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Identification of diversity-generating retroelements in human microbiomes
1Division of Computer Science, School of Informatics and Computing, Indiana University, Bloomington, IN 47405, USA. yye@indiana.edu.
International Journal of Molecular Sciences
|September 9, 2014
Summary
Diversity-generating retroelements (DGRs) accelerate host evolution via error-prone reverse transcription. This study identified 271 new DGR systems in the human microbiome, doubling known DGRs and revealing new target genes.
Area of Science:
- Microbiology
- Genomics
- Evolutionary Biology
Background:
- Diversity-generating retroelements (DGRs) enhance host evolution through a specialized reverse transcription process.
- DGRs, first found in Bordetella phage, are predicted in diverse viral and bacterial species.
- A minimal DGR system includes RTase, template (TR), and variable region (VR) genes.
Purpose of the Study:
- To develop a computational tool (DGRscan) for identifying DGR systems.
- To survey DGR systems within the human microbiome.
- To identify novel DGR-associated target genes.
Main Methods:
- Developed DGRscan for de novo and similarity-based DGR identification.
- Applied DGRscan to Human Microbiome Project (HMP) datasets.
- Analyzed identified DGR systems and their putative target genes.
Main Results:
- Identified 271 non-redundant DGR systems in the human microbiome, doubling the known count.
- Discovered 651 putative target genes potentially diversified by DGRs.
- Found DGRs are frequent in human-associated bacteria but rare in individual genomes.
Conclusions:
- DGRscan is effective for discovering DGR systems in large datasets.
- The human microbiome harbors a significant, previously uncharacterized DGR repertoire.
- This study provides functional insights into numerous unannotated genes involved in DGR systems.
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