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1.
PeerJ ; 12: e16925, 2024.
Artigo em Inglês | MEDLINE | ID: mdl-38371375

RESUMO

Pollution and its effects have been of major concern in recent decades. Many strategies and markers have been developed to assess their effects on biota. Cytochrome P450 (CYP) genes have received significant attention in this context because of their relationship with detoxification and activation of exogenous compounds. While their expression has been identified as a pollution exposure biomarker, in most cases, it has been tested only after acute exposures and for CYP genes associated with exogenous compounds. To elucidate CYP gene expression patterns under chronic pollution exposure, we have used the silverside Basilichthys microlepidotus as a model, which inhabits the Maipo River Basin, a freshwater system with different pollution levels. We performed next-generation RNA sequencing of liver and gill tissues from polluted and non-polluted populations. We found most CYP genes were not dysregulated by pollution, and the seven genes that were present and differentially expressed in liver and gill were mainly downregulated. Three CYP genes associated with exogenous compounds showed differential expression in the gill, while four CYP genes associated with endogenous compounds showed differential expression in the liver. The findings presented here highlight the importance of CYP genes, his family, tissues and his interaction in the context of pollution biomarkers use.


Assuntos
Sistema Enzimático do Citocromo P-450 , Peixes , Animais , Peixes/genética , Sistema Enzimático do Citocromo P-450/genética , Poluição Ambiental , Biomarcadores , Água Doce
2.
Mar Environ Res ; 193: 106253, 2024 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-37979403

RESUMO

Knowledge about connectivity between populations is essential for the fisheries management of commercial species. The lobster Jasus frontalis inhabits two oceanic island groups, the Juan Fernández Archipelago and the Desventuradas Islands, separated by 800 km. Since this species is primarily exploited in the Juan Fernández Archipelago, knowledge of the connectivity patterns among islands is foundational for species management. Here, we used variability at single-nucleotide polymorphisms (SNPs) and individual-based modeling (IBM) to estimate the genetic structure and connectivity between J. frontalis populations in these island groups. The variability at 9090 SNPs suggests two genetic populations, one in the Juan Fernández Archipelago and one in the Desventuradas Islands. Furthermore, IBM suggests an asymmetric connectivity pattern, with particles moving from the Juan Fernández Archipelago to the Desventuradas Islands but not vice versa. Since the IBM analysis suggests asymmetric larval movement between the islands, and the genetic analysis indicates isolation between the Juan Fernández Archipelago and the Desventuradas Islands, larval retention mechanisms such as small-scale oceanographic processes or behavior could hinder larval movement between islands. This study highlights the importance of using more than one methodology to estimate population connectivity.


Assuntos
Palinuridae , Animais , Palinuridae/genética , Ilhas , Metagenômica , Genética Populacional , Oceanos e Mares
3.
J Allergy Clin Immunol Pract ; 11(4): 1261-1280.e8, 2023 04.
Artigo em Inglês | MEDLINE | ID: mdl-36708766

RESUMO

BACKGROUND: Hereditary actin-related protein 2/3 complex subunit 1B deficiency is characterized clinically by ear, skin, and lung infections, bleeding, eczema, food allergy, asthma, skin vasculitis, colitis, arthritis, short stature, and lymphadenopathy. OBJECTIVE: We aimed to describe the clinical, laboratory, and genetic features of six patients from four Mexican families. METHODS: We performed exome sequencing in patients of four families with suspected actinopathy, collected their data from medical records, and reviewed the literature for reports of other patients with actin-related protein 2/3 complex subunit 1B deficiency. RESULTS: Six patients from four families were included. All had recurrent infections, mainly bacterial pneumonia, and cellulitis. A total of 67% had eczema whereas 50% had food allergies, failure to thrive, hepatomegaly, and bleeding. Eosinophilia was found in all; 84% had thrombocytopenia, 67% had abnormal-size platelets and anemia. Serum levels of IgG, IgA, and IgE were highly increased in most; IgM was normal or low. T cells were decreased in 67% of patients, whereas B and NK cells were increased in half of patients. Two of the four probands had compound heterozygous variants. One patient was successfully transplanted. We identified 28 other patients whose most prevalent features were eczema, recurrent infections, failure to thrive, bleeding, diarrhea, allergies, vasculitis, eosinophilia, platelet abnormalities, high IgE/IgA, low T cells, and high B cells. CONCLUSION: Actin-related protein 2/3 complex subunit 1B deficiency has a variable and heterogeneous clinical spectrum, expanded by these cases to include keloid scars and Epstein-Barr virus chronic hepatitis. A novel deletion in exon 8 was shared by three unrelated families and might be the result of a founder effect.


