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1.
J Econ Entomol ; 111(1): 120-126, 2018 02 09.
Artigo em Inglês | MEDLINE | ID: mdl-29267899

RESUMO

The fall armyworm, Spodoptera frugiperda (J.E. Smith) (Lepidoptera: Noctuidae), cannot survive prolonged periods of freezing temperatures, thereby limiting where it can overwinter in North America. Climate change is anticipated to reduce the frequency of freeze days in Florida over the decades, with the potential consequence of a significant expansion of the overwintering range, whose northern limit in North America was assessed between 27 and 28°N in the last century. To assess this possibility, the development of the fall armyworm on corn leaves, one of the main host plants in the United States, was determined at five constant temperatures ranging from 14 to 30°C. Based on the development time, the thermal constant and the lower threshold temperature were used to estimate the number of generations of fall armyworm at 42 locations in the state of Florida, from 2006 to 2016. Maps were constructed to provide a visual description of the interpolated data, using GIS (Geographic Information System). The highest number of generations was observed in the counties farther south, an area that showed the highest temperatures during the years and plays a strategic role in maintaining fall armyworm populations in corn fields. Additionally, we conclude that in the absence of freeze periods, the northern limit for fall armyworm overwintering should be between 28 and 29°N.


Assuntos
Mudança Climática , Cadeia Alimentar , Spodoptera/crescimento & desenvolvimento , Zea mays , Animais , Florida , Larva/crescimento & desenvolvimento , Estações do Ano , Temperatura , Zea mays/crescimento & desenvolvimento
2.
Insect Mol Biol ; 25(3): 324-37, 2016 06.
Artigo em Inglês | MEDLINE | ID: mdl-26991678

RESUMO

The noctuid moth Spodoptera frugiperda (the fall armyworm) is endemic to the Western Hemisphere and appears to be undergoing sympatric speciation to produce two subpopulations that differ in their choice of host plants. The 'rice strain' and 'corn strain' are morphologically indistinguishable, requiring the use of genetic markers for identification. Because fall armyworm is a major pest of corn and several other agricultural crops, characterizing the strains has important economic consequences. In this study, comparisons were made of the intron sequences from the triose-phosphate isomerase (Tpi) gene isolated from 85 fall armyworm specimens collected from two host plants. Sixteen new strain-specific haplotypes based on intron polymorphisms are described that can facilitate the characterization of fall armyworm populations associated with different host plants. Comparisons of genetic diversity within and between the strains provides evidence that the corn strain is undergoing active selection and supports the proposal of directional interstrain mating occurring in the wild. Comparisons of the polymorphisms indicate that each intron undergoes different patterns of mutation that in some cases corresponds to host plant preferences. The results confirm that intron sequence comparisons are an effective approach to study fall armyworm population genetics.


Assuntos
Especiação Genética , Mariposas/genética , Triose-Fosfato Isomerase/genética , Processamento Alternativo , Sequência de Aminoácidos , Animais , Sequência de Bases , Haplótipos , Íntrons , Dados de Sequência Molecular , Polimorfismo Genético
3.
Int J Biometeorol ; 60(2): 255-67, 2016 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-26045330

RESUMO

Fall armyworm, Spodoptera frugiperda (J.E. Smith), is a highly mobile insect pest of a wide range of host crops. However, this pest of tropical origin cannot survive extended periods of freezing temperature but must migrate northward each spring if it is to re-infest cropping areas in temperate regions. The northward limit of the winter-breeding region for North America extends to southern regions of Texas and Florida, but infestations are regularly reported as far north as Québec and Ontario provinces in Canada by the end of summer. Recent genetic analyses have characterized migratory pathways from these winter-breeding regions, but knowledge is lacking on the atmosphere's role in influencing the timing, distance, and direction of migratory flights. The Hybrid Single-Particle Lagrangian Integrated Trajectory (HYSPLIT) model was used to simulate migratory flight of fall armyworm moths from distinct winter-breeding source areas. Model simulations identified regions of dominant immigration from the Florida and Texas source areas and overlapping immigrant populations in the Alabama-Georgia and Pennsylvania-Mid-Atlantic regions. This simulated migratory pattern corroborates a previous migratory map based on the distribution of fall armyworm haplotype profiles. We found a significant regression between the simulated first week of moth immigration and first week of moth capture (for locations which captured ≥ 10 moths), which on average indicated that the model simulated first immigration 2 weeks before first captures in pheromone traps. The results contribute to knowledge of fall armyworm population ecology on a continental scale and will aid in the prediction and interpretation of inter-annual variability of insect migration patterns including those in response to climatic change and adoption rates of transgenic cultivars.


