bioRxiv Science⌕ Search

bioRxiv · 10.1101/2025.10.24.684117

The molecular architecture of the aquaglyceroporin gating system in Saccharomyces cerevisiae

Abstract

Aquaglyceroporins have been extensively studied in multiple systems. However, the molecular architecture and hence the precise mechanisms of action remain unknow. The yeast aquaglyceroporin Fps1 plays the main role in controlling cellular turgor. It is regulated by the two Rgc proteins which activate the Fps1 channel. To date, the molecular architecture and dynamics of the Fps1-Rgc gating system is unknown. We employed dual-coloured super-resolution millisecond fluorescence microscopy with a single-molecule sensitivity, to track Fps1 and Rgc2 in real time. Unlike previously believed, our data shows that Rgc2 mainly operates as a homodimer. At the same time, Rgc1, the seemingly redundant regulatory ortholog of Rgc2, has a clear effect on the architecture, colocalisation behaviour and molecular dynamics of the Fps1 and Rgc2 together. Moreover, Rgc1 seems to promote Rgc2 stability in response to hydrogen peroxide stress. Together, our results provide novel insights into the mechanism behind aquaglyceroporins regulation. ImportanceThe components of the Fps1 aquaglyceroporin gating system is conserved in Fungi and present in both bakers yeast Saccharomyces cerevisiae as well as common pathogenic included in the WHO fungal priority pathogens list: Candida albicans, Candida glabrata, Aspergillus fumigatus, Pichia kudriavzevii. For instance, in C. glabrata, the orthologs of both Fps1 and Rgc2 are involved in key pathogenic processes related to acetate tolerance, phagocytosis by macrophages, resistance to antifungal agents and overall drug uptake and efflux. As the Fps1 gating system is not present in metazoans, it constitutes an attractive drug target for antifungal agents. Thus, understanding the architecture and the finer mechanisms of the Fps1 pore regulation is a stepping stone in development of effective antifungal treatment and targeted antifungal drugs.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Andersson, M., Viaene, L., Albalate, A. M., Leake, M. C., Wollman, A. J., Shashkova, S.. 2025-10-24. The molecular architecture of the aquaglyceroporin gating system in Saccharomyces cerevisiae. https://doi.org/10.1101/2025.10.24.684117

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related preprints

SF3b inhibitors suppress proliferation of nonsmall cell lung cancer cells irrespective of EGFR mutation status

Epidermal growth factor receptor tyrosine kinase inhibitors (EGFR-TKIs) are standard care for EGFR-mutant non-small cell lung cancer (NSCLC), but acquired resistance limits their durability, and alternatives that do not depend on EGFR kinase activity are needed. We asked whether inhibitors of SF3b, a core component of the U2 small nuclear ribonucleoprotein particle, act on NSCLC cells regardless of EGFR genotype. Three lung adenocarcinoma lines were treated with pladienolide B or herboxidiene at 0.01, 0.1 and 1 uM: PC9 and HCC827, both carrying an EGFR exon 19 deletion and both inhibited by gefitinib at nanomolar concentrations, and A549, which is EGFR wild type and gefitinibin sensitive. Proliferation was followed for three days by crystal violet staining, EGFR intron 2 retention was assayed by RTPCR, and EGFR protein was measured by western blotting. Both compounds produced a concentration-dependent increase in the intron 2 retained product in all three lines, and both held proliferation at or near the day 0 cell number in all three, at concentrations down to 0.01 uM. EGFR protein was lost in PC9, reduced in A549, and only partly reduced in HCC827, where a residual band persisted in lanes whose growth was fully suppressed. Since A549 is EGFR wild-type, and published knockdown data show that removing EGFR does not suppress proliferation of wild-type lines, the growth inhibition cannot be attributed to loss of EGFR alone. We read EGFR intron 2 retention as a marker of target engagement rather than as the mechanism of the growth effect. These are the results of single experiments without replicates or statistical testing and should be read as preliminary.

molecular biology↗

Shared and Specific miRNA-mRNA in Human and Murine Acute Kidney Injury

Acute kidney injury (AKI) is managed as a single clinical entity despite substantial biological heterogeneity. We established a cross-species framework to define etiology-specific molecular programs and determine how these programs relate to molecular heterogeneity and pathobiology in human AKI. We performed parallel sequencing of totalRNA (mRNA) and miRNA (kidney, whole blood) in 3 murine models (mild AKI: ischemia-reperfusion injury, IRI; cecal-ligation and puncture, CLP; endotoxemia, LPS); kidney mRNA and miRNA clearly distinguished the models, blood mRNA maintained model-specific separation, and blood miRNA was less distinct. IRI was characterized by epithelial injury/repair, and extracellular matrix remodeling (i.e., miR-125b-1-3p, Vim, Sprr2g); CLP, broader inflammatory, metabolic programs (i.e., miR-692, Pfkfb3, Cdo1); LPS, inflammatory signaling (i.e., miR-155-5p, Irf7, Gbp3). We then compared these signatures to human whole blood RNAseq. Human blood samples varied along a shared gene axis that correlated to differing degrees with all three murine models, consistent with the heterogeneous nature of clinical AKI rather than discrete assignment to a single experimental etiology. Orthologs were linked to immune processes (i.e., SIGLEC14, DAAM2, CD177, DEFA3), and the presence of tubular casts in human biopsies, reflecting that mild murine AKI models capture etiology-specific biology relevant to severe human AKI. Integration of injury etiology, severity, and time may provide a framework for developing circulating biomarkers that may resolve the biological heterogeneity of human AKI.

molecular biology↗

Distinct labeling of host and viral genomes highlights redistribution of nuclear proteins during HSV-1 infection

Herpes simplex virus type 1 (HSV-1) coordinates viral and cellular proteins during infection. While proteins associated with HSV-1 genomes have been identified, changes in proteins associated with the host genome during infection remain poorly understood. We adapted accelerated native isolation of proteins on nascent DNA (aniPOND) to label and purify cellular and viral DNA then identify associated proteins by mass spectrometry. Using this approach, we confirm observations that cellular transcription, DNA replication, and repair proteins are enriched on viral genomes after the onset of viral DNA replication. We assessed how protein interactions with cellular DNA change during infection relative to protein abundance. Targets of the viral E3 ubiquitin ligase, ICP0, are depleted from the nucleus and cellular genome during infection. Transcription regulatory factors, Pol II, and the proteasome are depleted from the host genome, while association with DNA damage response and nuclear pore proteins increases. We also provide evidence for HSV-1 disruption of ribosome biogenesis. Results demonstrate reorganization of the nucleus during infection and validate this technique to identify changes to host genome-associated factors during infection.

molecular biology↗