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The PECAn image and statistical analysis pipeline identifies Minute cell competition genes and features

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  • Michael E. Baumgartner

    (University Walk
    University of Pennsylvania)

  • Paul F. Langton

    (University Walk)

  • Remi Logeay

    (University Walk)

  • Alex Mastrogiannopoulos

    (University Walk)

  • Anna Nilsson-Takeuchi

    (University Walk
    University of Southampton)

  • Iwo Kucinski

    (University of Cambridge
    University of Cambridge)

  • Jules Lavalou

    (University Walk)

  • Eugenia Piddini

    (University Walk)

Abstract

Investigating organ biology often requires methodologies to induce genetically distinct clones within a living tissue. However, the 3D nature of clones makes sample image analysis challenging and slow, limiting the amount of information that can be extracted manually. Here we develop PECAn, a pipeline for image processing and statistical data analysis of complex multi-genotype 3D images. PECAn includes data handling, machine-learning-enabled segmentation, multivariant statistical analysis, and graph generation. This enables researchers to perform rigorous analyses rapidly and at scale, without requiring programming skills. We demonstrate the power of this pipeline by applying it to the study of Minute cell competition. We find an unappreciated sexual dimorphism in Minute cell growth in competing wing discs and identify, by statistical regression analysis, tissue parameters that model and correlate with competitive death. Furthermore, using PECAn, we identify several genes with a role in cell competition by conducting an RNAi-based screen.

Suggested Citation

  • Michael E. Baumgartner & Paul F. Langton & Remi Logeay & Alex Mastrogiannopoulos & Anna Nilsson-Takeuchi & Iwo Kucinski & Jules Lavalou & Eugenia Piddini, 2023. "The PECAn image and statistical analysis pipeline identifies Minute cell competition genes and features," Nature Communications, Nature, vol. 14(1), pages 1-16, December.
  • Handle: RePEc:nat:natcom:v:14:y:2023:i:1:d:10.1038_s41467-023-38287-x
    DOI: 10.1038/s41467-023-38287-x
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    References listed on IDEAS

    as
    1. Agnes R. Banreti & Pascal Meier, 2020. "The NMDA receptor regulates competition of epithelial cells in the Drosophila wing," Nature Communications, Nature, vol. 11(1), pages 1-14, December.
    2. Iwo Kucinski & Michael Dinan & Golnar Kolahgar & Eugenia Piddini, 2017. "Chronic activation of JNK JAK/STAT and oxidative stress signalling causes the loser cell status," Nature Communications, Nature, vol. 8(1), pages 1-13, December.
    3. Vivek K. Dwivedi & Carlos Pardo-Pastor & Rita Droste & Ji Na Kong & Nolan Tucker & Daniel P. Denning & Jody Rosenblatt & H. Robert Horvitz, 2021. "Replication stress promotes cell elimination by extrusion," Nature, Nature, vol. 593(7860), pages 591-596, May.
    4. Nadja S. Katheder & Rojyar Khezri & Fergal O’Farrell & Sebastian W. Schultz & Ashish Jain & Mohammed M. Rahman & Kay O. Schink & Theodossis A. Theodossiou & Terje Johansen & Gábor Juhász & David Bilde, 2017. "Microenvironmental autophagy promotes tumour growth," Nature, Nature, vol. 541(7637), pages 417-420, January.
    5. Eduardo Moreno & Konrad Basler & Ginés Morata, 2002. "Cells compete for Decapentaplegic survival factor to prevent apoptosis in Drosophila wing development," Nature, Nature, vol. 416(6882), pages 755-759, April.
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