RESUMEN
Silkworm (Bombyx mori) larvae are expected to be useful as an ingredient in entomophagy. They are full of nutrients, including indigestible proteins; however, there have been few studies on the effects of the consumption of the entire body of silkworms on the intestinal microflora. We prepared a customized diet containing silkworm larval powder (SLP), and investigated the effects of ad libitum feeding of the SLP diet on the intestinal microbiota and the amount of short-chain fatty acids (SCFAs) in mice. We found that the diversity of the cecal and fecal microbiota increased in the mice fed the SLP diet (SLP group), and that the composition of their intestinal microbiota differed from that of the control mice. Furthermore, a genus-level microbiota analysis showed that in the SLP group, the proportions of Alistipes, Lachnospiraceae A2, and RF39, which are associated with the prevention of obesity, were significantly increased, while the proportions of Helicobacter and Anaerotruncus, which are associated with obesity, were significantly decreased. Additionally, the level of butyrate was increased in the SLP group, and Clostridia UCG 014 and Lachnospiraceae FCS020 were found to be associated with the level of butyrate, one of the major SCFAs. These findings indicated that silkworm powder may be useful as an insect food that might also improve obesity.
Asunto(s)
Bombyx , Ácidos Grasos Volátiles , Microbioma Gastrointestinal , Larva , Animales , Bombyx/microbiología , Bombyx/metabolismo , Larva/microbiología , Ratones , Ácidos Grasos Volátiles/metabolismo , Heces/microbiología , Bacterias/clasificación , Bacterias/metabolismo , Bacterias/genética , Polvos , Dieta , Ciego/microbiología , Ciego/metabolismo , Masculino , Obesidad/microbiología , Obesidad/metabolismo , Alimentación AnimalRESUMEN
The domestic silkworm, Bombyx mori, has been widely used in silk production for centuries. It is also used as a bioreactor by the textile and pharmaceutical industries to mass produce recombinant bioactive proteins containing silk-based materials. Furthermore, silkworms are well-known as a source of food and have also been orally administered to prevent and treat several human disorders. In this study, we aimed to investigate the inherent bio-physicochemical properties of edible silkworms to accurately evaluate their clinical and nutritional potential. We prepared raw powder from whole larvae of silkworm. The yield rate of the powder derived from dried larvae was almost 100% (98.1-99.1% in replicates). As "percentage yield" translates to "Budomari" in Japanese, this raw powder was named "B100rw." We further prepared B100dn that was denatured through autoclaving. Thereafter, we examined whether B100rw sustained the original bio-physicochemical properties by comparing it with B100dn. There was no significant difference in nutritional content between B100rw and B100dn. B100rw contained proteins derived from silkworm larvae and mulberry leaves, whereas the proteins of B100dn were mostly degraded. On measuring the enzymatic activity of both powders using trehalase as an indicator enzyme, B100rw was found to maintain trehalase activity. B100rw also maintained a random coil conformation, similar to that of liquid silk. This suggested that B100rw sustained the unique bio-physicochemical properties of living larvae. These findings may facilitate the development of novel food products or orally administered vaccines.
RESUMEN
The bivoltine strain of the domestic silkworm, Bombyx mori, exhibits a facultative diapause phenotype that is determined by maternal environmental conditions during embryonic and larval development. Although a recent study implicated a circadian clock gene period (per) in circadian rhythms and photoperiod-induced diapause, the roles of other core feedback loop genes, including timeless (tim), Clock (Clk), cycle (cyc), and cryptochrome2 (cry2), have to be clarified yet. Therefore, the aim of this study was to elucidate the roles of circadian clock genes in temperature-dependent diapause induction. To achieve this, per, tim, Clk, cyc, and cry2 knockout (KO) mutants were generated, and the percentages of diapause and non-diapause eggs were determined. The results show that per, tim, Clk, cyc, and cry2 regulated temperature-induced diapause by acting upstream of cerebral γ-aminobutyric acid (GABA)ergic and diapause hormone signaling pathways. Moreover, the temporal expression of the clock genes in wild-type (wt) silkworms was significantly different from that of thermosensitive transient receptor potential ankyrin 1 (TRPA1) KO mutants during embryonic development. Overall, the findings of this study provide target genes for regulating temperature-dependent diapause induction in silkworms.
