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HIV基因中人类编码微小RNA的靶标

Targets for human encoded microRNAs in HIV genes.

作者信息

Hariharan Manoj, Scaria Vinod, Pillai Beena, Brahmachari Samir K

机构信息

G.N. Ramachandran Knowledge Center for Genome Informatics, Institute of Genomics and Integrative Biology, Mall Road, Delhi 110 007, India.

出版信息

Biochem Biophys Res Commun. 2005 Dec 2;337(4):1214-8. doi: 10.1016/j.bbrc.2005.09.183. Epub 2005 Oct 7.

DOI:10.1016/j.bbrc.2005.09.183
PMID:16236258
Abstract

MicroRNAs (miRNAs) are increasingly being shown to play vital roles in development, apoptosis, and oncogenesis by interfering with gene expression at the post-transcriptional level. miRNAs, in principle, can contribute to the repertoire of host pathogen interactions during HIV-1 infection. Using a consensus scoring approach, high scoring miRNA-target pairs were selected which were identified by four well-established target prediction softwares. While hsa-mir-29a and 29b target the nef gene, hsa-mir-149 targets the vpr gene, hsa-mir-378 targets env, and hsa-mir-324-5p targets the vif gene. Not only were the minimum free energy values lowest for the bound complex, but also, the rules so far observed for microRNA-target pairing, viz., a continuous stretch of 6-7 base pairing towards the 5' end of the miRNA and incomplete complementarity with the target sequence, were found to be valid. The target regions were highly conserved across the various clades of HIV-1. microRNA expression profiles from previously reported microarray based experiments show that the five human miRNAs are expressed in T-cells, the normal site of infection of HIV-1 virus. This is the first report of human microRNAs which can target crucial HIV-1 genes including the nef gene, which plays an important role in delayed disease progression.

摘要

微小RNA(miRNA)越来越多地被证明在发育、细胞凋亡和肿瘤发生过程中通过在转录后水平干扰基因表达发挥重要作用。原则上,miRNA可在HIV-1感染期间参与宿主病原体相互作用。采用一致性评分方法,选择了由四种成熟的靶标预测软件鉴定出的高评分miRNA-靶标对。其中,hsa-mir-29a和29b靶向nef基因,hsa-mir-149靶向vpr基因,hsa-mir-378靶向env基因,hsa-mir-324-5p靶向vif基因。不仅结合复合物的最小自由能值最低,而且到目前为止观察到的miRNA-靶标配对规则,即miRNA 5'端连续6-7个碱基对的延伸以及与靶标序列的不完全互补,也被证明是有效的。这些靶标区域在HIV-1的各个进化分支中高度保守。先前基于微阵列实验报道的miRNA表达谱表明,这五种人类miRNA在T细胞中表达,而T细胞是HIV-1病毒的正常感染部位。这是关于人类miRNA可靶向包括nef基因在内的关键HIV-1基因的首次报道,nef基因在疾病进展延迟中起重要作用。

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