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PubMed2005

Molecular cloning and mRNA profile of insulin-like growth factor type 1 receptor in orange-spotted grouper, Epinephelus coioides.

The insulin-like growth factor type 1 receptor (IGF-IR) belongs to the tyrosine kinase (TK) receptor family. Besides being mitogenic, IGF-IR plays a crucial role in cell survival, transformation and maintenance of the malignant phenotype. In this study, we cloned the cDNA from the hypothalamus of the orange-spotted grouper (Epinephelus coioides) using reverse transcription PCR (RT-PCR) and the rapid amplification of cDNA ends (RACE) method. The deduced amino acid sequence showed that the receptor comprises 1413 amino acid residues. It contains cysteine-rich domains in its alpha-subunit, and a conserved transmembrane domain and TK domains in its beta-subunit. Comparison of the amino acid sequence with those of other species showed that the grouper IGF-IR shares 90.2%, 89.6%, 71.9% and 72% similarity with the IGF-IR of the Japanese flounder, turbot, zebrafish-a and zebrafish-b, respectively. When compared with its mammalian homologue, grouper IGF-IR contains a large insertion at its C-terminus. Phylogenetic analysis has revealed that the grouper IGF-IR belongs to the b-type IGF-IRs and has a higher similarity with flounder and turbot IGF-IR, and a lower similarity (<70%) with human, mouse and avian IGF-IR. Grouper IGF-IR transcripts were detected in the brain, peripheral tissues, embryos and early development larvae by semi-quantitative RT-PCR assay. It was observed that IGF-IR mRNA expression was greater in the brain than in peripheral tissues. The level of IGF-IR mRNA expression was much higher in retina, gonad, skeletal muscle and gill tissues than in liver, heart and thymus tissues. The expression of IGF-IR can be visualized as a ubiquitous signal in unfertilized eggs, embryos and early development larvae. The distribution pattern of IGF-IR mRNA in grouper development suggests that IGF-IR plays an important role in the embryo and early larval development stages.

Amino Acid Sequence↗
PubMed1996

Vertical transmission of chemoautotrophic symbionts in the bivalve Solemya velum (Bivalvia: Protobranchia).

Adults of the bivalve species Solemya velum live in symbiosis with chemoautotrophic bacteria in specialized gill bacteriocytes. The bacteria play an essential nutritional role in the mature association, fixing CO2 via the Calvin cycle with energy obtained through the oxidation of reduced sulfur compounds. To understand how the continuity of this partnership is maintained between host generations, we investigated the mode of symbiont transfer in S. velum. A diagnostic assay using the polymerase chain reaction and primers specific for the S. velum symbiont ribulose-1,5-bisphosphate carboxylase (RubisCO) gene consistently detected bacterial sequence in female gonad tissue, suggesting the presence of symbiont cells in host ovaries and a vertical mode of symbiont transmission from mother to offspring. Furthermore, intracellular bacteria were present in the developing gills of juveniles that had not yet hatched from the gelatinous capsule in which larval development occurs (11 days after fertilization). By 64 days postfertilization, the typical adult gill ultrastructure of alternating bacteriocytes and symbiont-free-intercalary cells was apparent. Knowledge about the mode of symbiont transfer in S. velum allows further study into the dynamics of host-symbiont interactions in chemoautotrophic associations.

Animals↗
PubMed1999

Functional analysis of dynamin isoforms in Drosophila melanogaster.

