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1.
Nucleic Acids Res ; 44(D1): D133-43, 2016 Jan 04.
Artículo en Inglés | MEDLINE | ID: mdl-26527724

RESUMEN

RegulonDB (http://regulondb.ccg.unam.mx) is one of the most useful and important resources on bacterial gene regulation,as it integrates the scattered scientific knowledge of the best-characterized organism, Escherichia coli K-12, in a database that organizes large amounts of data. Its electronic format enables researchers to compare their results with the legacy of previous knowledge and supports bioinformatics tools and model building. Here, we summarize our progress with RegulonDB since our last Nucleic Acids Research publication describing RegulonDB, in 2013. In addition to maintaining curation up-to-date, we report a collection of 232 interactions with small RNAs affecting 192 genes, and the complete repertoire of 189 Elementary Genetic Sensory-Response units (GENSOR units), integrating the signal, regulatory interactions, and metabolic pathways they govern. These additions represent major progress to a higher level of understanding of regulated processes. We have updated the computationally predicted transcription factors, which total 304 (184 with experimental evidence and 120 from computational predictions); we updated our position-weight matrices and have included tools for clustering them in evolutionary families. We describe our semiautomatic strategy to accelerate curation, including datasets from high-throughput experiments, a novel coexpression distance to search for 'neighborhood' genes to known operons and regulons, and computational developments.


Asunto(s)
Bases de Datos Genéticas , Escherichia coli K12/genética , Regulación Bacteriana de la Expresión Génica , Regulón , Análisis por Conglomerados , Escherichia coli K12/metabolismo , Redes Reguladoras de Genes , Operón , Posición Específica de Matrices de Puntuación , ARN Pequeño no Traducido/metabolismo , Factores de Transcripción/clasificación
2.
Nucleic Acids Res ; 41(Database issue): D203-13, 2013 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-23203884

RESUMEN

This article summarizes our progress with RegulonDB (http://regulondb.ccg.unam.mx/) during the past 2 years. We have kept up-to-date the knowledge from the published literature regarding transcriptional regulation in Escherichia coli K-12. We have maintained and expanded our curation efforts to improve the breadth and quality of the encoded experimental knowledge, and we have implemented criteria for the quality of our computational predictions. Regulatory phrases now provide high-level descriptions of regulatory regions. We expanded the assignment of quality to various sources of evidence, particularly for knowledge generated through high-throughput (HT) technology. Based on our analysis of most relevant methods, we defined rules for determining the quality of evidence when multiple independent sources support an entry. With this latest release of RegulonDB, we present a new highly reliable larger collection of transcription start sites, a result of our experimental HT genome-wide efforts. These improvements, together with several novel enhancements (the tracks display, uploading format and curational guidelines), address the challenges of incorporating HT-generated knowledge into RegulonDB. Information on the evolutionary conservation of regulatory elements is also available now. Altogether, RegulonDB version 8.0 is a much better home for integrating knowledge on gene regulation from the sources of information currently available.


Asunto(s)
Bases de Datos Genéticas , Escherichia coli K12/genética , Regulación Bacteriana de la Expresión Génica , Elementos Reguladores de la Transcripción , Transcripción Genética , Proteínas Bacterianas/metabolismo , Bases de Datos Genéticas/normas , Evolución Molecular , Genómica , Internet , Regiones Promotoras Genéticas , Regulón , Proteínas Represoras/metabolismo , Análisis de Secuencia de ARN , Factores de Transcripción/metabolismo , Sitio de Iniciación de la Transcripción
3.
PLoS One ; 12(4): e0174887, 2017.
Artículo en Inglés | MEDLINE | ID: mdl-28419102

RESUMEN

In prokaryotes, genomic distance is a feature that in addition to coregulation affects coexpression. Several observations, such as genomic clustering of highly coexpressed small regulons, support the idea that coexpression behavior of coregulated genes is affected by the distance between the coregulated genes. However, the specific contribution of distance in addition to coregulation in determining the degree of coexpression has not yet been studied systematically. In this work, we exploit the rich information in RegulonDB to study how the genomic distance between coregulated genes affects their degree of coexpression, measured by pairwise similarity of expression profiles obtained under a large number of conditions. We observed that, in general, coregulated genes display higher degrees of coexpression as they are more closely located on the genome. This contribution of genomic distance in determining the degree of coexpression was relatively small compared to the degree of coexpression that was determined by the tightness of the coregulation (degree of overlap of regulatory programs) but was shown to be evolutionary constrained. In addition, the distance effect was sufficient to guarantee coexpression of coregulated genes that are located at very short distances, irrespective of their tightness of coregulation. This is partly but definitely not always because the close distance is also the cause of the coregulation. In cases where it is not, we hypothesize that the effect of the distance on coexpression could be caused by the fact that coregulated genes closely located to each other are also relatively more equidistantly located from their common TF and therefore subject to more similar levels of TF molecules. The absolute genomic distance of the coregulated genes to their common TF-coding gene tends to be less important in determining the degree of coexpression. Our results pinpoint the importance of taking into account the combined effect of distance and coregulation when studying prokaryotic coexpression and transcriptional regulation.


Asunto(s)
Cromosomas Bacterianos/genética , Escherichia coli/genética , Regulación Bacteriana de la Expresión Génica , Genes Bacterianos/genética , Genoma Bacteriano/genética , Mapeo Cromosómico , Perfilación de la Expresión Génica , Modelos Genéticos , Operón/genética , Factores de Transcripción/metabolismo
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