# The kinase Bud32 regulates iron homeostasis in fungal pathogen Cryptococcus neoformans

**Authors:** Yuanyuan Ma, Bo Pan, Wenzhi Lei, Wenjie Fang, Weihua Pan, Wanqing Liao, Bin Xu, Peng Xue

PMC · DOI: 10.3389/fimmu.2025.1624237 · Frontiers in Immunology · 2025-07-25

## TL;DR

A kinase called Bud32 helps the fungus Cryptococcus neoformans manage iron, which is important for its ability to cause disease.

## Contribution

This study identifies Bud32 as a key regulator of iron homeostasis in C. neoformans through proteomic, metabolomic, and phosphoproteomic analyses.

## Key findings

- Deleting the BUD32 gene impairs growth in low-iron conditions and alters iron transport and iron-sulfur cluster proteins.
- Bud32 modulates iron-sulfur cluster assembly and affects proteins like Grx4, Cir1, and HapX.
- BUD32 deletion changes phosphorylation of iron regulators and reduces biliverdin levels in metabolites.

## Abstract

The ability to acquire iron and maintain iron homeostasis is crucial for the virulence of the human pathogenic fungus Cryptococcus neoformans. This study investigates the role of Bud32, a core virulence kinase and component of the KEOPS complex, within the iron regulatory network of C. neoformans.

We used gene deletion techniques to study the phenotypic effects of BUD32 gene knockout and conducted proteomic and metabolomic analyses to assess changes in protein expression and metabolite levels in the mutant. Additionally, we performed in vivo phosphoproteomics analysis to evaluate Bud32 impact on iron regulatory proteins.

Our findings revealed that deletion of BUD32 gene significantly impaired growth in iron-limiting environments, leading to notable alterations in the expression of iron transport and iron-sulfur cluster (ISC)-containing proteins. Specifically, Bud32 was shown to modulate ISC assembly and influence the activity of key iron-sulfur binding proteins, including Grx4, Cir1, and HapX. Metabolic profiling indicated changes in 696 metabolites, with reductions in biliverdin levels. Additionally, BUD32 gene deletion resulted in widespread changes in the phosphorylation status of numerous proteins, including the iron regulators Cir1 and Rim101.

These findings provide evidence for the involvement of the kinase Bud32 in regulating iron homeostasis in C. neoformans, thereby contributing to our understanding of its virulence mechanisms.

## Linked entities

- **Genes:** TP53RK (TP53 regulating kinase) [NCBI Gene 112858], GLRX3 (glutaredoxin 3) [NCBI Gene 10539], UBE2V1 (ubiquitin conjugating enzyme E2 V1) [NCBI Gene 7335], hapX (bZIP transcription factor HapX) [NCBI Gene 2868984], RIM101 (alkaline-responsive transcriptional regulator RIM101) [NCBI Gene 856358]
- **Proteins:** TP53RK (TP53 regulating kinase), GLRX3 (glutaredoxin 3), UBE2V1 (ubiquitin conjugating enzyme E2 V1), hapX (bZIP transcription factor HapX), RIM101 (alkaline-responsive transcriptional regulator RIM101)
- **Chemicals:** biliverdin (PubChem CID 251)
- **Species:** Cryptococcus neoformans (taxon 5207)

## Full-text entities

- **Chemicals:** iron (MESH:D007501), biliverdin (MESH:D001664)
- **Species:** Homo sapiens (human, species) [taxon 9606], Cryptococcus neoformans (Cryptococcus neoformans serotype A, species) [taxon 5207]

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC12332752/full.md

## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12332752/full.md

## References

68 references — full list in the complete paper: https://tomesphere.com/paper/PMC12332752/full.md

---
Source: https://tomesphere.com/paper/PMC12332752