Dynamin and dynamin-like proteins are required for endocytosis, synaptic vesicle recycling and membrane trafficking. From the shibire locus in Drosophila melanogaster, six different isoforms of dynamin are generated by alternative splicing. However, the roles of the individual isoforms in cellular processes are unknown. To investigate functional differences among the dynamin isoforms, transgenic lines were generated that individually expressed each of 3 different isoforms under UASGAL4 control. The expression of the isoforms was controlled by neural promoter (elav)-driven GAL4, or by a shibire-promoter driven GAL4 transgene. Reporter gene expression indicated that the shi promoter is active during embryogenesis, and in larvae, pupae, and adults in a pattern consistent with normal dynamin expression. To assay for the ability of dynamin isoforms to function in vivo, the isoforms expressed via these GAL4 drivers were tested for the ability to rescue shibire phenotypes. When expressed at very high levels all individual isoforms tested rescued the temperature-sensitive paralytic phenotype of shi(ts2) flies; however, this rescue was partial, suggesting that no single tested isoform is sufficient for synaptic vesicle recycling in vivo. When tested for ability to rescue lethality induced by heat-pulsing larvae during development, shi- promoter driven expression of individual isoforms conferred significant resistance to heat treatment during larval development. However, all 3 isoforms were unable to rescue the lethality of shi12-12B mutants which are severely hypomorphic (or null) for shibire function. Taken together, these observations suggest that individual shibire isoforms have specific molecular activities in vivo.

Alternative Splicing↗
PubMed1979

Incorporation of radioactive precursors into filarial larvae of Brugia developing in susceptible and refractory mosquitoes.

The incorporation of tritiated precursors injected into mosquito hosts parasitized by developing filarial larvae of Brugia patei has been studied by autoradiography in 2 species of mosquito, Aedes togoi in which filarial development was normal and Anopheles labranchiae atroparvus in which filarial development was abnormal. In both mosquito hosts there was significant incorporation into 4--5-day-old developing larvae of uridine and amino acids (isoleucine, leucine, valine, arginine, lysine, cystine, methionine, phenylalanine, tyrosine, tryptophan, histidine, and proline), although lower incorporation of methionine, tyrosine, and tryptophan was found during abnormal development. No incorporation of thymidine, hydroxytryptophan, dopa, or carbohydrate was found at this stage of larval development. Some incorporation of glucose and dopa was found in or around earlier stages of development in An. l. atroparvus. Mosquito flight muscle showed lower incorporation of glucose, but not of amino acids, around the site of filarial parasite development. The flight muscle of An. l. atroparvus showed a higher level of incorporation of lysine compared to that in A. togoi and higher levels of lysine and valine were found in the abnormally developing filarial larvae in the refractory mosquito.

Aedes↗
PubMed2002

Protobranch bivalves.

The subclass Protobranchia comprises more than 600 species of bivalves that occur throughout the world ocean. Mostly deposit feeders in soft sediments, they are abundant in the deep sea. Apomorphies that unite them as a group include gill structure, hinge conformation, shell microstructure, larval development, foot morphology, respiratory pigments, trophic mode and digestion. They are relatively small and highly conserved in form, originating in the Cambrian era. They may represent an ancestral, derived or paraphylectic group of the Bivalvia. The protobranchs include two orders, the Nuculoida and Solemyoida, which previously were classified separately in the subclasses Paleotaxodonta and Cryptodonta, respectively. They are of ecological interest and have a unique functional morphology. They feed mostly under the surface of the sediment with highly modified labial palps, but the degree to which they are selective in diet remains difficult to determine. They are important bioturbators in many soft-sediment assemblages; their feeding and locomotion affects sediment structure and community development. Solemyoids are unusual in inhabiting reducing environments and hydrocarbon seeps and in deriving their nutrition from endosymbiotic chemosynthetic bacteria. A variety of species of protobranchs are found in oceanic trenches, near hydrothermal vents, and in submarine caves. Protobranchs produce a lecithotrophic larval stage, the pericalymma, making their development unique among bivalves. The pericalymma remains in the plankton for a short time and presumably has low dispersal ability. Recruitment may be intermittent. Growth is rapid in post-larvae but decreases with age, though rates may not necessarily be slow, especially in continental shelf species. Life spans are commonly 1 to 2 decades, but deep-sea representatives may grow more slowly and live longer. Bottom fish, seastars and gastropods are their major predators and a few parasites and commensals have been documented. The predominance of protobranchs in deep-sea sediments may be a result of deep-sea origin or displacement from shallow waters by lamellibranchs. Their ability to deposit-feed, digest food extracellularly, and develop by means of lecithotrophic larvae make them particularly well adapted to cold and oligotrophic habitats.

