◽  
P.M. Macdonald
Keyword(s):  
Drosophila Melanogaster ◽  
Germ Cell ◽  
Cell Formation ◽  
Mrna Localization ◽  
Early Embryo ◽  
Posterior Pole ◽  
Early Embryogenesis ◽  
Drosophila Virilis ◽  
Pole Cell ◽  
Body Patterning

The Drosophila melanogaster gene oskar is required for both posterior body patterning and germline formation in the early embryo; precisely how oskar functions is unknown. The oskar transcript is localized to the posterior pole of the developing oocyte, and oskar mRNA and protein are maintained at the pole through early embryogenesis. The posterior maintenance of oskar mRNA is dependent upon the presence of oskar protein. We have cloned and characterized the Drosophila virilis oskar homologue, virosk, and examined its activity as a transgene in Drosophila melanogaster flies. We find that the cis-acting mRNA localization signals are conserved, although the virosk transcript also transiently accumulates at novel intermediate sites. The virosk protein, however, shows substantial differences from oskar: while virosk is able to rescue body patterning in a D. melanogaster oskar- background, it is impaired in both mRNA maintenance and pole cell formation. Furthermore, virosk induces a dominant maternal-effect lethality when introduced into a wild-type background, and interferes with the posterior maintenance of the endogenous oskar transcript in early embryogenesis. Our data suggest that virosk protein is unable to anchor at the posterior pole of the early embryo; this defect could account for all of the characteristics of virosk mentioned above. Our observations support a model in which oskar protein functions both by nucleating the factors necessary for the activation of the posterior body patterning determinant and the germ cell determinant, and by anchoring these factors to the posterior pole of the embryo. While the posterior body patterning determinant need not be correctly localized to provide body patterning activity, the germ cell determinant may need to be highly concentrated adjacent to the cortex in order to direct pole cell formation.

aubergineencodes aDrosophilapolar granule component required for pole cell formation and related to eIF2C

Development ◽  
2001 ◽  
Vol 128 (14) ◽  
pp. 2823-2832 ◽  
Author(s):  
Adam N. Harris ◽  
Paul M. Macdonald
Keyword(s):  
Polar Granule ◽  
Cell Formation ◽  
Posterior Pole ◽  
Translation Initiation Factor ◽  
Initiation Factor ◽  
Dependent Manner ◽  
Eukaryotic Translation ◽  
Pole Cell ◽  
Body Patterning ◽  
Pole Plasm

In Drosophila oocytes, activation of Oskar translation from a transcript localized to the posterior pole is an essential step in the organization of the pole plasm, specialized cytoplasm that contains germline and abdominal body patterning determinants. Oskar is a component of polar granules, large particles associated with the pole plasm and the germline precursor pole cells of the embryo. aubergine mutants fail to translate oskar mRNA efficiently and are thus defective in posterior body patterning and pole cell formation. We have found that Aubergine protein is related to eukaryotic translation initiation factor 2C and suggest how it may activate translation. In addition, we found that Aubergine was recruited to the posterior pole in a vas-dependent manner and is itself a polar granule component. Consistent with its presence in these structures, Aubergine is required for pole cell formation independently of its initial role in oskar translation. Unlike two other known polar granule components, Vasa and Oskar, Aubergine remains cytoplasmic after pole cell formation, suggesting that the roles of these proteins diverge during embryogenesis.

Polar granules and pole cells in the embryo of Calliphora erythrocephala: ultrastructure and [3H]leucine labelling

Development ◽  
1980 ◽  
Vol 57 (1) ◽  
pp. 79-93
Author(s):  
Anders Lundquist ◽  
Hadar Emanuelsson
Keyword(s):  
Cell Formation ◽  
Electron Microscopic ◽  
Electron Microscopic Autoradiography ◽  
Calliphora Erythrocephala ◽  
Pole Cell ◽  
Polar Granules ◽  
Pole Cells ◽  
Autoradiographic Analysis ◽  
Pole Plasm ◽  
Blastoderm Stage

The polar granules in Calliphora undergo a gradual fragmentation during early cleavage, but reaggregate after pole-cell formation. Autoradiographic analysis showed that the pole cells in Calliphora acquire a higher ‘3H’leucine label than the rest of the embryo during the blastoderm stage. Such an increased label was not seen in the pole plasm before pole-cell formation or in the pole cells during gastrulation. Electron microscopic autoradiography revealed that the polar granules are substantially labelled during the blastoderm stage. At the same time, characteristic nuclear blebs appear in the pole cells. The observations are consistent with the hypothesis that polar granules contain maternalmessenger RNA, which is released and translated into proteins.

