WormTagDB: A Systematic Survey of Endogenously Tagged Proteins in C. elegans and Roadmap Towards the Tagged Proteome

Endogenous protein tagging in Caenorhabditis elegans enables direct visualization and manipulation of proteins in vivo, providing native readouts of expression, localization, and dynamics. No coordinated effort currently exists to comprehensively tag proteins on a large scale, resulting in patchy coverage that limits comprehensive proteome analyses. We systematically reviewed 2,500 primary research articles, identifying 778 that report novel endogenous tags, and integrated these with the Caenorhabditis Genetics Center strain records to catalog >90% of all existing tagged alleles. In total, we found that 1,554 unique genes (~8% of the proteome) have been endogenously tagged. Gene Ontology enrichment analysis revealed that cytoskeletal proteins, transcription factors, and RNA-binding proteins dominate the tagged proteome, while membrane proteins, metabolic enzymes, and mitochondrial components remain largely untagged, reflecting both technical barriers and research priorities that have shaped the last decade of tagging efforts. We created WormTagDB (https://wormtagdb.rc.duke.edu), an interactive, community-updatable resource that consolidates all known endogenously tagged alleles and provides precomputed CRISPR guide and homology-arm primer designs for N- and C-terminal knock-ins across all protein-coding genes. This will enable researchers to easily identify existing alleles to prevent redundant strain generation and rapidly initiate new knock-in experiments. A systematic effort to tag every C. elegans gene would deliver the first complete metazoan visual proteome, providing comprehensive insights into protein localization, dynamics, and regulation, revealing new protein associations and molecular processes.

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Publication Details

Journal
bioRxiv (Cold Spring Harbor Laboratory)
Published
2025-12-05
DOI
https://doi.org/10.64898/2025.12.02.691955
Citations
4
Primary Topic
Genetics, Aging, and Longevity in Model Organisms
Type
article
Field-Weighted Citation Impact
3.81
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article

WormTagDB: A Systematic Survey of Endogenously Tagged Proteins in C. elegans and Roadmap Towards the Tagged Proteome

David R. Sherwood, Jake Leyhr, Qiuyi Chi, Lingling Zeng et al.
4 citations
bioRxiv (Cold Spring Harbor Laboratory)
Genetics, Aging, and Longevity in Model Organisms
3.81
article

WormTagDB: A Systematic Survey of Endogenously Tagged Proteins in C. elegans and Roadmap Towards the Tagged Proteome

David R. Sherwood, Jake Leyhr, Qiuyi Chi, Lingling Zeng, En-Zhi Shen, Wei Zou
article en
4 citations

Abstract

Endogenous protein tagging in Caenorhabditis elegans enables direct visualization and manipulation of proteins in vivo, providing native readouts of expression, localization, and dynamics. No coordinated effort currently exists to comprehensively tag proteins on a large scale, resulting in patchy coverage that limits comprehensive proteome analyses. We systematically reviewed 2,500 primary research articles, identifying 778 that report novel endogenous tags, and integrated these with the Caenorhabditis Genetics Center strain records to catalog >90% of all existing tagged alleles. In total, we found that 1,554 unique genes (~8% of the proteome) have been endogenously tagged. Gene Ontology enrichment analysis revealed that cytoskeletal proteins, transcription factors, and RNA-binding proteins dominate the tagged proteome, while membrane proteins, metabolic enzymes, and mitochondrial components remain largely untagged, reflecting both technical barriers and research priorities that have shaped the last decade of tagging efforts. We created WormTagDB (https://wormtagdb.rc.duke.edu), an interactive, community-updatable resource that consolidates all known endogenously tagged alleles and provides precomputed CRISPR guide and homology-arm primer designs for N- and C-terminal knock-ins across all protein-coding genes. This will enable researchers to easily identify existing alleles to prevent redundant strain generation and rapidly initiate new knock-in experiments. A systematic effort to tag every C. elegans gene would deliver the first complete metazoan visual proteome, providing comprehensive insights into protein localization, dynamics, and regulation, revealing new protein associations and molecular processes.

bioRxiv (Cold Spring Harbor Laboratory)
Duke University (US), Westlake University (CN), Duke Energy (United States) (US), Zhejiang University (CN)
Openalex Percentile: Top 6%
Genetics, Aging, and Longevity in Model Organisms
3.81
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