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1.
Am Nat ; 201(6): 841-850, 2023 06.
Artículo en Inglés | MEDLINE | ID: mdl-37229709

RESUMEN

AbstractOffspring desertion by parents generally occurs at an early stage of parental care, which is thought to minimize the costs of parental care prior to desertion. This study investigated the effects of endocrinological constraints on early total filial cannibalism by male Rhabdoblennius nitidus in the field, a paternal brooding blennid fish with androgen-dependent brood cycling. In brood reduction experiments, cannibal males showed low levels of plasma 11-ketotestosterone (11-KT) relative to noncannibals and also similar levels of 11-KT to males in the parental care phase. Since 11-KT regulates male courtship intensity, males with decreased courtship activity would exhibit total filial cannibalism. However, there is a possibility that a transient increase in 11-KT levels at the early stage of parental care delays total filial cannibalism. In contrast, total filial cannibalism could occur before a decline to the lowest 11-KT levels, at which point males might still be able to exhibit courtships, possibly to reduce the costs of parental care. To understand how much and when caregiving males exhibit mating and parental care behaviors, it is important to consider not only the presence of endocrinological constraints but also its intensity and flexibility.


Asunto(s)
Canibalismo , Perciformes , Animales , Masculino , Peces/fisiología , Reproducción , Cortejo , Conducta Sexual Animal
2.
Viruses ; 14(4)2022 04 15.
Artículo en Inglés | MEDLINE | ID: mdl-35458549

RESUMEN

Lamellarin α 20-sulfate is a cell-impenetrable marine alkaloid that can suppress infection that is mediated by the envelope glycoprotein of human immunodeficiency virus type 1. We explored the antiviral action and mechanisms of this alkaloid against emerging enveloped RNA viruses that use endocytosis for infection. The alkaloid inhibited the infection of retroviral vectors that had been pseudotyped with the envelope glycoprotein of Ebola virus and SARS-CoV-2. The antiviral effects of lamellarin were independent of the retrovirus Gag-Pol proteins. Interestingly, although heparin and dextran sulfate suppressed the cell attachment of vector particles, lamellarin did not. In silico structural analyses of the trimeric glycoprotein of the Ebola virus disclosed that the principal lamellarin-binding site is confined to a previously unappreciated cavity near the NPC1-binding site and fusion loop, whereas those for heparin and dextran sulfate were dispersed across the attachment and fusion subunits of the glycoproteins. Notably, lamellarin binding to this cavity was augmented under conditions where the pH was 5.0. These results suggest that the final action of the alkaloid against Ebola virus is specific to events following endocytosis, possibly during conformational glycoprotein changes in the acidic environment of endosomes. Our findings highlight the unique biological and physicochemical features of lamellarin α 20-sulfate and should lead to the further use of broadly reactive antivirals to explore the structural mechanisms of virus replication.


Asunto(s)
Alcaloides , Tratamiento Farmacológico de COVID-19 , Ebolavirus , Fiebre Hemorrágica Ebola , Alcaloides/farmacología , Antivirales/química , Sulfato de Dextran , Ebolavirus/metabolismo , Glicoproteínas , Fiebre Hemorrágica Ebola/tratamiento farmacológico , Heparina/farmacología , Humanos , SARS-CoV-2 , Internalización del Virus
3.
Mol Immunol ; 140: 240-249, 2021 12.
Artículo en Inglés | MEDLINE | ID: mdl-34773863

RESUMEN

We have previously reported that gamma-interferon inducible lysosomal thiolreductase (GILT) functions as a host defense factor against retroviruses by digesting disulfide bonds on viral envelope proteins. GILT is widely conserved even in plants and fungi as well as animals. The thiolreductase active site of mammalian GILT is composed of a CXXC amino acid motif, whereas the C-terminal cysteine residue is changed to serine in arthropods including shrimps, crabs, and flies. GILT from Penaeus monodon (PmGILT) also has the CXXS motif instead of the CXXC active site. We demonstrate here that a human GILT mutant (GILT C75S) with the CXXS motif and PmGILT significantly inhibit amphotropic murine leukemia virus vector infection in human cells without alterning its expression level and lysosomal localization, showing that the C-terminal cysteine residue of the active site is not required for the antiviral activity. We have reported that human GILT suppresses HIV-1 particle production by digestion of disulfide bonds on CD63. However, GILT C75S mutant and PmGILT did not digest CD63 disulfide bonds, and had no effect on HIV-1 virion production, suggesting that they do not have thiolreductase activity. Taken together, this study found that antiviral activity, but not thiolreductase activity, is conserved in arthropod GILT proteins. This finding provides a new insight that the common function of GILT is antiviral activity in many animals.