Assuntos
Migração Animal , Modelos Teóricos , Spodoptera , Animais , Feminino , Masculino , Estações do Ano , Estados Unidos , Zea mays
4.
J Econ Entomol ; 102(6): 2154-9, 2009 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-20069844

RESUMO

Observations of fall armyworm, Spodoptera frugiperda (J.E. Smith) (Lepidoptera: Noctuidae), larvae infesting plots of Miscanthus x giganteus Greef and Deuter ex Hodkinson and Renvoize prompted laboratory-based tests of survival, development, and feeding preferences on leaf tissue from M. x giganteus and switchgrass, Panicum virgatum L. Survival from hatch to pupation was >70 and 50% for fall armyworms reared on switchgrass and M. x giganteus, respectively, although survival of the S. frugiperda rice strain was significantly greater than the corn strain on both crops. Developmental times from hatch to pupation or adult emergence showed effects of crop and S. frugiperda host strain, but analysis of an interaction revealed developmental times for the rice strain were similar on both crops, whereas corn strain larvae showed delayed development on M. x giganteus relative to switchgrass. Analysis of larval (10 d) and pupal masses showed a similar pattern, with effects of crop and an interaction (at 10 d), but only the mass of corn strain larvae feeding on M. x giganteus was reduced relative to the other crop and strain combinations. In choice tests, neonates of both corn and rice strains showed a strong preference for feeding on young tissues rather than mature leaves of M. x giganteus or switchgrass, but they also clearly favored corn, Zea mays L., leaves over either of the perennial grasses. Results indicate both plants are potential hosts for S. frugiperda, but additional information is needed to understand under which scenarios and to what degree fall armyworms may damage perennial grasses grown for biofuel production.


Assuntos
Preferências Alimentares , Interações Hospedeiro-Parasita , Poaceae/parasitologia , Spodoptera/crescimento & desenvolvimento , Animais , Biocombustíveis
5.
Insect Mol Biol ; 12(5): 453-8, 2003 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-12974950

RESUMO

The fall armyworm, Spodoptera frugiperda, consists of two host strains (rice and corn) that differ in developmental, physiological and behavioural characteristics. However, because the strains are morphologically indistinguishable the investigation of strain-specific behaviour, particularly in the wild, is very difficult. This has spurred the isolation of diagnostic molecular markers. FR sequences are tandem-repeat genetic elements found in large clusters only in the rice strain. To facilitate their use as a strain marker we genetically mapped FR clusters and found they localized to the sex chromosomes. This represents one of the first examples of chromosome mapping in fall armyworm. The FR sequence and a strain-specific mitochondrial marker were then used to examine the distribution of different marker combinations in field specimens. These studies identified significant barriers to interstrain mating in the wild, specifically that corn strain females rarely, if ever, mate with rice strain males. The data also suggest that only a genetically distinct subset of the overwintering rice strain population in Florida annually migrate to Georgia. These studies demonstrate that the availability of genetically characterized molecular markers for strain identity makes possible studies on fall armyworm biology in the wild previously considered unfeasible.


