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bioRxiv · 10.1101/2021.01.06.425657

The SCFMet30 ubiquitin ligase senses cellular redox state to regulate the transcription of sulfur metabolism genes

Johnson, Z.·Wang, Y.·Sutter, B. M.·Tu, B. P.
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Abstract

In yeast, control of sulfur amino acid metabolism relies upon Met4, a transcription factor which activates the expression of a network of enzymes responsible for the biosynthesis of cysteine and methionine. In times of sulfur abundance, the activity of Met4 is repressed via ubiquitination by the SCFMet30 E3 ubiquitin ligase, but the mechanism by which the F-box protein Met30 senses sulfur status to tune its E3 ligase activity remains unresolved. Herein, we show that Met30 responds to flux through the transsulfuration pathway to regulate the MET gene transcriptional program. In particular, Met30 is responsive to the biological gas hydrogen sulfide, which is sufficient to induce ubiquitination of Met4 in vivo. Additionally, we identify important cysteine residues in Met30s WD-40 repeat region that sense the availability of sulfur in the cell. Our findings reveal how SCFMet30 dynamically senses the flow of sulfur metabolites through the transsulfuration pathway to regulate synthesis of these special amino acids.

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Johnson, Z., Wang, Y., Sutter, B. M., Tu, B. P.. 2021-01-07. The SCFMet30 ubiquitin ligase senses cellular redox state to regulate the transcription of sulfur metabolism genes. https://doi.org/10.1101/2021.01.06.425657

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