Resistance Gene-Guided Genome Mining Reveals RPL10 as the Target of Ligustrone A

The ribosome is essential for protein synthesis and targeting its function serves as a platform for many therapies. Resistance gene-guided genome mining for <i>a priori</i> target identification has emerged as a useful workflow in natural product drug discovery, allowing for identification of a compound's target before the time-consuming work of isolation and characterization is performed. In this work, we identify the previously unknown <i>lig</i> biosynthetic gene cluster (BGC) which contains a predicted resistance gene that shares sequence identity with the gene for human ribosomal protein RPL10. Through both heterologous expression and <i>in situ</i> BGC engineering, we identify ligustrone A (<b>1</b>) as this BGC's product. Utilizing chemical genetics and chemoproteomics, we validate that <b>1</b> engages RPL10. Taken together, via resistance gene-guided mining we both discover a new target for a known natural product and elucidate its biosynthesis.

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Publication Details

Journal
Journal of the American Chemical Society
Published
2025-06-16
DOI
https://doi.org/10.1021/jacs.5c03802
Citations
1
Primary Topic
Natural product bioactivities and synthesis
Type
article
Field-Weighted Citation Impact
0.81
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article

Resistance Gene-Guided Genome Mining Reveals RPL10 as the Target of Ligustrone A

Sheena C. Li, Joseph E. Spraker, Henry H. Le, Lawrence Hon et al.
1 citations
Journal of the American Chemical Society
Natural product bioactivities and synthesis
0.81
article

Resistance Gene-Guided Genome Mining Reveals RPL10 as the Target of Ligustrone A

Sheena C. Li, Joseph E. Spraker, Henry H. Le, Lawrence Hon, Cynthia Bailey, Colin J. B. Harvey, Danielle A. Yee, Michelle F. Grau, Bruno Perlatti, Samuel K. Oteng-Pabi, Ross D. Overacker, Clarence Hue Lok Yeung, Daniel Mummau, Amber Cornelius, Thomas Pavey, Adrianne Pigula
article en
1 citations

Abstract

The ribosome is essential for protein synthesis and targeting its function serves as a platform for many therapies. Resistance gene-guided genome mining for <i>a priori</i> target identification has emerged as a useful workflow in natural product drug discovery, allowing for identification of a compound's target before the time-consuming work of isolation and characterization is performed. In this work, we identify the previously unknown <i>lig</i> biosynthetic gene cluster (BGC) which contains a predicted resistance gene that shares sequence identity with the gene for human ribosomal protein RPL10. Through both heterologous expression and <i>in situ</i> BGC engineering, we identify ligustrone A (<b>1</b>) as this BGC's product. Utilizing chemical genetics and chemoproteomics, we validate that <b>1</b> engages RPL10. Taken together, via resistance gene-guided mining we both discover a new target for a known natural product and elucidate its biosynthesis.

Journal of the American Chemical SocietyVol. 147(25)
Menlo School (US), Hexagon (United States) (US), Hexagon (United Kingdom) (GB)
Zero hunger
Openalex Percentile: Top 27%
Natural product bioactivities and synthesis
0.81
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Resistance Gene-Guided Genome Mining Reveals RPL10 as the Target of Ligustrone A — Sheena C. Li, Joseph E. Spraker, et al. · Journal of the American Chemical Society (2025) | TGRS Research Map | TGRS