Formation of the amphibian grey crescent: Effects of colchicine and cytochalasin B

Summary The effects of colchicine and cytochalasin B on grey crescent formation in frog (Rana pipiens) and toad (Bufo arenarum) eggs were determined. Colchicine prevented the appearance of the grey crescent, but this inhibition was not due to the absence of an aster. Cytochalasin B did not inhibit grey crescent formation, nor did it inhibit certain activation events such as cortical granule breakdown or cortical contraction. Cytochalasin B caused a detachment of the cortex from the cytoplasm and induced the formation of a morphological grey crescent in non-activated eggs. The results suggest that microtubules may play several roles in grey crescent formation and that a change in the attachment of the cortex to the cytoplasm may also be involved.     

Involvement of the cytoskeleton in early grey crescent formation in axolotl oocytes

Summary Maturing axolotl oocytes which are treated with protein synthesis inhibitors or which are heat-shocked can be induced to reorganize their cytoplasm and to form an early grey crescent. The maturing axolotl oocyte has been used as a model system to study the role of the cytoskeleton in dorsoventral polarization as visualized by grey crescent formation. Results presented here provide evidence for the involvement of microtubules in the formation of the early grey crescent. Whereas inhibitors of microtubule polymerization and antibodies against tubulin both elicit early grey crescent formation, the effect of taxol shows that microtubule polymerization is required at a late stage in this event. The nucleus furnishes important factors required for early grey crescent formation and might play a role in microtubule polymerization.     

Early grey crescent formation experimentally induced by cycloheximide in the axolotl oocyte

Summary The effects of cycloheximide (CH) on grey crescent formation in artificially maturedAmbystoma mexicanum oocytes were determined. CH induced grey crescent formation after a few hours, especially after a 45° to 90° rotation from the vertical animal-vegetal axis. With low concentrations of CH (about 0.5 ng/oocyte), meiosis was still able to proceed normally to the stable second metaphase stage, but higher concentrations blocked it after 1st polar body extrusion and an interphasic nucleus appeared. Such effects were compared to those of inactone, an analogue of cycloheximide, which as a pure substance does not inhibit protein synthesis, but still contained a small amount of CH in the available samples. It is concluded that grey crescent formation can occur in non-activated oocytes. The effects of cycloheximide might be due to partial inhibition of protein synthesis and the presence of a proteinic inhibitor of the symmetry reaction in the normal oocyte is suggested.     

Ca2+ as a messenger of dorsal--ventral polarity formation in frog (Rana temporaria) eggs.

Three methods of Ca2+ administration were used to influence the location of the grey crescent and the dorsal lip of blastopore in R temporaria eggs, ie a Ca2+ microinjection into the subcortical cytoplasm, egg pricking in high Ca2+ solutions and Ca2+ ionophore A23187 microinjection and application. The treatments all induced grey crescent and dorsal lip of blastopore formation near the Ca2+ administration site. Inositol trisphosphate injections gave similar results. Colchicine injections into the eggs inhibited the appearance of both natural and Ca(2+)-induced grey crescents.     

豹蛙受精卵与未受精卵离心后的差别

1.豹蛙受精卵与未受精卵在用×1500g 左右离心后都形成四层:脂类物质层,原生质层,黑色粒层,和卵黄粒层。但切片的观察:黑色粒层与卵黄粒层的界限不明。可是越近植物極卵黄粒愈多,黑色粒愈少。2.未受精卵奥受精卵在用×1500g 左右离心后有内外部形态的不同。大部分未受精卵的脂类物质层是光滑的,而受精卵的脂类物质层是绉褶的。3.根据卵内物层和结构在离心卵内的分布可以测定他们的相对比重。它们相对的比重是:卵黄粒>黑色粒>原生质>脂类物质。受精卵的质膜和皮层的联合相对比重是等于或小于原生质的比重,但大于脂类物质的比重。未受精卵的质膜和皮层联合比重,在大多数未受精卵内因质膜与卵黄膜的关系不能正确确定。可是根据少数卵的情况,未受精卵的层膜与皮层的联合比重可能也大于未受精卵的脂灯物质小于或等于原生质的比重。4.我们提出了两个解释受精卵绉褶脂类物质层的形成假说,并加以讨论。可是在现在的实验资料情况下,我们还不能最后肯定那一个假说是完全正确的。     

