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Genetic Mapping of Thermotolerance Differences Between Species of Saccharomyces Yeast via Genome-Wide Reciprocal Hemizygosity Analysis
Published on: August 12, 2019
Intergenic Regions of Saccharomycotina Yeasts are Enriched in Potential to Encode Transmembrane Domains
Emilios Tassios1,2, Christoforos Nikolaou1, Nikolaos Vakirlis3
1Computational Genomics Group, Institute for Bioinnovation, Biomedical Sciences Research Center "Alexander Fleming", Vari, Greece.
Intergenic regions in yeast genomes show a surprising potential to form transmembrane domains. This TM-forming enrichment is linked to the emergence of new genes, suggesting a role in genomic evolution.
Area of Science:
- Genomics
- Molecular Evolution
- Yeast Biology
Background:
- Intergenic genomic regions possess regulatory and structural roles.
- Noncoding sequences can evolve into novel genes (de novo gene emergence).
- Saccharomyces cerevisiae intergenic regions exhibit "TM-forming enrichment"—a cryptic potential to form transmembrane domains.
Purpose of the Study:
- Investigate the TM-forming potential of intergenic regions across the Saccharomycotina budding yeast subphylum.
- Explain the source and biological relevance of TM-forming enrichment.
- Understand the evolutionary importance of this genomic feature.
Main Methods:
- Comparative genomic analysis across the Saccharomycotina subphylum.
- Assessment of TM-forming potential in intergenic regions.
- Correlation analysis between TM-forming enrichment and gene evolution.
Main Results:
- Pervasive, yet variable, TM-forming enrichment found across the Saccharomycotina subphylum.
- This enrichment is independent of sequence composition and intergenic region size.
- TM-forming enrichment, not just potential, correlates with more transmembrane domains in evolutionarily young genes.
Conclusions:
- The TM-forming enrichment of intergenic regions is a widespread phenomenon in budding yeasts.
- This property is not explained by simple sequence composition or regulatory elements.
- TM-forming enrichment may play a role in the evolution of new transmembrane proteins and genomic novelty.
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