RESUMEN
We established a knockout strain of a clock gene, period (per), by using TALEN in a bivoltine strain (Kosetsu) of Bombyx mori (Insecta, Lepidoptera), and examined the effect of per knockout on the circadian rhythm and photoperiodism. The generated per knockout allele was considered to be null, because a new stop codon was present in the insertion allele. The wild type (Kosetsu) showed clear circadian rhythms in eclosion and hatching, whereas the per knockout strain showed arrhythmic eclosion and hatching under constant darkness. In this strain, moreover, temporal expression changes of clock genes per and timeless were disrupted. The wild type showed a clear long-day response for induction of embryonic diapause: when larvae were reared under long-day and short-day conditions at 25°C, adults produced nondiapause and diapause eggs, respectively. However, the per knockout strain lost the sensitivity to photoperiod and laid nondiapause eggs under both conditions. We conclude that per plays an important role both in circadian rhythms and in photoperiodism of B. mori, indicating the involvement of the circadian clock consisting of per in the photoperiodism.
Asunto(s)
Bombyx , Relojes Circadianos , Animales , Bombyx/genética , Relojes Circadianos/genética , Ritmo Circadiano/genética , Insectos , FotoperiodoRESUMEN
The bivoltine strain of the domestic silkworm, Bombyx mori, has two generations per year. It shows a facultative diapause phenotype determined by environmental conditions, including photoperiod and temperature, and nutrient conditions during embryonic and larval development of the mother. However, it remains unclear how the environmental signals received during development are selectively utilized as cues to determine alternative diapause phenotypes. We performed a comparative analysis between the Kosetsu strain of B. mori and a Japanese population of the wild mulberry silkworm B. mandarina concerning the hierarchical molecular mechanisms in diapause induction. Our results showed that for the Kosetsu, temperature signals during the mother's embryonic development predominantly affected diapause determination through the thermosensitive transient receptor potential ankyrin 1 (TRPA1) and diapause hormone (DH) signaling pathways. However, embryonic diapause in B. mandarina was photoperiod-dependent, although the DH signaling pathway and thermal sensitivity of TRPA1 were conserved within both species. Based on these findings, we hypothesize that TRPA1-activated signals are strongly linked to the signaling pathway participating in diapause induction in Kosetsu to selectively utilize the temperature information as the cue because temperature-dependent induction was replaced by photoperiodic induction in the TRPA1 knockout mutant.
Asunto(s)
Bombyx , Morus , Fotoperiodo , Temperatura , Animales , Ritmo Circadiano , Diapausa , Regulación del Desarrollo de la Expresión Génica , FenotipoRESUMEN
Diapause represents a major developmental switch in insects and is a seasonal adaptation that evolved as a specific subtype of dormancy in most insect species to ensure survival under unfavorable environmental conditions and synchronize populations. However, the hierarchical relationship of the molecular mechanisms involved in the perception of environmental signals to integration in morphological, physiological, behavioral, and reproductive responses remains unclear. In the bivoltine strain of the silkworm Bombyx mori, embryonic diapause is induced transgenerationally as a maternal effect. Progeny diapause is determined by the environmental temperature during embryonic development of the mother. Here, we show that the hierarchical pathway consists of a γ-aminobutyric acid (GABA)ergic and corazonin signaling system modulating progeny diapause induction via diapause hormone release, which may be finely tuned by the temperature-dependent expression of plasma membrane GABA transporter. Furthermore, this signaling pathway possesses similar features to the gonadotropin-releasing hormone (GnRH) signaling system for seasonal reproductive plasticity in vertebrates.
