Skip to main content
bioRxiv
  • Home
  • About
  • Submit
  • ALERTS / RSS
Advanced Search
New Results

Using a Whole Genome Co-expression Network to Inform the Functional Characterisation of Predicted Genomic Elements from Mycobacterium tuberculosis Transcriptomic Data

View ORCID ProfileJennifer Stiens, Yen Yi Tan, Rosanna Joyce, View ORCID ProfileKristine B. Arnvig, View ORCID ProfileSharon L. Kendall, View ORCID ProfileIrene Nobeli
doi: https://doi.org/10.1101/2022.06.22.497203
Jennifer Stiens
1Institute of Structural and Molecular Biology, Biological Sciences, Birkbeck, University of London, London, UK
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
  • ORCID record for Jennifer Stiens
Yen Yi Tan
1Institute of Structural and Molecular Biology, Biological Sciences, Birkbeck, University of London, London, UK
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
Rosanna Joyce
1Institute of Structural and Molecular Biology, Biological Sciences, Birkbeck, University of London, London, UK
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
Kristine B. Arnvig
2Institute of Structural and Molecular Biology, Division of Biosciences, University College London, London, UK
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
  • ORCID record for Kristine B. Arnvig
Sharon L. Kendall
3Centre for Emerging, Endemic and Exotic Diseases, Pathobiology and Population Sciences, Royal Veterinary College, Hatfield, UK
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
  • ORCID record for Sharon L. Kendall
Irene Nobeli
1Institute of Structural and Molecular Biology, Biological Sciences, Birkbeck, University of London, London, UK
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
  • ORCID record for Irene Nobeli
  • For correspondence: i.nobeli@bbk.ac.uk
  • Abstract
  • Full Text
  • Info/History
  • Metrics
  • Supplementary material
  • Data/Code
  • Preview PDF
Loading

ABSTRACT

A whole genome co-expression network was created using Mycobacterium tuberculosis transcriptomic data from publicly available RNA-sequencing experiments covering a wide variety of experimental conditions. The network includes expressed regions with no formal annotation, including putative short RNAs and untranslated regions of expressed transcripts, along with the protein-coding genes. These unannotated expressed transcripts were among the best-connected members of the module sub-networks, making up more than half of the ‘hub’ elements in modules that include protein-coding genes known to be part of regulatory systems involved in stress response and host adaptation. This dataset provides a valuable resource for investigating the role of non-coding RNA, and conserved hypothetical proteins, in transcriptomic remodelling. Based on their connections to genes with known functional groupings and correlations with replicated host conditions, predicted expressed transcripts can be screened as suitable candidates for further experimental validation.

Competing Interest Statement

The authors have declared no competing interest.

Footnotes

  • updated supplemental table 2

  • https://doi.org/10.5281/zenodo.7319853

  • Abbreviations

    CDS
    coding sequence
    ME
    module eigengene
    MM
    module membership
    Mtb
    Mycobacterium tuberculosis
    MTBC
    Mycobacterium tuberculosis complex
    ncRNA
    non-coding RNA
    ORF
    open reading frame
    RNA-seq
    RNA sequencing
    RNAP
    RNA polymerase
    sORF
    short open reading frame
    sRNA
    short non-coding RNA
    TSS
    transcription start site
    TTS
    transcription termination site
    UTR
    untranslated region
    WGCNA
    weighted gene co-expression analysis
  • Copyright 
    The copyright holder for this preprint is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under a CC-BY-NC-ND 4.0 International license.
    Back to top
    PreviousNext
    Posted November 18, 2022.
    Download PDF

    Supplementary Material

    Data/Code
    Email

    Thank you for your interest in spreading the word about bioRxiv.

    NOTE: Your email address is requested solely to identify you as the sender of this article.

    Enter multiple addresses on separate lines or separate them with commas.
    Using a Whole Genome Co-expression Network to Inform the Functional Characterisation of Predicted Genomic Elements from Mycobacterium tuberculosis Transcriptomic Data
    (Your Name) has forwarded a page to you from bioRxiv
    (Your Name) thought you would like to see this page from the bioRxiv website.
    CAPTCHA
    This question is for testing whether or not you are a human visitor and to prevent automated spam submissions.
    Share
    Using a Whole Genome Co-expression Network to Inform the Functional Characterisation of Predicted Genomic Elements from Mycobacterium tuberculosis Transcriptomic Data
    Jennifer Stiens, Yen Yi Tan, Rosanna Joyce, Kristine B. Arnvig, Sharon L. Kendall, Irene Nobeli
    bioRxiv 2022.06.22.497203; doi: https://doi.org/10.1101/2022.06.22.497203
    Reddit logo Twitter logo Facebook logo LinkedIn logo Mendeley logo
    Citation Tools
    Using a Whole Genome Co-expression Network to Inform the Functional Characterisation of Predicted Genomic Elements from Mycobacterium tuberculosis Transcriptomic Data
    Jennifer Stiens, Yen Yi Tan, Rosanna Joyce, Kristine B. Arnvig, Sharon L. Kendall, Irene Nobeli
    bioRxiv 2022.06.22.497203; doi: https://doi.org/10.1101/2022.06.22.497203

    Citation Manager Formats

    • BibTeX
    • Bookends
    • EasyBib
    • EndNote (tagged)
    • EndNote 8 (xml)
    • Medlars
    • Mendeley
    • Papers
    • RefWorks Tagged
    • Ref Manager
    • RIS
    • Zotero
    • Tweet Widget
    • Facebook Like
    • Google Plus One

    Subject Area

    • Bioinformatics
    Subject Areas
    All Articles
    • Animal Behavior and Cognition (4682)
    • Biochemistry (10357)
    • Bioengineering (7670)
    • Bioinformatics (26330)
    • Biophysics (13523)
    • Cancer Biology (10683)
    • Cell Biology (15438)
    • Clinical Trials (138)
    • Developmental Biology (8497)
    • Ecology (12820)
    • Epidemiology (2067)
    • Evolutionary Biology (16851)
    • Genetics (11399)
    • Genomics (15478)
    • Immunology (10616)
    • Microbiology (25207)
    • Molecular Biology (10220)
    • Neuroscience (54463)
    • Paleontology (401)
    • Pathology (1668)
    • Pharmacology and Toxicology (2897)
    • Physiology (4342)
    • Plant Biology (9243)
    • Scientific Communication and Education (1586)
    • Synthetic Biology (2557)
    • Systems Biology (6780)
    • Zoology (1466)