Host egg pigmentation protects developing parasitoids from ultraviolet radiation

Parasites rely on their hosts not only for nutrition and reproduction, but also for protection against natural enemies and adverse climatic conditions. In host‐parasite interactions, protective characteristics of both players are important to consider regarding damaging effects of environmental hazards. While ultraviolet radiation (UVR) is pervasive and harmful to organisms in general, its impact on parasite fitness remains understudied. Moreover, studies that do examine the effects of UV exposure on parasitic organisms tend to neglect host traits, which may vary inter‐ or intra‐specifically and thus confer different levels of environmental protection. We examined in the laboratory whether the UV‐protective value of host egg pigmentation could also benefit parasitoids, using the egg parasitoid Telenomus podisi and the predatory stink bug Podisus maculiventris. This host species lays eggs of variable pigmentation levels from light to dark grey, an adaptation protecting its own embryos from UVR. We showed that higher levels of host egg pigmentation protect parasitoids subjected to a developmental exposure to UVR, increasing emergence rates by up to 86% and reducing development time by up to 4%. This protective effect of host pigmentation was context‐dependent, being less pronounced at low UVR intensity and towards the end of parasitoid development. Parasitoids that emerged from darker‐coloured eggs exposed to UVR were of slightly larger size than those developing in light‐coloured eggs, but other fitness‐related traits (fecundity, longevity, sex ratio) were unaffected. This study provides the first experimental evidence that host pigmentation can increase host suitability for parasitic organisms, and emphasizes the importance of considering trait variation in interacting species when investigating the susceptibility of ecological communities to important abiotic environmental factors.     

Inducing effects of the grey crescent region of early developmental stages of ambystoma mexicanum

Summary Parts of the grey crescent region of 1–2 cell, 8 cell and morula stages ofAmbystoma mexicanum were combined with presumptive gastrula ectoderm of the same species (sandwich method).Grey crescent material of the early cleavage stages induced neural tissues at a very low rate (6%–7%).From the morula stage onwards, the inducing ability of the grey crescent area increased and led to the formation of mesodermal as well as neural organs. The implanted area did not participate in the organ formations.

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Zusammenfassung Von Axolotl-Keimen wurden im 1–2 Zell-Stadium, im 8 Zell-Stadium und im Morula-Stadium Implantate aus der Region des grauen Halbmondes entnommen und mit präsumptivem Ektoderm aus frühen Gastrulen der gleichen Spezies kombiniert (Sandwich-Methode).Material aus dem grauen Halbmond früher Furchungsstadien induzierte nur wenig neurales Gewebe (6%–7% der Fälle).Vom Morula-Stadium an war die Induktionsrate höher. Neben neuralen wurden auch mesodermale Organe induziert. — Das implantierte Gewebe war nicht an den Organbildungen beteiligt.

     

Regional Morphological and Cytochemical Differentiation in the Fertilized Egg of Discoglossus pictus (Anura)

A vertical column of cytoplasm poor in yolk (CPY) is located in the centre of the animal region of the unfertilised and fertilised egg of Discoglossus pictus. At the base of this column is found a central region of CPY designated as "clear cytoplasm". Cytochemical methods show that the CPY in this whole region is rich in glycogen and RNA.
By 60 min post opposition (p.o.) the pigmented cortical layer starts moving towards the future ventral side. It attains its definitive position by 90 min p.o. when the grey crescent, visible from 75 min p.o. onwards, achieves its maximal extension on the future dorsal side. The cytoplasmic column is now tilted towards the future ventral side. It progressively loses its direct contact with the cell membrane and disappears.
From 90 min p.o. onwards, the "clear cytoplasm" is found progressively closer to the dorsal grey crescent cortex. When the first cleavage furrow appears at 135 min p.o., the "clear cytoplasm" is situated very near the dorsal cortex and even extends somewhat below the equator. In places a relatively thin layer of cytoplasm containing medium-sized and a few large yolk granules intervenes between the grey crescent cortex and the "clear cytoplasm".
These displacements suggest that sperm entry evokes a dorsally directed cytoplasmic movement in the animal half of the egg which, among other things, may facilitate an interaction between the vegetative yolk and the grey crescent cortex, or may directly influence the dorso-ventral polarisation of the vegetative yolk.     

