RESUMEN
Endocrine signal transduction occurs through cascades that involve the action of both ligand-dependent and ligand-independent nuclear receptors. In insects, two such nuclear receptors are HR3 and E75 that interact to transduce signals initiated by ecdysteroids. We have cloned these nuclear receptors from the crustacean Daphnia pulex to assess their function as regulators of gene transcription in this ecologically and economically important group of organisms. Both nuclear receptors from D. pulex (DappuHR3 (group NR1F) and DappuE75 (group NR1D)) exhibit a high degree of sequence similarity to other NR1F and NR1D group members that is indicative of monomeric binding to the RORE (retinoid orphan receptor element). DappuE75 possesses key amino acid residues required for heme binding to the ligand-binding domain. Next, we developed a gene transcription reporter assay containing a luciferase reporter gene driven by the RORE. DappuHR3, but not DappuE75, activated transcription of the luciferase gene in this system. Co-transfection experiments revealed that DappuE75 suppressed DappuHR3-dependent luciferase transcription in a dose-dependent manner. Electrophoretic mobility shift assays confirmed that DappuHR3 bound to the RORE. However, we found no evidence that DappuE75 similarly bound to the response element. These experiments further demonstrated that DappuE75 prevented DappuHR3 from binding to the response element. In conclusion, DappuHR3 functions as a transcriptional activator of genes regulated by the RORE and DappuE75 is a negative regulator of this activity. DappuE75 does not suppress the action of DappuHR3 by occupying the response element but presumably interacts directly with the DappuHR3 protein. Taken together with the previous demonstration that daphnid HR3 is highly induced by 20-hydroxyecdysone, these results support the premise that HR3 is a major component of ecdysteroid signaling in some crustaceans and is under the negative regulatory control of E75.
Asunto(s)
Daphnia/genética , Regulación de la Expresión Génica , Receptores Citoplasmáticos y Nucleares/genética , Secuencia de Aminoácidos , Animales , Secuencia de Bases , Clonación Molecular , Daphnia/metabolismo , Ensayo de Cambio de Movilidad Electroforética , Femenino , Immunoblotting , Datos de Secuencia Molecular , Filogenia , ARN Mensajero/biosíntesis , ARN Mensajero/genética , Receptores Citoplasmáticos y Nucleares/biosíntesis , Reacción en Cadena de la Polimerasa de Transcriptasa Inversa , Alineación de Secuencia , Transducción de Señal , TransfecciónRESUMEN
BACKGROUND: The nuclear receptor superfamily currently consists of seven gene subfamilies that encompass over 80 distinct receptor proteins. These transcription factors typically share a common five-domain structure with a highly conserved DNA-binding domain. Some nuclear receptors are ubiquitous among the metazoans, while others are unique to specific phylogenetic groups. Crustaceans represent the second largest group of arthropods with insects being the largest. However, relative to insects, little is known about the nuclear receptors of crustaceans. The aim of this study was to identify putative nuclear receptors from the first assembled genome of a crustacean Daphnia pulex http://wFleaBase.org. Nuclear receptor expression was evaluated and receptors were subjected to phylogenetic analyses to gain insight into evolution and function. RESULTS: Twenty-five putative nuclear receptors were identified in D. pulex based on the presence of a conserved DNA-binding domain. All of the nuclear receptor protein sequences contain a highly homologous DNA-binding domain and a less conserved ligand-binding domain with the exception of the NR0A group. These receptors lack a ligand-binding domain. Phylogenetic analysis revealed the presence of all seven receptor subfamilies. The D. pulex genome contains several nuclear receptors that have vertebrate orthologs. However, several nuclear receptor members that are represented in vertebrates are absent from D. pulex. Notable absences include receptors of the 1C group (peroxisome proliferators-activated receptors), the 3A group (estrogen receptor), and the 3C group (androgen, progestogen, mineralcorticoid, and glucocorticoid receptors). The D. pulex genome also contains nuclear receptor orthologs that are present in insects and nematodes but not vertebrates, including putative nuclear receptors within the NR0A group. A novel group of receptors, designated HR97, was identified in D. pulex that groups with the HR96/CeNHR8/48/DAF12 clade, but forms its own sub-clade. Gene products were detected in adult female D. pulex for 21 of the 25 receptors. CONCLUSION: Nuclear receptors are ancient proteins with highly conserved DNA-binding domains. The DNA-binding domains of the nuclear receptors of D. pulex contain the same degree of conservation that is typically found within nuclear receptors of other species. Most of the receptors identified in D. pulex have orthologs within the vertebrate and invertebrate lineages examined with the exception of the novel HR97 group and the Dappu-HR10 and potentially the Dappu-HR11 receptors found in D. pulex. These groups of receptors may harbour functions that are intrinsic to crustacean physiology.
