First evidence of Wolbachia infection in populations of grasshopper Podisma sapporensis (Orthoptera: Acrididae)

The brachypterous grasshopper Podisma sapporensis (Orthoptera: Acrididae) is distributed throughout the Sakhalin, Kunashir and Hokkaido Islands. Karyotypes of this species consist of two major chromosomal races with different sex chromosome systems, XO/XX and XY/XX. Molecular phylogeographic analysis of the chromosome races and subraces confirms the genetic divergence of the races and subraces in P. sapporensis. Here we first report that P. sapporensis is infected with Wolbachia consisting of three variants on wsp locus, while gatB locus was monomorphic. Furthermore, observation of cell tissue of P. sapporensis using electron microscopy confirmed the infection of Wolbachia that was inferred from polymerase chain reaction and revealed the distribution of the bacteria in the head, thorax and abdomen of P. sapporensis embryos. Our finding may shed new light on Wolbachia as a possible agent causing hybrid dysfunction resulting from experimental crosses between chromosome races or subraces of P. sapporensis.     

Asymmetric mating in the brachypterous grasshopper Podisma sapporensis

Crossing of genetically differentiated populations often results in assortative mating within populations. However, asymmetric sexual isolation or negative assortative mating has occasionally been reported. Previous studies suggested that sexual selection or sexual conflicts would lead to asymmetric mating when local populations are crossed. In order to evaluate the extent of assortative or disassortative mating in population crosses, we conducted laboratory crosses using the flightless grasshopper Podisma sapporensis. Crossing was conducted for all pairwise combinations of three populations, 150–240 km from one another – Teine, Shimokawa, and Akan. We found evidence for asymmetric mating for all the pairs of the populations. In particular, when the Teine and Akan populations were crossed, mating in the Teine male–Akan female cross was significantly more frequent than mating in both within‐population crosses, whereas mating in the Teine female–Akan male cross was significantly less frequent than mating in both within‐population crosses. We examined whether these results can be explained by any of the three hypotheses: (1) Kaneshiro's hypothesis, (2) differentiation in attractiveness, or (3) coevolution between male vigor and female receptivity. All the results were consistent with male vigor differing between populations balanced by different female potential to reject males. The available evidence suggests that antagonistic coevolution between the sexes has led local populations to different equilibria and that crossing of populations at different equilibria has resulted in asymmetry in mating frequencies.     

Expression of Maternally and Embryonically Derived Hypoxanthine Phosphoribosyl Transferase (Hprt) Activity in Mouse Eggs and Early Embryos

X-chromosome activity in early mouse development has been studied by a gene dosage method that involves measuring the activity level of the X-linked enzyme hypoxanthine phosphoribosyl transferase (HPRT) in single eggs and embryos from XO females and from females heterozygous for In(X)1H, a paracentric inversion of the X chromosome. The HPRT activity in oocytes increased threefold over a 24-hr period beginning after ovulation. Afterward, the activity plateaued in unfertilized eggs but continued to increase for at least 66 hr in presumed OY embryos. Both before and after ovulation, the level of activity in unfertilized eggs from In(X)/X females was twice that from XO females, and the distributions of activity in eggs for both sets of females remained unimodal. Beginning with the two-cell stage, distributions of activity for embryos from In(X)/X females were trimodal, which is evidence for embryonic activity. It is proposed that activation of a maternal mRNA or proenzyme is responsible for the HPRT activity increase in oocytes and early embryos and is supplemented by dosage-dependent activity of the embryonic Hprt gene as early as the two-cell stage.     

Daughters from daughterless mothers — Rescuing a female-lethal maternal effect by cytoplasmic transplantation inDrosophila embryos

Summary Daughterless is a temperature-sensitive, maternal effect mutation ofDrosophila melanogaster. Homozygousdaughterless females raised at temperatures above 22°C do not produce any female progeny. It was possible to rescue these female embryos by injecting cytoplasm from non-mutant unfertilized eggs into embryos fromdaughterless mothers. Cytoplasm from unfertilized eggs laid by homozygousdaughterless mothers was ineffective. Surprisingly, the cytoplasm from developing embryos with either wild-type ordaughterless mothers could also effect rescue. Based upon this data, we suggest that male and female embryos ofdaughterless mothers differ in their ability to initiate the synthesis of a product during the nuclear multiplication (cleavage) stage of embroniic development in the absence of a putativeda ⁺ maternally-synthesized factor, and that this is the basis for the sex-specific action of theda maternal effect.     

