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Interplay between HIV-1 infection and host microRNAs

机译:HIV-1感染与宿主microRNA之间的相互作用

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Using microRNA array analyses of in vitro HIV-1-infected CD4(+) cells, we find that several host microRNAs are significantly up- or downregulated around the time HIV-1 infection peaks in vitro. While microRNA-223 levels were significantly enriched in HIV-1-infected CD4(+)CD8(-) PBMCs, microRNA-29a/b, microRNA-155 and microRNA-21 levels were significantly reduced. Based on the potential for microRNA binding sites in a conserved sequence of the Nef-3'-LTR, several host microRNAs potentially could affect HIV-1 gene expression. Among those microRNAs, the microRNA-29 family has seed complementarity in the HIV-1 3'-UTR, but the potential suppressive effect of microRNA-29 on HIV-1 is severely blocked by the secondary structure of the target region. Our data support a possible regulatory circuit at the peak of HIV-1 replication which involves downregulation of microRNA-29, expression of Nef, the apoptosis of host CD4 cells and upregulation of microRNA-223.
机译:使用对体外HIV-1感染的CD4(+)细胞的microRNA阵列分析,我们发现,在HIV-1感染在体外达到高峰时,一些宿主microRNA被显着上调或下调。虽然microRNA-223的水平在HIV-1感染的CD4(+)CD8(-)PBMC中明显丰富,但microRNA-29a / b,microRNA-155和microRNA-21的水平却明显降低。基于Nef-3'-LTR保守序列中微小RNA结合位点的潜力,几种宿主微小RNA可能会影响HIV-1基因的表达。在这些microRNA中,microRNA-29家族在HIV-1 3'-UTR中具有种子互补性,但microRNA-29对HIV-1的潜在抑制作用被目标区域的二级结构严重阻断。我们的数据支持在HIV-1复制高峰期可能存在的调控回路,其中涉及microRNA-29的下调,Nef的表达,宿主CD4细胞的凋亡和microRNA-223的上调。

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