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Duplex stem-loop-containing quadruplex motifs in the human genome: a combined genomic and structural study

机译:人类基因组中含双链茎环的四链体基序:组合的基因组和结构研究

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Duplex stem-loops and four-stranded G-quadruplexes have been implicated in (patho)biological processes. Overlap of stem-loop- and quadruplex-forming sequences could give rise to quadruplex–duplex hybrids (QDH), which combine features of both structural forms and could exhibit unique properties. Here, we present a combined genomic and structural study of stem-loop-containing quadruplex sequences (SLQS) in the human genome. Based on a maximum loop length of 20 nt, our survey identified 80 307 SLQS, embedded within 60 172 unique clusters. Our analysis suggested that these should cover close to half of total SLQS in the entire genome. Among these, 48 508 SLQS were strand-specifically located in genic/promoter regions, with the majority of genes displaying a low number of SLQS. Notably, genes containing abundant SLQS clusters were strongly associated with brain tissues. Enrichment analysis of SLQS-positive genes and mapping of SLQS onto transcriptional/mutagenesis hotspots and cancer-associated genes, provided a statistical framework supporting the biological involvements of SLQS. In vitro formation of diverse QDH by selective SLQS hits were successfully verified by nuclear magnetic resonance?spectroscopy. Folding topologies of two SLQS were elucidated in detail. We also demonstrated that sequence changes at mutation/single-nucleotide polymorphism loci could affect the structural conformations adopted by SLQS. Thus, our predicted SLQS offer novel insights into the potential involvement of QDH in diverse (patho)biological processes and could represent novel regulatory signals.
机译:双链茎环和四链G-四链体与(病理)生物学过程有关。茎-环-和四链体形成序列的重叠可能会产生四链体-双链体杂种(QDH),它们结合了两种结构形式的特征,并可能表现出独特的特性。在这里,我们介绍了人类基因组中包含茎环的四链体序列(SLQS)的组合基因组和结构研究。基于最大回路长度20 nt,我们的调查确定了80307 SLQS,嵌入60172个唯一簇中。我们的分析表明,这些应覆盖整个基因组中接近总SLQS的一半。其中,48 508个SLQS特异性位于基因/启动子区域,大多数基因显示出低数量的SLQS。值得注意的是,含有大量SLQS簇的基因与脑组织密切相关。 SLQS阳性基因的富集分析以及将SLQS定位到转录/诱变热点和癌症相关基因上,提供了支持SLQS生物学参与的统计框架。通过选择性SLQS命中体外形成的各种QDH已通过核磁共振波谱成功地证实。详细说明了两个SLQS的折叠拓扑。我们还证明了突变/单核苷酸多态性基因座处的序列变化可能会影响SLQS采用的结构构象。因此,我们预测的SLQS为QDH在不同的(病理)生物学过程中的潜在参与提供了新颖的见解,并可能代表了新颖的调节信号。

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