Assuntos
Eczema , Eosinofilia , Infecções por Vírus Epstein-Barr , Vasculite , Humanos , Proteína 2 Relacionada a Actina , Actinas , Insuficiência de Crescimento , Herpesvirus Humano 4 , Imunoglobulina A , Imunoglobulina E , Reinfecção , Proteína 3 Relacionada a Actina/metabolismo
4.
Sci Rep ; 12(1): 14192, 2022 08 20.
Artigo em Inglês | MEDLINE | ID: mdl-35987816

RESUMO

Elucidating the processes responsible for maintaining the population connectivity of marine benthic species mediated by larval dispersal remains a fundamental question in marine ecology and fishery management. Understanding these processes becomes particularly important in areas with a biogeographic break and unidirectional water movement along the sides of the break. Based on variability at 4209 single-nucleotide polymorphisms in 234 individuals, we determine the genetic structure, temporal genetic stability, and gene flow among populations of the commercially important mola rock crab Metacarcinus edwardsii in a system in southern Chile with a biogeographic break at latitude 42°S. Specimens were collected at eight sites within its geographic distribution, with collection at four of these sites was performed twice. Using population genetic approaches, we found no evidence of geographic or temporal population differentiation. Similarly, we found no evidence of an effect on gene flow of the biogeographic break caused by the the West Wind Drift Current. Moreover, migration analyses supported gene flow among all sites but at different rates for different pairs of sites. Overall, our findings indicate that M. edwardsii comprises a single large population with high levels of gene flow among sites separated by over 1700 km and demonstrate temporal stability in its genetic structure.


Assuntos
Braquiúros , Genoma , Animais , Braquiúros/genética , Fluxo Gênico , Variação Genética , Genética Populacional , Filogeografia
5.
Rev Alerg Mex ; 69 Suppl 1: s81-s93, 2022.
Artigo em Espanhol | MEDLINE | ID: mdl-34998313

RESUMO

Betalactams are the most widely used antimicrobials for their safety and efficacy. These include the penicillins, cephalosporins, carbapenems, and monobactams. Penicillin allergy ranks first in relation to drug allergy. 10 to 20 % of the population is labeled as allergic to it, often wrongly. Cross reaction is reported in 2 to 5 % between penicillins and cephalosporin. There is no cross reaction between penicillins and aztreonam, but there is with ceftazidime. All the mechanisms of the Gell and Coombs classification are included in the pathophysiology of hypersensitivity reactions to penicillin. Stratification according to risk allows us to take the most objective behavior to label the patient as allergic to. In the natural history of penicillin allergy, 80-90 % of patients lose this sensitivity by 10 years. If necessary, the patient can undergo a desensitization protocol. The immuno-allergist is a key piece in the selection of the patient, the elaboration of the challenge and desensitization protocols, in a controlled environment.


Los betalactámicos son los antimicrobianos más utilizados por su seguridad y eficacia. En este grupo se incluyen las penicilinas, las cefalosporinas, los carbapenémicos y los monobactámicos. La penicilina constituye la primera causa de alergia a medicamentos: 10 a 20 % de la población se etiqueta como alérgica a la misma, en muchas ocasiones erróneamente. Se ha reportado reacción cruzada entre penicilinas y cefalosporina en 2 a 5 %. No hay reacción cruzada entre penicilinas y aztreonam, pero sí con ceftazidima. En la fisiopatología de las reacciones de hipersensibilidad a penicilina se incluyen todos los mecanismos de la clasificación de Gell y Coombs. La estratificación de acuerdo con el riesgo permite tomar la decisión más objetiva para etiquetar al paciente como alérgico. En la evolución natural de la alergia a la penicilina, 80 a 90 % de los pacientes pierde dicha sensibilidad a los 10 años. De ser indispensable, el paciente puede ser sometido a un protocolo de desensibilización. El médico inmunoalergologo es una pieza clave en la selección del paciente, la elaboración de los protocolos de reto y la desensibilización en un ambiente controlado.