Transcriptome Analysis of Honeybee (Apis Mellifera) Haploid and Diploid Embryos Reveals Early Zygotic Transcription during Cleavage

In honeybees, the haplodiploid sex determination system promotes a unique embryogenesis process wherein females develop from fertilized eggs and males develop from unfertilized eggs. However, the developmental strategies of honeybees during early embryogenesis are virtually unknown. Similar to most animals, the honeybee oocytes are supplied with proteins and regulatory elements that support early embryogenesis. As the embryo develops, the zygotic genome is activated and zygotic products gradually replace the preloaded maternal material. The analysis of small RNA and mRNA libraries of mature oocytes and embryos originated from fertilized and unfertilized eggs has allowed us to explore the gene expression dynamics in the first steps of development and during the maternal-to-zygotic transition (MZT). We localized a short sequence motif identified as TAGteam motif and hypothesized to play a similar role in honeybees as in fruit flies, which includes the timing of early zygotic expression (MZT), a function sustained by the presence of the zelda ortholog, which is the main regulator of genome activation. Predicted microRNA (miRNA)-target interactions indicated that there were specific regulators of haploid and diploid embryonic development and an overlap of maternal and zygotic gene expression during the early steps of embryogenesis. Although a number of functions are highly conserved during the early steps of honeybee embryogenesis, the results showed that zygotic genome activation occurs earlier in honeybees than in Drosophila based on the presence of three primary miRNAs (pri-miRNAs) (ame-mir-375, ame-mir-34 and ame-mir-263b) during the cleavage stage in haploid and diploid embryonic development.     

Persistence of maternal isoenzyme patterns of the lactate dehydrogenase and phosphoglucomutase system during early development of hybrid trout

Developmental changes in the isoenzyme patterns of LDH and PGM during early embryogenesis (until hatching) in two trout species (Salmo trutta and Salmo irideus) as well as in their reciprocal interspecific hybrids are reported, completing a previous study which had commenced from hatching onward (Hitzeroth et al., 1968). Isoenzymes of both systems occur in unfertilized eggs and in embryos from fertilization onward. Until about the Augenpunkt stage, the isoenzyme patterns remain unchanged and are identical to the patterns of unfertilized eggs; the reciprocal hybrids correspond to the respective maternal species. Additional isoenzymes appearing for the first time at about the Augenpunkt stage in the interspecific hybrids show the same electrophoretic mobility as those in the animals of the respective maternal species at this developmental stage. It is discussed whether the appearance of additional isoenzymes characterizes the activation of maternally derived alleles of the embryonic genome, or whether maternally derived cytoplasmic factors are responsible for the occurrence of these additional bands.Supported by the Deutsche Forschungsgemeinschaft.     

Diploid arrhenotoky and automictic thelytoky in soft scale insects (Lecaniidae: Coccoidea: Homoptera)

Parthenogenesis is reported in three soft scales with 2n=16. In the unfertilized eggs of all three, oogenesis is normal and diploidy is restored by the fusion of the division products of the haploid female pronucleus. In Lecanium putmani Phillips 12 of 13 uninseminated females collected in the wild produced only males. The 21 inseminated females produced 15% males. The males were diploid but contained one euchromatic (E) and one heterochromatic (H) chromosome set. Most of the eggs produced by the inseminated females contained sperm but a few did not. It was concluded, therefore, that females develop from fertilized eggs and males from unfertilized eggs and that the species was diploid arrhenotokous. In L. cerasifex Fitch only 18 of 56 females collected in the wild had been inseminated. The frequency of males among their embryos was 22%. The males were again diploid with one E and one H set of chromosomes. Among the 38 uninseminated females, 27 produced only males, and 10 produced only females. All the female producers contained needle-like bacterial symbionts. Most of the male producers, and most of the inseminated females contained no symbionts; the rest contained rod-like symbionts. It was concluded, therefore, that the females of L. cerasifex studied belonged to two races, a diploid arrhenotokous race and an obligate automictic thelytokous race. Eucalymantus tessellatus (Signoret) is obligate automictic thelytokous. All the females examined were uninseminated and produced only females.Supported by Grant GB 23665 from the National Science Foundation, Washington, D.C.     

Polyadenylic acid-containing of rna in unfertilized and fertilized eggs of the rabbit.

