Hormonal aspects of oögenesis in the flies Phormia regina and Sarcophaga bullata

The corpora allata (CA) and median neurosecretory cells (MNC) of Phormia regina and Sarcophaga bullata become active with increasing age of the fly, on a diet of sugar alone. To prevent or retard oögenesis the CA or MNCs must be removed shortly after emergence, with subsequent protein meals. Topical JH application partially compensates for CA or MNC removal. This shows that the MNC activate the CA, and not vice versa. The trauma of either operation slightly depresses egg development.Injection of ecdysone into both species in the stage of initial yolk deposition causes the primary oöcytes to degenerate. This leads to development of the penultimate oöcytes. Older and younger egg stages are not sensitive to ecdysone. In P. regina the application of JH to females with developing primary oöcytes stimulates yolk deposition in the penultimate oöcytes.     

Evidence for haemoglobin uptake by oöcytes of Chironomus thummi

Developing oöcytes of a haemoglobin-containing fly, Chironomus thummi, have been investigated using the 3,3′-diaminobenzidine method for their endogeneous peroxidase activity. In the previtellogenic oöcytes the reaction product, which is thought due to the peroxidatic activity of the haemoglobins, is not observed within the oöcytes. Vitellogenic oöcytes appear active in the uptake and incorporation of the externally derived peroxidese-active material into the yolk. The reaction product which is first visualized in the extracellular spaces within the follicle, then the pinosomes and multivesicular bodies of the oöcyte, is later seen in the mature yolk granules. These observations are discussed in terms of their relation to the accumulation of haemoglobin as a part of the yolk.     

Rate of follicle growth,change in follicle volume and stages of macromolecular synthesis during ovarian development in Musca domestica

At 21°C the first egg generation takes 6 days to develop. During this period the oöcyte volume increases by a factor of ×5000, and compared with an oögonium the growth factor amounts to ×100,000. The growth rate of the oöcyte increases with each stage of oögenesis, until at stage 5 it reaches 2.5 × 10⁶ μm³/hr. About 35% of the substance stored in the oöcyte originates from the nurse chamber. 30% of the volume is formed in the stage where the oöcyte synthesizes almost exclusively glycogen. Accordingly, about 30% of the volume is provided by the euplasmatic protein synthesis and by the yolk uptake.     

Vitellin and vitellogenin incorporation by isolated oöcytes of Locusta migratoria migratorioides (R.F.)

Vitellin and vitellogenin labelled in vitro with ¹²⁵I and in vivo with ³H were incorporated into yolk by locust oöcytes incubated in an in vitro system. This incorporation was specific and linear with the duration of incubation. Uptake of vitellin by oöcytes was 3–4 times higher than ¹²⁵I-bovine serum albumin in 2.1-mm oöcytes and 20 times higher than ¹²⁵I-bovine serum albumin in 4.0-mm long oöcytes. The uptake of the albumin was enhanced by the presence of vitellin in the incubation medium. ³H-labelled yolk protein was incorporated at higher rates than that labelled with ¹²⁵I. The addition of the juvenile hormone analogue ZR 515, caused the incorporation rates of vitellogenin to be increased. The amount of vitellin or vitellogenin taken up by the oöcytes increased with their length, and the rate of incorporation per unit surface area was highest in 3–4-mm long oöcytes. These results corroborate previously reported in vivo patterns of incorporation rates of developing oöcytes.     

Juvenile hormone-induced vitellogenesis in Apterous4, a non-vitellogenic mutant in Drosophila melanogaster

D. melanogaster females homozygous for the ap⁴ mutant synthesize yolk protein and circulate this protein in the haemolymph at concentrations not different from concentrations found in normal females. However, ap⁴ females deposit little or no yolk protein into developing oöcytes. Topical application of a juvenile hormone analogue (JHA), ZR-515, stimulated sequestration of yolk protein by developing oöcytes of ap⁴ females. JHA had no detectable effects on haemolymph concentrations of yolk protein in either normal or ap⁴ females nor on the protein profiles obtained from electrophoresis of haemolymph samples.     