Assuntos
Hipersensibilidade a Drogas , Penicilinas , Antibacterianos/efeitos adversos , Carbapenêmicos , Cefalosporinas/efeitos adversos , Reações Cruzadas , Hipersensibilidade a Drogas/diagnóstico , Hipersensibilidade a Drogas/epidemiologia , Hipersensibilidade a Drogas/etiologia , Humanos , Penicilinas/efeitos adversos , Testes Cutâneos
6.
Mol Ecol ; 31(5): 1389-1402, 2022 03.
Artigo em Inglês | MEDLINE | ID: mdl-34995392

RESUMO

Genetic differentiation depends on ecological and evolutionary processes that operate at different spatial and temporal scales. While the geographical context is likely to determine large-scale genetic variation patterns, habitat disturbance events will probably influence small-scale genetic diversity and gene flow patterns. Therefore, the genetic diversity patterns that we observe today result from the combination of both processes, but they are rarely assessed simultaneously. We determined the population structure and genetic diversity of a hemiparasitic mistletoe (Tristerix corymbosus) from the temperate rainforests of southern Chile to determine the effects of geographical context and habitat disturbance at a regional scale and if it is affected by the abundance and occurrence of its seed disperser mutualist (the arboreal marsupial Dromiciops gliroides). We genotyped 359 individuals from 12 populations using single nucleotide polymorphisms, across three different geographical contexts and four disturbance conditions. We also used camera traps to estimate the abundance and occurrence of the seed disperser. Our results suggest that genetic differences among populations are related more to geographical context than to habitat disturbance. However, as disturbance increased, D. gliroides abundance and occurrence decreased, and mistletoe inbreeding index (FIS ) increased. We also found highly uneven gene flow among study sites. Despite the high levels of disturbance that these temperate rainforests are facing, our results suggest that mistletoe genetic differentiation at a regional scale was more influenced by historical events. However, habitat disturbance can indirectly affect mistletoe population genetic differentiation via the seed dispersal process, which may increase levels of inbreeding.


Assuntos
Erva-de-Passarinho , Dispersão de Sementes , Ecossistema , Fluxo Gênico , Variação Genética/genética , Genética Populacional , Erva-de-Passarinho/genética , Árvores
7.
PLoS One ; 16(11): e0259595, 2021.
Artigo em Inglês | MEDLINE | ID: mdl-34735545

RESUMO

Most benthic marine invertebrates with sedentary benthic adult phases have planktonic larvae that permit connectivity between geographically isolated populations. Planktonic larval duration and oceanographic processes are vital to connecting populations of species inhabiting remote and distant islands. In the present study, we analyzed the population genetic structure of the sea urchin Centrostephanus sylviae, which inhabits only the Juan Fernández Archipelago and the Desventuradas islands, separated by more than 800 km. For 92 individuals collected from Robinson Crusoe and Selkirk Islands (Juan Fernández Archipelago) and San Ambrosio Island (Desventuradas Islands), 7,067 single nucleotide polymorphisms (SNPs) were obtained. The results did not show a spatial genetic structure for C. sylviae; relative high migration rates were revealed between the islands. An analysis of the water circulation pattern in the area described a predominant northward water flow with periods of inverted flow, suggesting that larvae could move in both directions. Overall, this evidence suggests that C. sylviae comprises a single large population composed of individuals separated by more than 800 km.