Molecular hybridization between ³H-polyuridylic acid and unlabeled RNA prepared from unfertilized rabbit eggs and 10-h postfertilization stage rabbit embryos has been used to measure the amount and subcellular localization of adenylated maternal RNA. The results reported indicate that there is poly (A)-containing RNA (putative messenger RNA) in unfertilized rabbit eggs. The amount of poly (A) in the RNA in rabbit eggs does not increase immediately after fertilization and is located primarily in the ribosomal fraction of the cell. The rate of protein synthesis in fertilized eggs is insensitive to α-amanitin at concentrations which inhibit RNA synthesis. These results suggest that maternal mRNA makes an important contribution to protein synthesis in early stages of cleavage in the rabbit embryo.     

Timing of Development During Epiboly in Embryos of Second-Generation Crosses and Backcrosses between Odd- and Even-Broodyear Pink Salmon, Oncorhynchus gorbuscha

Synopsis Odd- and even-year-spawning pink salmon (Oncorhynchus gorbuscha) are genetically isolated; their broodlines differ even in the same natal stream. Hybrids between broodlines exhibit outbreeding depression in survival. Variation in the time to completion of epiboly in embryos appears to be adaptive in both broodlines. We compared stage of development at a time near the completion of epiboly in families of second-generation offspring from crosses between odd- and even-year broodlines with development stages of within-broodyear controls and of backcrossed families. We observed embryos derived from matings of mature fish that were the results of fertilizations made 2 years earlier of eggs from females from the even brood year with semen from males from the even broodyear and with cryopreserved semen from males of the odd broodyear. The resulting fry had been released to the Pacific Ocean and recovered at maturity. Second generation embryos were produced by factorial matings of these mature fish involving (1) female and male controls, (2) female and male hybrids, and (3) both backcrosses. Analysis of variation of development time detected no effect of outbreeding, i.e., differences between controls and second generation hybrids (p > 0.05), but did detect variation between individual female parents (p < 0.03). Neither epistatic nor additive outbreeding depression could be detected in the rate of early embryonic development of pink salmon. However, effects on development rate attributable to female parents indicate that either a maternal effect or early additive genetic effects occurred before the expression of the paternal genome in embryos.     

CHANGE IN THE ACTIVITY OF LIPASE IN SEA URCHIN EGGS AND EMBRYOS DURING EARLY DEVELOPMENT*

During the early development of the sea urchin, Anthocidaris crassispina, the activity of lipase was maintained at the same level as in unfertilized eggs until the mesenchymal blastula stage (20 hr culture at 20°C) and then increased gradually after gastrulation. The activity in the embryos kept in SO^2?₄-free artificial sea water changed in a similar manner to that in those kept in normal sea water, during the development until 36 hr of fertilization. At 48 hr, the activity in the embryos, which had developed to the permanent blastulae in SO^2?₄-free sea water, was markedly lower than in normal plutei and was similar to that in unfertilized eggs. The lipase activity in fertilized eggs 30 min after fertilization, which was almost the same as that in unfertilized eggs was found mainly to be localized in the precipitate fraction obtained by the centrifugation at 12,000 x g for 20 min, whereas the activity in unfertilized eggs was found in the precipitate by the centrifugation at 105,000 x g for 60 min. Ca²⁺, adenosine 3′, 5′-cyclic monophosphate (cAMP) and guanosine 3′, 5′-cyclic monophosphate (cGMP) had no effect on the lipase activity.     

Plasticity and limitations of extended egg retention in oviparous Zootoca vivipara (Reptilia: Lacertidae)

The transition between oviparity and viviparity in reptiles is generally accepted to be a gradual process, the result of selection for increasingly prolonged egg retention within the oviduct. We examined egg retention plasticity in an oviparous strain of the lacertid lizard Zootoca vivipara, a species having both oviparous and viviparous populations. We forced a group of female Z. vivipara to retain their clutch in utero by keeping them in dry substrata, and assessed the effect on embryonic development and hatching success, along with offspring phenotype and locomotor performance. Forced egg retention for one additional week affected the developmental stage of embryos at oviposition, as well as hatchling robustness and locomotor performance. However, embryos from forced clutch retention treatment reached one stage unit more than control embryos at oviposition time. Embryos from control eggs were more developed than embryos from experimental eggs after approximately the same period of external incubation, showing that embryonic development is retarded during the period of extended egg retention, despite the high temperature inside the mother's body. Significant differences in external incubation time were only found in one of the two years of study. Hatching success was much lower in the experimental group with forced egg retention (21.1%) than in the control group (95.4%). Therefore, we conclude that there are limitations that hinder the advance of intrauterine embryonic development beyond the normal time of oviposition, and that extended egg retention does not represent clear advantages in this population of Z. vivipara. Nevertheless, the fact that some eggs are successful after forced egg retention could be advantageous for the females that are able to retain their clutch under unfavourable climatic conditions. © 2010 The Linnean Society of London, Biological Journal of the Linnean Society, 2011, 102 , 75–82.     

