Evolution of new enzymes by gene duplication and divergence

被引:88
作者
Copley, Shelley D. [1 ,2 ]
机构
[1] Univ Colorado, Dept Mol Cellular & Dev Biol, Campus Box 347, Boulder, CO 80309 USA
[2] Univ Colorado, Cooperat Inst Res Environm Sci, Campus Box 347, Boulder, CO 80309 USA
关键词
directed evolution; enzyme evolution; gene duplication; Innovation-amplification-divergence model; promiscuity; WHOLE-GENOME DUPLICATION; ESCHERICHIA-COLI; ENOLASE SUPERFAMILY; OPERON EXPRESSION; UNIVERSAL TREE; TRANSFER-RNA; COPY NUMBER; AMPLIFICATION; PROMISCUITY; MUTATION;
D O I
10.1111/febs.15299
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
Thousands of new metabolic and regulatory enzymes have evolved by gene duplication and divergence since the dawn of life. New enzyme activities often originate from promiscuous secondary activities that have become important for fitness due to a change in the environment or a mutation. Mutations that make a promiscuous activity physiologically relevant can occur in the gene encoding the promiscuous enzyme itself, but can also occur elsewhere, resulting in increased expression of the enzyme or decreased competition between the native and novel substrates for the active site. If a newly useful activity is inefficient, gene duplication/amplification will set the stage for divergence of a new enzyme. Even a few mutations can increase the efficiency of a new activity by orders of magnitude. As efficiency increases, amplified gene arrays will shrink to provide two alleles, one encoding the original enzyme and one encoding the new enzyme. Ultimately, genomic rearrangements eliminate co-amplified genes and move newly evolved paralogs to a distant region of the genome.
引用
收藏
页码:1262 / 1283
页数:22
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