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1.
Sci Rep ; 14(1): 3201, 2024 02 08.
Artículo en Inglés | MEDLINE | ID: mdl-38332158

RESUMEN

Previous research has extensively investigated why users spread misinformation online, while less attention has been given to the motivations behind sharing fact-checks. This article reports a four-country survey experiment assessing the influence of confirmation and refutation frames on engagement with online fact-checks. Respondents randomly received semantically identical content, either affirming accurate information ("It is TRUE that p") or refuting misinformation ("It is FALSE that not p"). Despite semantic equivalence, confirmation frames elicit higher engagement rates than refutation frames. Additionally, confirmation frames reduce self-reported negative emotions related to polarization. These findings are crucial for designing policy interventions aiming to amplify fact-check exposure and reduce affective polarization, particularly in critical areas such as health-related misinformation and harmful speech.


Asunto(s)
Emociones , Habla , Humanos , Motivación , Políticas , Sistemas de Lectura , Comunicación
2.
PLoS One ; 19(1): e0297061, 2024.
Artículo en Inglés | MEDLINE | ID: mdl-38285702

RESUMEN

A chain formation strategy based on mobile frames for a set of n differential drive mobile robots is presented. Considering two consecutive robots in the formation, robots Ri and Ri+1. It is intended that robot Ri+1 follows the delayed trajectory, τ units of time, of the leader robot Ri. In this way, the follower robot Ri+1 becomes the leader robot for robot Ri+ 2 in the formation and so on. With this formation policy, the trailing distance between two consecutive robots varies accordingly to the velocity of the Ri leader robot. Mobile frames are located on the body of the vehicles, in such a way that the position of robot Ri is determined with respect to the frame located on Ri+1 robot. The strategy relies on the fact that the general leader robot R1 describes any trajectory generated by bounded linear v1(t) and angular ω1(t) velocities. For the remaining vehicles in the string, the strategy considers a desired trajectory for the follower robot Ri+1 obtained by an estimation of the delayed trajectory of the leader robot Ri. This desired estimated trajectory is obtained under the knowledge of the actual and past input velocities of the Ri robot. To formally prove the convergence of the formation strategy, the equations describing the time variation of the relative posture between any pair of consecutive vehicles in the formation are obtained, and a feedback law based on local measurements is proposed to get the convergence of robot Ri+1 to the delayed trajectory, τ units of time, of the trajectory previously described by robot Ri. Lyapunov techniques are considered for this fact. The effectiveness of the chain formation solution is evaluated by means of numerical simulations and real time experiments showing an adequate convergence.


Asunto(s)
Robótica , Conocimiento , Políticas , Postura , Sistemas de Lectura
3.
Viruses ; 15(2)2023 01 25.
Artículo en Inglés | MEDLINE | ID: mdl-36851553

RESUMEN

Mitoviruses are small vertically transmitted RNA viruses found in fungi, plants and animals. Taxonomically, a total of 105 species and 4 genera have been formally recognized by ICTV, and recently, 18 new putative species have been included in a new proposed genus. Transcriptomic and metatranscriptomic studies are a major source of countless new virus-like sequences that are continually being added to open databases and these may be good sources for identifying new putative mitoviruses. The search for mitovirus-like sequences in the NCBI databases resulted in the discovery of more than one hundred new putative mitoviruses, with important implications for taxonomy and also for the evolutionary scenario. Here, we propose the inclusion of four new putative members to the genus Kvaramitovirus, and the existence of a new large basally divergent lineage composed of 144 members that lack internal UGA codons (subfamily "Arkeomitovirinae"), a feature not shared by the vast majority of mitoviruses. Finally, a taxonomic categorization proposal and a detailed description of the evolutionary history of mitoviruses were carried out. This in silico study supports the hypothesis of the existence of a basally divergent lineage that could have had an impact on the early evolutionary history of mitoviruses.


Asunto(s)
Evolución Biológica , Magnoliopsida , Animales , Sistemas de Lectura , Codón de Terminación , Bases de Datos Factuales , Perfilación de la Expresión Génica
4.
Nat Commun ; 13(1): 7452, 2022 12 02.
Artículo en Inglés | MEDLINE | ID: mdl-36460648

RESUMEN

The resolution of fluorescence microscopy images is limited by the physical properties of light. In the last decade, numerous super-resolution microscopy (SRM) approaches have been proposed to deal with such hindrance. Here we present Mean-Shift Super Resolution (MSSR), a new SRM algorithm based on the Mean Shift theory, which extends spatial resolution of single fluorescence images beyond the diffraction limit of light. MSSR works on low and high fluorophore densities, is not limited by the architecture of the optical setup and is applicable to single images as well as temporal series. The theoretical limit of spatial resolution, based on optimized real-world imaging conditions and analysis of temporal image stacks, has been measured to be 40 nm. Furthermore, MSSR has denoising capabilities that outperform other SRM approaches. Along with its wide accessibility, MSSR is a powerful, flexible, and generic tool for multidimensional and live cell imaging applications.


