# Overexpression of tRNA m7G modification methyltransferase complex promotes the biosynthesis of triterpene in yeast

**Authors:** Mengyu Ma, Jun Wang, Zhengwei Tan, Xiqin Liang, Bengui Fan, Lei Li, Huizhen Liang, Tianyue An, Guoli Wang

PMC · DOI: 10.3389/fmicb.2025.1557443 · Frontiers in Microbiology · 2025-03-31

## TL;DR

Overexpression of a tRNA modification complex in yeast boosts the production of valuable compounds like squalene and lupeol.

## Contribution

This study reveals that tRNA m7G modification can enhance terpenoid biosynthesis through metabolic regulation.

## Key findings

- Overexpression of Trm8/Trm82 increases squalene and lupeol production in yeast.
- Trm8/Trm82 upregulates genes in amino acid synthesis, glycolysis, and the TCA cycle.
- Enhanced glycolysis and acetyl-CoA biosynthesis contribute to increased terpenoid synthesis.

## Abstract

The sustainable production of valuable compounds using microbial cell factories is an effective approach, yet further metabolic engineering strategies are needed to enhance their biosynthetic potential. Recent studies suggest that RNA modifications can influence cellular metabolism, but their role in metabolic engineering remains largely unexplored.

The production of squalene and lupeol in different yeast strains was detected by gas chromatography-mass spectrometry (GC-MS) equipment. Transcriptomic analysis was performed to identify metabolic changes associated with the epigenetic modification. The transcriptional and translational expression of targeted genes were determined by real-time quantitative polymerase chain reaction and western blotting, respectively. The mRNA stability of targeted genes was measured by mRNA decay assay.

In this study, the overexpression of Trm8 and Trm82 complex, mediating the tRNA 7-methylguanosine (m7G) modification in yeast, significantly increased the production of squalene in CEN.PK2-1C. Transcriptome analysis indicated that Trm8/Trm82 overexpression upregulated the expression levels of genes involved in amino acid synthesis, glycolysis, and tricarboxylic acid cycle, and the enhanced glycolysis, upstream of acetyl-CoA biosynthesis, might be responsible for the promoted biosynthesis of squalene. Further investigation demonstrated that Trm8/Trm82 complex could increase the production of squalene and lupeol in engineered yeast.

These findings indicate that tRNA m7G modification can regulate central metabolism and enhance terpenoid biosynthesis. This study provides new insights into RNA modifications as a potential metabolic engineering strategy for improving the production of high-value compounds.

## Linked entities

- **Genes:** METTL1 (methyltransferase 1, tRNA methylguanosine) [NCBI Gene 4234], WDR4 (WDR4 tRNA N7-guanosine methyltransferase non-catalytic subunit) [NCBI Gene 10785]
- **Chemicals:** squalene (PubChem CID 638072), lupeol (PubChem CID 259846)

## Full-text entities

- **Genes:** TRM8 (tRNA (guanine46-N7)-methyltransferase) [NCBI Gene 851326], TRM82 (Trm82p) [NCBI Gene 851743]
- **Chemicals:** squalene (MESH:D013185), triterpene (MESH:D014315), m7G (MESH:C016578), terpenoid (MESH:D013729), lupeol (MESH:C010480), acetyl-CoA (MESH:D000105), tRNA 7-methylguanosine (-)
- **Species:** Saccharomyces cerevisiae (baker's yeast, species) [taxon 4932]

## Full text

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## Figures

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## References

46 references — full list in the complete paper: https://tomesphere.com/paper/PMC11996079/full.md

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Source: https://tomesphere.com/paper/PMC11996079