Unknown,Transcriptomics,Genomics,Proteomics

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Transcriptional profiles from Dickeya dadantii 3937 in various growth conditions


ABSTRACT: We have analysed the global gene expression of the plant pathogen Dickeya dadantii 3937 when grown in vitro under different growth and stress conditions. A multi-factorial design with 32 different experimental conditions was constructed, with two biological replicates for each condition. Cells were grown to exponential phase or stationary phases in four different growth media: M63 supplemented with 0.2% sucrose as carbon source, with or without 0.2% (w/v) polygalacturonate (PGA) and with or without 0.1% Saintpaulia leaf extracts (1 g leaves in 1 L M63). Cells grown in these four media were subjected to different stresses: (i) acid stress, by an incubation of 15 min in the presence of 30 mM malic acid; (ii) oxidative stress, by an incubation of 15 min in the presence of 100 _M H2O2 or (iii) osmotic stress, by an incubation of 15 min in the presence of 300 mM NaCl. The micro-arrays used in this study were custom designed and produced by Roche NimbleGen, Inc. (Madison, WI) based on the annotated sequence of D. dadantii, available at Genbank accession number nM-! CP002038, which comprises 4597 CDS. The 4plex expression micro-arrays consist of 60-mer oligonucleotides, triplicated in three blocks on the array (5 oligonucleotides per CDS).

ORGANISM(S): Dickeya dadantii 3937

SUBMITTER: Christine Oger 

PROVIDER: E-MTAB-541 | biostudies-arrayexpress |

REPOSITORIES: biostudies-arrayexpress

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Publications

lpxC and yafS are the most suitable internal controls to normalize real time RT-qPCR expression in the phytopathogenic bacteria Dickeya dadantii.

Hommais Florence F   Zghidi-Abouzid Ouafa O   Oger-Desfeux Christine C   Pineau-Chapelle Emilie E   Van Gijsegem Frederique F   Nasser William W   Reverchon Sylvie S  

PloS one 20110526 5


<h4>Background</h4>Quantitative RT-PCR is the method of choice for studying, with both sensitivity and accuracy, the expression of genes. A reliable normalization of the data, using several reference genes, is critical for an accurate quantification of gene expression. Here, we propose a set of reference genes, of the phytopathogenic bacteria Dickeya dadantii and Pectobacterium atrosepticum, which are stable in a wide range of growth conditions.<h4>Results</h4>We extracted, from a D. dadantii mi  ...[more]

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