Assuntos
Mapeamento Cromossômico , Variação Genética , Cromossomos Sexuais/genética , Spodoptera/genética , Sequências de Repetição em Tandem/genética , Animais , Cruzamentos Genéticos , Primers do DNA , Eletroforese em Gel de Ágar , Meio Ambiente , Florida , Georgia , Reação em Cadeia da Polimerase , Dinâmica Populacional , Spodoptera/fisiologia
6.
Insect Mol Biol ; 11(3): 241-8, 2002 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-12000643

RESUMO

The Drosophila ovarian tumour gene is required at multiple times in the germline for oogenesis. A second gene, Sex-lethal, controls sex determination in the soma and also has a separate germline function affecting similar oogenic stages as ovarian tumour. We demonstrate that ovarian tumour is not required for early Sex-lethal gene expression in the female germline, as had been previously reported. Instead, we provide evidence that ovarian tumour has a specific role in the developmentally regulated accumulation of SEX-LETHAL protein within the cytoplasm and nucleus. Furthermore, the examination of nurse cell polytene chromosomes produced by certain ovarian tumour mutations showed that SEX-LETHAL protein can associate with discrete chromosomal sites in the germline and that this pattern appears to change as the egg chamber matures. This is the first indication that SEX-LETHAL is capable of direct physical interactions with chromosomes (albeit in a mutant background) and is consistent with the developmentally regulated nuclear localization of SEX-LETHAL being important for oogenesis.


Assuntos
Proteínas de Drosophila , Proteínas de Insetos/metabolismo , Oogênese/fisiologia , Proteínas de Ligação a RNA/metabolismo , Animais , Cromossomos , Drosophila/genética , Drosophila/metabolismo , Feminino , Perfilação da Expressão Gênica , Proteínas de Insetos/genética , Líquido Intracelular , Oócitos , Proteínas de Ligação a RNA/genética
7.
Pediatr Int ; 43(5): 465-8, 2001 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-11737706

RESUMO

BACKGROUND: To evaluate the effects of an increase in glucose infusion rate of 2 mg/kg per min from the basal infusion rate on the prevention of hypoglycemia in very low-birthweight (VLBW) infants, following indomethacin therapy for patent ductus arteriosus (PDA). METHODS: Forty VLBW infants with PDA were given indomethacin 0.2 mg/kg intravenously up to three doses. In 15 of the 40 infants (supplemented group: between April 1995 and March 1996) the glucose infusion rate was increased in 2 mg/kg per min increments from the basal rate just before the initial indomethacin administration, compared with 25 historical control infants who received a fixed glucose infusion rate during the first 12 h after the initial dose. We evaluated the changes in blood glucose levels and glucose infusion rates in both groups. RESULTS: In the control group 11 of 25 (44%) infants had a blood glucose value below 40 mg/dL between 12 and 60 h (mean 32.7 h). In contrast only two out of 15 infants in the supplemented group reached the glucose level below 40 mg/dL between 72 and 96 h but both two were light-for-dates infants (defined as birthweight below the 10th percentile for gestational age on the standard intrauterine growth curve). Blood glucose values in the supplemented group were significantly higher than those in the control group between 12 and 96 h. However, glucose infusion rates were similar before and between 72 and 96 h. CONCLUSIONS: This retrospective study shows that an increase in glucose infusion rate of 2 mg/kg per min, in addition to the pre-existing stable maintenance glucose intake, might prevent against the occurrence of unexpected hypoglycemia in VLBW infants following indomethacin therapy.


Assuntos
Permeabilidade do Canal Arterial/tratamento farmacológico , Glucose/administração & dosagem , Hipoglicemia/prevenção & controle , Indometacina/efeitos adversos , Recém-Nascido de muito Baixo Peso , Glicemia , Feminino , Idade Gestacional , Glucose/uso terapêutico , Humanos , Hipoglicemia/induzido quimicamente , Indometacina/uso terapêutico , Recém-Nascido , Recém-Nascido de muito Baixo Peso/metabolismo , Infusões Intravenosas , Masculino , Gravidez , Estudos Retrospectivos
8.
Pediatr Int ; 43(1): 8-11, 2001 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-11207991

