Nomaguchi Masako, Doi Naoya, Yoshida Tomoya, Koma Takaaki, Adachi Shun, Ode Hirotaka, Iwatani Yasumasa, Yokoyama Masaru, Sato Hironori, Adachi Akio
Department of Microbiology, Graduate School of Medical Science, Tokushima University, Tokushima, Japan.
Department of Infectious Diseases and Immunology, Clinical Research Center, National Hospital Organization Nagoya Medical Center, Nagoya, Japan.
Front Microbiol. 2017 Dec 18;8:2542. doi: 10.3389/fmicb.2017.02542. eCollection 2017.
Genomic RNA of HIV-1 contains localized structures critical for viral replication. Its structural analysis has demonstrated a stem-loop structure, SLSA1, in a nearby region of HIV-1 genomic splicing acceptor 1 (SA1). We have previously shown that the expression level of mRNA is considerably altered by some natural single-nucleotide variations (nSNVs) clustering in SLSA1 structure. In this study, besides eleven nSNVs previously identified by us, we totally found nine new nSNVs in the SLSA1-containing sequence from SA1, splicing donor 2, and through to the start codon of Vif that significantly affect the mRNA level, and designated the sequence SA1D2prox (142 nucleotides for HIV-1 NL4-3). We then examined by extensive variant and mutagenesis analyses how SA1D2prox sequence and SLSA1 secondary structure are related to mRNA level. While the secondary structure and stability of SLSA1 was largely changed by nSNVs and artificial mutations introduced to restore the original NL4-3 form from altered ones by nSNVs, no clear association of the two SLSA1 properties with mRNA level was observed. In contrast, when naturally occurring SA1D2prox sequences that contain multiple nSNVs were examined, we attained significant inverse correlation between the level and SLSA1 stability. These results may suggest that SA1D2prox sequence adapts over time, and also that the altered SA1D2prox sequence, SLSA1 stability, and level are mutually related. In total, we show here that the entire SA1D2prox sequence and SLSA1 stability critically contribute to the modulation of mRNA level.
HIV-1的基因组RNA包含对病毒复制至关重要的局部结构。其结构分析已证明在HIV-1基因组剪接受体1(SA1)附近区域存在一个茎环结构,即SLSA1。我们之前已经表明,SLSA1结构中聚集的一些自然单核苷酸变异(nSNV)会显著改变mRNA的表达水平。在本研究中,除了我们之前鉴定出的11个nSNV外,我们在从SA1、剪接供体2一直到Vif起始密码子的含SLSA1序列中总共发现了9个新的nSNV,这些nSNV显著影响mRNA水平,并将该序列命名为SA1D2prox(针对HIV-1 NL4-3为142个核苷酸)。然后,我们通过广泛的变异和诱变分析来研究SA1D2prox序列和SLSA1二级结构如何与mRNA水平相关。虽然SLSA1的二级结构和稳定性因nSNV以及为从nSNV改变的形式恢复到原始NL4-3形式而引入的人工突变而发生了很大变化,但未观察到这两个SLSA1特性与mRNA水平有明确关联。相比之下,当检查包含多个nSNV的天然SA1D2prox序列时,我们发现水平与SLSA1稳定性之间存在显著负相关。这些结果可能表明SA1D2prox序列会随时间适应,并且改变的SA1D2prox序列、SLSA1稳定性和水平是相互关联的。总体而言,我们在此表明整个SA1D2prox序列和SLSA1稳定性对mRNA水平的调节起着关键作用。