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Small-Scale Plasma Membrane Preparation for the Analysis of Candida albicans Cdr1-mGFPHis
Published on: June 13, 2021
A functional portrait of Med7 and the mediator complex in Candida albicans
Faiza Tebbji1, Yaolin Chen2, Julien Richard Albert3
1Department of Biology, McGill University, Montreal, Quebec, Canada; Department of Biology, Concordia University, Montreal, Quebec, Canada.
Abstract:
Mediator is a multi-subunit protein complex that regulates gene expression in eukaryotes by integrating physiological and developmental signals and transmitting them to the general RNA polymerase II machinery. We examined, in the fungal pathogen Candida albicans, a set of conditional alleles of genes encoding Mediator subunits of the head, middle, and tail modules that were found to be essential in the related ascomycete Saccharomyces cerevisiae. Intriguingly, while the Med4, 8, 10, 11, 14, 17, 21 and 22 subunits were essential in both fungi, the structurally highly conserved Med7 subunit was apparently non-essential in C. albicans. While loss of CaMed7 did not lead to loss of viability under normal growth conditions, it dramatically influenced the pathogen's ability to grow in different carbon sources, to form hyphae and biofilms, and to colonize the gastrointestinal tracts of mice. We used epitope tagging and location profiling of the Med7 subunit to examine the distribution of the DNA sites bound by Mediator during growth in either the yeast or the hyphal form, two distinct morphologies characterized by different transcription profiles. We observed a core set of 200 genes bound by Med7 under both conditions; this core set is expanded moderately during yeast growth, but is expanded considerably during hyphal growth, supporting the idea that Mediator binding correlates with changes in transcriptional activity and that this binding is condition specific. Med7 bound not only in the promoter regions of active genes but also within coding regions and at the 3' ends of genes. By combining genome-wide location profiling, expression analyses and phenotyping, we have identified different Med7p-influenced regulons including genes related to glycolysis and the Filamentous Growth Regulator family. In the absence of Med7, the ribosomal regulon is de-repressed, suggesting Med7 is involved in central aspects of growth control.
Insights
The Mediator complex subunit Med7 is not essential for survival in Candida albicans but significantly impacts its virulence, including hyphal formation and host colonization. Mediator binding sites vary by growth condition, revealing condition-specific transcriptional regulation.
Area of Science:
- Molecular Biology
- Mycology
- Gene Regulation
Background:
- Mediator is a crucial multi-subunit complex regulating gene expression in eukaryotes.
- Essential Mediator subunits in Saccharomyces cerevisiae were investigated in Candida albicans.
Purpose of the Study:
- To investigate the role of the conserved Med7 subunit in Candida albicans, a fungal pathogen.
- To understand Mediator's genome-wide binding patterns and their relationship with gene expression and virulence.
Main Methods:
- Conditional alleles of Mediator subunit genes were analyzed.
- Epitope tagging and genome-wide location profiling (ChIP-seq) of Med7 were performed.
- Phenotypic analyses, including virulence assays and gene expression profiling, were conducted.
Main Results:
- Med7 was found to be non-essential for viability but critical for C. albicans virulence.
- Loss of Med7 affected carbon source utilization, hyphal development, biofilm formation, and host colonization.
- Med7 binding sites were condition-specific, expanding significantly during hyphal growth.
- Med7 influences glycolysis, Filamentous Growth Regulator family genes, and represses the ribosomal regulon.
Conclusions:
- Med7 plays a vital role in Candida albicans pathogenesis and growth control, despite not being essential for basic viability.
- Mediator binding is dynamic and condition-specific, correlating with transcriptional changes during different morphological states.
- Med7 is implicated in regulating key metabolic and virulence pathways in this fungal pathogen.