Asunto(s)
Algoritmos , Medicamentos Genéricos , Sistemas de Lectura , Microscopía Fluorescente , Colorantes Fluorescentes
5.
Rev. ecuat. pediatr ; 23(3): 239-248, 12 de Diciembre del 2022.
Artículo en Español | LILACS | ID: biblio-1411268

RESUMEN

Introducción: Las dificultades del aprendizaje son las alteraciones de mayor presencia en las aulas escolares y sus indicadores pueden diagnosticarse y prevenirse desde edades tempranas. El objetivo de esta investigación fue validar el Test para la detección temprana de las dificultades en el aprendizaje de la lectura y escritura. Métodos: El enfoque de la investigación fue cuantitativo, descriptivo y de corte transversal. Se utilizó la validez de constructo acorde con la propuesta original del test y de fiabilidad a través del Alpha de Cronbach en una muestra de 501 niños ecuatorianos de cuatro años. Resultados: La validación del instrumento evidencia una moderada correlación entre las sub-tareas y alta correlación entre las sub-tareas y el puntaje total. La fiabilidad es buena, α= 0.71, muy próxima a la de la población española α= 0.73. Por lo que, la prueba puede ser utilizada en el contexto ecuatoriano en su versión original, adecuando en las instrucciones dos palabras a la realidad lingüística del país y para la calificación los puntos de corte de dificultad. Conclusión: Considerando su valor y fácil aplicación se recomienda el uso de la prueba de lectura en contextos educativos y de salud.


Introduction: Learning difficulties are the alterations with the most significant presence in school classrooms, and their indicators can be diagnosed and prevented early. This research aimed to validate the test for the early detection of difficulties in learning to read and write. Methods: The research approach was quantitative, descriptive, and cross-sectional. Construct validity was used according to the original proposal of the test and reliability through Cronbach's alpha in a sample of 501 four-year-old Ecuadorian children. Results: The validation of the instrument shows a moderate correlation between the subtasks and a high correlation between the subtasks and the total score. The reliability is good, α = 0.71, very close to that of the Spanish population α = 0.73. Therefore, the test can be used in the Ecuadorian context in its original version, adapting two words in the instructions to the linguistic reality of the country and for the qualification of the cutoff points of difficulty. Conclusion: With the easy application of the "test of reading" in 4-year-old children, the authors recommended its application for the identification of dyslexia and phonological processing deficits in school children in Ecuador. The reading test's validity allows its application at a regional level.


Asunto(s)
Humanos , Preescolar , Trastornos de la Articulación , Lectura , Comprensión , Sistemas de Lectura Abierta , Sistemas de Lectura , Dislexia
6.
Arch Microbiol ; 201(1): 93-97, 2019 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-30255200

RESUMEN

Virulence factors of H. pylori, such as outer inflammatory protein A (oipA), are closely involved in the development of gastric diseases such as chronic gastritis and gastric cancer. The functional status of oipA is regulated by a repair mechanism based on CT dinucleotide repeats that influence the reading frame, thus granting the gene a functional or nonfunctional status; in other words, the functional status of the oipA gene seems to be associated with the development of gastric diseases. This study sought to detect the presence of the oipA gene and to determine its functional status in patients with gastric diseases. We analyzed 516 biopsy samples (101 with normal gastric tissue, 365 with chronic gastritis, and 50 with gastric cancer). The presence of oipA was determined by PCR, and the gene status was determined using sequencing reactions. The oipA gene was found to be associated with the development of chronic gastritis, and the "on" status of the gene was the most frequent in patients with gastric cancer who were from Western countries. The CT repeats revealed geographic characteristics, but it is the functional status of the oipA gene that seems to be involved in the development of gastric diseases and in the development of gastric cancer in particular.


