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<p>Epithelial-to-Mesenchymal Transition (EMT) is a critical biological process by which cells acquire enhanced migratory and invasive properties. A key signaling pathway involved in EMT phenotypes includes transforming growth factor β (TGFβ) and transcription factors (TFs) such as <i>SNAIL</i>, <i>ZEB</i>, and <i>TWIST</i>. Additionally, microRNAs (miRNAs) – small, non-coding molecules that regulate gene expression by targeting mRNA transcripts – directly regulate genes central to the EMT process. Notably, miR-22 has been identified as a significant regulator of EMT through direct inhibition of EMT drivers like <i>SNAI1</i> and indirect regulation of upstream genes. In this study, we performed CRISPR-based network rewiring by selectively removing an edge—the connection between two nodes—to investigate its impact on EMT dynamics. Specifically, we disrupted the connection between miR-22 and <i>SNAI1</i> without affecting other interactions involving miR-22 or <i>SNAI1</i> and examined the resulting effects on EMT. We demonstrate that the removal of the miR-22 target site from the <i>SNAI1</i> gene renders cells more sensitive to TGFβ-mediated EMT. This finding highlights the unique advantage of edge-specific perturbation by ablating the direct regulatory connection between miR-22 and <i>SNAI1</i>. We demonstrate that all measured downstream effects on EMT can be attributed to this single interaction, independent of miR-22’s influence on other targets or indirect pathways. More generally, our results underscore the importance of CRISPR-mediated edge ablation for exploring the interactions that govern biological networks and highlight an underexplored opportunity to develop edge-based therapeutic modalities.</p>

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Rewiring miR-22/SNAI1 via CRISPR-based edge editing destabilizes the epithelial phenotype

  • 期刊论文

  • 出版模式：

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  • 发表日期：

    2026年4月29日

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  • John T. Nguyen,
  • Lijia Huang,
  • Herbert Levine,
  • Mingyang Lu,
  • Leonidas Bleris

摘要

Epithelial-to-Mesenchymal Transition (EMT) is a critical biological process by which cells acquire enhanced migratory and invasive properties. A key signaling pathway involved in EMT phenotypes includes transforming growth factor β (TGFβ) and transcription factors (TFs) such as SNAIL, ZEB, and TWIST. Additionally, microRNAs (miRNAs) – small, non-coding molecules that regulate gene expression by targeting mRNA transcripts – directly regulate genes central to the EMT process. Notably, miR-22 has been identified as a significant regulator of EMT through direct inhibition of EMT drivers like SNAI1 and indirect regulation of upstream genes. In this study, we performed CRISPR-based network rewiring by selectively removing an edge—the connection between two nodes—to investigate its impact on EMT dynamics. Specifically, we disrupted the connection between miR-22 and SNAI1 without affecting other interactions involving miR-22 or SNAI1 and examined the resulting effects on EMT. We demonstrate that the removal of the miR-22 target site from the SNAI1 gene renders cells more sensitive to TGFβ-mediated EMT. This finding highlights the unique advantage of edge-specific perturbation by ablating the direct regulatory connection between miR-22 and SNAI1. We demonstrate that all measured downstream effects on EMT can be attributed to this single interaction, independent of miR-22’s influence on other targets or indirect pathways. More generally, our results underscore the importance of CRISPR-mediated edge ablation for exploring the interactions that govern biological networks and highlight an underexplored opportunity to develop edge-based therapeutic modalities.