Asunto(s)
Bombyx/metabolismo , Diapausa/genética , Desarrollo Embrionario/genética , Proteínas Transportadoras de GABA en la Membrana Plasmática/metabolismo , Proteínas de Insectos/metabolismo , Neuropéptidos/metabolismo , Ácido gamma-Aminobutírico/metabolismo , Secuencia de Aminoácidos , Animales , Bombyx/embriología , Bombyx/genética , Membrana Celular/metabolismo , Proteínas Transportadoras de GABA en la Membrana Plasmática/genética , Antagonistas de Receptores de GABA-A/farmacología , Neuronas GABAérgicas/efectos de los fármacos , Neuronas GABAérgicas/metabolismo , Proteínas de Insectos/genética , Neuropéptidos/genética , Óvulo/efectos de los fármacos , Óvulo/metabolismo , Filogenia , Receptores de GABA-A/metabolismo , Transducción de Señal/genética , Transducción de Señal/fisiologíaRESUMEN
Insulin family peptides are known to be key regulators of growth and metabolism in insects and vertebrates. Insects have two types of insulin family peptides: insulin-like peptides and insulin-like growth factor (IGF)-like peptides (IGFLPs). We recently demonstrated that an IGFLP in the silkmoth, Bombyx mori (BIGFLP) promotes the growth of the genital imaginal disc ex vivo. However, the role of BIGFLP in the regulation of insect growth remains unclear because no in vivo study has been performed. Therefore, we analysed the functions of BIGFLP in vivo by constructing BIGFLP knock-out (KO) B. mori using the clustered regularly interspaced palindromic repeats (CRISPR) and CRISPR-associated protein 9 (CRISPR-Cas9) system. The KO moths exhibited decreased body weights and size of the appendages compared wild-type (wt) moths. Interestingly, KO females also had drastically lower ovary weights and number of eggs than wt females. However, mutant ovaries that were transplanted into wt host pupae reached a similar weight to wt ovaries that were transplanted into the wt hosts, suggesting that IGFLP in the haemolymph promotes ovarian development. These findings show that BIGFLP regulates the growth and development of adult organs, particularly the ovaries, in B. mori.
Asunto(s)
Bombyx/fisiología , Proteínas de Insectos/metabolismo , Ovario/crecimiento & desarrollo , Péptidos/metabolismo , Somatomedinas/metabolismo , Animales , Femenino , Técnicas de Silenciamiento del Gen , Hemolinfa/metabolismo , Discos Imaginales/crecimiento & desarrollo , Proteínas de Insectos/genética , Diferenciación Sexual/fisiología , Somatomedinas/genéticaRESUMEN
The insect neuropeptide family FXPRLa, which carries the Phe-Xaa-Pro-Arg-Leu-NH2 sequence at the C-terminus, is involved in many physiological processes. Although ligand-receptor interactions in FXPRLa signaling have been examined using in vitro assays, the correlation between these interactions and in vivo physiological function is unclear. Diapause in the silkworm, Bombyx mori, is thought to be elicited by diapause hormone (DH, an FXPRLa) signaling, which consists of interactions between DH and DH receptor (DHR). Here, we performed transcription activator-like effector nuclease (TALEN)-based mutagenesis of the Bombyx DH-PBAN and DHR genes and isolated the null mutants of these genes in a bivoltine strain. All mutant silkworms were fully viable and showed no abnormalities in the developmental timing of ecdysis or metamorphosis. However, female adults oviposited non-diapause eggs despite diapause-inducing temperature and photoperiod conditions. Therefore, we conclude that DH signaling is essential for diapause induction and consists of highly sensitive and specific interactions between DH and DHR selected during ligand-receptor coevolution in Bombyx mori.
