De novo emergence of adaptive membrane proteins from thymine-rich genomic sequences.
basic_science · Level V
Where this comes from
- Record sourced from PubMed, PMID 32034123.
- Also identified by DOI 10.1038/s41467-020-14500-z and PMC identifier 7005711.
- Licence recorded as CC BY.
- The licence permits redistribution, so the abstract is shown in full and the full text is available from the publisher.
Abstract
Recent evidence demonstrates that novel protein-coding genes can arise de novo from non-genic loci. This evolutionary innovation is thought to be facilitated by the pervasive translation of non-genic transcripts, which exposes a reservoir of variable polypeptides to natural selection. Here, we systematically characterize how these de novo emerging coding sequences impact fitness in budding yeast. Disruption of emerging sequences is generally inconsequential for fitness in the laboratory and in natural populations. Overexpression of emerging sequences, however, is enriched in adaptive fitness effects compared to overexpression of established genes. We find that adaptive emerging sequences tend to encode putative transmembrane domains, and that thymine-rich intergenic regions harbor a widespread potential to produce transmembrane domains. These findings, together with in-depth examination of the de novo emerging YBR196C-A locus, suggest a novel evolutionary model whereby adaptive transmembrane polypeptides emerge de novo from thymine-rich non-genic regions and subsequently accumulate changes molded by natural selection.
Medical subject headings
- Evolution, Molecular
- Membrane Proteins
- Saccharomyces cerevisiae Proteins
- TATA-Binding Protein Associated Factors
- Thymine
- Transcription Factor TFIID