Asunto(s)
Proteínas de la Membrana Bacteriana Externa/genética , Gastritis/microbiología , Infecciones por Helicobacter/microbiología , Helicobacter pylori/genética , Helicobacter pylori/patogenicidad , Sistemas de Lectura/genética , Neoplasias Gástricas/microbiología , Antígenos Bacterianos/genética , Repeticiones de Dinucleótido/genética , Femenino , Humanos , Masculino , Persona de Mediana Edad , Reacción en Cadena de la Polimerasa , Factores de Virulencia/genética
7.
Clinics (Sao Paulo) ; 73(suppl 1): e479s, 2018 09 06.
Artículo en Inglés | MEDLINE | ID: mdl-30208166

RESUMEN

While cancer immunotherapy has gained much deserved attention in recent years, many areas regarding the optimization of such modalities remain unexplored, including the development of novel approaches and the strategic combination of therapies that target multiple aspects of the cancer-immunity cycle. Our own work involves the use of gene transfer technology to promote cell death and immune stimulation. Such immunogenic cell death, mediated by the combined transfer of the alternate reading frame (p14ARF in humans and p19Arf in mice) and the interferon-ß cDNA in our case, was shown to promote an antitumor immune response in mouse models of melanoma and lung carcinoma. With these encouraging results, we are now setting out on the road toward translational and preclinical development of our novel immunotherapeutic approach. Here, we outline the perspectives and challenges that we face, including the use of human tumor and immune cells to verify the response seen in mouse models and the incorporation of clinically relevant models, such as patient-derived xenografts and spontaneous tumors in animals. In addition, we seek to combine our immunotherapeutic approach with other treatments, such as chemotherapy or checkpoint blockade, with the goal of reducing dosage and increasing efficacy. The success of any translational research requires the cooperation of a multidisciplinary team of professionals involved in laboratory and clinical research, a relationship that is fostered at the Cancer Institute of Sao Paulo.


Asunto(s)
Técnicas de Transferencia de Gen , Terapia Genética/métodos , Inmunoterapia/métodos , Interferón beta/uso terapéutico , Neoplasias/terapia , Sistemas de Lectura/genética , Muerte Celular/genética , Inhibidor p16 de la Quinasa Dependiente de Ciclina/genética , Humanos , Neoplasias/inmunología , Proteína p14ARF Supresora de Tumor/genética
8.
Eur J Haematol ; 100(6): 529-535, 2018 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-29319890

RESUMEN

Hemoglobinopathies are the most common autosomal recessive disorders and are mostly inherited in a recessive manner. However, certain mutations can affect the globin chain stability, leading to dominant forms of thalassemia. The aim of this work was the molecular and structural characterization of two heterozygous in-frame deletions, leading to ß-globin variants in pediatric patients in Argentina. The HBB gene of the probands and their parents was sequenced, and other markers of globin chain imbalance were analyzed. Several structural analyses were performed, and the effect of the mutations on the globin chain stability was analyzed. In Hb JC-Paz, HBB:c.29_37delCTGCCGTTA (p.Ala10_Thr12del), detected in an Argentinean boy, one α-helix turn is expected to be lost. In Hb Tavapy, HBB:c.182_187delTGAAGG (p.Val60_Lys61del), the deleted residues are close to distal histidine (His63) in the heme pocket. Both mutations are predicted to have a destabilizing effect. The development of computational structural models and bioinformatics algorithms is expected to become a useful tool to understand the impact of the mutations leading to dominant thalassemia.


Asunto(s)
Sustitución de Aminoácidos , Hemoglobinas Anormales/genética , Sistemas de Lectura , Eliminación de Secuencia , Globinas beta/genética , Niño , Preescolar , Análisis Mutacional de ADN , Índices de Eritrocitos , Femenino , Hemoglobinopatías/sangre , Hemoglobinopatías/diagnóstico , Hemoglobinopatías/genética , Hemoglobinopatías/terapia , Hemoglobinas Anormales/química , Humanos , Masculino , Modelos Moleculares , Conformación Proteica , Pliegue de Proteína , Globinas beta/química
9.
Clinics ; Clinics;73(supl.1): e479s, 2018. graf
Artículo en Inglés | LILACS | ID: biblio-952830