Animals↗
PubMed2002

Embryogenesis and development of Epimenia babai (Mollusca Neomeniomorpha).

Neomenioid aplacophorans (= Solenogastres) constitute one of the main lineages of molluscs. Developmental data of early embryogenesis and larval development of neomenioids are available for some species based on histological sections. I used other techniques to study the development of Epimenia babai Salvini-Plawen, 1997, and here I report new data on neomenioid development. The embryos of E. babai are lecithotrophic and cleavage is spiral, unequal, and holoblastic. Two polar lobes are formed, one at the first cleavage stage and one at the second cleavage stage. No evidence of external metameric iteration is visible through scanning electron microscopy or histology at any stage. A ciliated foot, a pedal pit, and aragonitic spicules develop from the definitive ectoderm. A spicule begins as a solid tip, continues to an open-ended hollow spicule, and finally becomes a closed-ended hollow spicule. The free-swimming trochophore larvae of E. babai have been considered unusual in lacking the characteristic neomenioid cellular test, an outer locomotory structure within which the entire definitive adult body develops. However, through the use of scanning electron and light microscopy, semithin sections, Hoechst nuclear staining, and programmed cell death staining to study the ontogeny and fate of the apical cells, I show that the entire pre-oral sphere (the apical cap) of the larvae is similar to the test of the other neomenioids. The results suggest that the test of the neomenioid larvae is an enlarged pre-oral sphere of a trochophore. The test morphologies of neomenioid larvae are compared to those of pericalymma larvae of protobranch bivalves, and the homology and evolution of molluscan larval tests is discussed.

Animals↗
PubMed1993

Diffusion patterns on domains representing developing Xenopus retina.

The retinotectal map of mature Xenopus frogs has linear metrics. The regions of the Xenopus retina were modeled during embryonic and early larval development with a set of standard geometrical shapes. A disk was used to model the entire early retina, rings of various thickness were used to model the ciliary margin (the growth zone of the larval retina), and portions of a sphere were used to model the entire late embryonic and larval retina. Gradients produced by several reaction-diffusion pattern-generating configurations were considered: Gierer-Meinhardt and Kauffman-type activator-inhibitor systems; an ideal Turing-like two morphogen system; a point source with diffuse sinks; and variously placed point source-point sink combinations. A few special arrangements produced linear metrics: a point source-point sink system produced linear angular metrics on a thin ring; and ideal Turing system produced linear cartesian metrics on a thin ring; and carefully configured multiple sources and sinks produced linear metrics on a disk. These cases could lead to linear map metrics, but are biologically implausible. Thus linear map metrics are probably not a direct consequence of linear positional values, and more generally, most embryonic tissues probably use non-linear gradients of positional information. Formation of linear map metrics may be functionally important for Xenopus frogs, accounting in part for the evolutionary preservation of mechanisms for interactions among neighboring retinal fibers.

Animals↗
PubMed1985

[Morpho-anatomic and functional sectorization of Schistosoma mansoni daughter sporocysts].

During the larval development of S. mansoni in the snail host, morpho-anatomic changes occur in the daughter sporocyst by a sectorization of this larval stage. Three sectors can be distinguished: an anterior zone with a well-differentiated birth pore; dilated zones containing the developing cercariae; constricted zones without cercarial embryo. The photonic and electronic microscopical study shows variations in the tegumental structure of these sectors. This evolution of the daughter sporocysts is discussed in relation with the dynamics of larval stages and the replication process of sporocysts.

Animals↗
PubMed2001

Isolation of genes involved in ascidian metamorphosis: epidermal growth factor signaling and metamorphic competence.