Assuntos
Ouriços-do-Mar/genética , Animais , Oceanografia , Polimorfismo de Nucleotídeo Único/genética
8.
Proc Biol Sci ; 288(1954): 20210754, 2021 07 14.
Artigo em Inglês | MEDLINE | ID: mdl-34229490

RESUMO

Marine species may exhibit genetic structure accompanied by phenotypic differentiation related to adaptation despite their high mobility. Two shape-based morphotypes have been identified for the green turtle (Chelonia mydas) in the Pacific Ocean: the south-central/western or yellow turtle and north-central/eastern or black turtle. The genetic differentiation between these morphotypes and the adaptation of the black turtle to environmentally contrasting conditions of the eastern Pacific region has remained a mystery for decades. Here we addressed both questions using a reduced-representation genome approach (Dartseq; 9473 neutral SNPs) and identifying candidate outlier loci (67 outlier SNPs) of biological relevance between shape-based morphotypes from eight Pacific foraging grounds (n = 158). Our results support genetic divergence between morphotypes, probably arising from strong natal homing behaviour. Genes and enriched biological functions linked to thermoregulation, hypoxia, melanism, morphogenesis, osmoregulation, diet and reproduction were found to be outliers for differentiation, providing evidence for adaptation of C. mydas to the eastern Pacific region and suggesting independent evolutionary trajectories of the shape-based morphotypes. Our findings support the evolutionary distinctness of the enigmatic black turtle and contribute to the adaptive research and conservation genomics of a long-lived and highly mobile vertebrate.


Assuntos
Tartarugas , Adaptação Fisiológica/genética , Animais , Deriva Genética , Oceano Pacífico , Tartarugas/genética
9.
Evol Appl ; 13(6): 1183-1194, 2020 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-32684954

RESUMO

Human activity has caused a deterioration in the health and population size of riverine species; thus, public policies have been implemented to mitigate the anthropogenic impacts of water use, watercourse transformation, and pollution. We studied the Maipo River Basin, one of the most polluted with untreated wastewater in Chile, for a period of 12 years (2007-2019). Since the implementation of new public policies, including the operation of a wastewater collector (2012), the Maipo River Basin is currently much less polluted by untreated water than before. To analyze the impact of wastewater reduction in this river basin, we studied the native silverside (Basilichthys microlepidotus), which inhabits both polluted and unpolluted areas of the river basin. Previous studies reported the overexpression of the ornithine decarboxylase (odc) gene, heterozygote deficit, and high frequency of a homozygote odc genotype in silverside populations that inhabit wastewater-polluted sites, suggesting a phenotypic change and genotypic selection in response to pollution. Here, a population affected and another population unaffected by wastewater were studied before and after implementing the wastewater collector. The physicochemical data of water samples, changes in odc expression and microsatellite variability, and odc genotype frequencies were analyzed. The results showed physicochemical changes in the affected site before and after the operation of the wastewater collector. The microsatellite loci showed no changes in either population. The odc expression in the affected site was higher before the operation of the wastewater collector. Significant changes in the genotype frequencies of the odc gene before and after the wastewater collector operation were detected only at the affected site, wherein the homozygous dominant genotype decreased from >59% to <25%. Our results suggest that public policies aimed at mitigating aquatic pollution can indirectly affect both gene expression and genotype frequencies of important functional genes.

10.
J Cell Sci ; 132(22)2019 11 14.
Artigo em Inglês | MEDLINE | ID: mdl-31636114

RESUMO

Cajal bodies are nuclear organelles involved in the nuclear phase of small nuclear ribonucleoprotein (snRNP) biogenesis. In this study, we identified the splicing factor TCERG1 as a coilin-associated factor that is essential for Cajal body integrity. Knockdown of TCERG1 disrupts the localization of the components of Cajal bodies, including coilin and NOLC1, with coilin being dispersed in the nucleoplasm into numerous small foci, without affecting speckles, gems or the histone locus body. Furthermore, the depletion of TCERG1 affects the recruitment of Sm proteins to uridine-rich small nuclear RNAs (snRNAs) to form the mature core snRNP. Taken together, the results of this study suggest that TCERG1 plays an important role in Cajal body formation and snRNP biogenesis.