RESUMO

BACKGROUND: The purpose of the present study was to evaluate the effect of intravenous albumin administration on the serum total and unbound bilirubin values in term non-hemolytic hyperbilirubinemic neonates during intensive phototherapy. METHODS: Fifty-eight infants (gestational age 39.4 +/- 1.4 weeks; birth weight 3,245 +/- 435 g) were given phototherapy with similar light energy. Twenty infants (control group) received only phototherapy, while 38 others (albumin-treated group) were also given human albumin at 1 g/kg bodyweight, i.v., during the first 2 h of phototherapy. RESULTS: When comparing changes in total and unbound bilirubin values 0, 2, 6 and 24 h after entering the study between the albumin-treated group and the control group, there was a significant reduction in the serum unbound bilirubin values at the end of albumin treatment and at 6 and 24 h. However, there was no significant reduction in total serum bilirubin values during the study period. In the albumin-treated group, the mean serum unbound bilirubin reduction from the baseline level at the end of albumin treatment and at 6 and 24 h was 0.40 +/- 0.19, 0.41 +/- 0.20 and 0.43 +/- 0.20 microg/dL, respectively. CONCLUSIONS: The results suggest that albumin priming may be effective for an immediate reduction in serum unbound bilirubin values, the fraction that is potentially neurotoxic.


Assuntos
Albuminas/uso terapêutico , Bilirrubina/sangue , Icterícia Neonatal/terapia , Fototerapia , Albuminas/farmacologia , Humanos , Recém-Nascido , Infusões Intravenosas , Icterícia Neonatal/sangue , Fototerapia/métodos , Valores de Referência , Estudos Retrospectivos , Resultado do Tratamento
9.
Biol Neonate ; 78(2): 121-8, 2000.
Artigo em Inglês | MEDLINE | ID: mdl-10971005

RESUMO

We hypothesized that anti-CD18 monoclonal antibody, R15.7, a murine IgG(1) antibody which blocks leukocyte-endothelial cell adherence, might ameliorate the cardiopulmonary manifestations of sepsis secondary to group B streptococci (GBS). Twenty-six anesthetized, mechanically ventilated newborn piglets received a continuous infusion of GBS (7.5 x 10(9) cfu/kg/min) and were randomly assigned to a treatment group receiving R15.7 (1 mg/kg i.v.) 15 min prior to GBS infusion or to a control group. Cardiopulmonary measurements, arterial blood gases and peripheral blood leukocytes were obtained over 120 min of R15.7 infusion. GBS infusion caused significant increases in pulmonary artery and systemic arterial blood (Psa) pressures, pulmonary vascular (PVR) and systemic vascular (SVR) resistances, and PVR/SVR ratio with decreases in cardiac output and stroke volume. R15.7-treated piglets maintained significantly higher Psa (p < 0.003), dynamic lung compliance (p < 0.04), PaO2 and pH (p < 0.05), and lower total lung resistance (p < 0.01) and PaCO2 (p < 0.04). A longer median survival time was observed in the treatment group (p < 0.01). These data suggest that administration of a CD18-blocking agent prolongs survival in a young animal model of GBS sepsis, possibly secondary to improved tissue perfusion, lung mechanics and acid-base status.


Assuntos
Anticorpos Monoclonais/uso terapêutico , Antígenos CD18/imunologia , Sistema Cardiovascular/fisiopatologia , Pulmão/fisiopatologia , Infecções Estreptocócicas/terapia , Streptococcus agalactiae , Animais , Pressão Sanguínea , Débito Cardíaco , Artéria Pulmonar/fisiopatologia , Sepse/microbiologia , Sepse/fisiopatologia , Sepse/terapia , Infecções Estreptocócicas/fisiopatologia , Volume Sistólico , Suínos , Resistência Vascular
11.
Mech Dev ; 88(1): 3-14, 1999 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-10525184

RESUMO

The ovo and ovarian tumor genes are required during early and late stages of Drosophila oogenesis. The ovo product, a zinc-finger transcription factor, can bind to sites and influence the level of expression of the ovarian tumor promoter. Our examination of ovo null mutant organelles demonstrate that it is required for the differentiation of XX germ cells during larval gonial stages, in addition to its known role in maintaining germ cell numbers. In contrast, ovarian tumor is required during pupal and adult stages for the cystocyte divisions that give rise to the egg chamber. Studies on sexually transformed flies indicate that both the ovo and ovarian tumor null mutant phenotypes are distinctive from and more severe than the germline defects produced when male germ cells develop in female soma. This suggests that ovo and ovarian tumor have oogenic functions other than their putative role in germline sex determination. We also demonstrate that the regulation of ovarian tumor by ovo is stage-specific, as ovarian tumor promoter activity does not require ovo during larval stages but becomes ovo-dependent in the adult ovary. This coincides with when the ovarian tumor promoter becomes responsive to sex-specific signals from the soma suggesting a convergence of somatic and germline regulatory pathways on ovarian tumor during oogenesis.