Although embryonic development in ascidians has been studied for over a century, the signals involved in coordinating post-larval development and metamorphosis are just beginning to be investigated. In this paper, we demonstrate that transcription is necessary for both the acquisition of metamorphic competence and the completion of the initial events of metamorphosis in Boltenia villosa. Transcripts expressed during metamorphic competence were isolated by a suppressive PCR subtraction of Boltenia villosa larval cDNAs. One of these transcripts is homologous to cornichon. Cornichon has a crucial but undefined role in epidermal growth factor (EGF) signaling during Drosophila embryogenesis. In situ hybridization demonstrates that Boltenia cornichon (Cnib) is expressed in the anterior papillary region of larvae as they gain competence. Our hypothesis is that Cnib acts to potentiate EGF signaling, thereby allowing Boltenia larvae to respond to cues for metamorphosis. Further research into the role of Cnib in urochordate metamorphosis may provide insight into the function of cornichon in other organisms. A better molecular understanding of urochordate metamorphosis will also provide a foundation for exploring the role of metamorphosis in chordate evolution.

Amino Acid Sequence↗
PubMed2001

Induction of stress by the swimbladder nematode Anguillicola crassus in European eels, Anguilla anguilla, after repeated experimental infection.

The purpose of this study was to determine under laboratory conditions over a period of 311 days if infection with the nematode Anguillicola crassus induces stress in European eels (Anguilla anguilla), and stimulates the endocrine stress axis as measured by serum cortisol levels. Eels were experimentally infected with 3rd-stage larvae (L3) in different doses to simulate natural conditions with varying infection pressures. Blood samples were drawn from the caudal vein every 2 weeks and serum cortisol concentrations were determined by radioimmunoassay (RIA). The results showed that the application of L3 resulted in a significant increase in the cortisol levels. The period of time at which elevated cortisol values were observed was consistent with the time of larval development and the appearance of adult A. crassus. Thus, there is a stress response to the larval and young adult stages, but no chronic response to older adults. Therefore, it is likely that infection of eels under natural conditions especially with a high number of larvae may be a considerable stressor, in combination with different environmental factors like water temperature, pH, oxygen concentration, pollution and interindividual relationships.

Air Sacs↗
PubMed2001

Caenorhabditis elegans MES-3 is a target of GLD-1 and functions epigenetically in germline development.

The maternal-effect sterile (MES) proteins are maternally supplied regulators of germline development in Caenorhabditis elegans. In the hermaphrodite progeny from mes mutant mothers, the germline dies during larval development. On the basis of the similarities of MES-2 and MES-6 to known transcriptional regulators and on the basis of the effects of mes mutations on transgene expression in the germline, the MES proteins are predicted to be transcriptional repressors. One of the MES proteins, MES-3, is a novel protein with no recognizable motifs. In this article we show that MES-3 is localized in the nuclei of embryos and germ cells, consistent with its predicted role in transcriptional regulation. Its distribution in the germline and in early embryos does not depend on the wild-type functions of the other MES proteins. However, its nuclear localization in midstage embryos and its persistence in the primordial germ cells depend on wild-type MES-2 and MES-6. These results are consistent with biochemical data showing that MES-2, MES-3, and MES-6 associate in a complex in embryos. The distribution of MES-3 in the adult germline is regulated by the translational repressor GLD-1: MES-3 is absent from the region of the germline where GLD-1 is known to be present, MES-3 is overexpressed in the germline of gld-1 mutants, and GLD-1 specifically binds the mes-3 3' untranslated region (3' UTR). Analysis of temperature-shifted mes-3(bn21ts) worms and embryos indicates that MES-3 function is required in the mother's germline and during embryogenesis to ensure subsequent normal germline development. We propose that MES-3 acts epigenetically to induce a germline state that is inherited through both meiosis and mitosis and that is essential for survival of the germline.

3' Untranslated Regions↗
PubMed1985

The development of the dendritic organization of primary and secondary motoneurons in the spinal cord of Xenopus laevis. An HRP study.