RESUMEN

While cancer immunotherapy has gained much deserved attention in recent years, many areas regarding the optimization of such modalities remain unexplored, including the development of novel approaches and the strategic combination of therapies that target multiple aspects of the cancer-immunity cycle. Our own work involves the use of gene transfer technology to promote cell death and immune stimulation. Such immunogenic cell death, mediated by the combined transfer of the alternate reading frame (p14ARF in humans and p19Arf in mice) and the interferon-β cDNA in our case, was shown to promote an antitumor immune response in mouse models of melanoma and lung carcinoma. With these encouraging results, we are now setting out on the road toward translational and preclinical development of our novel immunotherapeutic approach. Here, we outline the perspectives and challenges that we face, including the use of human tumor and immune cells to verify the response seen in mouse models and the incorporation of clinically relevant models, such as patient-derived xenografts and spontaneous tumors in animals. In addition, we seek to combine our immunotherapeutic approach with other treatments, such as chemotherapy or checkpoint blockade, with the goal of reducing dosage and increasing efficacy. The success of any translational research requires the cooperation of a multidisciplinary team of professionals involved in laboratory and clinical research, a relationship that is fostered at the Cancer Institute of Sao Paulo.


Asunto(s)
Humanos , Terapia Genética/métodos , Sistemas de Lectura/genética , Interferón beta/uso terapéutico , Técnicas de Transferencia de Gen , Inmunoterapia/métodos , Neoplasias/terapia , Muerte Celular/genética , Inhibidor p16 de la Quinasa Dependiente de Ciclina/genética , Proteína p14ARF Supresora de Tumor/genética , Neoplasias/inmunología
10.
Antonie Van Leeuwenhoek ; 110(2): 291-296, 2017 Feb.
Artículo en Inglés | MEDLINE | ID: mdl-27771809

RESUMEN

Volatile phenols are aromatic compounds produced by some yeasts of the genus Brettanomyces as defense against the toxicity of hydroxycinnamic acids (p-coumaric acid, ferulic acid and caffeic acid). The origin of these compounds in winemaking involves the sequential action of two enzymes: coumarate decarboxylase and vinylphenol reductase. The first one converts hydroxycinnamic acids into hydroxystyrenes, which are then reduced to ethyl derivatives by vinylphenol reductase. Volatile phenols derived from p-coumaric acid (4-vinylphenol and 4-ethylphenol) have been described as the major contributors to self-defeating aromas associated with stable, gouache, wet mouse, etc., which generates large economic losses in the wine industry. The gene responsible for the production of 4-vinylphenol from p-coumaric acid has been identified as PAD1, which encodes a phenylacrylic acid decarboxylase. PAD1 has been described for many species, among them Candida albicans, Candida dubliniensis, Debaryomyces hansenii and Pichia anomala. In Brettanomyces bruxellensis LAMAP2480, a 666 bp reading frame (DbPAD) encodes a coumarate decarboxylase. Recent studies have reported the existence of a new reading frame belonging to DbPAD called DbPAD2 of 531 bp, which could encode a protein with similar enzymatic activity to PAD1. The present study confirmed that the transformation of Saccharomyces cerevisiae strain BY4722 with reading frame DbPAD2 under the control of the B. bruxellensis ACT1 promoter, encodes an enzyme with coumarate decarboxylase activity. This work has provided deeper insight into the origin of aroma defects in wine due to contamination by Brettanomyces spp.


Asunto(s)
Brettanomyces/enzimología , Brettanomyces/genética , Carboxiliasas/genética , Microbiología de Alimentos , Proteínas Fúngicas/genética , Proteínas Fúngicas/metabolismo , Carboxiliasas/metabolismo , Fenoles/metabolismo , Sistemas de Lectura/genética , Saccharomyces cerevisiae/genética , Compuestos Orgánicos Volátiles/metabolismo , Vino/microbiología
12.
Eur J Hum Genet ; 22(5): 644-51, 2014 May.
Artículo en Inglés | MEDLINE | ID: mdl-24105372

RESUMEN

Oligophrenin-1 (OPHN1) is one of at least seven genes located on chromosome X that take part in Rho GTPase-dependent signaling pathways involved in X-linked intellectual disability (XLID). Mutations in OPHN1 were primarily described as an exclusive cause of non-syndromic XLID, but the re-evaluation of the affected individuals using brain imaging displayed fronto-temporal atrophy and cerebellar hypoplasia as neuroanatomical marks. In this study, we describe clinical, genetic and neuroimaging data of a three generation Brazilian XLID family co-segregating a novel intragenic deletion in OPHN1. This deletion results in an in-frame loss of exon 7 at transcription level (c.781_891del; r.487_597del), which is predicted to abolish 37 amino acids from the highly conserved N-terminal BAR domain of OPHN1. cDNA expression analysis demonstrated that the mutant OPHN1 transcript is stable and no abnormal splicing was observed. Features shared by the affected males of this family include neonatal hypotonia, strabismus, prominent root of the nose, deep set eyes, hyperactivity and instability/intolerance to frustration. Cranial MRI scans showed large lateral ventricles, vermis hypoplasia and cystic dilatation of the cisterna magna in all affected males. Interestingly, hippocampal alterations that have not been reported in patients with loss-of-function OPHN1 mutations were found in three affected individuals, suggesting an important function for the BAR domain in the hippocampus. This is the first description of an in-frame deletion within the BAR domain of OPHN1 and could provide new insights into the role of this domain in relation to brain and cognitive development or function.


