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The folding of 5′-UTR human G-quadruplexes possessing a long central loop

机译:具有长中心环的5-UTR人类G-四链体的折叠

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摘要

G-quadruplexes are widespread four-stranded structures that are adopted by G-rich regions of both DNA and RNA and are involved in essential biological processes such as mRNA translation. They are formed by the stacking of two or more G-quartets that are linked together by three loops. Although the maximal loop length is usually fixed to 7 nt in most G-quadruplex-predicting software, it has already been demonstrated that artificial DNA G-quadruplexes containing two distal loops that are limited to 1 nt each and a central loop up to 30 nt long are likely to form in vitro. This report demonstrates that such structures possessing a long central loop are actually found in the 5′-UTRs of human mRNAs. Firstly, 1453 potential G-quadruplex-forming sequences (PG4s) were identified through a bioinformatic survey that searched for sequences respecting the requirement for two 1-nt long distal loops and a long central loop of 2–90 nt in length. Secondly, in vitro in-line probing experiments confirmed and characterized the folding of eight candidates possessing central loops of 10–70 nt long. Finally, the biological effect of several G-quadruplexes with a long central loop on mRNA expression was studied in cellulo using a luciferase gene reporter assay. Clearly, the actual definition of G-quadruplex-forming sequences is too conservative and must be expanded to include the long central loop. This greatly expands the number of expected PG4s in the transcriptome. Consideration of these new candidates might aid in elucidating the potentially important biological implications of the G-quadruplex structure.
机译:G-四链体是广泛的四链结构,被DNA和RNA的富含G的区域所采用,并参与基本的生物过程,例如mRNA翻译。它们是由两个或多个G四重奏的堆叠形成的,它们通过三个循环链接在一起。尽管在大多数G四联体预测软件中,最大环长度通常固定为7 nt,但已经证明,人工DNA G四联体包含两个远端环,每个环限制为1 nt,中央环最多30 nt长时间可能会在体外形成。该报告证明,实际上在人mRNA的5'-UTR中发现了具有长中央环的此类结构。首先,通过生物信息学调查确定了1453个潜在的G-四链体形成序列(PG4),该序列搜索的序列符合两个1-nt长的远端环和一个长2–90 nt的长中心环的要求。其次,体外在线探测实验确认并表征了具有10-70 nt长的中央环的8个候选分子的折叠。最后,使用萤光素酶基因报告基因测定法,研究了纤维素中具有中央长环的几个G-四链体对mRNA表达的生物学效应。显然,G-四链体形成序列的实际定义过于保守,必须扩展以包括较长的中心环。这大大扩展了转录组中预期的PG4的数量。考虑这些新的候选物可能有助于阐明G-四链体结构的潜在重要生物学意义。

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