Asunto(s)
Daphnia/genética , Regulación de la Expresión Génica , Filogenia , Receptores Citoplasmáticos y Nucleares/genética , Secuencia de Aminoácidos , Animales , Daphnia/fisiología , Evolución Molecular , Femenino , Genoma , Humanos , Datos de Secuencia Molecular , Partenogénesis/genética , ARN Mensajero/genética , ARN Mensajero/metabolismo , Receptores Citoplasmáticos y Nucleares/química , Receptores Citoplasmáticos y Nucleares/metabolismoRESUMEN
BACKGROUND: Environmental signals to maternal organisms can result in developmental alterations in progeny. One such example is environmental sex determination in Branchiopod crustaceans. We previously demonstrated that the hormone methyl farnesoate could orchestrate environmental sex determination in the early embryo to the male phenotype. Presently, we identify a transcription factor that is activated by methyl farnesoate and explore the extent and significance of this transgenerational signaling pathway. METHODOLOGY/PRINCIPAL FINDINGS: Several candidate transcription factors were cloned from the water flea Daphnia pulex and evaluated for activation by methyl farnesoate. One of the factors evaluated, the complex of two bHLH-PAS proteins, dappuMet and SRC, activated a reporter gene in response to methyl farnesoate. Several juvenoid compounds were definitively evaluated for their ability to activate this receptor complex (methyl farnesoate receptor, MfR) in vitro and stimulate male sex determination in vivo. Potency to activate the MfR correlated to potency to stimulate male sex determination of offspring (pyriproxyfen>methyl farnesoate>methoprene, kinoprene). Daphnids were exposed to concentrations of pyriproxyfen and physiologic responses determined over multiple generations. Survivial, growth, and sex of maternal organisms were not affected by pyriproxyfen exposure. Sex ratio among offspring (generation 2) were increasingly skewed in favor of males with increasing pyriproxyfen concentration; while, the number of offspring per brood was progressively reduced. Female generation 2 daphnids were reared to reproductive maturity in the absence of pyriproxyfen. Sex ratios of offspring (generation 3) were not affected in this pyriproxyfen lineage, however, the number of offspring per brood, again, was significantly reduced. CONCLUSIONS: Results reveal likely components to a hormone/receptor signaling pathway in a crustacean that orchestrates transgenerational modifications to important population metrics (sex ratios, fecundity of females). A model is provided that describes how these signaling processes can facilitate population sustainability under normal conditions or threaten sustainability when perturbed by environmental chemicals.
Asunto(s)
Crustáceos/metabolismo , Sistema Endocrino/metabolismo , Transducción de Señal , Secuencia de Aminoácidos , Animales , Clonación Molecular , Crustáceos/efectos de los fármacos , Daphnia/efectos de los fármacos , Daphnia/fisiología , Sistema Endocrino/efectos de los fármacos , Ácidos Grasos Insaturados/farmacología , Femenino , Fertilidad , Genes Reporteros , Estadios del Ciclo de Vida/efectos de los fármacos , Ligandos , Luciferasas/metabolismo , Masculino , Datos de Secuencia Molecular , Densidad de Población , Piridinas/farmacología , Procesos de Determinación del Sexo/efectos de los fármacos , Razón de Masculinidad , Transducción de Señal/efectos de los fármacos , Factores de Transcripción/químicaRESUMEN
OBJECTIVE: To investigate the detection and characterization of micro-vessels within the carotid atherosclerotic plaque using B-flow imaging (BFI) ultrasound with contrast-enhanced ultrasound (CEU) as the reference standard. METHODS: Between August 2008 and July 2011, 78 patients with carotid atherosclerosis that were admitted at the Department of Ultrasonography in ZhongNan Hospital of Wuhan University, Wuhan, China underwent standard and BFI examination. Fifty-one patients received both BFI and CEU. We evaluated the relationship between BFI findings, and clinical symptoms in ischemic stroke, or transient ischemic attack patients. The correlation of cerebrovascular symptoms, stenosis, and plaque type on the detection of neovessels by BFI were statistically evaluated using χ2 test (McNemar test). The agreement of the 2 sonographic methods was assessed by K coefficient. The diagnostic efficacy of BFI for carotid atherosclerotic micro-vessel detection was also calculated. RESULTS: The BFI findings of micro-vessel were correlated to patient's symptom. The agreement between BFI and CEU for diagnosis of microvascularization was good (K=0.406). The following was calculated: sensitivity (0.483); specificity (0.955); positive predictive value (0.933); negative predictive value (0.583); and accuracy of BFI (0.686). Logistic regression demonstrated a significant association between cerebrovascular events and the presence of BFI signals within carotid plaques (B: 2.422; 95% confidence interval: 1.728-73.407). CONCLUSION: Compared with CEU, the BFI is less sensitive, however, it is a valid and practical method for detection of carotid atherosclerotic micro-vessels.
