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Published on: April 18, 2021
Genetic and epigenetic mechanisms underlying cell-surface variability in protozoa and fungi
Kevin J Verstrepen1, Gerald R Fink
1Laboratory for Systems Biology, VIB, B-3001 Leuven, Belgium. kevin.verstrepen@biw.vib-kuleuven.be
Abstract:
Eukaryotic microorganisms have evolved ingenious mechanisms to generate variability at their cell surface, permitting differential adherence, rapid adaptation to changing environments, and evasion of immune surveillance. Fungi such as Saccharomyces cerevisiae and the pathogen Candida albicans carry a family of mucin and adhesin genes that allow adhesion to various surfaces and tissues. Trypanosoma cruzi, T. brucei, and Plasmodium falciparum likewise contain large arsenals of different cell surface adhesion genes. In both yeasts and protozoa, silencing and differential expression of the gene family results in surface variability. Here, we discuss unexpected similarities in the structure and genomic location of the cell surface genes, the role of repeated DNA sequences, and the genetic and epigenetic mechanisms-all of which contribute to the remarkable cell surface variability in these highly divergent microbes.
Insights
Microbial cell surface variability, crucial for adaptation and immune evasion, is achieved through similar gene structures and epigenetic mechanisms in diverse eukaryotes like fungi and protozoa.
Area of Science:
- Microbiology
- Molecular Biology
- Genetics
Background:
- Eukaryotic microorganisms utilize cell surface variability for adaptation and immune evasion.
- Fungi (e.g., Saccharomyces cerevisiae, Candida albicans) and protozoa (e.g., Trypanosoma cruzi, Plasmodium falciparum) possess large gene families encoding cell surface adhesins.
Purpose of the Study:
- To investigate unexpected similarities in cell surface gene families across divergent microbial eukaryotes.
- To explore the role of genomic organization, repetitive DNA, and regulatory mechanisms in generating cell surface diversity.
Main Methods:
- Comparative analysis of cell surface gene families in yeasts and protozoa.
- Examination of gene structure, genomic location, and repetitive DNA elements.
- Investigation of genetic and epigenetic regulatory mechanisms controlling gene expression.
Main Results:
- Identified conserved structural features and genomic locations of cell surface adhesin gene families.
- Highlighted the significant role of repetitive DNA sequences in facilitating gene family expansion and variation.
- Demonstrated that differential gene expression and silencing contribute to cell surface variability.
Conclusions:
- Despite evolutionary divergence, microbes share common strategies for generating cell surface variability.
- Genomic architecture and epigenetic control are key drivers of microbial surface diversity, impacting adherence and immune evasion.
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