Vitellogenesis by the American cockroach: Electrophoretic and antigenic characterization of haemolymph and oöcyte proteins

Several peptides have been found in the haemolymph which are antigenically similar to peptides found in the terminal oöcyte during vitellogenesis. There appear to be two major peptides. labeled A and D, in the oöcyte with a stoichiometry of A₂D₁. These two proteins are also found in the haemolymph. Several other prominent proteins found in the haemolymph during the six day cycle are not found to be immunochemically similar to yolk antisera.The possibility of a precursor protein found in both the haemolymph and terminal oöcyte with a molecular weight of 189,000 is discussed.     

Yolk deposition in Douglas-fir beetle oöcytes: Possible rôle of RNA synthesis in the follicular epithelium

RNA synthesis and morphological changes in the follicular epithelial cells of oöcytes of Douglas-fir beetle, Dendroctonus pseudotsugae were studied during the reproductive phase. Inhibition of synthesis of DNA dependent RNA by actinomycin D injections blocked yolk deposition in the oöcytes as well as oviposition within the normal period. A mixture of radioactively labelled haemolymph and ovarial proteins was deposited as yolk proteins in the oöcytes of normal beetles. Such proteins were not deposited in the oöcytes of females injected with actinomycin D; the blockage of yolk deposition persisted even when such females were treated extraneously with juvenile hormone.     

Extra-ovariolar egg resorption in a dung beetle, Euoniticellus intermedius

Most oösorption in the dung beetle Euoniticellus intermedius takes place in the haemocoele, oöcytes being extruded from the ovariole before the deposition of the chorion. Oösorption can be induced in the laboratory both by prevention of oviposition and by starvation. For up to two days after the onset of starvation the terminal oöcyte appears normal. After three days the prechorionic oöcyte may move through the ovariole wall; the yolk spheres are then disrupted. On the fourth day little yolk remains in the extruded oöcyte, and most of the extruded cells are degenerating. We suggest that extra-ovariolar egg resorption may be a mechanism for ensuring that the single ovariole is not occluded when conditions are suitable for oviposition.     

Inhibition of oöcyte development during pregnancy in the cockroach Eublaberus posticus

The corpora allata are inhibited during pregnancy in ovoviviparous Eublaberus posticus, and yolk is not deposited in the basal oöcytes for the entire or almost the entire gestation period.Precocious oöcyte development occurs if the oötheca is removed but this can be prevented by substituting a plastic oötheca for the true egg case in the uterus. Implantation of a uterus containing an oötheca into the abdomen of a female whose oötheca is removed does not prevent precocious oöcyte development even though many of the eggs in the implant grow and stretch the donor uterus. These experiments argue against the hypothesis that an ‘agent’ from the uterine eggs or stretched uterus inhibits the activity of the corpora allata (CA), and supports the hypothesis that inhibition from the uterus is mechanical.Cyclical activity of neurosecretory cells in certain abdominal ganglia in one species of ovoviviparous cockroach has been correlated with the cyclical inhibition of the oöcytes during pregnancy. Mechanoreceptors are found in the uteri of several ovoviviparous species including Eublaberus.In Eublaberus transecting the nerve cord between various ganglia in pregnant females only results in a marked decrease in the percentage of famales showing precocious oöcyte development when the nerves posterior to the sixth abdominal ganglion are severed. However, the results are the same if these nerves are severed after removing the oötheca. It is suggested that pressure of the oötheca on mechanoreceptors in the uterus, or cessation of pressure (after removal of the oötheca), result in sensory information being transmitted to the last abdominal ganglion which affect the CA, perhaps indirectly by controlling the activity of the neurosecretory cells in various abdominal ganglia.     