Ion currents and membrane domains in the cleaving Xenopus egg

We used an extracellular vibrating probe to measure ion currents through the cleaving Xenopus laevis egg. Measurements indicate sharp membrane heterogeneities. Current leaves the first cleavage furrow after new, unpigmented membrane is inserted. This outward current may be carried by K+ efflux. No direct involvement of the Na+,K+-ATPase in the generation of this outward current is detected at first cleavage. Inward current enters the old, pigmented membrane; however, it does not enter uniformly. The inward current is largest at the old membrane bordering the new membrane. This suggests a heterogeneous ion channel distribution within the old membrane. Experiments suggest that the inward current may be carried by Na+ influx, Ca2+ influx, and Cl- efflux. No steady currents were detected during grey crescent formation, the surface contraction waves preceding cleavage, or with groove formation at the beginning of cleavage.     

Destruction of components of the neural induction system of the amphibian egg with ultraviolet irradiation

Ultraviolet irradiation of the vegetal hemisphere of the fertilized amphibian (Xenopus laevis) egg prior to first cleavage results in the embryo developing an incomplete set of neural structures. The effects of irradiation on various morphogenetic processes, including cell division, formation of the dorsal lip, invagination at gastrulation, and neural induction by the primary organizer, were examined. A decrease in the capacity for invagination during gastrulation and a diminution in the neural inducing capacity of the primary organizer were found to account for defective neurulation in irradiated embryos. Consequently, irradiation of the uncleaved egg leads to interference with the events of both gastrulation and neurulation.     

Ultraviolet irradiation initiates ectopic foot formation in regenerating hydra and promotes budding

We have studied the effects of ultraviolet-C (UVC) and Ultraviolet-B (UVB) on growth and pattern formation inPelmatohydra oligactis. UVC brings about a significant increase in budding in intact hydra while UVB does not exhibit such an effect. Excessive budding could be a response for survival at wavelengths that damage biological tissues. If the head or base piece of a bisected hydra is irradiated and recombined with the unirradiated missing part, regeneration proceeds normally indicating that exposure of a body part with either an intact head or foot to UVC does not influence pattern formation. Most significantly, in the middle piece, but not in the head or the base piece of a trisected hydra, UVC leads to initiation of ectopic feet formation in almost one third of the cases. Thus, UV irradiation interferes with pattern formation in regenerating hydra, possibly by changing positional values, and promotes budding in intact hydra. This is the first report on induction of ectopic feet formation by UV in regenerating hydra and opens up the possibility of using UV irradiation as a tool to understand pattern formation in the enigmatic hydra     

Changes in the dorsoventral polarity in frog eggs (Rana temporaria) under the influence of Ca2+ injections. The conditions for effecting a response

The effect of local injections of Ca2+ solutions into Rana temporaria eggs during the period from fertilization to 1st cleavage division was studied. In most cases, microinjection of 2-5 nl of 1-20 mM Ca2+ solution into subcortical cytoplasm determined formation of the grey crescent (and the dorsal blastopore lip) at the site of injection. Injection of 0.1 mM Ca2+ or Ca(2+)-free solutions had no effect on the formation of the dorso-ventral axis. The effect of Ca2+ is more pronounced when the injection is made into vegetal part of the egg, close to the boundary between pigmented and non-pigmented zones, than into animal-equatorial part. Injections made during the 0.10-0.15 period of the first cell cycle produced greater effect than those made during the 0.40-0.45 period of the same cycle.     

