Regulation of the branched-chain amino acid pathway and its crosstalk to carbon metabolism in yeast

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This study profiled protein and metabolite dynamics during yeast diauxic shift, finding the leucine-committed BCAA branch shows a fermentative signature and that dysregulation disrupts carbon metabolism.

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AI-generated deep summary by claude@2026-07, 2026-07-15 · read from full text

The study examined how the branched-chain amino acid (BCAA) pathway is regulated during the diauxic shift in Saccharomyces cerevisiae, a transition governed by TORC1 from rapid fermentation to respiration. Using a GFP-tagged BCAA pathway strain library, high-throughput flow cytometry, and untargeted LC-MS metabolomics integrated with a thermodynamically curated genome-scale model, the authors profiled protein and metabolite dynamics in wild-type and mutants affecting non-essential BCAA biosynthesis genes. They found the BCAA pathway functioned in two branches, with only the leucine-committed branch showing a fermentative signature consistent with TORC1 activity, and they identified regulatory elements where BCAA dysregulation disrupted distant central carbon metabolic circuits. A key limitation is that the work is entirely in yeast with model-based integration rather than direct measurement in human or disease tissue. The paper does not explicitly discuss endometriosis or adenomyosis; it was included in the corpus via a keyword match in the upstream search index.

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Abstract

ABSTRACT In Saccharomyces cerevisiae, the TORC1 pathway regulates the transition from rapid fermentative growth to respiration during the diauxic shift, by tightly coordinating energy- and biomass-producing pathways. Although leucine and other components of the branched-chain amino acid (BCAA) pathway are known TORC1 regulators, how the BCAA pathway is controlled across this transition and influences the crosstalk between central carbon and amino acid metabolism remains unclear. By integrating high-throughput flow cytometry and untargeted LC-MS metabolomics into a thermodynamically curated genome-scale model, we profiled protein levels, metabolite dynamics, and cellular context during the diauxic shift of a GFP-tagged strain library of the BCAA pathway in wild-type and mutants lacking non-essential genes for BCAA biosynthesis. This analysis revealed that the BCAA pathway operates in two branches, with only the leucine-committed branch exhibiting a fermentative signature aligned with TORC1 activity. We further identified key regulatory elements and showed that dysregulation of the BCAA pathway disrupts distant metabolic circuits, including central carbon metabolism. Our findings highlight the dynamic role of the BCAA pathway in metabolic network integration during the diauxic shift.
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ABSTRACT In Saccharomyces cerevisiae, the TORC1 pathway regulates the transition from rapid fermentative growth to respiration during the diauxic shift, by tightly coordinating energy- and biomass-producing pathways. Although leucine and other components of the branched-chain amino acid (BCAA) pathway are known TORC1 regulators, how the BCAA pathway is controlled across this transition and influences the crosstalk between central carbon and amino acid metabolism remains unclear. By integrating high-throughput flow cytometry and untargeted LC-MS metabolomics into a thermodynamically curated genome-scale model, we profiled protein levels, metabolite dynamics, and cellular context during the diauxic shift of a GFP-tagged strain library of the BCAA pathway in wild-type and mutants lacking non-essential genes for BCAA biosynthesis. This analysis revealed that the BCAA pathway operates in two branches, with only the leucine-committed branch exhibiting a fermentative signature aligned with TORC1 activity. We further identified key regulatory elements and showed that dysregulation of the BCAA pathway disrupts distant metabolic circuits, including central carbon metabolism. Our findings highlight the dynamic role of the BCAA pathway in metabolic network integration during the diauxic shift.

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europepmc
last seen: 2026-05-20T01:45:00.602351+00:00
unpaywall
last seen: 2026-05-26T02:00:01.498150+00:00
License: Public-Domain