Asunto(s)
Isquemia Encefálica/complicaciones , Enfermedades de las Arterias Carótidas/diagnóstico por imagen , Microvasos/patología , Adulto , Anciano , Anciano de 80 o más Años , Enfermedades de las Arterias Carótidas/complicaciones , Enfermedades de las Arterias Carótidas/patología , Medios de Contraste , Femenino , Humanos , Masculino , Persona de Mediana Edad , Sensibilidad y Especificidad , UltrasonografíaRESUMEN
One of the great challenges facing modern toxicology is in predicting the hazard associated with chemical mixtures. The development of effective means of predicting the toxicity of chemical mixtures requires an understanding of how chemicals interact to produce nonadditive outcomes (e.g., synergy). We hypothesized that tributyltin would elicit toxicity in daphnids (Daphnia magna) by exaggerating physiological responses to 20-hydroxyecdysone signaling via synergistic activation of the retinoid X receptor (RXR):ecdysteroid receptor (EcR) complex. Using reporter gene assays, we demonstrated that RXR, alone, is activated by a variety of ligands including tributyltin, whereas RXR:EcR heterodimers were not activated by tributyltin. However, tributyltin, in combination with the daphnid EcR ligand 20-hydroxyecdysone, caused concentration-dependent, synergistic activation of the RXR:EcR reporter. Electrophoretic mobility shift assays revealed that tributyltin did not enhance the activity of 20-hydroxyecdysone by increasing binding of the receptor complex to a DR-4 DNA-binding site. Exposure of daphnids to elevated concentrations of 20-hydroxyecdysone caused premature and incomplete ecdysis resulting in death. Tributyltin exaggerated this effect of exogenous 20-hydroxyecdysone. Further, exposure of daphnids to tributyltin enhanced the inductive effects of 20-hydroxyecdysone on expression of the 20-hydroxyecdysone-inducible gene HR3. Continuous, prolonged exposure of maternal daphnids to concentrations of tributyltin resulted in mortality concurrent with molting. Taken together, these results demonstrate that xenobiotics, such as tributyltin, can interact with RXR to influence gene expression regulated by the heterodimeric partner to RXR. The result of such interactions can be toxicity due to inappropriate or exaggerated hormonal signaling. The application of the in vitro/in vivo approach used in this study is discussed in relation to modeling of nonadditive interactions among constituents of chemical mixtures.
Asunto(s)
Ecdisterona/toxicidad , Compuestos de Trialquiltina/toxicidad , Contaminantes Químicos del Agua/toxicidad , Animales , Células Cultivadas , Daphnia , Relación Dosis-Respuesta a Droga , Sinergismo Farmacológico , Ecdisterona/metabolismo , Femenino , Expresión Génica/efectos de los fármacos , Muda/efectos de los fármacos , Receptores de Esteroides/genética , Receptores de Esteroides/metabolismo , Receptores X Retinoide/genética , Receptores X Retinoide/metabolismo , Transducción de SeñalRESUMEN
The induction of vitellogenin in oviparous vertebrates has become the gold standard biomarker of exposure to estrogenic chemicals in the environment. This biomarker of estrogen exposure also has been used in arthropods, however, little is known of the factors that regulate the expression of vitellogenin in these organisms. We investigated changes in accumulation of mRNA products of the vitellogenin gene Vtg2 in daphnids (Daphnia magna) exposed to a diverse array of chemicals. We further evaluated the involvement of hormonal factors in the regulation of vitellogenin expression that may be targets of xenobiotic chemicals. Expression of the Vtg2 gene was highly responsive to exposure to various chemicals with an expression range spanning approximately four orders of magnitude. Chemicals causing the greatest induction were piperonyl butoxide, chlordane, 4-nonylphenol, cadmium, and chloroform. Among these, only 4-nonylphenol is recognized to be estrogenic. Exposure to several chemicals also suppressed Vtg2 mRNA levels, as much as 100-fold. Suppressive chemicals included cyproterone acetate, acetone, triclosan, and atrazine. Exposure to the estrogens diethylstilbestrol and bisphenol A had little effect on vitellogenin mRNA levels further substantiating that these genes are not induced by estrogen exposure. Exposure to the potent ecdysteroids 20-hydroxyecdysone and ponasterone A revealed that Vtg2 was subject to strong suppressive control by these hormones. Vtg2 mRNA levels were not significantly affected from exposure to several juvenoid hormones. Results indicate that ecdysteroids are suppressors of vitellogenin gene expression and that vitellogenin mRNA levels can be elevated or suppressed in daphnids by xenobiotics that elicit antiecdysteroidal or ecdysteroidal activity, respectively. Importantly, daphnid Vtg2 is not elevated in response to estrogenic activity.
