The citron homology domain as a scaffold for Rho1 signaling.
basic_science · Level V
Where this comes from
- Record sourced from PubMed, PMID 34544876.
- Also identified by DOI 10.1073/pnas.2110298118 and PMC identifier 8488606.
- Licence recorded as CC BY.
- The licence permits redistribution, so the abstract is shown in full and the full text is available from the publisher.
Abstract
<i>Aspergillus fumigatus</i> is a human opportunistic pathogen showing emerging resistance against a limited repertoire of antifungal agents available. The GTPase Rho1 has been identified as an important regulator of the cell wall integrity signaling pathway that regulates the composition of the cell wall, a structure that is unique to fungi and serves as a target for antifungal compounds. Rom2, the guanine nucleotide exchange factor to Rho1, contains a C-terminal citron homology (CNH) domain of unknown function that is found in many other eukaryotic genes. Here, we show that the Rom2 CNH domain interacts directly with Rho1 to modulate β-glucan and chitin synthesis. We report the structure of the Rom2 CNH domain, revealing that it adopts a seven-bladed β-propeller fold containing three unusual loops. A model of the Rho1-Rom2 CNH complex suggests that the Rom2 CNH domain interacts with the Rho1 Switch II motif. This work uncovers the role of the Rom2 CNH domain as a scaffold for Rho1 signaling in fungal cell wall biosynthesis.
Medical subject headings
- Aspergillus fumigatus
- Basic-Leucine Zipper Transcription Factors
- Cell Wall
- Fungal Proteins
- Intracellular Signaling Peptides and Proteins
- Protein Serine-Threonine Kinases
- rho GTP-Binding Proteins