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Simultaneous Mapping and Quantitation of Ribonucleotides in Human Mitochondrial DNA
Published on: November 14, 2017
mtR_find: A Parallel Processing Tool to Identify and Annotate RNAs Derived from the Mitochondrial Genome
Asan M S H Mohideen1, Steinar D Johansen1, Igor Babiak1
1Genomics Group, Faculty of Biosciences and Aquaculture, Nord University, P.O. Box 1490, 8049 Bodø, Norway.
We developed mtR_find, a tool to identify mitochondrial RNAs, including small RNAs (mt-sRNAs) and long non-coding RNAs (mt-lncRNAs). This tool aids in discovering novel RNA biomarkers associated with diseases like cancer and obesity.
Area of Science:
- Genomics
- Molecular Biology
- Bioinformatics
Background:
- Mitochondrial RNAs are prevalent in sequencing data, but their unique features pose challenges for analysis.
- Existing tools struggle to accurately identify and annotate mitochondrial small RNAs (mt-sRNAs) and long non-coding RNAs (mt-lncRNAs).
Purpose of the Study:
- To develop a novel computational tool, mtR_find, for the detection and annotation of mitochondrial RNAs.
- To establish a standardized nomenclature for accurate annotation of mt-sRNAs.
- To explore the potential of mt-ncRNAs as diagnostic or prognostic markers.
Main Methods:
- Developed mtR_find, a tool utilizing a novel method for counting RNA sequences from adapter-trimmed reads.
- Applied mtR_find to analyze existing transcriptomic datasets.
- Benchmarked mtR_find using simulated datasets for validation.
Main Results:
- Identified mt-sRNAs significantly associated with hepatocellular carcinoma and obesity.
- Discovered novel mt-sRNAs and mt-lncRNAs in mouse early development.
- Demonstrated the tool's ability to extract novel biological insights from existing data.
Conclusions:
- mtR_find provides unprecedented resolution and simplicity for analyzing mt-ncRNA transcriptomes.
- The tool facilitates re-analysis of transcriptomic databases, uncovering disease-associated RNAs.
- mt-ncRNAs show promise as potential diagnostic or prognostic markers in medicine.
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