Asunto(s)
Proteínas del Citoesqueleto/genética , Proteínas Activadoras de GTPasa/genética , Hipocampo/metabolismo , Discapacidad Intelectual/genética , Proteínas Nucleares/genética , Dominios y Motivos de Interacción de Proteínas/genética , Sistemas de Lectura , Eliminación de Secuencia , Adolescente , Adulto , Encéfalo/metabolismo , Niño , Hibridación Genómica Comparativa , Proteínas del Citoesqueleto/química , Análisis Mutacional de ADN , Facies , Femenino , Proteínas Activadoras de GTPasa/química , Hipocampo/patología , Humanos , Discapacidad Intelectual/diagnóstico , Imagen por Resonancia Magnética , Masculino , Persona de Mediana Edad , Proteínas Nucleares/química , Linaje , Fenotipo , Inactivación del Cromosoma X , Adulto Joven
13.
Psychol. av. discip ; 5(2): 57-67, dic. 2011. ilus, graf, tab
Artículo en Español | LILACS | ID: lil-659466

RESUMEN

La investigación explora las relaciones entre las características de las interacciones establecidas para propiciar la interpretación de un texto narrativo y las inferencias que los niños hacen sobre él. Ésta se enmarca en la psicología educativa, cognitiva y cultural. 4 grupos de preescolar participaron en el estudio con un total de 48 niños. El diseño fue descriptivo exploratorio. Se hizo un análisis cualitativo - análisis del discurso - y uno cuantitativo - análisis de redes sociales - para procesar los datos. Se encontró que los niños cuya maestra propiciaba más interacciones alrededor del texto buscando una comprensión como transacción texto -lector, lograron mayor elaboración inferencial y los niños cuyas docentes propusieron interacciones en las que planteaban discusiones sobre información explícita en el texto, realizaron pocas inferencias y de menor complejidad.


This research explores the relationship between the characteristics of interactions established to favor the narrative text interpretation and the inferences that children make on it. This is marked in the educative, cognitive and cultural psychologist. In this research participated four groups of kinder garden with a total of forty eight children. This was a descriptive and explorative design. Was realized a discursive analysis and a social nets analysis to process information. It was find that children which teacher favor more interactions and better interactions raised a textual analyses got a high inferencial elaboration, and children which teachers proposed low interaction raised discussions about explicit information in the text, realized a few inferences and with a low level of elaboration.


Asunto(s)
Desarrollo Infantil , Preescolar , Sistemas de Lectura , Comprensión , Relaciones Interpersonales , Escuelas de Párvulos , Docentes , Construcción Social del Género , Análisis de Redes Sociales
14.
Acta Virol ; 55(1): 45-53, 2011.
Artículo en Inglés | MEDLINE | ID: mdl-21434704

RESUMEN

Influenza A virus (IAV) PB1-F2 protein is encoded by an alternative reading frame (+1) within the PB1 gene. PB1-F2 has been shown to contribute to the pathogenesis of influenza virus infection as well as to the secondary bacterial infection. More recently has been shown that PB1-F2 protein may regulate a viral RNA (vRNA) polymerase activity by the interaction with PB1 protein. We proved that PB1-F2 protein increased the level of expression of PB1 protein and vRNA in the infected cells. Moreover, we demonstrated that a higher level of vRNA expression resulted in the increase of expression of multiple viral proteins, including NP, M1, and NS1. Finally, we used plasmids expressing N-terminal (1-50 aa) or C-terminal (51-87 aa) region of the PB1-F2 molecule for transfection of MDCK cells co-infected with influenza A/Puerto Rico/8/34 (H1N1) virus deficient in the PB1-F2 protein expression (PR8ΔPB1-F2). These experiments clearly showed that N-terminal region of PB1-F2 protein was responsible for the increase in PB1 protein expression. C-terminal region of PB1-F2 protein had no effect. Thus, we have identified the important function for N-terminal region of PB1-F2 protein.


