Department of Biochemistry and Biophysics, and the Center for RNA Biology, University of Rochester School of Medicine and Dentistry, Rochester, NY, USA.
RNA Biol. 2011 Mar-Apr;8(2):230-6. doi: 10.4161/rna.8.2.14802. Epub 2011 Mar 1.
After HIV-1 enters a human cell, its RNA genome is converted into double stranded DNA during the multistep process of reverse transcription. First (minus) strand DNA synthesis is initiated near the 5' end of the viral RNA, where only a short fragment of the genome is copied. In order to continue DNA synthesis the virus employs a complicated mechanism, which enables transferring of the growing minus strand DNA to a remote position at the genomic 3' end. This is called minus strand DNA transfer. The transfer enables regeneration of long terminal repeat sequences, which are crucial for viral genomic DNA integration into the host chromosome. Numerous factors have been identified that stimulate minus strand DNA transfer. In this review we focus on describing protein-RNA and RNA-RNA interactions, as well as RNA structural features, known to facilitate this step in reverse transcription.
HIV-1 进入人体细胞后,其 RNA 基因组在逆转录的多步过程中转化为双链 DNA。首先,在病毒 RNA 的 5' 端附近起始(-)链 DNA 的合成,其中仅复制基因组的一小段。为了继续 DNA 合成,病毒采用了一种复杂的机制,能够将生长中的(-)链 DNA 转移到基因组 3' 端的远程位置。这称为(-)链 DNA 转移。这种转移使长末端重复序列得以再生,这对于病毒基因组 DNA 整合到宿主染色体中至关重要。已经鉴定出许多刺激(-)链 DNA 转移的因素。在这篇综述中,我们专注于描述蛋白质-RNA 和 RNA-RNA 相互作用以及 RNA 结构特征,这些特征已知有助于逆转录中的这一步骤。