Predicting evolutionary outcomes through the probability of accessing sequence variants

被引:2
|
作者
Gunnarsson, P. Alexander [1 ,2 ,3 ]
Babu, M. Madan [1 ,2 ,3 ]
机构
[1] MRC Lab Mol Biol, Francis Crick Ave, Cambridge CB2 0QH, England
[2] St Jude Childrens Res Hosp, Dept Struct Biol, Memphis, TN 38105 USA
[3] St Jude Childrens Res Hosp, Ctr Excellence Data Driven Discovery, Memphis, TN 38105 USA
基金
英国医学研究理事会;
关键词
INFLUENZA-VIRUS; PEPTIDE MOTIFS; FITNESS; REPLICATION; MUTATION; PHOSPHORYLATION; ADAPTATION; DYNAMICS; BIASES;
D O I
10.1126/sciadv.ade2903
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Natural selection can only operate on available genetic variation. Thus, determining the probability of accessing different sequence variants from a starting sequence can help predict evolutionary trajectories and outcomes. We define the concept of "variant accessibility" as the probability that a set of genotypes encoding a particular protein function will arise through mutations before subject to natural selection. This probability is shaped by the mutational biases of nucleotides and the structure of the genetic code. Using the influenza A virus as a model, we discuss how a more accessible but less fit variant can emerge as an adaptation rather than a more fit variant. We describe a genotype-accessibility landscape, complementary to the genotype-fitness landscape, that informs the likelihood of a starting sequence reaching different parts of genotype space. The proposed framework lays the foundation for predicting the emergence of adaptive genotypes in evolving systems such as viruses and tumors.
引用
收藏
页数:12
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