Transcriptome analysis of the mobile genome ICEclc in Pseudomonas knackmussii B13.
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Type
Article: article from journal or magazin.
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Publications
Institution
Title
Transcriptome analysis of the mobile genome ICEclc in Pseudomonas knackmussii B13.
Journal
BMC Microbiology
ISSN
1471-2180[electronic], 1471-2180[linking]
Publication state
Published
Issued date
2010
Volume
10
Pages
153
Language
english
Abstract
Background: Integrative and conjugative elements (ICE) form a diverse group of DNA elements that are integrated in the chromosome of the bacterial host, but can occasionally excise and horizontally transfer to a new host cell. ICE come in different families, typically with a conserved core for functions controlling the element's behavior and a variable region providing auxiliary functions to the host. The ICEclc element of Pseudomonas knackmussii strain B13 is representative for a large family of chromosomal islands detected by genome sequencing approaches. It provides the host with the capacity to degrade chloroaromatics and 2-aminophenol.
Results: Here we study the transcriptional organization of the ICEclc core region. By northern hybridizations, reverse-transcriptase polymerase chain reaction (RT-PCR) and Rapid Amplification of cDNA Ends (5'-RACE) fifteen transcripts were mapped in the core region. The occurrence and location of those transcripts were further confirmed by hybridizing labeled cDNA to a semi-tiling micro-array probing both strands of the ICEclc core region. Dot blot and semi-tiling array hybridizations demonstrated most of the core transcripts to be upregulated during stationary phase on 3-chlorobenzoate, but not on succinate or glucose.
Conclusions: The transcription analysis of the ICEclc core region provides detailed insights in the mode of regulatory organization and will help to further understand the complex mode of behavior of this class of mobile elements. We conclude that ICEclc core transcription is concerted at a global level, more reminiscent of a phage program than of plasmid conjugation.
Results: Here we study the transcriptional organization of the ICEclc core region. By northern hybridizations, reverse-transcriptase polymerase chain reaction (RT-PCR) and Rapid Amplification of cDNA Ends (5'-RACE) fifteen transcripts were mapped in the core region. The occurrence and location of those transcripts were further confirmed by hybridizing labeled cDNA to a semi-tiling micro-array probing both strands of the ICEclc core region. Dot blot and semi-tiling array hybridizations demonstrated most of the core transcripts to be upregulated during stationary phase on 3-chlorobenzoate, but not on succinate or glucose.
Conclusions: The transcription analysis of the ICEclc core region provides detailed insights in the mode of regulatory organization and will help to further understand the complex mode of behavior of this class of mobile elements. We conclude that ICEclc core transcription is concerted at a global level, more reminiscent of a phage program than of plasmid conjugation.
Keywords
Bacterial Proteins/genetics, Bacterial Proteins/metabolism, Chromosome Mapping, Chromosomes, Bacterial, DNA Transposable Elements/genetics, DNA Transposable Elements/physiology, Gene Expression Regulation, Bacterial, Genome, Bacterial, Genomic Instability, Genomic Islands, Oligonucleotide Array Sequence Analysis, Pseudomonas/genetics, Pseudomonas/metabolism, Reverse Transcriptase Polymerase Chain Reaction, Transcription, Genetic
Pubmed
Web of science
Open Access
Yes
Create date
11/01/2011 15:07
Last modification date
20/08/2019 13:46