During embryonic and larval development of the clawed toad, Xenopus laevis, two different populations of motoneurons appear in the spinal cord. In this study the development of primary motoneurons which innervate the axial musculature (used during embryonic locomotion) and of secondary motoneurons which innervate the extremity musculature (used for locomotion during metamorphosis and thereafter) was analyzed with horseradish peroxidase (HRP) as a neuronal marker. After application of HRP to the axial musculature (rostral five postotic myotomes) the first labeled primary motoneurons were found at stage 24/25. During development gradually more labeled neurons were observed. These primary motoneurons send their dendrites into the marginal zone (white matter). At first only dorsal and lateral dendrites develop (stages 25-33), followed by ventral dendrites (stage 37/38). Up till stage 48 the developing dendrites extend throughout the marginal zone. Hereafter the marginal zone increases particularly at the dorsolateral edge, a development which is not followed by the dendrites of the primary motoneurons. The dendrites of mature primary motoneurons (stages 58-62) occupy the ventral and ventrolateral parts of the marginal zone. At stage 48, shortly after the hindlimb bud arises (stage 46, early metamorphosis), the first neurons related to this developing extremity could be labeled in the ventrolateral part of the lumbar spinal cord. At first these secondary motoneurons bear only a few dorsal dendrites of which only the tips reache out in the adjacent white matter. Already at stage 50 these dorsal dendrites have invaded the whole dorsolateral part of the marginal zone. Also the first ventral dendrites were observed at this stage. Later, at stage 53/54 also some ventral dendrites have reached the white matter together with a few lateral dendrites. At these early metamorphic stages already some primary afferent fibers were found making contact with the dorsomedial dendrites. At stage 58 for the first time recurrent axon collaterals were found, which extend into the ventromedial part of the marginal zone. The development of motoneurons in the spinal cord seems to be characterized by two phases: (1) establishment of contacts between motoneurons and target muscles, and (2) subsequent formation of connections of these motoneurons with other nerve cells within the central nervous system. The dendrites of primary motoneurons follow the development of the marginal zone, while dendrites of secondary motoneurons develop into an already well developed marginal zone.(ABSTRACT TRUNCATED AT 400 WORDS)

Animals↗
PubMed2006

Cadmium exposures during early development: do they lead to reproductive impairment in fathead minnows?

The primary objective of this study was to determine whether cadmium (Cd) exposures during embryonic and larval development alter the reproductive performance, reproductive physiology, and sex ratio of fathead minnows (Pimephales promelas). Embryonic exposures were conducted by exposing adult female fathead minnows to 0, 25, or 100 microg/L Cd for 8 d prior to breeding. Larval exposures were conducted by exposing the larvae to waterborne Cd at 0, 12.5, 25, or 50 microg/L from 8 to 29 d posthatch (the time period associated with female sexual differentiation). Minnows from each exposure period were raised to maturity, at which time their reproductive success, secondary sexual characteristics, gonadosomatic index (GSI), plasma 11-ketotestosterone (11-KT) concentrations, and sex ratios were assessed. Results from the embryonic study reveal that Cd exposures alter the secondary sexual characteristics of male fathead minnows but do not alter reproductive performance, GSI, 11-KT concentrations, or sex ratios. Larval exposures, during the period of female sexual differentiation, significantly reduce the frequency of adult spawning and increase clutch size but do not alter fecundity, secondary sexual characteristics, GSI, or 11-KT. Subtle alterations in sex ratio were observed, indicating that larval Cd exposures may increase the proportion of females in an exposed population.

Animals↗
PubMed2004

Ciona intestinalis Hox gene cluster: Its dispersed structure and residual colinear expression in development.