Asunto(s)
Antivirales/metabolismo , Artrópodos/enzimología , Artrópodos/virología , Interferón gamma/farmacología , Oxidorreductasas/metabolismo , Secuencias de Aminoácidos , Animales , Baculoviridae/fisiología , Células COS , Chlorocebus aethiops , Secuencia Conservada , Endosomas/metabolismo , VIH-1/fisiología , Células HeLa , Humanos , Interferón gamma/metabolismo , Virus de la Leucemia Murina/fisiología , Lisosomas/metabolismo , Oxidorreductasas/química , Penaeidae/virología , Especificidad por Sustrato , Virión/fisiología
4.
Biosci Biotechnol Biochem ; 85(3): 703-713, 2021 Feb 24.
Artículo en Inglés | MEDLINE | ID: mdl-33624778

RESUMEN

In larviculture facilities, rotifers are generally used as an initial food source, while a proper size of live feeds to connect rotifer and Artemia associated with fish larval growth is needed. The improper management of feed size and density induces mass mortality and abnormal development of fish larvae. To improve the survival and growth of target larvae, this study applied carbon and argon heavy-ion-beam irradiation in mutation breeding to select rotifer mutants with larger lorica sizes. The optimal irradiation conditions of heavy-ion beam were determined with lethality, reproductivity, mutant frequency, and morphometric characteristics. Among 56 large mutants, TYC78, TYC176, and TYA41 also showed active population growth. In conclusion, (1) heavy-ion-beam irradiation was defined as an efficient tool for mutagenesis of rotifers and (2) the aforementioned 3 lines that have larger lorica length and active population growth may be used as a countermeasure of live feed size gap during fish larviculcure.


Asunto(s)
Iones Pesados , Rotíferos/efectos de la radiación , Alimentación Animal , Animales , Acuicultura , Larva/crecimiento & desarrollo , Larva/efectos de la radiación , Mutación , Radiación Ionizante , Rotíferos/genética , Rotíferos/crecimiento & desarrollo , Rotíferos/fisiología
5.
Mar Drugs ; 17(9)2019 Aug 24.
Artículo en Inglés | MEDLINE | ID: mdl-31450557

RESUMEN

In this study, we aimed to find chemicals from lower sea animals with defensive effects against human immunodeficiency virus type 1 (HIV-1). A library of marine natural products consisting of 80 compounds was screened for activity against HIV-1 infection using a luciferase-encoding HIV-1 vector. We identified five compounds that decreased luciferase activity in the vector-inoculated cells. In particular, portimine, isolated from the benthic dinoflagellate Vulcanodinium rugosum, exhibited significant anti-HIV-1 activity. Portimine inhibited viral infection with an 50% inhibitory concentration (IC50) value of 4.1 nM and had no cytotoxic effect on the host cells at concentrations less than 200 nM. Portimine also inhibited vesicular stomatitis virus glycoprotein (VSV-G)-pseudotyped HIV-1 vector infection. This result suggested that portimine mainly targeted HIV-1 Gag or Pol protein. To analyse which replication steps portimine affects, luciferase sequences were amplified by semi-quantitative PCR in total DNA. This analysis revealed that portimine inhibits HIV-1 vector infection before or at the reverse transcription step. Portimine has also been shown to have a direct effect on reverse transcriptase using an in vitro reverse transcriptase assay. Portimine efficiently inhibited HIV-1 replication and is a potent lead compound for developing novel therapeutic drugs against HIV-1-induced diseases.


Asunto(s)
Fármacos Anti-VIH/farmacología , Organismos Acuáticos/química , Dinoflagelados/química , Infecciones por VIH/tratamiento farmacológico , VIH-1/efectos de los fármacos , Iminas/farmacología , Compuestos de Espiro/farmacología , Fármacos Anti-VIH/aislamiento & purificación , Fármacos Anti-VIH/uso terapéutico , Evaluación Preclínica de Medicamentos , Células HEK293 , VIH-1/fisiología , Células HeLa , Humanos , Iminas/aislamiento & purificación , Iminas/uso terapéutico , Concentración 50 Inhibidora , Compuestos de Espiro/aislamiento & purificación , Compuestos de Espiro/uso terapéutico , Replicación Viral/efectos de los fármacos
6.
G3 (Bethesda) ; 6(4): 1095-106, 2016 04 07.
Artículo en Inglés | MEDLINE | ID: mdl-26865699

