Viral Recombination Section, HIV Dynamics and Replication Program, National Cancer Institute, Frederick, MD 21702, USA.
Viral Mutation Section, HIV Dynamics and Replication Program, National Cancer Institute, Frederick, MD 21702, USA.
Virology. 2018 Jan 15;514:1-8. doi: 10.1016/j.virol.2017.10.020. Epub 2017 Nov 9.
The HIV-1 RNA genome contains complex structures with many structural elements playing regulatory roles during viral replication. A recent study has identified multiple RNA structures with unknown functions that are conserved among HIV-1 and two simian immunodeficiency viruses. To explore the roles of these conserved RNA structures, we introduced synonymous mutations into the HIV-1 genome to disrupt each structure. These mutants exhibited similar particle production, viral infectivity, and replication kinetics relative to the parent NL4-3 virus. However, when replicating in direct competition with the wild-type NL4-3 virus, mutations of RNA structures at inter-protein domain junctions can cause fitness defects. These findings reveal the ability of HIV-1 to tolerate changes in its sequences, even in apparently highly conserved structures, which permits high genetic diversity in HIV-1 population. Our results also suggest that some conserved RNA structures may function to fine-tune viral replication.
HIV-1 RNA 基因组包含复杂的结构,许多结构元件在病毒复制过程中发挥调节作用。最近的一项研究鉴定了多个具有未知功能的 RNA 结构,它们在 HIV-1 和两种猿猴免疫缺陷病毒中保守。为了探索这些保守 RNA 结构的作用,我们在 HIV-1 基因组中引入同义突变来破坏每个结构。这些突变体相对于亲本 NL4-3 病毒表现出相似的颗粒产生、病毒感染力和复制动力学。然而,当与野生型 NL4-3 病毒直接竞争复制时,蛋白结构域连接处的 RNA 结构突变会导致适应性缺陷。这些发现揭示了 HIV-1 能够耐受其序列的变化,即使在明显高度保守的结构中,这使得 HIV-1 群体具有高度的遗传多样性。我们的结果还表明,一些保守的 RNA 结构可能有助于精细调节病毒复制。