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Hidden messages in the nef gene of human immunodeficiency virus type I suggest a novel RNA secondary structure

机译:人类免疫缺陷病毒I型的nef基因中的隐藏信息提示一种新的RNA二级结构

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The coexistence of multiple codes in the genome of human immunodeficiency virus type 1 (HIV-1) was analyzed. We explored factors constraining the variability of the virus genome primarily in relation to conserved RNA secondary structures overlapping coding sequences, and used a simple combination of algorithms for RNA secondary structure prediction based on the nearest-neighbor thermodynamic rules and a statistical approach. In our previous study, we applied this combination to a non-redundant data set of env nucleotide sequences, confirmed the conservative secondary structure of the rev-responsive element (RRE) and found a new RNA structure in the first conserved (C1) region of the env gene. In this study, we analyzed the variability of putative RNA secondary structures inside the nef gene of HIV-1 by applying these algorithms to a non-redundant data set of 104 nef sequences retrieved from the Los Alamos HIV database, and predicted the existence of a novel functional RNA secondary structure in the β3/β4 regions of nef. The predicted RNA fold in the β3/β4 region of nef appears in two forms with different loop sizes. The loop of the first fold consists of seven nucleotides (positions 494-500), with consensus UCAAGCU appearing in 79% of sequences. The other has a five-base loop (positions 495-499) with consensus CAAGC. The difference in size between these two loops may reflect the difference between respective counterparts in the hairpin recognition. This may also have an adaptive biological significance.
机译:分析了人类1型免疫缺陷病毒(HIV-1)基因组中多个密码的共存。我们探索了主要与保守的RNA二级结构重叠的编码序列有关的因素来限制病毒基因组的变异性,并基于最近邻的热力学规则和统计方法,使用简单的算法组合来预测RNA二级结构。在先前的研究中,我们将此组合应用于env核苷酸序列的非冗余数据集,确认了rev响应元件(RRE)的保守二级结构,并在该基因的第一个保守(C1)区发现了新的RNA结构。 env基因。在这项研究中,我们通过将这些算法应用于从洛斯阿拉莫斯HIV数据库中检索到的104个nef序列的非冗余数据集,分析了HIV-1 nef基因内部推定RNA二级结构的变异性,并预测了nef的β3/β4区域具有新颖的功能性RNA二级结构。 nef的β3/β4区域中的预测RNA折叠以两种形式出现,并具有不同的环大小。第一个折叠的环由七个核苷酸(第494-500位)组成,共有UCAAGCU出现在79%的序列中。另一个具有五基循环(位置495-499),并具有一致的CAAGC。这两个循环之间的大小差异可以反映发夹识别中相应副本之间的差异。这也可能具有适应性生物学意义。

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