Mandal Dibyakanti, Exline Colin M, Feng Zehua, Stoltzfus C Martin
Department of Microbiology, University of Iowa, Iowa City, Iowa 52242, USA.
J Virol. 2009 Jun;83(12):6067-78. doi: 10.1128/JVI.02231-08. Epub 2009 Apr 8.
The human immunodeficiency virus type 1 (HIV-1) accessory protein Vif is encoded by an incompletely spliced mRNA resulting from splicing of the major splice donor in the HIV-1 genome, 5' splice site (5'ss) D1, to the first splice acceptor, 3'ss A1. We have shown previously that splicing of HIV-1 vif mRNA is tightly regulated by suboptimal 5'ss D2, which is 50 nucleotides downstream of 3'ss A1; a GGGG silencer motif proximal to 5'ss D2; and an SRp75-dependent exonic splicing enhancer (ESEVif). In agreement with the exon definition hypothesis, mutations within 5'ss D2 that are predicted to increase or decrease U1 snRNP binding affinity increase or decrease the usage of 3'ss A1 (D2-up and D2-down mutants, respectively). In this report, the importance of 5'ss D2 and ESEVif for avoiding restriction of HIV-1 by APOBEC3G (A3G) was determined by testing the infectivities of a panel of mutant viruses expressing different levels of Vif. The replication of D2-down and ESEVif mutants in permissive CEM-SS cells was not significantly different from that of wild-type HIV-1. Mutants that expressed Vif in 293T cells at levels greater than 10% of that of the wild type replicated similarly to the wild type in H9 cells, and Vif levels as low as 4% were affected only modestly in H9 cells. This is in contrast to Vif-deleted HIV-1, whose replication in H9 cells was completely inhibited. To test whether elevated levels of A3G inhibit replication of D2-down and ESEVif mutants relative to wild-type virus replication, a Tet-off Jurkat T-cell line that expressed approximately 15-fold-higher levels of A3G than control Tet-off cells was generated. Under these conditions, the fitness of all D2-down mutant viruses was reduced relative to that of wild-type HIV-1, and the extent of inhibition was correlated with the level of Vif expression. The replication of an ESEVif mutant was also inhibited only at higher levels of A3G. Thus, wild-type 5'ss D2 and ESEVif are required for production of sufficient Vif to allow efficient HIV-1 replication in cells expressing relatively high levels of A3G.
1型人类免疫缺陷病毒(HIV-1)辅助蛋白Vif由一种不完全剪接的mRNA编码,该mRNA是由HIV-1基因组中的主要剪接供体、5'剪接位点(5'ss)D1与第一个剪接受体、3'ss A1剪接产生的。我们之前已经表明,HIV-1 vif mRNA的剪接受次优5'ss D2严格调控,5'ss D2位于3'ss A1下游50个核苷酸处;一个靠近5'ss D2的GGGG沉默子基序;以及一个依赖SRp75的外显子剪接增强子(ESEVif)。与外显子定义假说一致,预测会增加或降低U1 snRNP结合亲和力的5'ss D2内的突变分别增加或降低了3'ss A1的使用(分别为D2上调和D2下调突变体)。在本报告中,通过测试一组表达不同水平Vif的突变病毒的感染性,确定了5'ss D2和ESEVif对于避免APOBEC3G(A3G)对HIV-1的限制的重要性。D2下调和ESEVif突变体在允许的CEM-SS细胞中的复制与野生型HIV-1没有显著差异。在293T细胞中表达的Vif水平高于野生型10%的突变体在H9细胞中的复制与野生型相似,在H9细胞中低至4%的Vif水平仅受到轻微影响。这与缺失Vif的HIV-1形成对比,其在H9细胞中的复制被完全抑制。为了测试相对于野生型病毒复制,A3G水平升高是否会抑制D2下调和ESEVif突变体的复制,构建了一种Tet-off Jurkat T细胞系,其表达的A3G水平比对照Tet-off细胞高约15倍。在这些条件下,所有D2下调突变病毒的适应性相对于野生型HIV-1都降低了,并且抑制程度与Vif表达水平相关。ESEVif突变体的复制也仅在较高水平的A3G时受到抑制。因此,野生型5'ss D2和ESEVif是产生足够的Vif以允许HIV-1在表达相对高水平A3G的细胞中有效复制所必需的。