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Updated: Jul 31, 2026

High Throughput Yeast Strain Phenotyping with Droplet-Based RNA Sequencing
Published on: May 21, 2020
A Candida albicans gene expressed in Saccharomyces cerevisiae results in a distinct pattern of mRNA processing
A Iborra1, R Sentandreu, D Gozalbo
1Departament de Microbiologia i Ecologia, Facultat de Farmàcia, Universitat de València, Burjassot, España.
Abstract:
Two plasmids (derived from YCplac22 and YEplac112) carrying a Candida albicans gene (including the 5' non-coding promoter sequences) coding for a 30 kDa membrane-bound protein, were used to transform Saccharomyces cerevisiae cells. A 30 kDa protein was immunodetected by Western blot in the membrane fraction of transformants. Northern analysis showed the presence of three mRNA species (of about 1.1, 0.7 and 0.5 kb) hybridizing with the C. albicans gene as a probe. The same result was obtained using the 5' and 3' regions of the gene as probes, whereas only a 1.1 kb mRNA was found in C. albicans and none was detected in S. cerevisiae control transformants. Thus, heterologous expression of this gene in S. cerevisiae results in a distinct pattern of mRNA processing, either due to the location on plasmid vectors and/or to differences in the mRNA processing systems in the two microorganisms.
Insights
Heterologous expression of a Candida albicans gene in Saccharomyces cerevisiae yielded a 30 kDa protein. Distinct mRNA processing patterns were observed in the yeast transformants, suggesting differences in gene expression systems.
Area of Science:
- Molecular Biology
- Microbiology
- Genetics
Background:
- Investigating gene expression and protein production in different yeast species is crucial for understanding molecular mechanisms.
- Candida albicans and Saccharomyces cerevisiae are important model organisms in eukaryotic research.
Purpose of the Study:
- To examine the heterologous expression of a Candida albicans gene in Saccharomyces cerevisiae.
- To analyze the mRNA processing and protein production of the C. albicans gene in S. cerevisiae.
Main Methods:
- Transformation of Saccharomyces cerevisiae with plasmids containing a Candida albicans gene.
- Immunodetection of the expressed protein using Western blot analysis.
- Northern blot analysis to study mRNA species and processing.
Main Results:
- A 30 kDa membrane-bound protein was successfully immunodetected in S. cerevisiae transformants.
- Northern analysis revealed three distinct mRNA species (1.1, 0.7, and 0.5 kb) in transformants, unlike C. albicans (1.1 kb) or control S. cerevisiae.
- The presence of multiple mRNA species suggests altered mRNA processing in the heterologous host.
Conclusions:
- Heterologous expression of the C. albicans gene in S. cerevisiae leads to unique mRNA processing.
- Differences in mRNA processing may be attributed to plasmid vector effects or inherent differences in yeast mRNA processing systems.
- This study highlights the complexities of inter-species gene expression and regulation.
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