Asunto(s)
Metamorfosis Biológica/fisiología , Mutagénesis , Neuropéptidos/genética , Receptores de Péptidos/genética , Transducción de Señal , Secuencia de Aminoácidos , Animales , Secuencia de Bases , Bombyx , Femenino , Proteínas de Insectos/genética , Metamorfosis Biológica/genética , Datos de Secuencia Molecular , MutaciónRESUMEN
In the bivoltine strain of the silkworm, Bombyx mori, embryonic diapause is induced transgenerationally as a maternal effect. Progeny diapause is determined by the environmental temperature during embryonic development of the mother; however, its molecular mechanisms are largely unknown. Here, we show that the Bombyx TRPA1 ortholog (BmTrpA1) acts as a thermosensitive transient receptor potential (TRP) channel that is activated at temperatures above â¼ 21 °C and affects the induction of diapause in progeny. In addition, we show that embryonic RNAi of BmTrpA1 affects diapause hormone release during pupal-adult development. This study identifying a thermosensitive TRP channel that acts as a molecular switch for a relatively long-term predictive adaptive response by inducing an alternative phenotype to seasonal polyphenism is unique.
Asunto(s)
Bombyx/embriología , Bombyx/metabolismo , Diapausa de Insecto/genética , Embrión no Mamífero/metabolismo , Patrón de Herencia/genética , Proteínas de Insectos/metabolismo , Canales Catiónicos TRPC/metabolismo , Temperatura , Animales , Peso Corporal , Bombyx/genética , Desarrollo Embrionario/genética , Perfilación de la Expresión Génica , Regulación del Desarrollo de la Expresión Génica , Técnicas de Silenciamiento del Gen , Células HEK293 , Humanos , Proteínas de Insectos/genética , Activación del Canal Iónico , Datos de Secuencia Molecular , Células Neuroendocrinas/citología , Células Neuroendocrinas/metabolismo , Neuropéptidos/metabolismo , Fenotipo , Pupa/citología , Pupa/metabolismo , Interferencia de ARN , Canales Catiónicos TRPC/genéticaRESUMEN
Many promoters have been used to drive expression of heterologous transgenes in insects. One major obstacle in the study of non-model insects is the dearth of useful promoters for analysis of gene function. Here, we investigated whether the promoter of the immediate-early gene, ie1, from the Bombyx mori nucleopolyhedrovirus (BmNPV) could be used to drive efficient transgene expression in a wide variety of insects. We used a piggyBac-based vector with a 3xP3-DsRed transformation marker to generate a reporter construct; this construct was used to determine the expression patterns driven by the BmNPV ie1 promoter; we performed a detailed investigation of the promoter in transgene expression pattern in Drosophila melanogaster and in B. mori. Drosophila and Bombyx belong to different insect orders (Diptera and Lepidoptera, respectively); however, and to our surprise, ie1 promoter-driven expression was evident in several tissues (e.g., prothoracic gland, midgut, and tracheole) in both insects. Furthermore, in both species, the ie1 promoter drove expression of the reporter gene from a relatively early embryonic stage, and strong ubiquitous ie1 promoter-driven expression continued throughout the larval, pupal, and adult stages by surface observation. Therefore, we suggest that the ie1 promoter can be used as an efficient expression driver in a diverse range of insect species.