Mutations in a newly identified Drosophila melanogaster gene, mago nashi, disrupt germ cell formation and result in the formation of mirror-image symmetrical double abdomen embryos

Development ◽  
1991 ◽  
Vol 113 (1) ◽  
pp. 373-384 ◽  
Author(s):  
R.E. Boswell ◽  
M.E. Prout ◽  
J.C. Steichen
Keyword(s):  
Drosophila Melanogaster ◽  
Germ Cell ◽  
Cell Formation ◽  
Temperature Shift ◽  
Longitudinal Axis ◽  
Posterior Pole ◽  
Mirror Image ◽  
Sensitive Period ◽  
Temperature Sensitive ◽  
Mago Nashi

The mago nashi (mago) locus is a newly identified strict maternal effect, grandchildless-like, gene in Drosophila melanogaster. In homozygous mutant mago females reared at 17 degrees C, mago+ function is reduced, the inviable embryos lack abdominal segments and 84–98% of the embryos die. In contrast, at 25 degrees C, some mago alleles produce a novel gene product capable of inducing the formation of symmetrical double abdomen embryos. Reciprocal temperature-shift experiments indicate that the temperature-sensitive period is during oogenetic stages 7–14. Furthermore, embryos collected from mago1 homozygous females contain no apparent functional posterior determinants in the posterior pole. In viable F1 progeny from mago mutant females, regardless of genotype and temperature, polar granules are reduced or absent and germ cells fail to form (the grandchildless-like phenotype). Thus, we propose that the mago+ product is a component of the posterior determinative system, required during oogenesis, both for germ cell determination and delineation of the longitudinal axis of the embryo.

Staphylococcal infection and pathomurfological characteristic of the pituitary-adrenal-thyroid system

2020 ◽  
Vol 03 (04) ◽  
pp. 69-73
Author(s):  
Samira Mammadhasan Yagubova ◽  
◽  
Elchin Chingiz Akbarov ◽  
Tarana Nadir Mirzayeva ◽  
◽  
...  
Keyword(s):  
Structural Changes ◽  
Adrenal Glands ◽  
Early Stage ◽  
Morphological Changes ◽  
Endocrine System ◽  
Staphylococcal Infection ◽  
The Body ◽  
Glandular Cells ◽  
Exogenous Factors ◽  
Specific Symptoms

During the staphylococcal infection, changes in the interaction of glandular cells, dystrophic and disorganizing pathologies in tissues, especially acute structural and hemodynamic changes in the stroma of the glands in the pituitary-adrenal-thyroid system, develop from the first day of the experiment. At the end of the experiment, on the background of a decrease in exudative processes, fibroplastic reactions are significantly activated, resulting in signs of incomplete regeneration – mainly sclerotic processes and cystic-atrophic changes in the parenchyma. Structural changes in tissues in the early stages of staphylococcal infection and the dynamics of development are characterized by specific symptoms in each of the glands. Since the pituitary gland is exposed to endogenous and exogenous factors earlier and more often than the adrenal glands, and the adrenal glands are earlier than the thyroid gland, dystrophic and destructive changes in the pituitary and adrenal glands are more pronounced at the early stage of the experiment. These morphological changes can change the hormonal status of the body and lead to dysfunction of the endocrine system as a whole – a decrease in the functional activity of the glands to some extent, and even inhibition of adenohypophyseal cells. Key words: staphylococcal infection, peritonitis, pituitary, adrenal and thyroid glands

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