Travers Simon A A, Tully Damien C, McCormack Grace P, Fares Mario A
Molecular Evolution and Bioinformatics Laboratory, Department of Biology, National University of Ireland, Maynooth, Ireland.
Mol Biol Evol. 2007 Dec;24(12):2787-801. doi: 10.1093/molbev/msm213. Epub 2007 Oct 5.
The env gene of human immunodeficiency virus (HIV) is a functionally important gene responsible for the production of protein products (gp120 and gp41) involved in host cell recognition, binding, and entry. This occurs through a complex and, as yet, not fully understood process of protein-protein interaction and within and between protein functional communication. Exposure on the surface of active HIV virions means the gp120-gp41 complexes are subjected to intense immune system pressure and have, therefore, evolved mechanisms to avoid neutralization. Using protein-coding sequences representing all the HIV type-1 (HIV-1) group M subtypes, we have identified amino acids within the env gene whose evolution is inextricably linked over the entire HIV-1 group M epidemic. We identified 848 pairs of coevolving residues (involving 263 out of 764 amino acid sites), which represent 0.29% of all possible pairs. Of the coevolving pairs, 68% were significantly correlated by hydrophobicity, molecular weight, or both hydrophobicity and molecular weight. Subsequent grouping of coevolving pairs resulted in the identification of 290 groups of amino acid residues, with the size of these groups ranging from 2 to 10 amino acid residues. Many of these dependencies are correlated by function including CD4 binding, coreceptor binding, glycosylation, and protein-protein interaction. This analysis provides important information regarding the functional dependencies observed within all the HIV-1 group M subtypes and may assist in the identification of functional protein domains and therapeutic targets within the HIV-1 env gene.
人类免疫缺陷病毒(HIV)的env基因是一个功能重要的基因,负责产生参与宿主细胞识别、结合和进入的蛋白质产物(gp120和gp41)。这一过程通过蛋白质-蛋白质相互作用的复杂且尚未完全理解的过程发生,涉及蛋白质功能的内部和之间的通讯。活跃的HIV病毒粒子表面的暴露意味着gp120-gp41复合物受到免疫系统的强烈压力,因此进化出了避免被中和的机制。利用代表所有HIV-1 M组亚型的蛋白质编码序列,我们在env基因中鉴定出了一些氨基酸,其进化在整个HIV-1 M组流行过程中有着千丝万缕的联系。我们鉴定出了848对共同进化的残基(涉及764个氨基酸位点中的263个),占所有可能配对的0.29%。在共同进化的配对中,68%在疏水性、分子量或疏水性和分子量两者方面显著相关。随后对共同进化配对的分组导致鉴定出290组氨基酸残基,这些组的大小从2到10个氨基酸残基不等。这些依赖性中的许多在功能上相关,包括CD4结合、共受体结合、糖基化和蛋白质-蛋白质相互作用。该分析提供了关于在所有HIV-1 M组亚型中观察到的功能依赖性的重要信息,并可能有助于识别HIV-1 env基因内的功能蛋白结构域和治疗靶点。