Fan Jun, Negroni Matteo, Robertson David L
Faculty of Life Sciences, University of Manchester, Michael Smith Building, Oxford Road, Manchester M13 9PT, UK.
Infect Genet Evol. 2007 Dec;7(6):717-23. doi: 10.1016/j.meegid.2007.07.012. Epub 2007 Jul 28.
We find that recombination breakpoints are non-randomly distributed across the genomes of HIV-1 intersubtype recombinants. In particular we find two recombination prone regions, "hot spots", located approximately either side of the envelope gene. To investigate this, we test whether there is a correlation between the distribution of the recombinant breakpoints with (1) genetic similarity, (2) predicted locations of secondary RNA structure, (3) regions identified as recombinant hot spots from experimental studies and (4) the predicted locations of positively selected sites. No detectable relationship with RNA secondary structure was found. A weak relationship with genetic similarity exists but it does not account for the recombination hot spots. The comparison with the published experimental studies indicated that the identified recombination hot spots differ in their locations, indicating that selection is having an impact on HIV-1 recombinant structures in infected individuals. We observe an association between recombination prone regions and strong positive selection across the envelope gene in support of this hypothesis.
我们发现重组断点在HIV-1亚型间重组体的基因组中呈非随机分布。特别是,我们发现两个重组倾向区域,即“热点”,分别位于包膜基因两侧。为了对此进行研究,我们测试了重组断点的分布与以下因素之间是否存在相关性:(1)遗传相似性;(2)预测的RNA二级结构位置;(3)实验研究确定的重组热点区域;(4)正选择位点的预测位置。未发现与RNA二级结构有可检测到的关系。与遗传相似性存在微弱关系,但这并不能解释重组热点。与已发表的实验研究的比较表明,确定的重组热点在位置上有所不同,这表明选择对感染个体中的HIV-1重组结构有影响。我们观察到重组倾向区域与包膜基因上的强烈正选择之间存在关联,支持这一假设。