The role of factors from the head in the regulation of egg development in the mosquito Aedes aegypti

The relationships between the release of factors from the head after blood-feeding, subsequent levels of ecdysteroids and vitellin, and the ultimate maturation of eggs in Aedes aegypti were investigated. Females were decapitated at various times after a blood meal, at 20 or 48 h after feeding the animals were dissected and divided into two groups, those with arrested oöcytes (yolk length < 100 μm) and those with maturing oöcytes (yolk length > 100 μm). These yolk lengths correspond with the levels of oöcyte growth believed to accompany the proposed initiation and promotion phases of egg development. Animals dissected at 20 h were assayed for ecdysteroid by radioimmunoassay; those dissected at 48 h were assayed for vitellin by rocket immunoelectrophoresis.Non-blood-fed unoperated females contained 8% as much ecdysteroid as blood-fed controls and no measurable vitellin. Females with arrested oöcytes (< 100 μm) were obtained only if decapitations were performed before 8 h; these females had about 20% of the ecdysteroids and 8% of the vitellogenin normally found in blood-fed animals. Females decapitated between 2 and 8 h with maturing oöcytes contained 50–60% as much ecdysteroid and vitellin as blood-fed unoperated controls. Normal ecdysteroid and vitellin levels were reached only when decapitations were delayed for 12 and 24 h, respectively. The number of developing oöcytes was also decreased by early decapitation and was closely correlated with vitellin levels.We conclude that the egg development neurosecretory hormone is released twice, once before 8 h and once after 8 h, to control ecdysteroid levels. We also suggest the presence of other factors from the head that control vitellin levels, the number of developing oöcytes, and the early growth of the oöcyte (initiation).     

Effects of electrocoagulation of cerebral neurosecretory cells and implantation of corpora allata on oöcyte development in Locusta migratoria

The implantation of active corpora allata into intact Locusta females during growth accelerates pre-vitellogenic oöcyte growth and vitellogenesis. Localised stimulation of yolk deposition follows the implantation of active corpora allata between the ovarioles demonstrating a gonadotrophic rôle for the corpus allatum hormone. Electrocoagulation of the median neurosecretory cells of the brain prevents vitellogenesis whilst pre-vitellogenic oöcyte growth occurs normally. Implantation of active corpora allata into females with ablated cerebral neurosecretory cells promotes vitellogenesis in a proportion of test animals although mature oöcytes are never produced.It is suggested that the rôle of the median neurosecretory cells during egg development in Locusta is primarily concerned with the activation and maintenance of activity of the corpora allata. The corpus allatum hormone acts both metabolically and gonadotrophically.     

Isolement,action biologique et evolution des substances paragoniales contenues dans le spermatophore d'Acanthoscelides obtectus (Coleoptère)

In Acanthoscelides obtectus, some male secretions deposited in the spermatophore during mating reach the blood of the females and stimulate oögenesis. Water extracts from spermatophores injected into a female abdomen stimulate oögenesis but do not influence egg-laying or sexual receptivity. After column chromatograph of spermatophores, aqueous extracts on Sephadex G 25 Coarse, G 25 Superfine, and G 15, an active fraction has been isolated. This injected into the abdomen of virgin females stimulates oögenesis at low concentrations, but it is toxic at higher concentrations. This fraction was examined by paper electrophoresis at low voltage and then chromatographed on G 10 Sephadex. Two peaks were obtained: the first corresponds to the paragonial substance A which stimulates oögenesis at 0,2 10^?3 μg/μl concentration. The second contains the paragonial substance B. At a 0,3 10^?3 ug/μl concentration this substance is toxic. First this toxicity inhibits oögenesis and then causes the death of most females at higher concentrations. The toxic effect appears 2 or 3 days after injection. These two substances are purified on paper chromatography and the biological activities are contained in a zone of R_f 0.25 to 0.45 (paragonial substance A) and in a zone of 0.16–0.30 R_f (paragonial substance B).The paragonial substances disappear from the spermatophore after mating. Aqueous extracts of spermatophores obtained 6 hr after mating do not stimulate oögenesis and do not have any toxic effect. The chemical nature of these both fractions is not yet determined because the quantity of extracts obtained at the end of the purification is very low.The action of both paragonial substances is similar to the action of hormones. The paragonial substances influence unknown receptors at low concentration after a latent period. The origin of the paragonial B substance was not determined, but this substance which inhibits oögenesis at low concentrations could be an antagonist of paragonial A substance.     