Assuntos
Corpos Enovelados/fisiologia , Fatores de Processamento de RNA/genética , Ribonucleoproteínas Nucleares Pequenas/metabolismo , Fatores de Elongação da Transcrição/genética , Humanos , Splicing de RNA , Ribonucleoproteínas Nucleares Pequenas/genética , Fatores de Elongação da Transcrição/metabolismo
11.
Sci Rep ; 9(1): 3459, 2019 03 05.
Artigo em Inglês | MEDLINE | ID: mdl-30837616

RESUMO

To understand the role of gene expression in adaptive variation, it is necessary to examine expression variation in an ecological context. Quantitative real-time PCR (qPCR) is considered the most accurate and reliable technique to measure gene expression and to validate the data obtained by RNA-seq; however, accurate normalization is crucial. In Chile, the freshwater silverside fish Basilichthys microlepidotus inhabits both polluted and nonpolluted areas, showing differential gene expression related to pollution. In this study, we infer the stability of six potential reference genes (tubulin alpha, hypoxanthine-guanine phosphoribosyltransferase, glyceraldehyde-3-phosphate dehydrogenase, beta-actin, 60S ribosomal protein L13, and 60S ribosomal protein L8) in the gills and liver of silverside individuals inhabiting polluted and nonpolluted areas. To validate the reference genes selected, the most and least stable reference genes were used to normalize two target transcripts, one for each organ. The RefFinder tool was used to analyze and identify the most stably expressed genes. The 60S ribosomal protein L8 gene was ranked as the most stable gene for both organs. Our results show that reference gene selection influences the detection of differences in the expression levels of target genes in different organs and, also highlighting candidate reference genes that could be used in field studies.


Assuntos
Peixes/genética , Perfilação da Expressão Gênica , Regulação da Expressão Gênica , Brânquias/metabolismo , Fígado/metabolismo , Transcriptoma , Poluição da Água , Animais , Regulação da Expressão Gênica/efeitos dos fármacos , Especificidade de Órgãos , Estabilidade de RNA , Poluição Química da Água
12.
Int J Mol Sci ; 20(5)2019 Feb 26.
Artigo em Inglês | MEDLINE | ID: mdl-30813527

RESUMO

Integrins are transmembrane cell receptors involved in two crucial mechanisms for successful fertilization, namely, mammalian intracellular signaling and cell adhesion. Integrins α6ß4, α3ß1 and α6ß1 are three major laminin receptors expressed on the surface of mammalian cells including gametes, and the presence of individual integrin subunits α3, α6, ß1 and ß4 has been previously detected in mammalian sperm. However, to date, proof of the existence of individual heterodimer pairs in sperm and their detailed localization is missing. The major conclusion of this study is evidence that the ß4 integrin subunit is expressed in mouse sperm and that it pairs with subunit α6; additionally, there is a detailed identification of integrin heterodimer pairs across individual membranes in an intact mouse sperm head. We also demonstrate the existence of ß4 integrin mRNAs in round spermatids and spermatogonia by q-RT-PCR, which was further supported by sequencing the PCR products. Using super-resolution microscopy accompanied by colocalization analysis, we located integrin subunits as follows: α6/ß4-inner apical acrosomal membrane and equatorial segment; α3, α6/ß1, ß4-plasma membrane overlaying the apical acrosome; and α3/ß1-outer acrosomal membrane. The existence of α6ß4, α3ß1 and α6ß1 heterodimers was further confirmed by proximity ligation assay (PLA). In conclusion, we delivered detailed characterization of α3, α6, ß1 and ß4 integrin subunits, showing their presence in distinct compartments of the intact mouse sperm head. Moreover, we identified sperm-specific localization for heterodimers α6ß4, α3ß1 and α6ß1, and their membrane compartmentalization and the presented data show a complexity of membranes overlaying specialized microdomain structures in the sperm head. Their different protein compositions of these individual membrane rafts may play a specialized role, based on their involvement in sperm-epithelium and sperm-egg interaction.


Assuntos
Compartimento Celular , Integrinas/metabolismo , Multimerização Proteica , Espermatozoides/metabolismo , Animais , Integrinas/química , Masculino , Camundongos Endogâmicos C57BL , Modelos Biológicos , Domínios Proteicos , Subunidades Proteicas/metabolismo
14.
Int J Biochem Cell Biol ; 91(Pt B): 194-202, 2017 10.
Artigo em Inglês | MEDLINE | ID: mdl-28600144

RESUMO

Studies of the spatial organization of the highly compartmentalized eukaryotic nucleus and dynamics of transcription and RNA processing within it are fundamental for fully understanding how gene expression is regulated in the cell. Although some progress has been made in deciphering the functional consequences of this complex network of interacting molecules in the context of nuclear organization, how proteins and RNA move in the nucleus and how the transcription and RNA processing machineries find their targets are important questions that remain largely unexplored. Here, we review major hallmarks and novel insights regarding the movement of RNA and proteins in the context of nuclear organization as well as the mechanisms by which the proteins involved in RNA processing localize to specific nuclear compartments.


