Structure and function of naturally evolved de novo proteins

被引:38
作者
Bornberg-Bauer, Erich [1 ,2 ]
Hlouchova, Klara [3 ,4 ]
Lange, Andreas [1 ]
机构
[1] Univ Munster, Inst Evolut & Biodivers, Huefferstr 1, D-48149 Munster, Germany
[2] MPI Dev Biol, Dept Prot Evolut, Tubingen, Germany
[3] Charles Univ Prague, Fac Sci, Dept Cell Biol, Biocev, Prague, Czech Republic
[4] Czech Acad Sci, Gilead Sci & IOCB Res Ctr, Inst Organ Chem & Biochem, Flemingovo Nam 2, Prague 16610, Czech Republic
关键词
ANTIFREEZE GLYCOPROTEINS; SEQUENCE SPACE; EVOLUTION; GENE; DESIGN; AGGREGATION; ORIGINATION; UNDERSTAND; EMERGENCE; SELECTION;
D O I
10.1016/j.sbi.2020.11.010
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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.
引用
收藏
页码:175 / 183
页数:9
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