RESUMEN

The mangrove killifish Kryptolebias marmoratus, and its close relative Kryptolebias hermaphroditus, are the only vertebrate species known to reproduce by self-fertilization due to functional ovotestis development. To improve our understanding of their genomes, we constructed a genetic map. First, a single F1 fish was made by artificial fertilization between K. marmoratus and K. hermaphroditus strains. F2 progeny were then obtained by self-fertilization of the F1 fish. We used RAD-seq to query genomic DNAs from the two parental strains, the F1 individual and 49 F2 progeny. Results identified 9904 polymorphic RAD-tags (DNA markers) that mapped to 24 linkage groups, corresponding to the haploid chromosome number of these species. The total length of the map was 1248 cM, indicating that about one recombination occurred for each of the 24 homologous chromosome pairs in each meiosis. Markers were not evenly distributed along the chromosomes: in all chromosomes, many markers (> 8% of the total markers for each chromosome) mapped to chromosome tips. Centromeres suppress recombination, and this uneven distribution is probably due to the species' acrocentric chromosomes. Mapped marker sequences were compared to genomic sequences of medaka and platyfish, the next most closely related species with sequenced genomes that are anchored to genetic maps. Results showed that each mangrove killifish chromosome corresponds to a single chromosome of both platyfish and medaka, suggesting strong conservation of chromosomes over 100 million years of evolution. Our genetic map provides a framework for the K. marmoratus/K. hermaphroditus genome sequence and an important resource for understanding the biology of hermaphroditism.


Asunto(s)
Mapeo Cromosómico , Estudios de Asociación Genética , Autofecundación/genética , Vertebrados/genética , Animales , Centrómero , Evolución Molecular , Ligamiento Genético , Genoma , Genómica , Filogenia , Recombinación Genética , Sintenía , Vertebrados/clasificación
7.
Mar Genomics ; 20: 25-31, 2015 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-25703093

RESUMEN

Rotifer resting eggs often have to endure harsh environmental conditions during the diapause phase. They are stimulated by light to hatch. In order to study the hatching mechanism, we observed resting eggs and measured their transcriptional expression under different light exposure periods (total darkness, and after 30 min, and 4h light). By using differential-display reverse transcription PCR (DDRT-PCR), we isolated 80 genes that displayed different expression patterns in response to the three light treatments: 20 genes were expressed in total darkness, 40 different genes were differentially expressed under 30 min light, and 20 further genes were expressed after 4h of light. The resting eggs showed no phenotypic differences in embryonic development during the 4h illumination period. In general, the expression patterns of the analyzed genes in resting eggs were differentially modulated by light exposure time. In total darkness, resting eggs mainly expressed genes encoding cell defense and homeostasis functions. In the 30 min illumination group, we found enriched expression of genes encoding fatty acid metabolism-related components, including Acyl-CoA dehydrogenase (ACAD). Genes encoding cellular and embryonic developmental functions were highly observed in the 30 min-illuminated group but were not observed in the 4h-illuminated group. Real-time RT-PCR revealed that several transcripts such as encoding V-type H(+)-translocating pyrophosphatase (V-PPase) and Meckelin had prolonged expression levels when exposed to light for 4h. In the 4h illuminated group, the RecQ protein-like 5 (RECQL5) gene was enriched. This RECQL5 gene may be expressed to protect the developing embryo from continuous light exposure. The data presented in this study indicate that DDRT-PCR-aided gene screening can be helpful to isolate candidate genes involved in the hatching process.


Asunto(s)
Regulación de la Expresión Génica/fisiología , Luz , Óvulo/fisiología , Rotíferos/fisiología , Animales , Reacción en Cadena de la Polimerasa/métodos
8.
Mitochondrial DNA ; 25(1): 29-30, 2014 Feb.
Artículo en Inglés | MEDLINE | ID: mdl-23488916

RESUMEN

The complete mitochondrial genome was obtained from the assembled genome data sequenced by next generation sequencing (NGS) technology from the monogonont rotifer Brachionus koreanus. The mitochondrial genome of B. koreanus was composed of two circular chromosomes designated as mtDNA-I (10,421 bp) and mtDNA-II (11,923 bp). The gene contents of B. koreanus were identical with previously reported B. plicatilis mitochondrial genomes. However, gene orders of B. koreanus showed one rearrangement between the two species. Of 12 protein-coding genes (PCGs), 3 genes (ATP6, ND1, and ND3) had an incomplete stop codon. The A + T base composition of B. koreanus mitochondrial genome was high (68.81%). They also showed anti-G bias (12.03% and 10.97%) on the second and third position of PCGs as well as slight anti-C bias (15.96% and 14.31%) on the first and third position of PCGs.