Dehiscence of Coelomomyces psorophorae sporangia from Aedes taeniorhynchus: Induction by amines and amino acids

The effect of various chemicals on induction of dehiscence of nonsterile Coelomomyces psorophorae sporangia from Aedes taeniorhynchus larvae was examined. Tests were made with various salts, reducing agents, chelating agents, buffers, alcohols, carbohydrates, fatty acids and derivatives, amino acids and derivatives, peptides, amines, purines and pyrimidines, antibiotics, and plant hormones. The most active compound was Tris [tris(hydroxymethyl)aminomethane]. Tris was most effective at pH 8–9, and a concentration of 1–20 mM. Structure-activity studies indicated that active compounds had a basic requirement for NH₂ and either COOH or CH₂OH attached to the alpha carbon, but only certain amino acids and amines were highly active. Preparations virtually free of host debris were not responsive to Tris, but addition of bacteria-free homogenates of A. taeniorhynchus larvae restored responsiveness. Dehiscence of C. psorophorae sporangia from Psorophora howardii was also enhanced by exposure to Tris.     

Sterol accumulation in developing ovaries of the silkworm Bombyx mori in relation to the diapause hormone

Ovary sterol of the silkworm Bombyx mori during pupal-adult development was investigated using ‘diapause’ and ‘non-diapause’ ovaries. It is composed of cholesterol with high relative concentration of more than 80%, β-sitosterol less than 20% and a trace of campesterol. Cholesterol and β-sitosterol contents per pair of ovaries increased strikingly as ovary development proceeded. In sterol concentration per wet weight of ovaries, free forms of cholesterol and β-sitosterol did not increase, or rather inclined to decrease in the former and were almost constant in the latter. However, the ester forms, especially cholesterol ester, increased remarkably during oöcyte maturation. This suggests that this ester may preferably be deposited in oöcyte yolk.Furthermore, the accumulation of sterol esters especially cholesterol ester was higher in ‘diapause’ than ‘non-diapause’ ovaries. It is highly probable that the diapause hormone stimulates the accumulation of cholesterol ester in oöcytes undergoing oögenesis.     

Corpus allatum activity during overlapping cycles of oöcyte growth in adult female Melanoplus sanguinipes

Cycles of oögenesis in Melanoplus sanguinipes overlap to the extent that there are always 2 and occasionally 3 sets of vitellogenic oöcytes in the ovarioles at any one time. Three phases of vitellogenic oöcyte development can be distinguished: (1) An initial 24-hour phase of slow development (1.0–1.2 mm, 0.05–0.10 mm³). (2) A phase of rapid oöcyte growth (1.2–3.5 mm, 0.1–1.3 mm³). The duration of this phase is 2 days in the first cycle and 3 days in subsequent cycles. (3) A final phase of rapid oöcyte growth and maturation (3.5–4.5 mm, 1.3–2.8 mm³). Including the time taken for oviposition the duration of this latter phase is 3 days. Phases 1, 2 and 3 of cycles n + 2, n + 1 and n, respectively, overlap entirely. Activity of the corpora allata was measured using a radio-biosynthetic technique. A period of increased corpus allatum activity coincides with the initial part of phase 2 in each cycle. Each set of oöcytes is, thus, subject to 2 and occasionally 3 peaks of corpus allatum activity during development. Using these data a model of the control of oöcyte development has been devised     

Reproductive allocation by the blow fly Lucilia sericata in response to protein limitation

Adult females of the anautogenous blow fly Lucilia sericata (Meigen) (Diptera: Calliphoridae) were fed standardized meals of liquidized liver, in quantities shown to range around the minimum required to initiate yolk deposition. Females from each feeding regime were dissected at daily intervals between 4 and 11 days of age; the number and stage of development of all oöcytes were recorded. Once an initial threshold quantity of protein was ingested, yolk deposition was initiated in all available oöcytes. Subsequently, one of two distinct developmental pathways was followed: arrested development in all oöcytes at an early stage of yolk deposition, or more extensive yolk deposition followed by progressive oösorbtion and the maturation of small batches of eggs. The proportion of females showing oösorbtion relative to arrested follicular development increased with increasing protein meal size, suggesting that the difference in response may be triggered by a second protein threshold, either side of which the arrested development or oösorbtion pathways are followed. The behaviour observed may reflect strategies to maximize reproductive output in this short‐lived, resource‐limited insect species. Flies that display arrested development may have sufficient protein to mature few if any complete eggs, but may subsequently be able to mature a full egg‐batch if they obtain further protein meals; this possibility is offset by the risk of death before finding such a meal. Flies that show oöcyte development and oösorbtion produce smaller egg batches more quickly and hence have a higher probability of achieving at least some reproductive output. By initiating yolk deposition in all oöcytes, female L. sericata retain the potential to adopt either developmental pathway, depending on subsequent protein intake.     