Asunto(s)
Baculoviridae/genética , Bombyx/genética , Drosophila melanogaster/genética , Expresión Génica , Genes Inmediatos-Precoces/genética , Regiones Promotoras Genéticas , Transgenes/genética , Animales , Animales Modificados Genéticamente , Bombyx/embriología , ADN/genética , Embrión no Mamífero/metabolismo , Genes Reporteros , Genoma de los Insectos/genética , Proteínas Fluorescentes Verdes/metabolismo , Larva/genética , Mutagénesis Insercional/genética , Transformación GenéticaRESUMEN
The white spotted tussock moth, Orgyia thyellina, is a typical insect that exhibits seasonal polyphenisms in morphological, physiological, and behavioral traits, including a life-history tradeoff known as oogenesis-flight syndrome. However, the developmental processes and molecular mechanisms that mediate developmental plasticity, including life-history tradeoff, remain largely unknown. To analyze the molecular mechanisms involved in reproductive polyphenism, including the diapause induction, we first cloned and characterized the diapause hormone-pheromone biosynthesis activating neuropeptide (DH-PBAN) cDNA encoding the five Phe-X-Pro-Arg-Leu-NH(2) (FXPRLa) neuropeptides: DH, PBAN, and α-, ß-, and γ-SGNPs (subesophageal ganglion neuropeptides). This gene is expressed in neurosecretory cells within the subesophageal ganglion whose axonal projections reach the neurohemal organ, the corpus cardiacum, suggesting that the DH neuroendocrine system is conserved in Lepidoptera. By injection of chemically synthetic DH and anti-FXPRLa antibody into female pupae, we revealed that not only does the Orgyia DH induce embryonic diapause, but also that this neuropeptide induces seasonal polyphenism, participating in the hypertrophy of follicles and ovaries. In addition, the other four FXPRLa also induced embryonic diapause in O. thyellina, but not in Bombyx mori. This is the first study showing that a neuropeptide has a pleiotropic effect in seasonal reproductive polyphenism to accomplish seasonal adaptation. We also show that a novel factor (i.e., the DH neuropeptide) acts as an important inducer of seasonal polyphenism underlying a life-history tradeoff. Furthermore, we speculate that there must be evolutionary conservation and diversification in the neuroendocrine systems of two lepidopteran genera, Orgyia and Bombyx, in order to facilitate the evolution of coregulated life-history traits and tradeoffs.
Asunto(s)
Neuropéptidos/fisiología , Reproducción , Estaciones del Año , Secuencia de Aminoácidos , Animales , Evolución Biológica , Femenino , Hormonas de Insectos/biosíntesis , Mariposas Nocturnas , Neuropéptidos/genética , Sistemas Neurosecretores , PupaRESUMEN
In the silkworm Bombyx mori and other insects, prothoracicotropic hormone (PTTH) plays a central role in controlling molting and metamorphosis by stimulating the prothoracic glands to synthesize and release the molting hormone ecdysone. Using an AcNPV (Autographa californica nucleopolyhedrovirus)-mediated transient gene transfer system, we identified a cis-regulatory element that participates in the decision to switch expression of PTTH on or off in PTTH-producing neurosecretory cells (PTPCs). The nucleotide sequence of this cis-regulatory element is similar to a cis-regulatory element that participates in direction of expression of diapause hormone-pheromone biosynthesis activating neuropeptide gene (DH-PBAN) (Shiomi et al., 2007). Furthermore, we found that B. mori Pitx (BmPitx), a bicoid-like homeobox transcription factor, binds the element and activates PTTH expression. Therefore, we propose that the cell-specific expression of two neuropeptide hormone genes, PTTH and DH-PBAN, is activated by the Pitx transcription factor, which may act as a pan-activator in the insect neuroendocrine system and in vertebrate pituitary cells.