Assuntos
Núcleo Celular/metabolismo , Proteínas/metabolismo , Processamento Pós-Transcricional do RNA , RNA/genética , RNA/metabolismo , Transcrição Gênica , Animais , Sequência de Bases , Humanos
15.
Mol Neurobiol ; 54(10): 7808-7823, 2017 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-27844289

RESUMO

TCERG1 is a highly conserved human protein implicated in interactions with the transcriptional and splicing machinery that is associated with neurodegenerative disorders. Biochemical, neuropathological, and genetic evidence suggests an important role for TCERG1 in Huntington's disease (HD) pathogenesis. At present, the molecular mechanism underlying TCERG1-mediated neuronal effects is unknown. Here, we show that TCERG1 depletion led to widespread alterations in mRNA processing that affected different types of alternative transcriptional or splicing events, indicating that TCERG1 plays a broad role in the regulation of alternative splicing. We observed considerable changes in the transcription and alternative splicing patterns of genes involved in cytoskeleton dynamics and neurite outgrowth. Accordingly, TCERG1 depletion in the neuroblastoma SH-SY5Y cell line and primary mouse neurons affected morphogenesis and resulted in reduced dendritic outgrowth, with a major effect on dendrite ramification and branching complexity. These defects could be rescued by ectopic expression of TCERG1. Our results indicate that TCERG1 affects expression of multiple mRNAs involved in neuron projection development, whose misregulation may be involved in TCERG1-linked neurological disorders.


Assuntos
Citoesqueleto/metabolismo , Neuroblastoma/metabolismo , Crescimento Neuronal/fisiologia , Neurônios/metabolismo , Fatores de Elongação da Transcrição/biossíntese , Processamento Alternativo/fisiologia , Animais , Linhagem Celular Tumoral , Células Cultivadas , Citoesqueleto/genética , Citoesqueleto/patologia , Feminino , Células HEK293 , Humanos , Masculino , Camundongos , Neuroblastoma/genética , Neuroblastoma/patologia , Neurônios/patologia , RNA Mensageiro/biossíntese , RNA Mensageiro/genética , Fatores de Elongação da Transcrição/deficiência , Fatores de Elongação da Transcrição/genética
16.
PLoS One ; 11(11): e0166029, 2016.
Artigo em Inglês | MEDLINE | ID: mdl-27814382

RESUMO

For marine invertebrates with a benthic adult form and a planktonic larva phase, the connectivity among populations is mainly based on larval dispersal. While an extended larval phase will promote gene flow, other factors such as an intensive fishery and geographical barriers could lead to changes in genetic variability. In this study, the population genetic structure of the commercial crab Metacarcinus edwardsii was analyzed along 700 km of the Chilean coast. The analysis, based on eight microsatellite loci genotyped from megalopae and adult crabs, considered temporal and spatial patterns of genetic variation. The results showed no evidence of spatial patterns in genetic structure, suggesting high connectivity among the sampling sites. The temporal analysis showed no evidence of changes in allele frequencies and no evidence of a recent bottleneck. The lack of spatial structure and allele variation over time could be explained by the interaction of factors such as i) low reproductive variance due to the capability of females to store sperm in the seminal receptacle, which can be used for successive broods, ii) high larval dispersal and iii) high individual reproductive output. Using our data as priors, a genetic modelling approach coincided, predicting this temporal and spatial stability. The same analysis showed that a reduction in population size leads to the loss of genetic variability in populations, as well as of the genetic cohesiveness between populations, pointing out the importance management for species under exploitation, such as M. edwardsii.


