Department of Biochemistry, University of Texas Southwestern Medical Center, Dallas, TX 75390-9038, USA.
Genetics. 2024 Nov 6;228(3). doi: 10.1093/genetics/iyae154.
In yeast, control of sulfur amino acid metabolism relies upon Met4, a transcription factor that 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 trans-sulfuration 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 Met30's 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 trans-sulfuration pathway to regulate the synthesis of these special amino acids.
在酵母中,硫氨基酸代谢的控制依赖于 Met4,这是一种转录因子,它激活了一组负责半胱氨酸和蛋氨酸生物合成的酶的表达。在硫充足的情况下,Met4 的活性通过 SCFMet30 E3 泛素连接酶的泛素化受到抑制,但 F-box 蛋白 Met30 如何感知硫状态以调节其 E3 连接酶活性的机制仍未解决。在此,我们表明 Met30 响应转硫途径中的通量来调节 MET 基因转录程序。具体来说,Met30 对生物气体硫化氢有反应,硫化氢足以在体内诱导 Met4 的泛素化。此外,我们确定了 Met30 的 WD-40 重复区域中重要的半胱氨酸残基,这些残基可以感知细胞中硫的可用性。我们的发现揭示了 SCFMet30 如何动态感知转硫途径中硫代谢物的流动,以调节这些特殊氨基酸的合成。