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2.
Arch Surg ; 131(5): 566-8, 1996 May.
Artículo en Inglés | MEDLINE | ID: mdl-8624207

RESUMEN

Intra-abdominal cysts may rise from a variety of organs. However, foreign-body reaction and cyst formation should be considered in the differential diagnosis. In this report, we describe the finding of a preoperatively undetected gossypiboma. A gossypiboma is a mass within the body that is composed of a cotton matrix; in this case, an unmarked laparotomy sponge. The evaluation, findings, and prevention of gossypiboma are discussed.


Asunto(s)
Abdomen , Quistes/etiología , Reacción a Cuerpo Extraño/complicaciones , Tapones Quirúrgicos de Gaza , Abdomen/cirugía , Quistes/diagnóstico por imagen , Quistes/cirugía , Humanos , Radiografía Abdominal , Tomografía Computarizada por Rayos X
3.
Science ; 263(5143): 75-7, 1994 Jan 07.
Artículo en Inglés | MEDLINE | ID: mdl-8272867

RESUMEN

Activation of transcription initiation by the cI protein of phage lambda is thought to be mediated by a direct interaction between cl and RNA polymerase at the PRM promoter. Two negatively charged amino acid residues in the DNA binding domain of cI play a key role in activation, suggesting that these residues contact RNA polymerase. The subunit of RNA polymerase involved was identified by selecting polymerase mutants that restored the activation function of a mutant form of cI protein. Although previous studies suggest that several activators interact with the alpha subunit of RNA polymerase, the results here suggest that cI interacts with the sigma subunit. An arginine to histidine change near the carboxyl terminus of sigma specifically suppresses an aspartic acid to asparagine change in the activation region of cI. This finding supports the direct-contact model and suggests that a cluster of positively charged residues near the carboxyl terminus of sigma is the target of the negatively charged activation region of cI.


Asunto(s)
Bacteriófago lambda/genética , Proteínas de Unión al ADN , Proteínas Represoras/genética , Factor sigma/genética , Factores de Transcripción/genética , Activación Transcripcional , Bacteriófago P22/genética , Secuencia de Bases , ARN Polimerasas Dirigidas por ADN/genética , ARN Polimerasas Dirigidas por ADN/metabolismo , Modelos Genéticos , Datos de Secuencia Molecular , Regiones Promotoras Genéticas , Proteínas Represoras/química , Proteínas Represoras/metabolismo , Factor sigma/química , Factor sigma/metabolismo , Supresión Genética , Factores de Transcripción/química , Factores de Transcripción/metabolismo , Proteínas Virales , Proteínas Reguladoras y Accesorias Virales
4.
J Bacteriol ; 173(6): 1944-50, 1991 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-2001998

RESUMEN

Oligonucleotide-directed mutagenesis was used to complete a collection of mutations in the -35 and -10 hexamers of the ant promoter of Salmonella phage P22. The effects of all 36 single-base-pair substitutions on promoter strength in vivo were measured in strains carrying the mutant promoters fused to an ant-lacZ gene on a single-copy prophage. The results of these assays show that certain consensus base pairs are more important than others; in general, the least-critical positions are among the most poorly conserved. Some mutations within the hexamers have smaller effects on promoter strength than certain mutations outside the hexamers in this and other promoters. Several different patterns of base pair preferences are observed. These hierarchies of base pair preferences correlate well (but not perfectly) with the hierarchies defined by the frequency distribution of base pairs at each position among wild-type promoters. The hierarchies observed in the ant promoter also agree well with most of the available information on base pair preferences in other promoters.


Asunto(s)
Regiones Promotoras Genéticas , Fagos de Salmonella/genética , Secuencia de Bases , Clonación Molecular , Análisis Mutacional de ADN , Regulación Viral de la Expresión Génica , Enlace de Hidrógeno , Datos de Secuencia Molecular , Relación Estructura-Actividad
5.
J Mol Biol ; 206(4): 579-90, 1989 Apr 20.
Artículo en Inglés | MEDLINE | ID: mdl-2661827

RESUMEN

A mutation is described that alters the promoter specificity of sigma 70, the primary sigma factor of Escherichia coli RNA polymerase. In strains carrying both the mutant and wild-type sigma gene (rpoD), the mutant sigma causes a large increase in the activity of mutant P22 ant promoters with A.T or C.G instead of the wild-type, consensus G.C base-pair at position -33, the third position of the consensus -35 hexamer 5'-TTGACA-3'. There is little or no effect on the activities of the wild-type and 23 other mutant ant promoters, including one with T.A at -33. The mutant sigma also activates E. coli lac promoters with A.T or C.G, but not T.A, at the corresponding position. The rpoD mutation (rpoD-RH588) changes a CGT codon to CAT. The corresponding change in sigma 70 is Arg588----His. This residue is in a region that is conserved among most sigma factors, a region that is also homologous with the helix-turn-helix motif of DNA-binding proteins. These results suggest that this region of sigma 70 is directly involved in recognition of the -35 hexamer.


Asunto(s)
ARN Polimerasas Dirigidas por ADN/genética , Escherichia coli/genética , Regiones Promotoras Genéticas , Factor sigma/genética , Factores de Transcripción/genética , Secuencia de Bases , Deleción Cromosómica , Genes Bacterianos , Operón Lac , Datos de Secuencia Molecular , Mutación
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