Assuntos
Braquiúros/genética , Frequência do Gene/genética , Variação Genética/genética , Animais , Feminino , Pesqueiros , Fluxo Gênico/genética , Genética Populacional/métodos , Genótipo , Geografia , Larva/genética , Masculino , Repetições de Microssatélites/genética , Oceano Pacífico , Densidade Demográfica , Dinâmica Populacional
17.
Drug Saf Case Rep ; 3(1): 9, 2016 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-27747689

RESUMO

An 81-year-old male and a 47-year-old female experienced recurrent severe bullous dermatosis secondary to an intake of drugs and alternative medicines indicated for arthralgias. The first patient had previously presented with Stevens-Johnson/toxic epidermal necrolysis (TEN) overlap syndrome in 2007 secondary to ingestion of trimethoprim/sulfamethoxazole indicated for a urinary tract infection; 6 years later, he presented with the same syndrome 2 days after ingestion of oral naproxen tablets 250 mg twice daily. The second patient had presented 5 years previously with TEN after receiving trimethoprim/sulfamethoxazole. In 2014, she presented with arthralgias and received a xenobiotic oral called 'miracle pills' (dosage is unknown); 3 weeks later, she again experienced TEN. Both patients were treated with intravenous immunoglobulin 400 mg/kg/day; duration of treatment was 5 days for the first patient and 3 days for the second. However, the male patient died from severe sepsis; the female patient experienced a favorable outcome. There are many risk factors for the development of cutaneous adverse drug reactions; a history of allergic reactions is one important risk factor, and both patients had it. This article reviews the scientific literature on this topic and analyzes the possible causes, including infectious processes, immunological defects, and immunogenetic factors.

18.
Edumecentro ; 8(2): 134-148, abr.-jun. 2016. ilus
Artigo em Espanhol | LILACS | ID: lil-778872

RESUMO

Fundamento: algunos textos de José Martí constituyen fuentes del conocimiento histórico que deben ser consultados y aprovechados por los educadores, en el proceso enseñanza aprendizaje de la Historia de Cuba. Objetivo: elaborar tareas docentes para la enseñanza de Historia de Cuba I integrando en ellas fragmentos de la obra martiana, en correspondencia con el contenido que se trate. Métodos: se realizó una investigación cualitativa en la Filial de Ciencias Médicas "Lidia Doce Sánchez" en el curso 2014-2015. Se emplearon métodos teóricos: análisis-síntesis, inducción-deducción e histórico-lógico, y empíricos: análisis documental, encuesta en forma de cuestionario a estudiantes de segundo año de la carrera y de entrevista a profesores de Historia de Cuba. Los resultados fueron triangulados metodológicamente. Resultados: en los programas se constató la necesidad de utilizar las obras martianas para un aprendizaje desarrollador, y el reforzamiento de valores humanos y revolucionarios; los alumnos coinciden en que no se ofrece un adecuado tratamiento a la obra martiana en los diferentes temas de Historia de Cuba I, y los profesores reconocen la importancia de incluir su análisis en las distintas formas organizativas de la enseñanza, y el estudio de su amplia bibliografía para valorar sus aportes sobre el pensamiento revolucionario cubano, por lo que se propusieron tareas docentes, las cuales fueron valoradas por criterio de especialistas. Conclusiones: las tareas docentes resultaron adecuadas por su carácter científico-pedagógico, su pertinencia y su funcionalidad para lograr un aprendizaje desarrollador e influir en el fortalecimiento de valores del futuro egresado de la carrera de Medicina.


Background: some of José Martí´s texts constitute sources of the historical knowledge that should be consulted and used by the professors, in the teaching-learning process of the History of Cuba. Objective: to elaborate teaching tasks for the teaching of History of Cuba I integrating in them fragments of Marti's work, in correspondence with the matching content. Methods: it was carried out a qualitative investigation in"Lidia Doce Sánchez" Medical Sciences University Site in the academic year 2014-2015. Theoretical methods were used: analysis-synthesis, induction-deduction and historical-logical, and empiric ones: documental analysis, a survey in questionnaire form was applied to students of second year of the career and in interview form to professors of History of Cuba. The results were methodologically triangulated. Results: the necessity of using Marti´s works was verified in the programs for a developing learning, and the reinforcement of human and revolutionary values; the students coincide in the sense that it isn't offered an appropriate treatment to Marti´s works in the different topics of History of Cuba I, and the professors recognize the importance of including its analysis in the different organizational forms of teaching, and the study of his wide bibliography to value his contributions on the Cuban revolutionary thought, teaching tasks were proposed , which were valued by the specialists' criteria. Conclusions: the teaching tasks were adequate because of their scientific-pedagogic character, their pertinence and functionality to achieve a developing learning and to influence in the strengthening of values of the future graduates of the Medicine career.


