Prostova Maria A, Gmyl Anatoly P, Bakhmutov Denis V, Shishova Anna A, Khitrina Elena V, Kolesnikova Marina S, Serebryakova Marina V, Isaeva Olga V, Agol Vadim I
a M P Chumakov Institute of Poliomyelitis and Viral Encephalitides ; Moscow Russia.
b M V Lomonosov Moscow State University ; Moscow Russia.
RNA Biol. 2015;12(12):1338-54. doi: 10.1080/15476286.2015.1100794.
Since replication of RNA-viruses is generally a low-fidelity process, it would be advantageous, if specific interactions of their genomic cis-elements with dedicated ligands are relatively tolerant to mutations. The specificity/promiscuity trade-off of such interactions was addressed here by investigating structural requirements of the oriL (also known as the clover leaf-like element), of poliovirus RNA, a replicative cis-element containing a conserved essential tetraloop functionally interacting with the viral protein 3CD. The sequence of this tetraloop and 2 adjacent base-pairs was randomized in the viral genome, and viable viruses were selected in susceptible cells. Strikingly, each position of this octanucleotide in 62 investigated viable viruses could be occupied by any nucleotide (with the exception of one position, which lacked U), though with certain sequence preferences, confirmed by engineering mutant viral genomes whose phenotypic properties were found to correlate with the strength of the cis-element/ligand interaction. The results were compatible with a hypothesis that functional recognition by 3CD requires that this tetraloop should stably or temporarily adopt a YNMG-like (Y=U/C, N=any nucleotide, M=A/C) fold. The fitness of "weak" viruses could be increased by compensatory mutations "improving" the tetraloops. Otherwise, the recognition of "bad" tetraloops might be facilitated by alterations in the 3CD protein. The virus appeared to tolerate mutations in its cis-element relaying on either robustness (spatial structure degeneracy) or resilience (a combination of dynamic RNA folding, low-fidelity replication modifying the cis-element or its ligand, and negative selection). These mechanisms (especially resilience involving metastable low-fit intermediates) can also contribute to the viral evolvability.
由于RNA病毒的复制通常是一个低保真度的过程,因此,如果其基因组顺式元件与特定配体的特异性相互作用对突变相对耐受,那将是有利的。本文通过研究脊髓灰质炎病毒RNA的oriL(也称为苜蓿叶状元件)的结构要求,探讨了这种相互作用的特异性/混杂性权衡,oriL是一种复制性顺式元件,含有一个保守的必需四环,可与病毒蛋白3CD发生功能相互作用。该四环的序列及其相邻的两个碱基对在病毒基因组中被随机化,并在易感细胞中筛选出存活病毒。令人惊讶的是,在62种被研究的存活病毒中,这个八核苷酸的每个位置都可以被任何核苷酸占据(有一个位置除外,该位置缺少尿嘧啶),尽管有一定的序列偏好,通过构建突变病毒基因组得到证实,其表型特性与顺式元件/配体相互作用的强度相关。结果与一个假设相符,即3CD的功能识别要求这个四环应稳定或暂时采用YNMG样(Y = U/C,N = 任何核苷酸,M = A/C)折叠。“弱”病毒的适应性可以通过“改善”四环的补偿性突变来提高。否则,3CD蛋白的改变可能会促进对“不良”四环的识别。病毒似乎能够耐受其顺式元件中的突变,这依赖于稳健性(空间结构简并性)或恢复力(动态RNA折叠、修饰顺式元件或其配体的低保真复制以及负选择的组合)。这些机制(特别是涉及亚稳态低适应性中间体的恢复力)也有助于病毒的进化能力。