Asunto(s)
Genoma Mitocondrial/genética , Rotíferos/genética , Animales , Composición de Base/genética , Secuencia de Bases , Codón/genética , Orden Génico/genética , Secuenciación de Nucleótidos de Alto Rendimiento , Datos de Secuencia Molecular , República de Corea , Especificidad de la Especie
9.
Comp Biochem Physiol B Biochem Mol Biol ; 164(4): 229-35, 2013 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-23313744

RESUMEN

The hermaphroditic fish, Kryptolebias marmoratus is known as a unique vertebrate that reproduces by internal self-fertilization, resulting in genetic homogeneity. In this study, we characterized two strains, PAN-RS (13 and 20 days after hatching, dah) and DAN (20 dah), that show different growth rates and morphometric parameters. In the same period (20 dah), the PAN-RS strain showed significantly faster growth rate than the DAN strain in all the parameters measured in this study. In the case of the 13 dah of PAN-RS strain, they showed similar morphometries and growth rate with the DAN strain (20 dah). To investigate why they showed different growth rates in both strains, we analyzed the transcript profile of several genes, such as growth-, hypothalamic-pituitary-gonadal axis-, vitellogenesis-, steroidogenesis-, and sex-related gene for both strains. Based on our results, the different growth rates with several reproduction parameters would be associated with transcript profiles of some gene batteries as the first trigger for the related protein expression in both strains. In addition, this study would provide a better understanding of the physiology and endocrinology in K. marmoratus, particularly, of the transcriptional regulation of growth- and reproduction-related genes with clonal difference.


Asunto(s)
Ciprinodontiformes/metabolismo , Familia de Multigenes , ARN Mensajero/metabolismo , Animales , Ciprinodontiformes/genética , Ciprinodontiformes/crecimiento & desarrollo , Autofecundación , Vitelogénesis/genética
10.
Mol Biol Evol ; 25(6): 1129-37, 2008 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-18326862

RESUMEN

The monogonont rotifer Brachionus plicatilis is an emerging model system for a diverse array of questions in limnological ecosystem dynamics, the evolution of sexual recombination, cryptic speciation, and the phylogeny of basal metazoans. We sequenced the complete mitochondrial genome of B. plicatilis sensu strictu NH1L and found that it is composed of 2 circular chromosomes, designated mtDNA-I (11,153 bp) and mtDNA-II (12,672 bp). Hybridization to DNA isolated from mitochondria demonstrated that mtDNA-I is present at 4 times the copy number of mtDNA-II. The only nucleotide similarity between the 2 chromosomes is a 4.9-kbp region of 99.5% identity including a transfer RNA (tRNA) gene and an extensive noncoding region that contains putative D-loop and control sequence. The mtDNA-I chromosome encodes 4 proteins (ATP6, COB, NAD1, and NAD2), 13 tRNAs, and the large and small subunit ribosomal RNAs; mtDNA-II encodes 8 proteins (COX1-3, NAD3-6, and NAD4L) and 9 tRNAs. Gene order is not conserved between B. plicatilis and its closest relative with a sequenced mitochondrial genome, the acanthocephalan Leptorhynchoides thecatus, or other sequenced mitochondrial genomes. Polymerase chain reaction assays and Southern hybridization to DNA from 18 strains of Brachionus suggest that the 2-chromosome structure has been stable for millions of years. The novel organization of the B. plicatilis mitochondrial genome into 2 nearly equal chromosomes of 4-fold different copy number may provide insight into the evolution of metazoan mitochondria and the phylogenetics of rotifers and other basal animal phyla.


Asunto(s)
Evolución Molecular , Genoma de los Helmintos , Genoma Mitocondrial , Cromosomas en Anillo , Rotíferos/genética , Animales , Secuencia de Bases , Mapeo Cromosómico , Codón/genética , Secuencia Conservada , Orden Génico , Genes de ARNr , Filogenia , ARN de Transferencia/genética , Rotíferos/clasificación , Análisis de Secuencia de ADN , Regiones no Traducidas/genética
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