Assuntos
Proteínas de Ligação a DNA/genética , Proteínas de Drosophila , Drosophila/fisiologia , Proteínas de Insetos/genética , Oogênese/genética , Fatores de Transcrição/genética , Animais , Animais Geneticamente Modificados , Diferenciação Celular/genética , Aberrações Cromossômicas , Proteínas de Ligação a DNA/metabolismo , Feminino , Regulação da Expressão Gênica no Desenvolvimento , Proteínas de Insetos/metabolismo , Masculino , Mutação , Oócitos/patologia , Oócitos/fisiologia , Ovário/fisiologia , Regiões Promotoras Genéticas , Fatores de Transcrição/metabolismo
12.
Mech Dev ; 88(2): 159-72, 1999 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-10534615

RESUMO

The reaper and head involution defective genes can induce apoptotic death in several Drosophila cell types, including portions of the embryo and eye. By a combination of FLP recombinase and the yeast Gal4/UAS transcription activation system, we expressed both cell death genes in discrete clones in the adult ovarian follicle cell layer. The expression of either reaper or head involution defective induced follicle cell apoptosis during all oogenic stages. Unexpectedly, the disruption of the follicle layer led to the induced degeneration of the nurse cells in an apoptotic manner, demonstrating a germline-somatic interaction required for germ cell viability. The germline apoptosis initiates at a specific time in oogenesis, coinciding with the beginning of vitellogenesis. This observation is intriguing given previous suggestions of a process to eliminate defective egg chambers at these same oogenic stages. The induce germline degeneration initiates with the transient formation of a network of filamentous actin around the nurse cell nucleus, in close association with a product of the adducin-related hu-li tai shao gene. This was immediately followed by nuclear condensation and DNA fragmentation, both characteristics diagnostic of apoptosis. Occurring concomitantly with the nuclear phenotypes were the disorganization of ring canals, and the degradation of Armadillo protein (a beta-catenin homolog) and filamentous actin. Germ cells degenerating as a normal consequence of oogenesis displayed a similar set of phenotypes, suggesting that a common apoptotic mechanism may underlie these different germline death phenomena.


Assuntos
Apoptose/genética , Proteínas de Drosophila , Drosophila/genética , Óvulo/patologia , Transativadores , Actinas/metabolismo , Animais , Animais Geneticamente Modificados , Proteínas do Domínio Armadillo , Proteínas de Ligação a Calmodulina/genética , Proteínas de Ligação a Calmodulina/metabolismo , Citoplasma/genética , Citoplasma/patologia , Proteínas do Citoesqueleto/genética , Proteínas do Citoesqueleto/metabolismo , Feminino , Regulação da Expressão Gênica no Desenvolvimento , Proteínas Inibidoras de Apoptose , Proteínas de Insetos/genética , Proteínas de Insetos/metabolismo , Neuropeptídeos/genética , Ovário , Óvulo/citologia , Óvulo/fisiologia , Peptídeos/genética , Fatores de Transcrição , Proteínas Virais/genética , Proteínas Virais/metabolismo , beta Catenina , beta-Galactosidase/genética , beta-Galactosidase/metabolismo
13.
Pediatr Int ; 41(5): 525-8, 1999 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-10530066

RESUMO

PURPOSE: To evaluate the effects of indomethacin on blood glucose values in premature infants with patent ductus arteriosus (PDA). METHODS: Twenty-five very low birthweight infants with PDA were given 0.2 mg/kg, i.v., indomethacin for up to three doses. We examined the relationship between blood glucose values and glucose infusion rate before and after indomethacin therapy. RESULTS: There was a significant reduction in blood glucose values between 12 and 96 h following i.v. indomethacin therapy. Eleven of 25 infants (44%) had blood glucose values below 40 mg/dL between 12 and 60 h (mean 32.7 h) after the initial dose. Although the glucose infusion rate during the first 12 h was constant (3.56 +/- 0.98 mg/kg per min), the blood glucose values decreased from 96 +/- 32 mg/dL at the starting point to 75 +/- 29 mg/dL at 12 h (P < 0.05). The maximum blood glucose reduction was 51.6 +/- 34.7 mg/dL and the maximum blood glucose reduction rate was 50.4 +/- 20.2%. CONCLUSIONS: The results suggest that blood glucose values should be measured at least every 6 h for 72 h until they stabilize in order to prevent unexpected hypoglycemia.