Asunto(s)
Bombyx/metabolismo , Regulación de la Expresión Génica , Proteínas de Homeodominio/metabolismo , Hormonas de Insectos , Proteínas de Insectos/metabolismo , Neuropéptidos/metabolismo , Precursores de Proteínas/metabolismo , Secuencia de Aminoácidos , Animales , Secuencia de Bases , Bombyx/genética , Clonación Molecular , Técnicas de Transferencia de Gen , Proteínas de Homeodominio/genética , Hormonas de Insectos/biosíntesis , Hormonas de Insectos/genética , Proteínas de Insectos/genética , Larva/genética , Larva/metabolismo , Microinyecciones , Datos de Secuencia Molecular , Muda/genética , Neuropéptidos/genética , Sistemas Neurosecretores/metabolismo , Nucleopoliedrovirus , Precursores de Proteínas/genética , Pupa/genética , Pupa/metabolismo , Factores de Transcripción/genética , Factores de Transcripción/metabolismoRESUMEN
In the silkworm Bombyx mori, the diapause hormone-pheromone biosynthesis activating neuropeptide gene, DH-PBAN, is a neuropeptide gene that encodes a polypeptide precursor consisting in five Phe-X-Pro-Arg-Leu-NH(2) (FXPRL) amide (FXPRLa) neuropeptides; DH (diapause hormone), PBAN (pheromone-biosynthesis-activating neuropeptide) and α-, ß- and γ-SGNPs (subesophageal ganglion neuropeptides). These neuropeptides are synthesized in DH-PBAN-producing neurosecretory cells contained within three neuromeres, four mandibular cells, six maxillary cells, two labial cells (SLb) and four lateral cells of the subesophageal ganglion. DH is solely responsible, among the FXPRLa peptide family, for embryonic diapause. Functional differentiation has been previously suggested to occur at each neuromere, with the SLb cells releasing DH through brain innervation in order to induce embryonic diapause. We have investigated the immunoreactive intensity of DH in the SLb when thermal (25°C or 15°C) and light (continuous illumination or darkness) conditions are altered and following brain surgery that induces diapause or non-diapause eggs in the progeny. We have also examined the immunoreactivity of the other FXPRLa peptides by using anti-ß-SGNP and anti-PBAN antibodies. Pupal SLb somata immunoreactivities seem to be affected by both thermal and light conditions during embryogenesis. Thus, we have been able to identify a close correlation between the immunoreactive intensity of neuropeptides and environmental conditions relating to the determination of embryonic diapause in B. mori.
Asunto(s)
Bombyx/embriología , Bombyx/metabolismo , Proteínas de Insectos/metabolismo , Neuropéptidos/metabolismo , Animales , Bombyx/genética , Oscuridad , Ensayo de Inmunoadsorción Enzimática , Técnica del Anticuerpo Fluorescente , Regulación del Desarrollo de la Expresión Génica , Proteínas de Insectos/genética , Luz , Neuropéptidos/genética , Neuropéptidos/inmunología , Fenotipo , Precursores de Proteínas/genética , Precursores de Proteínas/metabolismo , TemperaturaRESUMEN
A defensin-like gene, BmdefA, was rediscovered in the silkworm genome and expressed sequence tags databases. The open reading frame of BmdefA encodes a prepropeptide consisting of a 22-residue signal peptide, a 34-residue propeptide, and a 36-residue mature peptide with a molecular mass of 4.0 kDa. The mature peptide possesses the characteristic six-cysteine motif of insect defensins, and its predicted isoelectric point is 4.12, indicating it is a novel anionic defensin. An intron is present in BmdefA and several cis-regulatory elements are in the regulating region. It is transcribed constitutively at a high level in the hemocyte, silk gland, head, and ovary of the silkworm larvae, and in the fat body of early-stage pupae and moth. BmdefA is also strongly induced by immune challenge. These results suggest that BmdefA plays an important role in both immunity and metamorphosis.
