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Single-cell microRNA-mRNA co-sequencing reveals non-genetic heterogeneity and mechanisms of microRNA regulation

Author

Listed:
  • Nayi Wang

    (Yale University
    Yale University School of Medicine
    Yale Cancer Center)

  • Ji Zheng

    (Yale University School of Medicine
    Yale Cancer Center
    Third Military Medical University)

  • Zhuo Chen

    (Yale University
    Yale University School of Medicine
    Yale Cancer Center)

  • Yang Liu

    (Yale University School of Medicine
    Yale Cancer Center)

  • Burak Dura

    (Yale University)

  • Minsuk Kwak

    (Yale University)

  • Juliana Xavier-Ferrucio

    (Yale Cancer Center
    Yale University School of Medicine)

  • Yi-Chien Lu

    (Yale Cancer Center
    Yale University School of Medicine)

  • Miaomiao Zhang

    (Yale University School of Medicine
    Third Military Medical University
    Jiangsu University)

  • Christine Roden

    (Yale University School of Medicine
    Yale Cancer Center)

  • Jijun Cheng

    (Yale University School of Medicine
    Yale Cancer Center)

  • Diane S. Krause

    (Yale Cancer Center
    Yale University School of Medicine)

  • Ye Ding

    (New York State Department of Health)

  • Rong Fan

    (Yale University
    Yale Cancer Center)

  • Jun Lu

    (Yale University School of Medicine
    Yale Cancer Center
    Yale Center for RNA Science and Medicine
    Yale Cooperative Center of Excellence in Hematology)

Abstract

Measuring multiple omics profiles from the same single cell opens up the opportunity to decode molecular regulation that underlies intercellular heterogeneity in development and disease. Here, we present co-sequencing of microRNAs and mRNAs in the same single cell using a half-cell genomics approach. This method demonstrates good robustness (~95% success rate) and reproducibility (R2 = 0.93 for both microRNAs and mRNAs), yielding paired half-cell microRNA and mRNA profiles, which we can independently validate. By linking the level of microRNAs to the expression of predicted target mRNAs across 19 single cells that are phenotypically identical, we observe that the predicted targets are significantly anti-correlated with the variation of abundantly expressed microRNAs. This suggests that microRNA expression variability alone may lead to non-genetic cell-to-cell heterogeneity. Genome-scale analysis of paired microRNA-mRNA co-profiles further allows us to derive and validate regulatory relationships of cellular pathways controlling microRNA expression and intercellular variability.

Suggested Citation

  • Nayi Wang & Ji Zheng & Zhuo Chen & Yang Liu & Burak Dura & Minsuk Kwak & Juliana Xavier-Ferrucio & Yi-Chien Lu & Miaomiao Zhang & Christine Roden & Jijun Cheng & Diane S. Krause & Ye Ding & Rong Fan &, 2019. "Single-cell microRNA-mRNA co-sequencing reveals non-genetic heterogeneity and mechanisms of microRNA regulation," Nature Communications, Nature, vol. 10(1), pages 1-12, December.
  • Handle: RePEc:nat:natcom:v:10:y:2019:i:1:d:10.1038_s41467-018-07981-6
    DOI: 10.1038/s41467-018-07981-6
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    Cited by:

    1. Hotaka Kobayashi & Robert H. Singer, 2022. "Single-molecule imaging of microRNA-mediated gene silencing in cells," Nature Communications, Nature, vol. 13(1), pages 1-14, December.

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