Assuntos
Fármacos Cardiovasculares/efeitos adversos , Permeabilidade do Canal Arterial/tratamento farmacológico , Hipoglicemia/induzido quimicamente , Indometacina/efeitos adversos , Recém-Nascido Prematuro , Feminino , Humanos , Recém-Nascido , Recém-Nascido de muito Baixo Peso , Masculino , Estudos Retrospectivos , Estatísticas não Paramétricas
14.
Development ; 126(5): 861-71, 1999 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-9927588

RESUMO

In Drosophila, compatibility between the sexually differentiated state of the soma and the sex chromosome constitution of the germline is required for normal gametogenesis. In this study, we defined important aspects of the soma-germline interactions controlling early oogenesis. In particular, the sex-specific germline activity of the ovarian tumor promoter was found to be dependent upon somatic factors controlled by the somatic sex differentiation gene transformer. This regulation defines whether there is sufficient ovarian tumor expression in adult XX germ cells to support oogenesis. In addition, the ovarian tumor function required for female germline differentiation is dependent on the activity of another germline gene, ovo, whose regulation is transformer-independent. These and other data indicate that ovarian tumor plays a central role in coordinating regulatory inputs from the soma (as regulated by transformer) with those from the germline (involving ovo). We also demonstrate that transformer-dependent interactions influence whether XX germ cells require ovarian tumor or ovo functions to undergo early gametogenic differentiation. These results are incorporated into a model hypothesizing that the functions of ovarian tumor and ovo are dependent on an early sex determination decision in the XX germline that is at least partially controlled by somatic transformer activity.


Assuntos
Proteínas de Ligação a DNA/genética , Proteínas de Drosophila , Drosophila/genética , Regulação da Expressão Gênica no Desenvolvimento , Proteínas de Insetos/genética , Proteínas Nucleares/genética , Fatores de Transcrição/genética , Animais , Proteínas de Ligação a DNA/fisiologia , Feminino , Masculino , Fenótipo , Regiões Promotoras Genéticas , Proteínas de Ligação a RNA/genética , Espermatozoides , Fatores de Transcrição/fisiologia
15.
J Perinat Med ; 27(5): 399-403, 1999.
Artigo em Inglês | MEDLINE | ID: mdl-10642962

RESUMO

We describe the case of a patient with a neonatal giant cutaneous hemangioma with high-output cardiac failure and Kasabach-Merritt syndrome and successfully treated with transcutaneous arterial embolization aimed at controlling severe congestive heart failure and consumption coagulopathy. A patient was admitted to the neonatal care unit on the first day of age because of a large hemangioma on his right lateral chest wall and respiratory distress, associated with cardiac failure resulting from arteriovenous shunting. On the second day of age the platelet count decreased to 5.7 x 10(4)/microliter and fibrinogen level was 85 mg/dl. The values of prothrombin time and activated partial thromboplastin time were prolonged. Intravenous predonisone therapy was started immediately, but bleeding tendency was getting worse and the evidence of congestive heart failure persisted. On the third day the patient then underwent embolization of feeding arteries with microcoils. The cardiac failure and thrombocytopenic coagulopathy had improved significantly without complications. We conclude that transcutaneous arterial embolization is an effective and safe treatment in this neonate and should be considered for the treatment of control high-output cardiac failure and coagulopathy in infants with hemangioma and Kasabach-Merritt syndrome.