Asunto(s)
Bombyx/química , Bombyx/metabolismo , Defensinas/química , Defensinas/metabolismo , Regulación de la Expresión Génica/genética , Secuencia de Aminoácidos , Animales , Aniones/química , Secuencia de Bases , Bombyx/genética , Secuencia Conservada , Defensinas/clasificación , Defensinas/genética , Genoma de los Insectos/genética , Datos de Secuencia Molecular , Alineación de Secuencia , Transcripción Genética/genéticaRESUMEN
Spider dragline silk is a unique fibrous protein with combination of tensile strength and elasticity, but the isolation of large amount of silk from spiders is not feasible. In this paper, we used a newly established Bac-to-Bac/BmNPV Baculovirus expression system to express the recombinant spider (Nephila clavata) dragline silk protein (MaSp1) fused EGFP in BmN cells and larvae of silkworm. A 70 kDa fusion protein was visualized after rBacmid/BmNPV/drag infection by SDS-PAGE and immunoblotting analysis. Fusion protein expressed in the BmN cells probably occupied five percent of the cell total protein; In a silkworm larva, approximately 6 mg fusion proteins were expressed. Solubility analysis of the expressed spider dragline silk protein indicated that 60% fusion protein is insoluble. EGFP fluorescence showed that fusion protein is tend to form aggregate by self assemblage. The results indicated the solubility is the primary limit for spider dragline proteins yield. It also suggested that directly produce fibrous spider silk in the secreting-silk organs of the transgenic silkworm larvae might be a better method.
Asunto(s)
Bombyx/metabolismo , Fibroínas/metabolismo , Expresión Génica/genética , Proteínas Recombinantes de Fusión/metabolismo , Arañas/metabolismo , Secuencia de Aminoácidos , Animales , Secuencia de Bases , Bombyx/genética , Línea Celular , ADN Complementario/genética , Fibroínas/química , Fibroínas/genética , Fibroínas/aislamiento & purificación , Genes Reporteros/genética , Larva/genética , Larva/metabolismo , Datos de Secuencia Molecular , Proteínas Recombinantes de Fusión/química , Proteínas Recombinantes de Fusión/genética , Proteínas Recombinantes de Fusión/aislamiento & purificación , Solubilidad , Arañas/química , Arañas/genéticaRESUMEN
The diapause hormone-pheromone biosynthesis activating neuropeptide gene, DH-PBAN, is expressed exclusively in seven pairs of DH-PBAN-producing neurosecretory cells (DHPCs) on the terminally differentiated processes of the subesophageal ganglion (SG). To help reveal the regulatory mechanisms of cell-specific DH-PBAN expression, we identified a cis-regulatory element that regulates expression in DHPCs using the recombinant AcNPV-mediated gene transfer system and a gel-mobility shift assay. Bombyx mori Pitx (BmPitx), a bicoid-like homeobox transcription factor, binds this element and activates DH-PBAN expression. The BmPitx was expressed in various tissues, including DHPCs in the SG. Suppression of DH-PBAN expression by silencing of the BmPitx successfully induced non-diapaused eggs from a diapause egg producer. To the best of our knowledge, this report is the first to identify a neuropeptide-encoding gene as a target of the Pitx transcriptional regulator in invertebrates. Thus, it is tempting to speculate that functional conservation of Pitx family members on neuropeptide gene expression occurs through a "combinational code mechanism" in both vertebrate and invertebrate in neuroendocrine systems.
Asunto(s)
Bombyx/genética , Regulación de la Expresión Génica/fisiología , Genes Homeobox/fisiología , Proteínas de Insectos/metabolismo , Neuropéptidos/metabolismo , Precursores de Proteínas/metabolismo , Animales , Clonación Molecular , Proteínas Fluorescentes Verdes/metabolismo , Larva , Datos de Secuencia Molecular , Interferencia de ARN/fisiología , Reacción en Cadena de la Polimerasa de Transcriptasa Inversa/métodosRESUMEN
Previously, we showed that chilling of diapausing Bombyx eggs activated ERK/MAPK in yolk cells coincidentally with acquisition of developmental competence, and that ERK regulates diapause termination via activating transcription of key enzyme genes for ecdysteroid and sorbitol metabolism. To further elucidate the molecular mechanisms of temperature signaling and diapause termination, effects of different temperatures on diapause termination, yolk morphology, and ERK and p38 MAPK phosphorylation were analyzed. We confirmed the coincidence of diapause termination and changes of phosphorylated levels of ERK and p38 MAPK at various temperatures. Our study also shows that different temperatures have distinct effects on diapause termination and yolk morphology, however, these two effects did not always coincide. Our analyses suggest the possibility that the effects on diapause termination and yolk morphology are independently regulated by ERK. We observed that a temperature shift alters diapause intensity reversibly, and coincidental changes of phosphorylated ERK levels suggest that ERK may have a role in regulating the diapause intensity. The present study suggests that ERK and p38 MAPK have roles for transmitting the temperature signals that are important for diapause termination.