Vitellogenic arrest in the cockroach, Blatta orientalis

Starvation stimulated vitellogenic arrest occurs in the cockroach Blatta orientalis after 5 days. This is characterized by cessation of yolk uptake and oöcyte growth.After 5 days of starvation, protein and RNA synthesis decrease, but some macromolecular synthesis continues during the entire starvation period. No oöcyte resorption occurs for up to 15 days of starvation. In contrast to starvation, injection of actinomycin-D results in resorption within 8 hr. The results suggest that B. orientalis copes with starvation by maintaining arrested oöcytes as an alternative to immediate resorption.     

Synthesis and deposition of yolk protein in adult Drosophila melanogaster

Newly eclosed Drosophila melanogaster females contain only previtellogenic stage oöcytes and no immunologically detectable female specific haemolymph protein. During the subsequent 48 hr the concentration of female specific protein in the haemolymph rises to a plateau value of 21 μg/μl; at this time yolk protein represents about one third of the total haemolymph protein in adult females. The first mature (stage 14) oöcytes are observed at 48 hr post eclosion. The female specific haemolymph protein and the major protein from mature oöcytes are electophoretically and immunologically the same or very similar. Injection of alpha amanitin into newly eclosed females inhibits the development of mature oöcytes and the degree of inhibition depends on the age of the female at the time of injection. Phenocopies of non-vitellogenic mutants result when alpha amanitin is injected into newly eclosed females; after 36 hr post eclosion no visible inhibition of vitellogenesis (as observed morphologically at 72 hr post eclosion) can be produced by alpha amanitin.     

Vitellogenin accumulation in the fat body and haemolymph of Locusta migratoria in relation to egg maturation

Vitellogenins first appear in the fat body of Locusta migratoria during subphase I of vitellogenesis and increase to a constant level during subphase II. A second increase occurs shortly before the oöcyte attains maximal size. Vitellogenin content of fat body subsequently returns to that of subphase I, appropriate to the size of the subterminal oöcyte. The absolute amount of vitellogenin in the fat body is low compared to that found in the haemolymph. Fat body and haemolymph vitellogenins have immunological properties similar to oöcyte yolk proteins—when challenged with oöcyte protein antiserum. They exhibit similar electrophoretic mobility in polyacrylamide gel electrophoresis and are complex glyco-lipoproteins.     

Vitellogenin fluctuations in haemolymph and fat body and dynamics of uptake into oöcytes during the reproductive cycle of Diploptera punctata

Haemolymph and fat body soluble protein titres have been examined during the reproductive cycle of Diploptera punctata, with particular emphasis on the occurrence of vitellogenin and its uptake into the developing oöcytes. Vitellogenin was first detected in the haemolymph of mated females 2 days after adult eclosion at about the same time that vitellin deposition in basal oöcytes began. Peak haemolymph titres of vitellogenin occurred on day 6, correlated with the completion of yolk uptake. Thereafter vitellogenin levels declined and were generally undetectable throughout most of gestation, rising again shortly before parturition in association with the second gonotrophic cycle. Total haemolymph protein levels were not correlated with vitellogenesis.Soluble fat body vitellogenin titres of mated females remained low during the first oöcyte growth period but then rose several-fold at its completion and remained high throughout pregnancy and the second gonotrophic cycle. Total fat body soluble proteins decline after adult eclosion in association with oöcyte growth.Vitellin accumulation in basal oöcytes was related linearly to increase in volume until the onset of chorion formation. Thus no post-vitellogenic growth period was detected.