Induction of homologous recombination in Saccharomyces cerevisiae

Summary We have investigated the effects of UV irradiation of Saccharomyces cerevisiae in order to distinguish whether UV-induced recombination results from the induction of enzymes required for homologous recombination, of the production of substrate sites for recombination containing regions of DNA damage. We utilized split-dose experiments to investigate the induction of proteins required for survival, gene conversion, and mutation in a diploid strain of S. cerevisiae. We demonstrate that inducing doses of UV irradiation followed by a 6 h period of incubation render the cells resistant to challenge doses of UV irradiation. The effects of inducing and challenge doses of UV irradiation upon interchromosomal gene conversion and mutation are strictly additive. Using the yeast URA3 gene cloned in non-replicating single- and double-stranded plasmid vectors that integrate into chromosomal genes upon transformation, we show that UV irradiation of haploid yeast cells and homologous plasmid DNA sequences each stimulate homologous recombination approximately two-fold, and that these effects are additive. Non-specific DNA damage has little effect on the stimulation of, homologous recombination, as shown by studies in which UV-irradiated heterologous DNA was included in transformation/recombination experiments. We further demonstrate that the effect of competing single- and double-stranded heterologous DNA sequences differs in UV-irradiated and unirradiated cells, suggesting an induction of recombinational machinery in UV-irradiated S. cerevisiae cells.     

Androgenesis and homozygous gynogenesis in muskellunge (Esox masquinongy): Evaluation using flow cytometry

The purpose of this work was to study the effects of ultraviolet (UV) irradiation on denucleation of eggs and investigate the heat-shock conditions for diploidization for induction of androgenesis in muskellunge, Esox masquinongy. Several egg incubation media, including saline, Ringer's solution, and Ringer's solution supplemented with bovine serum albumin (BSA), were found suitable to maintain the egg fertility as high as in muskellunge ovarian fluid. The optimal doses of UV radiation were 660–1320 J/m², at which 100% haploid larvae were produced at a hatching rate of 22.5 ± 2.8%. UV irradiation at low doses (165–330 J/m²) generated abnormal larvae, which were morphologically identical to haploids. Using a flow cytometry method, it was found that cellular DNA content of these larvae was close to that of diploids but significantly lower in value and had a wider distribution (expressed as coefficient of variation) than that of control fish. This suggested that a low dose of UV irradiation might cause gene mutations, alteration of chromosomal conformation and fragmentation, but did not prevent maternal DNA from participating in mitotic division. Interference of maternal DNA residues could be another reason for the poor viability of androgenetic fish. A high dose of UV radiation (1980 J/m²) caused development of severely deformed embryos, indicating that UV radiation also damaged molecules in the eggs other than the denucleation. Our results suggest that classic color and allozyme markers might not be sufficient to prove a complete androgenesis. In order to optimize time and duration of shock for induced diploidization, we investigated the heat-shock conditions for inhibiting the first mitotic cleavage through induction of homozygous gynogenesis. We found that heat-shock treatment at 31°C for 9 min starting at 1.4τ₀ (a dimensionless factor describing progress in embryo development) after fertilization produced the highest percentage of diploids at hatching. Mol. Reprod. Dev. 49:10–18, 1998. © 1998 Wiley-Liss, Inc.     

Effects of irradiation on the reproductive ability of Zonitoides arboreus, a snail pest of orchid roots

The effect of irradiation on the reproductive ability of the orchid snail, Zonitoides arboreus, a serious pest of potted orchids in Hawaii, was investigated. Weekly egg production averaged between 0.8 and 1.9 over a 9–wk period for snails not exposed to irradiation, and egg hatch averaged 61%. In comparison to untreated controls, irradiation of snails at the lowest dose tested (34–37 Gy) reduced egg production and egg hatch by 63% and 94%, respectively over a 9–wk period. None of the snails treated with levels of irradiation ≥ 69 Gy produced viable eggs. This is the first study measuring the effect of ionising irradiation on a terrestrial snail or slug species using sterilising doses. Overall, the results show that the reproductive ability of this snail species is affected by irradiation in a similar manner as for Biomphalaria glabrata, an aquatic snail for which the effects of irradiation have been studied in detail.     