Assuntos
Ensino , Educação Médica , Aprendizagem
19.
Edumecentro ; 8(2)abr.-jun. 2016.
Artigo em Espanhol | CUMED | ID: cum-69321

RESUMO

Fundamento: algunos textos de José Martí constituyen fuentes del conocimiento histórico que deben ser consultados y aprovechados por los educadores, en el proceso enseñanzaaprendizaje de la Historia de Cuba.Objetivo: elaborar tareas docentes para la enseñanza de Historia de Cuba I integrando en ellas fragmentos de la obra martiana, en correspondencia con el contenido que se trate. Métodos: se realizó una investigación cualitativa en la Filial de Ciencias Médicas Lidia DoceSánchez en el curso 2014-2015. Se emplearon métodos teóricos: análisis-síntesis, inducción-deducción e histórico-lógico, y empíricos: análisis documental, encuesta en forma de cuestionario a estudiantes de segundo año de la carrera y de entrevista a profesores de Historia de Cuba. Los resultados fueron triangulados metodológicamente. Resultados: en los programas se constató la necesidad de utilizar las obras martianas paraun aprendizaje desarrollador, y el reforzamiento de valores humanos y revolucionarios; los alumnos coinciden en que no se ofrece un adecuado tratamiento a la obra martiana en losdiferentes temas de Historia de Cuba I, y los profesores reconocen la importancia de incluir su análisis en las distintas formas organizativas de la enseñanza, y el estudio de su ampliabibliografía para valorar sus aportes sobre el pensamiento revolucionario cubano, por lo que se propusieron tareas docentes, las cuales fueron valoradas por criterio de especialistas.Conclusiones: las tareas docentes resultaron adecuadas por su carácter científico-pedagógico, su pertinencia y su funcionalidad para lograr un aprendizaje desarrollador e influir en el fortalecimiento de valores del futuro egresado de la carrera de Medicina(AU)


Assuntos
Ensino , História , Educação Médica
20.
RNA ; 22(4): 571-82, 2016 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-26873599

RESUMO

Coupling between transcription and RNA processing is key for gene regulation. Using live-cell photobleaching techniques, we investigated the factor TCERG1, which coordinates transcriptional elongation with splicing. We demonstrate that TCERG1 is highly mobile in the nucleoplasm and that this mobility is slightly decreased when it is associated with speckles. Dichloro-1-ß-D-ribofuranosylbenzimidazole (DRB) but not α-amanitin treatment reduced the mobility of TCERG1, which suggests interaction with paused transcription elongation complexes. We found that TCERG1 mobility is rapid at the transcription site (TS) of a reporter that splices post-transcriptionally and that TCERG1 is recruited to the active TS independent of the CTD of RNAPII, thus excluding phosphorylated CTD as a requirement for recruiting this factor to the TS. Importantly, the mobility of TCERG1 is reduced when the reporter splices cotranscriptionally, which suggests that TCERG1 forms new macromolecular complexes when splicing occurs cotranscriptionally. In this condition, spliceostatin A has no effect, indicating that TCERG1 rapidly binds and dissociates from stalled spliceosomal complexes and that the mobility properties of TCERG1 do not depend on events occurring after the initial spliceosome formation. Taken together, these data suggest that TCERG1 binds independently to elongation and splicing complexes, thus performing their coupling by transient interactions rather than by stable association with one or the other complexes. This finding has conceptual implications for understanding the coupling between transcription and RNA processing.


Assuntos
Splicing de RNA , Elongação da Transcrição Genética , Fatores de Elongação da Transcrição/fisiologia , Núcleo Celular/metabolismo , Genes Reporter , Células HEK293 , HIV-1/genética , Humanos , Transporte Proteico
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