Interspecific hybridization of phaseolus vulgaris with P. lunatus and P. acutifolius

Summary The influence of genotypic combinations on the growth of hybrid embryos between Phaseolus vulgaris and P. lunatus, and between P. vulgaris and P. acutifolius was examined. All embryos obtained from P. vulgaris × P. lunatus crosses developed only to a stage which appears to be comparable to the pre-heart-shape stage of selfed embryos. Reciprocal crosses were attempted, but pods abscised at a very early stage. Embryos derived from P. vulgaris × P. acutifolius and reciprocal crosses attained the cotyledon stage although no mature seeds were formed. A distinct characteristic of these embryos was the uneven development of the two cotyledons. The rate of growth and final size of these hybrid embryos seemed to be influenced by the genotypes of both parents.Immature embryos were cultured on defined medium and the effects of glutamine and gibberellin (GA₃) were examined. Glutamine was effective in increasing the survival rate; gibberellin had no apparent effect. Plants derived from cultured embryos of P. vulgaris × P. lunatus, P. vulgaris × P. acutifolius and P. acutifolius × P. vulgaris were obtained.Technical paper No. 00 of the Oregon Agricultural Experiment Station. Research was supported by the Oregon Agricultural Experiment Station, the Research Council of Oregon State University (National Institute of Health Biomedical Research Support Grant RR07079) and the Processor Research Council of Oregon. A.R. is supported by an African Graduate Fellowship from the African-American Institute     

Repair of a genetically-caused defect in oogenesis in Drosophila melanogaster by transplantation of cytoplasm from wild-type eggs and by injection of pyrimidine nucleosides

Eggs produced by homozygous mutant rudimentary (r⁹, 154.5) females of Drosophila melanogaster die during embryogenesis, apparently because the mutant female fails to incorporate certain substances into the egg during oogenesis. These eggs can be rescued by injecting them at the preblastoderm stage with wild-type nuclei and cytoplasm or wild-type cytoplasm alone from unfertilized eggs. Some preblastoderm eggs injected with 1.5% of egg volume of cytoplasm from unfertilized wild-type eggs were able to complete both embryonic and postembryonic development and emerged as adults, whereas not a single uninjected control egg was able to complete embryonic development. The eggs of rudimentary mothers can also be rescued by injecting each egg at the blastoderm stage with 0.01 μg of pyrimidine nucleosides. The results demonstrate that a pyrimidine deficiency is the cause of abortive embryogenesis, and confirm the previous finding that the rudimentary mutation leads to pyrimidine auxotrophy.     

A 4-year summary of the nonsurgical recovery of baboon embryos: A report on 498 eggs

A nonsurgical embryo recovery procedure, developed to allow the economical acquisition of cleavage stage baboon embryos, has been successfully used for 4 years. With this technique, 498 eggs have been recovered from 979 uterine flushes (50.9%) on 71 baboons. Of 467 eggs recovered from mated baboons, 290 (62.1%) were fertilized. Papio anubis females provided a higher percentage of fertilized eggs (75.3%) than did Papio hamadryas (47.8%) or Papio cynocephalus (44.3%) females following exposure to males during estrus, although sexual preference may be responsible for the reduced fertilization rate in the P. cynocephalus females. Recovery rates from individual baboons ranged from 0% (n = 11) to between 66% and 93% for ten baboons from each of which 12–33 eggs have been recovered. Fertilized eggs were at the two-cell (n = 23) to blastocyst (n = 53) stage at recovery 1–6 days postdeturgescence (PD) of the sex skin, with morulae (n = 84) being the most frequent cell stage recovered (30%). The optimum time for performing the procedure was the third day PD, when 113 (40%) embryos were recovered. The abilities of baboons to become pregnant and to provide fertilized embryos were significantly related (P < 0.005), allowing the embryo recovery technique to be used as a screening procedure for evaluating baboon fertility.     

