dFlpTag, a RMCE-based tool for simultaneous endogenous protein tagging and cell labeling in Drosophila

Conditional protein tagging is a potent technique for elucidating protein expression patterns. The existing MiMIC and CRIMIC insertion collections in Drosophila genome offer a foundation for rapidly generating conditional protein tagging strains. In this study, we introduce dFlpTag, a new tool designed to create both constitutive and conditional protein tagging strains from MiMic or CRIMIC insertions. Moreover, dFlpTag enables co-labeling of the source cells of the protein of interest in a cell type-specific or sparse fashion. To demonstrate its utility, we generated strains for tagging the pre-synaptic protein Brp, the post-synaptic and polarity protein Dlg1, and the transmembrane protein Dpr12, thereby revealing their expression across multiple or a specific neuropil in the Drosophila central nervous system, individual synaptic boutons at the neuromuscular junction, and in large and small patches of epithelial cells within larval wing discs. We advocate for the straightforward application of this tool to tag thousands of genes that already possess MiMic or CRIMIC insertions within a coding intron.

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Publication Details

Journal
Scientific Reports
Published
2025-11-27
DOI
https://doi.org/10.1038/s41598-025-30193-0
Primary Topic
Neurobiology and Insect Physiology Research
Type
article
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article

dFlpTag, a RMCE-based tool for simultaneous endogenous protein tagging and cell labeling in Drosophila

Miranda C. Dyson, Yina Ruan, Jiekun Yan, Sha Liu et al.
Scientific Reports
Neurobiology and Insect Physiology Research
article

dFlpTag, a RMCE-based tool for simultaneous endogenous protein tagging and cell labeling in Drosophila

Miranda C. Dyson, Yina Ruan, Jiekun Yan, Sha Liu, Xiaojun Xie, Ling Li, Fran Laenen
article en

Abstract

Conditional protein tagging is a potent technique for elucidating protein expression patterns. The existing MiMIC and CRIMIC insertion collections in Drosophila genome offer a foundation for rapidly generating conditional protein tagging strains. In this study, we introduce dFlpTag, a new tool designed to create both constitutive and conditional protein tagging strains from MiMic or CRIMIC insertions. Moreover, dFlpTag enables co-labeling of the source cells of the protein of interest in a cell type-specific or sparse fashion. To demonstrate its utility, we generated strains for tagging the pre-synaptic protein Brp, the post-synaptic and polarity protein Dlg1, and the transmembrane protein Dpr12, thereby revealing their expression across multiple or a specific neuropil in the Drosophila central nervous system, individual synaptic boutons at the neuromuscular junction, and in large and small patches of epithelial cells within larval wing discs. We advocate for the straightforward application of this tool to tag thousands of genes that already possess MiMic or CRIMIC insertions within a coding intron.

Scientific ReportsVol. 15(1)
Children's Hospital of Zhejiang University (CN), VIB-KU Leuven Center for Brain & Disease Research (BE), KU Leuven (BE)
Openalex Percentile: Top 60%
Neurobiology and Insect Physiology Research
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