Matrix regulation: a plug-and-tune method for combinatorial regulation in Saccharomyces cerevisiae

Transcriptional fine-tuning of long pathways is complex, even in the extensively applied cell factory Saccharomyces cerevisiae. Here, we present Matrix Regulation (MR), a CRISPR-mediated pathway fine-tuning method enabling the construction of 6<sup>8</sup> gRNA combinations and screening for the optimal expression levels across up to eight genes. We first identify multiple tRNAs with efficient gRNA processing capacities to assemble a gRNA regulatory matrix combinatorially. Then, we expand the target recognition of CRISPR regulation from NGG PAM to NG PAM by characterizing dCas9 variants. To increase the dynamic range of modulation, we test 101 candidate activation domains followed by mutagenesis and screening the best one to further enhance its activation capability in S. cerevisiae by 3-fold. The regulations generate combinatorial strain libraries for both the mevalonate pathway and the heme biosynthesis pathway and increase squalene production by 37-fold and heme by 17-fold, respectively, demonstrating the versatility of our method and its applicability in fundamental research.

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Publication Details

Journal
Nature Communications
Published
2025-08-15
DOI
https://doi.org/10.1038/s41467-025-62886-5
Citations
2
Primary Topic
CRISPR and Genetic Engineering
Type
article
Field-Weighted Citation Impact
1.61

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Matrix regulation: a plug-and-tune method for combinatorial regulation in Saccharomyces cerevisiae

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article

Matrix regulation: a plug-and-tune method for combinatorial regulation in Saccharomyces cerevisiae

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article en
2 citations

Abstract

Transcriptional fine-tuning of long pathways is complex, even in the extensively applied cell factory Saccharomyces cerevisiae. Here, we present Matrix Regulation (MR), a CRISPR-mediated pathway fine-tuning method enabling the construction of 6<sup>8</sup> gRNA combinations and screening for the optimal expression levels across up to eight genes. We first identify multiple tRNAs with efficient gRNA processing capacities to assemble a gRNA regulatory matrix combinatorially. Then, we expand the target recognition of CRISPR regulation from NGG PAM to NG PAM by characterizing dCas9 variants. To increase the dynamic range of modulation, we test 101 candidate activation domains followed by mutagenesis and screening the best one to further enhance its activation capability in S. cerevisiae by 3-fold. The regulations generate combinatorial strain libraries for both the mevalonate pathway and the heme biosynthesis pathway and increase squalene production by 37-fold and heme by 17-fold, respectively, demonstrating the versatility of our method and its applicability in fundamental research.

Nature CommunicationsVol. 16(1)
BioInnovation Institute (DK), China Agricultural University (CN), Chalmers University of Technology (SE), Beijing University of Chemical Technology (CN)
National Natural Science Foundation of China, Novo Nordisk, Novo Nordisk Fonden, Fundamental Research Funds for the Central Universities
Openalex Percentile: Top 15%
CRISPR and Genetic Engineering
1.61
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