Helmy Mohab, Hatlen Andrea, Marco Antonio
School of Biological Sciences, University of Essex, Colchester CO4 3SQ, UK.
Noncoding RNA. 2019 Jun 22;5(2):42. doi: 10.3390/ncrna5020042.
The impact of population variation in the analysis of regulatory interactions is an underdeveloped area. MicroRNA target recognition occurs via pairwise complementarity. Consequently, a number of computational prediction tools have been developed to identify potential target sites that can be further validated experimentally. However, as microRNA target predictions are done mostly considering a reference genome sequence, target sites showing variation among populations are neglected. Here, we studied the variation at microRNA target sites in human populations and quantified their impact in microRNA target prediction. We found that African populations carry a significant number of potential microRNA target sites that are not detectable in the current human reference genome sequence. Some of these targets are conserved in primates and only lost in Out-of-Africa populations. Indeed, we identified experimentally validated microRNA/transcript interactions that are not detected in standard microRNA target prediction programs, yet they have segregating target alleles abundant in non-European populations. In conclusion, we show that ignoring population diversity may leave out regulatory elements essential to understand disease and gene expression, particularly neglecting populations of African origin.
群体变异在调控相互作用分析中的影响是一个尚未充分发展的领域。微小RNA的靶标识别通过成对互补性发生。因此,已经开发了许多计算预测工具来识别可以通过实验进一步验证的潜在靶位点。然而,由于微小RNA靶标的预测大多是基于参考基因组序列进行的,所以群体间存在变异的靶位点被忽视了。在这里,我们研究了人类群体中微小RNA靶位点的变异,并量化了它们在微小RNA靶标预测中的影响。我们发现非洲人群携带大量在当前人类参考基因组序列中无法检测到的潜在微小RNA靶位点。其中一些靶标在灵长类动物中是保守的,仅在走出非洲的人群中丢失。事实上,我们鉴定出了在标准微小RNA靶标预测程序中未检测到的经实验验证的微小RNA/转录本相互作用,但它们具有在非欧洲人群中大量存在的分离靶标等位基因。总之,我们表明忽略群体多样性可能会遗漏理解疾病和基因表达所必需的调控元件,尤其是忽略了非洲裔人群。