Effects of selected physical and chemical treatments of Colorado potato beetle eggs on host acceptance and development of the parasitic wasp, Edovum puttleri

Effects of various physical and chemical treatments of Colorado potato beetle [Leptinotarsa decemlineata (Coleoptera: Chrysomelidae)] eggs on parasitization and development of the egg parasitoid Edovum puttleri (Hymenoptera: Eulophidae) were investigated. UV irradiation did not affect host acceptance but reduced host suitability for UV exposure times 90 min. Susceptibility of host eggs to UV irradiation varied with host age; eggs were most vulnerable to damage from irradiation at 12, 18, and 24 h post-oviposition. The rate of parasitization also was influenced by host age. Percent parasitization was greatest in freshly laid eggs and 24–30 h old eggs. Seventy-seven percent of host eggs frozen at –20 °C (5 min) were parasitized by E. puttleri, but extended exposure of eggs to –20 °C reduced both acceptance and suitability. Host eggs that had been washed with hexane (removal of kairomone and sticky layer) also were parasitized. After 5 min of washing, application of kairomone significantly increased the rate of parasitism (from 74.7% to 88.2%), but with longer periods of washing, kairomone application had no significant effect on percent parasitism. Thus, the sticky material(s) coating the egg did not appear to be essential for parasitization to occur. Our results provide effective methods and times for treating Colorado potato beetle eggs to maximize parasitization and development of E. puttleri.     

Inhibition of protein synthesis elicits early grey crescent formation in the axolotl oocyte

Summary In the axolotl (Ambystoma mexicanum Shaw), it was recently shown that cycloheximide (CH) could induce early grey crescent formation (EGC) in non-activated oocytes, maturing in vitro (Grinfeld and Beetschen 1982). Since it was not proved that EGC was a consequence of protein synthesis inhibition rather than a side-effect of the drug, experiments were performed using microinjections of a quite different inhibitor, diphtheria toxin (DT). This toxin also appeared to elicit EGC. Incorporation of (³H) leucine into oocyte proteins in the presence of increasing DT concentrations (10^–11 to 10^–6 M) was then investigated. The frequency of EGC closely parallels the level of protein synthesis inhibition, which is higher in symmetrized oocytes. The lowest CH concentration which can still elicit EGC also exerts a fairly strong inhibition of (³H) leucine incorporation into proteins. It is concluded that protein synthesis inhibition in the late maturing oocyte actually creates specific conditions which allow cytoplasmic rearrangements to occur, leading to grey crescent formation. These results support the interpretation that (a) proteinic inhibitor (s) of symmetrization could be synthesized in the normal maturing oocyte.     

Effects of cytoskeletal inhibitors on ooplasmic segregation and microtubule organization during fertilization and early development in the ascidian Molgula occidentalis

The effects of microtubule and microfilament inhibitors on ooplasmic segregation and microtubule organization were examined during fertilization, parthenogenetic activation, and early development in the ascidian Molgula occidentalis. At fertilization the egg cortex contracts as the first phase movement and shortly after mitochondria migrate as the myoplasmic crescent develops in the second phase. The microtubule inhibitors colcemid and nocodazole inhibit the second phase, but not the first phase, of ooplasmic segregation. The microfilament inhibitor cytochalasin E has the reciprocal effect of inhibiting the first, but not the second, phase. It appears that sperm may initially bind at any site on the egg surface and that the contractile activities at the first phase and during polar body formation occur independent of the microtubule system. Since the second phase migration occurs as the sperm astral microtubules assemble and since microtubule, but not microfilament, inhibitors arrest this aspect of ooplasmic segregation, microtubules appear necessary for mitochondrial migration. These results demonstrate that the two phases of ascidian ooplasmic segregation are mediated by different systems, the first by microfilaments and the second by microtubules. The microtubule and microfilament systems appear to operate independent of one another and their combined actions result in the completion of ooplasmic segregation. A model is proposed in which the cortical contraction following fertilization is important not only as the motive force for the first phase movement but also as a method to unite the myoplasm with the entering sperm which can initially bind anywhere on the egg surface. The association between myoplasmic components and the growing sperm aster would ensure that the migration and the spatial distribution of myoplasm in the second phase results in the formation of the myoplasmic crescent.