The evolution of genome compression and genomic novelty in RNA viruses

被引:120
作者
Belshaw, Robert
Pybus, Oliver G.
Rambaut, Andrew
机构
[1] Univ Oxford, Dept Zool, Oxford OX1 3PS, England
[2] Univ Edinburgh, Inst Evolut Biol, Edinburgh EH9 3JT, Midlothian, Scotland
基金
英国惠康基金;
关键词
D O I
10.1101/gr.6305707
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
The genomes of RNA viruses are characterized by their extremely small size and extremely high mutation rates ( typically 10 kb and 10(-4)/ base/ replication cycle, respectively), traits that are thought to be causally linked. One aspect of their small size is the genome compression caused by the use of overlapping genes ( where some nucleotides code for two genes). Using a comparative analysis of all known RNA viral species, we show that viruses with larger genomes tend to have less gene overlap. We provide a numerical model to show how a high mutation rate could lead to gene overlap, and we discuss the factors that might explain the observed relationship between gene overlap and genome size. We also propose a model for the evolution of gene overlap based on the co- opting of previously unused ORFs, which gives rise to two types of overlap: ( 1) the creation of novel genes inside older genes, predominantly via + 1 frameshifts, and ( 2) the incremental increase in overlap between originally contiguous genes, with no frameshift preference. Both types of overlap are viewed as the creation of genomic novelty under pressure for genome compression. Simulations based on our model generate the empirical size distributions of overlaps and explain the observed frameshift preferences. We suggest that RNA viruses are a good model system for the investigation of general evolutionary relationship between genome attributes such as mutational robustness, mutation rate, and size.
引用
收藏
页码:1496 / 1504
页数:9
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