Ascidians, belonging to the subphylum Urochordata, the earliest branch from the lineage to the vertebrates, exhibit a prototypical morphogenesis of chordates in the larval development, although they subsequently metamorphose into adults with a unique body structure. Recent draft genome analysis of the ascidian Ciona intestinalis has identified 9 Hox genes, which, however, have been located on five scaffolds. Similarly, expression patterns of Ciona Hox genes are largely unknown, although some data have been available for a few Hox member genes. Thus, the cluster structure and colinearity of Hox genes are still an enigma in C. intestinalis. To address these issues, we used fluorescence in situ hybridization and whole-mount in situ hybridization techniques and examined the genomic organization and spatiotemporal expression of all Hox as well as extended Hox member genes (Evx and Mox) of C. intestinalis. We found that seven of nine Ciona Hox genes are located on a single chromosome with some ordering exceptions, and the other genes, including Evx and Mox, are located on three other chromosomes. Some Ciona Hox genes, if not all, exhibited spatially coordinated expression within the larval central nervous system and the gut of the juvenile. In light of these observations, we suggest that the cluster organization and colinearity of the Hox genes are under dispersing and disintegrating conditions in C. intestinalis.

Animals↗
PubMed1998

Overcrowding of Culex sitiens (Diptera: Culicidae) larvae: population regulation by chemical factors or mechanical interference.

Crowding of Culex sitiens Wiedemann larvae was investigated to determine whether pupation was delayed by the presence of chemical factors in the water or by mechanical interference. As the larval density increased from 0.05 to 1.0 larvae per milliliter of water, the duration of larval development increased from 7.5 to 23.0 d and larvae mortality increased from 1.7 to 99.6%. At high larval densities (2 larvae per milliliter), the larvae did not pupate, but remained alive as 4th instars for at least 50 d, even after their abundance subsequently declined due to mortality. When not crowded, 80% of the larvae fed at the surface; the remainder fed mainly on the bottom (even at a depth of 35 cm). Removal of chemical retardants by changing the water daily increased pupation to 65% (compared with 4% in controls, in which the water was not changed), but this was less than the effect of reducing mechanical interference by increasing the surface area, which increased pupation to 98%. Therefore, the main density-dependent factor was mechanical interference during feeding, but prolonged development to 19 d showed that chemical retardants also were important. The chemical retardant was not stable, so that 2nd generation larvae reared in the same water were unaffected, but its effect was irreversible, because most crowded larvae moved to clean water and a lower density did not pupate.

Animals↗
PubMedDate not supplied

Recent developments in research into the Cyathostominae and Anoplocephala perfoliata.

Intestinal helminths are an important cause of equine disease. Of these parasites, the Cyathostominae are the commonest group that infect horses. These nematodes consist of a complex tribe of 51 species, although individual horses tend to harbour 10 or so common species, in addition to a few rarer species. The Cyathostominae can be extremely pathogenic, and high levels of infection result in clinical symptoms ranging from chronic weight loss to colic, diarrhoea and death. As part of their life cycle, immature cyathostomins penetrate the large intestinal wall, where they can enter a state of inhibited larval development. These larvae can exist in this state for months to years, after which they subsequently re-emerge. If larvae re-emerge in large numbers (i.e. several million), severe pathological consequences ensue. The inhibited larvae are also relatively refractory to several of the currently available anthelmintics, so that horses treated previously with anthelmintics can still carry life-threatening burdens of these parasitic stages. Little is known about the cyathostomin larvae during their mucosal phase, and current research efforts are focused on investigating the biology of these stages. Much of the research described here highlights this area of research and details studies aimed at investigating the host immune responses that the mucosal larvae invoke. As part of this research effort, molecular tools have been developed to facilitate the identification of larval and egg stages of cyathostomins. These molecular tools are now proving very useful in the investigation of the relative contributions that individual, common cyathostomin species make to the pathology and epidemiology of mixed helminth infections. At the more applied level, research is also in progress to develop an immunodiagnostic test that will allow numbers of mucosal larvae to be estimated. This test utilises antigen-specific IgG(T) serum antibody responses as markers of infection. As anthelmintic resistance will be the major constraint on the future control of the Cyathostominae, researchers are now actively investigating this area and studies aimed at elucidating the molecular mechanisms of drug resistance are described. Another parasite which has assumed a clinically important role in horses is the tapeworm, Anoplocephala perfoliata. This parasite is prevalent world-wide and has been shown to be a significant cause of equine colic. Because previous methods of estimating the infection intensity of tapeworm were inaccurate, recent research has been directed at developing an immunodiagnostic ELISA for these cestodes. Specific IgG(T) responses to antigens secreted by adult tapeworms have been shown to provide a reasonable indication of infection intensity. An ELISA based on these responses is now commercially available. The steps involved in the development of this ELISA are described here. In addition to these recent advances in research, this review also outlines the principle areas for future research into these important equine parasites.

