Unknown,Transcriptomics,Genomics,Proteomics

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MNNG treated Excherichia coli reveal new up or down regulated genes belonging to the Ada regulon


ABSTRACT: An oligonucleotide tiling array technology is utilized to measure the entire Escherichia coli transcriptome and its transcriptional changes after induction of the adaptive response by the alkylating agent N-methyl-N'-nitro-N-nitrosoguanidine (MNNG). Keywords: Gene expression during the adaptive response in Escherichia coli Escherichia coli K-12 MG1655 single colony in five parallells was grown to mid-log phase and exposed to the ada-response inducer MNNG. Total RNA was extracted from induced and uninduced cells and cDNA was prepared, fragmented and labelled prior to hybridizing to arrays. The Escherichia coli genome was split in two; sequences encoding proteins, tRNAs or rRNAs with a known function on either strand, and sequences without such annotation. A selective tiling approach was used to ensure sufficient coverage of unnanotated genomic regions due to the limited number of array probes.

ORGANISM(S): Escherichia coli str. K-12 substr. MG1655

SUBMITTER: Knut Kristiansen 

PROVIDER: E-GEOD-13830 | biostudies-arrayexpress |

REPOSITORIES: biostudies-arrayexpress

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Publications

Custom design and analysis of high-density oligonucleotide bacterial tiling microarrays.

Thomassen Gard O S GO   Rowe Alexander D AD   Lagesen Karin K   Lindvall Jessica M JM   Rognes Torbjørn T  

PloS one 20090617 6


<h4>Background</h4>High-density tiling microarrays are a powerful tool for the characterization of complete genomes. The two major computational challenges associated with custom-made arrays are design and analysis. Firstly, several genome dependent variables, such as the genome's complexity and sequence composition, need to be considered in the design to ensure a high quality microarray. Secondly, since tiling projects today very often exceed the limits of conventional array-experiments, resear  ...[more]

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