Assuntos
Débito Cardíaco Elevado/etiologia , Embolização Terapêutica , Hemangioma/terapia , Neoplasias Torácicas/terapia , Fibrinogênio/metabolismo , Hemangioma/complicações , Humanos , Recém-Nascido , Masculino , Contagem de Plaquetas , Síndrome , Neoplasias Torácicas/complicações , Trombocitopenia/complicações
16.
Dev Biol ; 190(2): 153-64, 1997 Oct 15.
Artigo em Inglês | MEDLINE | ID: mdl-9344535

RESUMO

The ovarian tumor gene is required during both early and late stages of oogenesis. Mutations produce a range of phenotypes, including agametic ovarioles, tumorous egg chambers, and late stage oogenic arrest. We demonstrate that each of these phenotypes is associated with specific aberrations in actin distribution. In the earliest case, ovarian tumor mutations cause actin filaments to accumulate ectopically in the fusome. This correlates with abnormal fusome morphology and arrested germ cell development in the germaria. Similarly, ovarian tumor function is required for the localization of actin that is essential for the maturation of ring canals. This defect gives rise to tumorous egg chambers in which germ cell numbers and morphology are profoundly aberrant. We also confirm that ovarian tumor is required for the formation of the nurse cell cytoplasmic actin array that is essential for the nonspecific transport of cytoplasmic contents to the oocyte during late oogenesis. Our data suggest that at this stage ovarian tumor controls the site where actin filaments initiate. Taken together, these studies suggest that the diverse ovarian tumor mutant phenotypes derive from the mislocalization of actin filaments, indicating a role for this gene in organizing the female germline cytoskeleton, and that the misregulation of actin can have profound effects on germ cell division and differentiation.


Assuntos
Actinas/metabolismo , Proteínas de Drosophila , Drosophila/genética , Proteínas de Insetos/genética , Oncogenes , Oogênese , Alelos , Animais , Diferenciação Celular , Citoesqueleto/metabolismo , Feminino , Modelos Biológicos , Mutação , Neoplasias Ovarianas/etiologia , Neoplasias Ovarianas/genética , Ovário/crescimento & desenvolvimento , Ovário/ultraestrutura , Fenótipo
17.
Genetics ; 141(3): 1061-74, 1995 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-8582613

RESUMO

P elements are widely used as insertional mutagens to tag genes, facilitating molecular cloning and analyses. We modified a P element so that it carried two copies of the suppressor of Hairy-wing [su(Hw)] binding regions isolated from the gypsy transposable element. This transposon was mobilized, and the genetic consequences of its insertion were analyzed. Gene expression can be altered by the su(Hw) protein as a result of blocking the interaction between enhancer/silencer elements and their promoter. These effects can occur over long distances and are general. Therefore, a composite transposon (SUPor-P for suppressor-P element) combines the mutagenic efficacy of the gypsy element with the controllable transposition of P elements. We show that, compared to standard P elements, this composite transposon causes an expanded repertoire of mutations and produces alleles that are suppressed by su(Hw) mutations. The large number of heterochromatic insertions obtained is unusual compared to other insertional mutagenesis procedures, indicating that the SUPor-P transposon may be useful for studying the structural and functional properties of heterochromatin.


Assuntos
Elementos de DNA Transponíveis/genética , Proteínas de Ligação a DNA/genética , Drosophila melanogaster/genética , Genes de Insetos , Genes Supressores , Mutagênese Insercional , Proteínas Nucleares/genética , Animais , Cromossomos/ultraestrutura , DNA Recombinante/genética , Proteínas de Drosophila , Feminino , Regulação da Expressão Gênica , Teste de Complementação Genética , Marcadores Genéticos , Masculino , Proteínas Repressoras , Retroelementos/genética
18.
Genetics ; 141(1): 191-202, 1995 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-8536967

RESUMO

Severe alleles of the ovarian tumor (otu) and ovo genes result in female sterility in Drosophila melanogaster, producing adult ovaries that completely lack egg chambers. We examined the developmental stage in which the agametic phenotype first becomes apparent. Germ cell development in embryos was studied using a strategy that allowed simultaneous labeling of pole cells with the determination of embryonic genotype. We found that ovo- or otu- XX embryonic germ cells were indistinguishable in number and morphology from those present in wild-type siblings. The effects of the mutations were not consistently manifested in the female germline until pupariation, and there was no evidence that either gene was required for germ cell viability at earlier stages of development. The requirement for otu function in the pupal and adult ovary is supported by temperature-shift experiments using a heat-inducible otu gene construct. We demonstrate that otu activity limited to prepupal stages was not sufficient to support oogenesis, while induction during the pupal and adult periods caused suppression of the otu mutant phenotype.


