# The Yeast Gsk-3 Kinase Mck1 Is Necessary for Cell Wall Remodeling in Glucose-Starved and Cell Wall-Stressed Cells

**Authors:** Fan Zhang, Yingzhi Tang, Houjiang Zhou, Kaiqiang Li, James A. West, Julian L. Griffin, Kathryn S. Lilley, Nianshu Zhang

PMC · DOI: 10.3390/ijms26083534 · 2025-04-09

## TL;DR

The study shows that the Mck1 kinase in yeast helps strengthen cell walls during stress by working with other pathways and regulating metabolism.

## Contribution

The paper reveals novel roles of Mck1 in metabolic reprogramming and cell wall remodeling under stress.

## Key findings

- Mck1 cooperates with Slt2 to promote cell wall thickening in glucose-starved cells.
- Mck1 is required for UDP-glucose accumulation through stress and metabolic regulons.
- Mck1 regulates cytoskeleton-dependent processes and transcription via PKA inhibition and SAGA activation.

## Abstract

The cell wall integrity (CWI) pathway is responsible for transcriptional regulation of cell wall remodeling in response to cell wall stress. How cell wall remodeling mediated by the CWI pathway is effected by inputs from other signaling pathways is not well understood. Here, we demonstrate that the Mck1 kinase cooperates with Slt2, the MAP kinase of the CWI pathway, to promote cell wall thickening in glucose-starved cells. Integrative analyses of the transcriptome, proteome and metabolic profiling indicate that Mck1 is required for the accumulation of UDP-glucose (UDPG), the substrate for β-glucan synthesis, through the activation of two regulons: the Msn2/4-dependent stress response and the Cat8-/Adr1-mediated metabolic reprogram dependent on the SNF1 complex. Analysis of the phosphoproteome suggests that similar to mammalian Gsk-3 kinases, Mck1 is involved in the regulation of cytoskeleton-dependent cellular processes, metabolism, signaling and transcription. Specifically, Mck1 may be implicated in the Snf1-dependent metabolic reprogram through PKA inhibition and SAGA (Spt-Ada-Gcn5 acetyltransferase)-mediated transcription activation, a hypothesis further underscored by the significant overlap between the Mck1- and Gcn5-activated transcriptomes. Phenotypic analysis also supports the roles of Mck1 in actin cytoskeleton-mediated exocytosis to ensure plasma membrane homeostasis and cell wall remodeling in cell wall-stressed cells. Together, these findings not only reveal the novel functions of Mck1 in metabolic reprogramming and polarized growth but also provide valuable omics resources for future studies to uncover the underlying mechanisms of Mck1 and other Gsk-3 kinases in cell growth and stress response.

## Linked entities

- **Genes:** MCK1 (serine/threonine/tyrosine protein kinase MCK1) [NCBI Gene 855409], SLT2 (mitogen-activated serine/threonine-protein kinase SLT2) [NCBI Gene 856425], MSN2 (stress-responsive transcriptional activator MSN2) [NCBI Gene 855053], MSN4 (stress-responsive transcriptional activator MSN4) [NCBI Gene 853803], CAT8 (cationic amino acid transporter 8) [NCBI Gene 838282], adr-1 (A-to-I RNA editing regulator adr-1) [NCBI Gene 172542], snf-1 (Sodium: Neurotransmitter symporter Family) [NCBI Gene 172119], KAT2A (lysine acetyltransferase 2A) [NCBI Gene 2648]
- **Proteins:** MCK1 (serine/threonine/tyrosine protein kinase MCK1), SLT2 (mitogen-activated serine/threonine-protein kinase SLT2), KAT2A (lysine acetyltransferase 2A)
- **Chemicals:** UDP-glucose (PubChem CID 8629)
- **Species:** Saccharomyces cerevisiae (taxon 4932)

## Full-text entities

- **Genes:** KAT2A (lysine acetyltransferase 2A) [NCBI Gene 2648] {aka GCN5, GCN5L2, PCAF-b, hGCN5}, ADA (adenosine deaminase) [NCBI Gene 100] {aka ADA1}, AGXT (alanine--glyoxylate aminotransferase) [NCBI Gene 189] {aka AGT, AGT1, AGXT1, PH1, SPAT, SPT}
- **Chemicals:** Glucose (MESH:D005947), beta-glucan (MESH:D047071), UDP-glucose (MESH:D014532)
- **Species:** Saccharomyces cerevisiae (baker's yeast, species) [taxon 4932]

## Figures

8 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12027387/full.md

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Source: https://tomesphere.com/paper/PMC12027387