Asunto(s)
Bombyx/embriología , Bombyx/enzimología , Quinasas MAP Reguladas por Señal Extracelular/metabolismo , Temperatura , Proteínas Quinasas p38 Activadas por Mitógenos/metabolismo , Animales , Quinasas MAP Reguladas por Señal Extracelular/análisis , Regulación del Desarrollo de la Expresión Génica , Regulación Enzimológica de la Expresión Génica , Óvulo/citología , Óvulo/enzimología , Óvulo/crecimiento & desarrollo , Fosforilación , Factores de Tiempo , Proteínas Quinasas p38 Activadas por Mitógenos/análisisRESUMEN
The eggs of the silkworm Bombyx mori undergo a state of suspended overt development and diminished metabolism called "diapause" to escape adverse environmental conditions. Termination of Bombyx embryonic diapause requires 2-3 months of low temperature (5 degrees C), but the molecular mechanisms underlying diapause termination are unknown. Diapause termination requires a decrease in the sorbitol concentration, which arrests embryonic development, and the secretion factors from yolk cells that promote embryonic development. In the present study, we report that 20-hydroxyecdysone promoted the development of denuded embryos and that ecdysteroid-phosphate phosphatase (EPPase), which is a key enzyme for active ecdysteroid production, was induced by incubation of diapausing eggs at 5 degrees C. In dechorionated egg cultures, extracellular signal-regulated kinase (ERK), which is activated by incubating diapausing eggs at 5 degrees C, regulated sorbitol-glycogen conversion, ecdysteroid secretion via gene transcription of key enzymes, sorbitol dehydrogenase-2, and EPPase, suggesting that ERK has a key role in diapause termination.
Asunto(s)
Bombyx/embriología , Ecdisteroides/metabolismo , Desarrollo Embrionario/fisiología , Quinasas MAP Reguladas por Señal Extracelular/fisiología , Sorbitol/metabolismo , Animales , Bombyx/metabolismo , Bombyx/fisiología , Frío , Ecdisteroides/fisiología , Ecdisterona/fisiología , Yema de Huevo/fisiología , Femenino , Expresión Génica , Glucógeno/biosíntesis , Monoéster Fosfórico Hidrolasas/metabolismoRESUMEN
Araneoid spiders use specialized abdominal glands to produce up to seven different protein-based silks/glues that have various mechanical properties. To date, the fibroin sequences encoding egg case fibers have not been fully determined. To gain further understanding of a recently reported spider silk protein gene family, several novel strategies were utilized in this study to isolate two full-length cDNAs of egg case silk proteins, cylindrical silk protein 1 (CySp1, 9.1 kb) and cylindrical silk protein 2 (CySp2, 9.8 kb), from the wasp spider, Argiope bruennichi. Northern blotting analysis demonstrated that CySp1 and CySp2 are selectively expressed in the cylindrical glands. The amino acid composition of raw egg case silk was closely consistent with the deduced amino acid composition based on the sequences of CySp1 and CySp2, which supports the assertion that CySp1 and CySp2 represent two major components of egg case silk. CySp1 and CySp2 are primarily composed of remarkable homogeneous assemble repeats that are 180 residues in length and consist of several complex subrepeats, and they contain highly homologous C-termini and markedly different N-termini. Our results suggest a possible link between CySp1 and CySp2. In addition, comparisons of stress/strain curves for dragline and egg case silk from Argiope bruennichi showed obvious differences in ultimate strength and extensibility, and similarities in toughness.