Structure and function of naturally evolved de novo proteins
Language English Country England, Great Britain Media print-electronic
Document type Journal Article, Research Support, Non-U.S. Gov't, Review
PubMed
33567396
DOI
10.1016/j.sbi.2020.11.010
PII: S0959-440X(20)30213-X
Knihovny.cz E-resources
- MeSH
- Genomics MeSH
- Evolution, Molecular * MeSH
- Proteins * genetics MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Review MeSH
- Names of Substances
- Proteins * MeSH
Comparative evolutionary genomics has revealed that novel protein coding genes can emerge randomly from non-coding DNA. While most of the myriad of transcripts which continuously emerge vanish rapidly, some attain regulatory regions, become translated and survive. More surprisingly, sequence properties of de novo proteins are almost indistinguishable from randomly obtained sequences, yet de novo proteins may gain functions and integrate into eukaryotic cellular networks quite easily. We here discuss current knowledge on de novo proteins, their structures, functions and evolution. Since the existence of de novo proteins seems at odds with decade-long attempts to construct proteins with novel structures and functions from scratch, we suggest that a better understanding of de novo protein evolution may fuel new strategies for protein design.
References provided by Crossref.org
High-throughput Selection of Human de novo-emerged sORFs with High Folding Potential
Toxin rescue by a random sequence
Experimental characterization of de novo proteins and their unevolved random-sequence counterparts
Modern and prebiotic amino acids support distinct structural profiles in proteins