In situ Development of Perch Eggs,Perca fluviutilis L. (Pisces,Percidae) in a Small Eutrophic Lake,Lake Plussee,Holstein, Germany

Naturally spawned egg strands of perch, Perca fluviatilis L. were sampled from exposed fir trees submerged in Lake Plußsee, Holstein, Northern Germany from April to May 1989. These were incubated in situ and in the laboratory to estimate the viability, development and abnormalities of the embryos. From the in siru incubated eggs 91.6% embryos were viable, the nonviable portion comprising 1.1 % unfertilized eggs, 5.1 % dead and 2.2 % with abnormalities. As compared to the eggs incubated in the laboratory with 84.1 % viable embryos, the nonviable portion consisting 1.1 % unfertilized eggs, 11.3 % dead and 3.5 % with abnormalities. Incubation rate of P. fluviatilis embryos both in situ and laboratory, ranged from 200-210 ATUs (10°C in situ and 8°C in the laboratory) with incubation period of 20-27 days from fertilization to 50 % hatching.     

Temperature Dependence of Membrane Lipid Composition in Early Blastula Embryos of Lytechinus pictus: Selective Sorting of Phospholipids into Nascent Plasma Membranes

Lytechinus pictus eggs were fertilized and incubated at 10, 16, and 23°C until the early blastula stage of embryonic development. The phospholipid composition of the embryos and control unfertilized eggs remain identical and unchanged as incubating temperatures are varied; thus, neither incubating temperature, fertilization nor membrane assembly affect their total phospholipid composition. This result agrees with metabolic studies by others, using only a single incubation temperature, and indicates that embryonic development to the early blastula stage occurs with little, if any, de novo phospholipid biosynthesis. However, as in all poikilotherms, the phospholipid composition of the nascent plasma membranes varies with the incubation temperature. Thus, until the blastula stage of embryonic development, the lipids of these newly formed plasma membranes are derived from lipid pools within the embryo whose phospholipid composition is static. The variation of plasma membrane composition is primarily reflected in an increase in the phosphatidylethanolamine (PE): phosphatidylcholine (PC) ratio as incubating temperatures decrease; this is achieved by an exchange of PE for PC. Several mechanisms are considered for the specificity of the selective sorting and assembly of these phospholipids into the nascent plasma membranes. Received: 16 March 1999/Revised: 15 May 1999     

Developmental potencies of nuclei from cleavage,preblastoderm, and syncytial blastoderm transplanted into unfertilized eggs ofDrosophila melanogaster

Summary Wild-type nuclei from eggs ofDrosophila melanogaster at various developmental stages and from different regions of the egg—cleavage nuclei, pole nuclei from preblastoderm, and lateral nuclei from syncytial blastoderm—were singly implanted into unfertilizedy w sn ³ lz _50e eggs to determine their developmental potencies.All three types of transplanted nuclei were almost equally effective in initiating development of unfertilized eggs. Development was arrested in one of five critieal embryonic stages or in one of the three larval instars. The frequency of individuals reaching a distinct stage was approximately the same for all three types of donor nuclei. The stage-specific pattern of defects was independent of the type of nucleus transplanted.The deviations from normal development were broadly similar to those seen in controls developing from fertilized eggs which had only been punctured or into which cytoplasm had been injected. Many defective embryos also occurred in these control experiments. These and other observations indicate that a large proportion of irregularly developed individuals found after nuclear transfer can be ascribed to loss of egg material, disturbances in the internal organization of the egg during nuclear implantation, and the difficulty the implanted nucleus has in adjusting to the autonomous processes within the egg, such as the formation and migration of cytoplasmic islands.Some of the defective embryos and larvae originating from nuclear transfer were implanted into adult hosts. After culture for 14 days the early embryonic stages had formed several larval structures, and the late embryonic and larval stages had developed all larval organs. The proliferated imaginal primordia of thesein vivo cultured embryos and larvae, as well as the imaginal disks of the third instar larva, were then implanted into larval hosts with which they passed through metamorphosis and differentiated into imaginal structures. All three types of donor nuclei were capable of producing all adult structures derivedin situ from imaginal disks. The phenotype of these structures waswild-type, thus demonstrating their origin from the transplanted nuclei.The problem as to why not all transplanted nuclei initiated development, and why development after nuclear transplantation was arrested at the third larval instar, at the latest, is discussed.This article is dedicated to Professor Friedrich Seidel on the occasion of his 75th birthday.