Assuntos
Proteínas de Ligação a DNA/genética , Proteínas de Drosophila , Drosophila melanogaster/genética , Hormônios de Inseto/genética , Oogênese/genética , Fatores de Transcrição/genética , Animais , Diferenciação Celular , Sobrevivência Celular , Drosophila melanogaster/embriologia , Feminino , Genes de Insetos , Células Germinativas , Proteínas de Choque Térmico HSP70/genética , Larva , Mutação , Regiões Promotoras Genéticas , Zigoto
19.
Genetics ; 140(1): 207-17, 1995 May.
Artigo em Inglês | MEDLINE | ID: mdl-7635286

RESUMO

Phenotypic and genetic analyses demonstrate that fs (1) Yb activity is required in the soma for the development of a subset of ovarian follicle cells and to support later stages of egg maturation. Mutations in fs (1) Yb cause a range of ovarian phenotypes, from the improper segregation of egg chambers to abnormal dorsal appendage formation. The mutant phenotypes associated with fs (1) Yb are very similar to the ovarian aberrations produced by temperature-sensitive alleles of Notch and Delta. Possible functional or regulatory interactions between fs (1) Yb and Notch are suggested by genetic studies. A duplication of the Notch locus partially suppresses the female-sterility caused by fs (1) Yb mutations, while reducing Notch dosage makes the fs (1) Yb mutant phenotype more severe. In addition, fs (1) Yb alleles also interact with genes that are known to act with or regulate Notch activity, including Delta, daughterless, and mastermind. However, differences between the mutant ovarian phenotype of fs (1) Yb and that of Notch or Delta indicate that the genes do not have completely overlapping functions in the ovary. We propose that fs (1) Yb acts as an ovary-specific factor that determines follicle cell fate.


Assuntos
Drosophila melanogaster/genética , Hormônios de Inseto/fisiologia , Proteínas de Membrana/genética , Família Multigênica , Alelos , Animais , Proteínas de Drosophila , Drosophila melanogaster/fisiologia , Feminino , Genes de Insetos , Infertilidade Feminina/genética , Hormônios de Inseto/genética , Peptídeos e Proteínas de Sinalização Intracelular , Proteínas de Membrana/fisiologia , Oogênese , Especificidade de Órgãos , Folículo Ovariano , Ovário/crescimento & desenvolvimento , Ovário/ultraestrutura , Receptores Notch
20.
Genetics ; 139(3): 1309-20, 1995 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-7768440

RESUMO

The small ovary gene (sov) is required for the development of the Drosophila ovary. Six EMS-induced recessive alleles have been identified. Hypomorphic alleles are female sterile and have no effect on male fertility, whereas more severe mutations result in lethality. The female-sterile alleles produce a range of mutant phenotypes that affect the differentiation of both somatic and germline tissues. These mutations generally produce small ovaries that contain few egg cysts and disorganized ovarioles, and in the most extreme case no ovarian tissue is present. The mutant egg cysts that develop have aberrant morphology, including abnormal numbers of nurse cells and patches of necrotic cells. We demonstrate that sov gene expression is not required in the germline for the development of functional egg cysts. This indicates that the sov function is somatic dependent. We present evidence using loss-of-function and constitutive forms of the somatic sex regulatory genes that sov activity is essential for the development of the somatic ovary regardless of the chromosomal sex of the fly. In addition, the genetic mapping of the sov locus is presented, including the characterization of two lethal sov alleles and complementation mapping with existing rearrangements.


Assuntos
Drosophila/genética , Genes de Insetos , Alelos , Animais , Mapeamento Cromossômico , Drosophila/crescimento & desenvolvimento , Feminino , Fertilidade/genética , Dosagem de Genes , Genes Letais/genética , Genes Recessivos , Masculino , Mutação , Oócitos/crescimento & desenvolvimento , Ovário/citologia , Ovário/crescimento & desenvolvimento , Fenótipo
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