Animals↗
PubMed1995

LET-23-mediated signal transduction during Caenorhabditis elegans development.

We are using Caenorhabditis elegans vulval induction to study intercellular signaling and its regulation. Genes required for vulval induction include the LIN-3 transforming alpha-like growth factor, the LET-23 epidermal growth factor (EGF)-receptor-like transmembrane tyrosine kinase, the SEM-5 adaptor protein, LET-60 Ras, and the LIN-45 Raf serine/threonine kinase. Inactivation of this pathway results in a failure of vulval differentiation, the "vulvaless" phenotype. Activation of this pathway either by overexpression of LIN-3, a point mutation in the LET-23 extracellular domain, or hyperactivity of LET-60 Ras results in excessive vulval differentiation, the "multivulva" phenotype. In addition to searching for new genes that act positively in this signaling pathway, we have also characterized genes that negatively regulate this inductive signaling pathway. We find that such negative regulators are functionally redundant: mutation of only one of these negative regulators has no effect on vulval differentiation; however, if particular combinations of these genes are inactivated, excessive vulval differentiation occurs. The LIN-15 locus encodes two functionally redundant products, LIN-15A and LIN-15B, that formally act upstream of the LET-23 receptor to prevent its activity in the absence of inductive signal. The LIN-15A and B proteins are novel and unrelated to each other. The unc-101, sli-1, and rok-1 genes encode a distinct set of negative regulators of vulval differentiation. The unc-101 gene encodes an adaptin, proposed to be involved in intracellular protein trafficking. The sli-1 gene encodes a protein with similarity to c-cbl, a mammalian proto-oncogene not previously linked with a tyrosine kinase-Ras-mediated signaling pathway. LIN-3 and LET-23 are required for several aspects of C. elegans development--larval viability, P12 neuroectoblast specification, hermaphrodite vulval induction and fertility, and three inductions during male copulatory spicule development. Fertility and vulval differentiation appear to be mediated by distinct parts of the cytoplasmic tail of LET-23, and by distinct signal transduction pathways.

Animals↗
PubMed1999

The effect of sex steroids on primary and secondary sex differentiation in the sexually dichromatic reedfrog (Hyperolius argus: Hyperolidae) from the Arabuko Sokoke Forest of Kenya.

The current study examined the role of steroids in primary and secondary sex differentiation in the African reedfrog (Hyperolius argus: Hyperolidae). This species is sexually dimorphic: males have a solid green dorsum and females are reddish-brown with large white spots. This study is the first to report the effects of sex steroids on the development of a sexually dichromatic species and the first to examine the role of sex steroids on development of the vocal sac. Both males and females metamorphosed solid green without spots. Approximately 2 months after metamorphosis, control females transformed to the female-typical color pattern. Control males never developed this color pattern (remained green), but developed vocal sacs. To examine the role of sex steroid hormones on primary (gonadal differentiation) and secondary (vocal sac development and dorsal coloration) sex differentiation, testosterone (T) or estradiol-17beta (E(2)) were administered throughout larval development. At metamorphosis, 53% of the controls were males, based on gross gonadal morphology and histology of a subsample. Both doses of T produced 100% males. All E(2)-treated animals had ovarian cavities and/or follicles when examined histologically (at both doses) but 50% had testicular tissue in addition to these ovarian characteristics. Both doses of T induced vocal sac development and both doses of E(2) induced female coloration. Thus, both T and E(2) induced secondary sex characteristics (vocal sac development and dorsal color change, respectively) but E(2) produced hermaphroditic gonads, whereas T induced complete sex reversal.

Animals↗