Basic Sciences Division and Computational Biology Program, Fred Hutchinson Cancer Research Center, Seattle, United States.
Molecular and Cellular Biology PhD program, University of Washington, Seattle, United States.
Elife. 2018 Mar 28;7:e34420. doi: 10.7554/eLife.34420.
The immediate evolutionary space accessible to HIV is largely determined by how single amino acid mutations affect fitness. These mutational effects can shift as the virus evolves. However, the prevalence of such shifts in mutational effects remains unclear. Here, we quantify the effects on viral growth of all amino acid mutations to two HIV envelope (Env) proteins that differ at [Formula: see text]100 residues. Most mutations similarly affect both Envs, but the amino acid preferences of a minority of sites have clearly shifted. These shifted sites usually prefer a specific amino acid in one Env, but tolerate many amino acids in the other. Surprisingly, shifts are only slightly enriched at sites that have substituted between the Envs-and many occur at residues that do not even contact substitutions. Therefore, long-range epistasis can unpredictably shift Env's mutational tolerance during HIV evolution, although the amino acid preferences of most sites are conserved between moderately diverged viral strains.
HIV 可立即利用的进化空间在很大程度上取决于单个氨基酸突变如何影响适应性。这些突变效应会随着病毒的进化而发生变化。然而,这种突变效应变化的流行程度尚不清楚。在这里,我们量化了对两种 HIV 包膜 (Env) 蛋白中所有氨基酸突变的影响,这两种蛋白在 [Formula: see text]100 个残基处存在差异。大多数突变对两种 Env 蛋白的影响相似,但少数位点的氨基酸偏好明显发生了变化。这些发生变化的位点通常在一种 Env 中偏爱特定的氨基酸,但在另一种 Env 中可以容忍许多氨基酸。令人惊讶的是,这些变化在 Env 之间发生取代的位点上的富集程度仅略有增加,并且许多变化发生在甚至不接触取代的残基上。因此,尽管在中度分化的病毒株之间大多数位点的氨基酸偏好是保守的,但长程上位性可以不可预测地改变 HIV 进化过程中 Env 的突变耐受性。