Division Viral Transformation Mechanisms, Research Focus Infection, Inflammation and Cancer, German Cancer Research Center (Deutsches Krebsforschungszentrum, DKFZ), 69120 Heidelberg, Germany.
Core Facility Omics IT and Data Management, German Cancer Research Center (Deutsches Krebsforschungszentrum, DKFZ), 69120 Heidelberg, Germany.
Viruses. 2020 Nov 2;12(11):1250. doi: 10.3390/v12111250.
In addition to regulatory or accessory proteins, some complex retroviruses gain a repertoire of micro-RNAs (miRNAs) to regulate and control virus-host interactions for efficient replication and spread. In particular, bovine and simian foamy viruses (BFV and SFV) have recently been shown to express a diverse set of RNA polymerase III-directed miRNAs, some with a unique primary miRNA double-hairpin, dumbbell-shaped structure not known in other viruses or organisms. While the mechanisms of expression and structural requirements have been studied, the functional importance of these miRNAs is still far from understood. Here, we describe the in silico identification of BFV miRNA targets and the subsequent experimental validation of bovine Ankyrin Repeat Domain 17 (ANKRD17) and Bax-interacting factor 1 (Bif1) target genes in vitro and, finally, the suppression of ANKRD17 downstream genes in the affected pathway. Deletion of the entire miRNA cassette in the non-coding part of the U3 region of the long terminal repeats attenuated replication of corresponding BFV mutants in bovine cells. This repression can be almost completely trans-complemented by the most abundant miRNA BF2-5p having the best scores for predicted and validated BFV miRNA target genes. Deletion of the miRNA cassette does not grossly affect particle release and overall particle composition.
除了调节蛋白或辅助蛋白外,一些复杂的逆转录病毒还获得了一系列微小 RNA(miRNA),以调节和控制病毒-宿主相互作用,从而实现有效的复制和传播。特别是,牛和猿猴泡沫病毒(BFV 和 SFV)最近被证明能够表达一系列不同的 RNA 聚合酶 III 指导的 miRNA,其中一些具有独特的初级 miRNA 双链发夹,哑铃形结构在其他病毒或生物体中尚未发现。虽然已经研究了表达的机制和结构要求,但这些 miRNA 的功能重要性仍远未被理解。在这里,我们描述了 BFV miRNA 靶标的计算机识别,以及随后在体外对牛锚蛋白重复域 17(ANKRD17)和 Bax 相互作用因子 1(Bif1)靶基因的实验验证,最后是对受影响途径中 ANKRD17 下游基因的抑制。在长末端重复 U3 区非编码部分的整个 miRNA 盒缺失会削弱相应 BFV 突变体在牛细胞中的复制。这种抑制作用可以通过最丰富的 miRNA BF2-5p 几乎完全进行反式补偿,该 miRNA 具有针对预测和验证的 BFV miRNA 靶基因的最佳评分。miRNA 盒缺失不会严重影响颗粒释放和整体颗粒组成。