Asunto(s)
Daphnia/metabolismo , Contaminantes Ambientales/toxicidad , Vitelogeninas/genética , Xenobióticos/toxicidad , Animales , Cadmio/toxicidad , Daphnia/efectos de los fármacos , Daphnia/genética , Ecdisteroides/toxicidad , Ecdisterona/toxicidad , Estrógenos/toxicidad , Expresión Génica/efectos de los fármacos , Compuestos Heterocíclicos/toxicidad , Compuestos Policíclicos/toxicidad , ARN Mensajero/metabolismo , Vitelogeninas/metabolismoRESUMEN
While a functional role for the sesquiterpenoid hormone methyl farnesoate in arthropods has been recognized for decades, the identification of a receptor that mediates the action of this hormone remains equivocal. Luciferase reporter assays were used in the present study to evaluate the ability of methyl farnesoate and other putative ligands to activate gene transcription associated with the retinoid X receptor (RXR) and RXR:EcR heterodimeric complexes from the crustacean (Daphnia magna). The daphnid RXR constructs, transfected into HepG2 cells along with the reporter construct, significantly activated luciferase gene expression in response to tributyltin indicating that the crustacean RXR is indeed ligand activated. However, RXR was not activated by methyl farnesoate or other putative RXR ligands. Cells co-transfected with the daphnid RXR and EcR produced luciferase in response to ecdysteroids and this activation was significantly enhanced when cells were also provided either methyl farnesoate or other putative RXR ligands. This synergy among RXR and EcR ligands was not dependent upon the co-activator SRC-1 and did not correlate to a physiological response of daphnids to juvenoid hormones (male sex determination). Results indicate that methyl farnesoate, along with compounds that are functionally similar to methyl farnesoate synergize with ecdysteroids to activate the RXR:EcR receptor complex. However, this effect appears to be unrelated to the ability of these compounds to stimulate male sex determination.
Asunto(s)
Daphnia/metabolismo , Ácidos Grasos Insaturados/metabolismo , Receptores X Retinoide/metabolismo , Secuencia de Aminoácidos , Animales , Secuencia de Bases , ADN Complementario/genética , ADN Complementario/aislamiento & purificación , Daphnia/efectos de los fármacos , Ecdisterona/farmacología , Genes Reporteros , Humanos , Ligandos , Luciferasas/metabolismo , Masculino , Datos de Secuencia Molecular , Sistemas de Lectura Abierta/genética , Receptores de Esteroides/metabolismo , Receptores X Retinoide/química , Receptores X Retinoide/genética , Alineación de Secuencia , Homología de Secuencia de Aminoácido , Procesos de Determinación del Sexo , Razón de Masculinidad , Activación Transcripcional/efectos de los fármacosRESUMEN
Terpenoid hormones function as morphogens throughout the animal kingdom and many of these activities are mediated through members of the retinoid X group of nuclear receptors (RXR; NR2B). In the present study, RXR was cloned from the water flea Daphnia magna, a primitive crustacean of the class Branchiopoda, and characterized with respect to phylogeny, developmental expression, and hormonal regulation. The full length daphnid RXR cDNA was cloned by initial PCR amplification of a cDNA fragment from the highly conserved DNA-binding domain followed by extension of the fragment using RACE PCR. The full length cDNA was 1888 base pairs in length and coded for a 400 amino acid protein that exhibited the five-domain structure of a nuclear receptor superfamily member. The RXR protein shared significant identity with other NR2B group members. Phylogenetic analyses of the ligand-binding domain of the receptor revealed that daphnid RXR clustered with RXR from decapod crustaceans on a branch of the phylogenetic tree that was distinct from RXRs known to bind retinoic acids and juvenile hormones. Daphnid RXR mRNA levels were greatest in embryos that were early in development and progressively declined through the initial five stages of embryo development. Adult females expressed higher levels of RXR mRNA than did males and exposure of females to the terpenoid mimic pyriproxyfen reduced RXR mRNA to levels approaching levels in males. RXR mRNA levels in males were refractory to pyriproxyfen. These results show that branchiopod crustaceans dynamically express RXR which should be evaluated as a candidate receptor for the terpenoid hormone methyl farnesoate which functions as a sex determinant in these organisms.