Asunto(s)
Subtipo H1N1 del Virus de la Influenza A/metabolismo , Proteínas Virales/biosíntesis , Proteínas Virales/metabolismo , Secuencia de Aminoácidos , Animales , Células Cultivadas , ARN Polimerasas Dirigidas por ADN/metabolismo , Perros , Femenino , Humanos , Subtipo H1N1 del Virus de la Influenza A/genética , Ratones , Ratones Endogámicos BALB C , Puerto Rico , ARN Viral/genética , Sistemas de Lectura , Vacunas de ADN/genética , Proteínas Virales/genética
15.
Gene ; 448(1): 1-6, 2009 Dec 01.
Artículo en Inglés | MEDLINE | ID: mdl-19699281

RESUMEN

Kynureninase has been described in bacteria, fungi and animals as an enzyme involved in the catabolic degradation pathway of l-tryptophan. This pyridoxal 5'-phosphate (PLP)-dependent enzyme catalyzes the hydrolytic cleavage of l-kynurenine and 3-hydroxy-l-kynurenine to yield l-alanine and either anthranilic or 3-hydroxyanthranilic acid, respectively. We identified a putative kynureninase gene from a Trypanosoma cruzi project aiming at the structural and functional characterization of more than 100 proteins differentially expressed during metacyclogenesis. This gene encodes a protein similar in size and sequence to kynureninases from other sources. This open reading frame was cloned and the recombinant enzyme was overexpressed. Recombinant T. cruzi kynureninase was purified to homogeneity and its identity was confirmed by mass spectrometry. The apparent molecular mass of the native T. cruzi kynureninase was estimated by gel filtration, suggesting that the protein is a homodimer. Circular dichroism spectrum indicated a mixture of alpha-helix and beta-sheet structure, expected for an aminotransferase fold. l-kynurenine, preferentially hydrolyzed by prokaryotic inducible kynureninases, and 3-hydroxy-l-kynurenine, the preferred substrate in fungi and vertebrates, are both catabolized equally well by T. cruzi kynureninase. Further experimental assays will be performed to fully understand the importance of this enzyme for T. cruzi metabolism.


Asunto(s)
Bases de Datos de Proteínas , Hidrolasas/metabolismo , Trypanosoma cruzi/enzimología , Secuencia de Aminoácidos , Animales , Cromatografía en Gel , Dicroismo Circular , Humanos , Hidrolasas/química , Hidrolasas/genética , Hidrolasas/aislamiento & purificación , Modelos Moleculares , Datos de Secuencia Molecular , Estructura Terciaria de Proteína , Sistemas de Lectura , Proteínas Recombinantes/química , Proteínas Recombinantes/genética , Proteínas Recombinantes/aislamiento & purificación , Proteínas Recombinantes/metabolismo , Alineación de Secuencia , Homología de Secuencia de Aminoácido
16.
J Biotechnol ; 101(2): 173-80, 2003 Mar 06.
Artículo en Inglés | MEDLINE | ID: mdl-12568746

RESUMEN

The efficient production of recombinant proteins in Escherichia coli requires a proper termination of translation to ensure the synthesis of only the desired product. During the recombinant production of Bacillus subtilis flgM in E. coli, we detected an additional polypeptide of molecular mass higher than the expected, corresponding to a product of a translational readthrough of the UGA stop codon. In this paper we show that the readthrough was abolished when the synthesis of the recombinant protein was carried out at 25 degrees C. The possible causes that contribute to reduce the proportion of readthrough protein species against the correct terminated product are discussed.


Asunto(s)
Proteínas Bacterianas/biosíntesis , Escherichia coli/genética , Escherichia coli/metabolismo , Regulación Bacteriana de la Expresión Génica/fisiología , Temperatura , Bacillus subtilis/genética , Bacillus subtilis/metabolismo , Proteínas Bacterianas/química , Proteínas Bacterianas/genética , Proteínas Bacterianas/aislamiento & purificación , Secuencia de Bases , Células Cultivadas , Clonación Molecular , Codón de Terminación/genética , Codón de Terminación/fisiología , Regulación Bacteriana de la Expresión Génica/genética , Datos de Secuencia Molecular , Mutagénesis Insercional/métodos , Mutación , Biosíntesis de Proteínas/fisiología , Control de Calidad , Sistemas de Lectura , Proteínas Recombinantes/biosíntesis , Proteínas Recombinantes/genética
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