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Analyzing Gene Expression from Marine Microbial Communities using Environmental Transcriptomics
Published on: February 18, 2009
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Comparative transcriptomics of two environmentally relevant cyanobacteria reveals unexpected transcriptome diversity.
Karsten Voigt1, Cynthia M Sharma2, Jan Mitschke1
1Faculty of Biology, University of Freiburg, Freiburg, Germany.
The ISME Journal
|April 18, 2014
Summary
Marine cyanobacteria Prochlorococcus exhibit extensive antisense transcription, with over 75% of genes transcribed from both strands. This reveals significant gene expression complexity in these abundant ocean microbes.
Area of Science:
- Marine microbiology
- Genomics
- Transcriptomics
Background:
- Prochlorococcus are abundant, ecologically vital marine cyanobacteria.
- Two strains, adapted to high- and low-light, represent major ecotypes.
- Their transcriptomes show adaptations to specific environmental constraints.
Purpose of the Study:
- Compare transcriptome structure and composition of two Prochlorococcus strains.
- Map genome-wide transcriptional start sites (TSS) for both strains.
- Investigate gene expression complexity and regulation.
Main Methods:
- Genome-wide mapping of transcriptional start sites (TSS).
- Comparative analysis of transcriptome data between two Prochlorococcus strains (MED4 and MIT9313).
- Analysis of 5' untranslated regions and translation initiation mechanisms.
Main Results:
- Antisense transcription observed for ~75% of genes, exceeding other bacteria.
- Hundreds of TSS found within genes, including prochlorosin genes.
- Very little conservation in TSS location and non-coding transcripts between strains.
- Extremely short 5' untranslated regions detected (median 27-29 nt).
- Leaderless and S1-dependent translation suggested as initiation mechanisms.
Conclusions:
- Genome-wide antisense transcription is a major feature of Prochlorococcus.
- Significant complexity and variability in transcriptional architecture exist.
- These findings challenge traditional views of bacterial gene expression.
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