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人类微小RNA发夹前体中二级结构元件的分析

Analysis of secondary structural elements in human microRNA hairpin precursors.

作者信息

Liu Biao, Childs-Disney Jessica L, Znosko Brent M, Wang Dan, Fallahi Mohammad, Gallo Steven M, Disney Matthew D

机构信息

Department of Chemistry, Scripps Florida, The Scripps Research Institute, 130 Scripps Way 3A1, Jupiter, FL, 33458, USA.

Center for Personalized Medicine, Roswell Park Cancer Institute, Buffalo, NY, 14263, USA.

出版信息

BMC Bioinformatics. 2016 Mar 1;17:112. doi: 10.1186/s12859-016-0960-6.

Abstract

BACKGROUND

MicroRNAs (miRNAs) regulate gene expression by targeting complementary mRNAs for destruction or translational repression. Aberrant expression of miRNAs has been associated with various diseases including cancer, thus making them interesting therapeutic targets. The composite of secondary structural elements that comprise miRNAs could aid the design of small molecules that modulate their function.

RESULTS

We analyzed the secondary structural elements, or motifs, present in all human miRNA hairpin precursors and compared them to highly expressed human RNAs with known structures and other RNAs from various organisms. Amongst human miRNAs, there are 3808 are unique motifs, many residing in processing sites. Further, we identified motifs in miRNAs that are not present in other highly expressed human RNAs, desirable targets for small molecules. MiRNA motifs were incorporated into a searchable database that is freely available. We also analyzed the most frequently occurring bulges and internal loops for each RNA class and found that the smallest loops possible prevail. However, the distribution of loops and the preferred closing base pairs were unique to each class.

CONCLUSIONS

Collectively, we have completed a broad survey of motifs found in human miRNA precursors, highly expressed human RNAs, and RNAs from other organisms. Interestingly, unique motifs were identified in human miRNA processing sites, binding to which could inhibit miRNA maturation and hence function.

摘要

背景

微小RNA(miRNA)通过靶向互补mRNA进行降解或翻译抑制来调节基因表达。miRNA的异常表达与包括癌症在内的多种疾病相关,因此使其成为有趣的治疗靶点。构成miRNA的二级结构元件的组合有助于设计调节其功能的小分子。

结果

我们分析了所有人类miRNA发夹前体中存在的二级结构元件或基序,并将它们与具有已知结构的高表达人类RNA以及来自各种生物体的其他RNA进行比较。在人类miRNA中,有3808个独特的基序,许多位于加工位点。此外,我们在miRNA中鉴定出其他高表达人类RNA中不存在的基序,这些是小分子的理想靶点。miRNA基序已被纳入一个可免费获取的可搜索数据库中。我们还分析了每种RNA类别中最常见的凸起和内环,发现可能的最小环占主导。然而,环的分布和首选的闭合碱基对在每个类别中都是独特的。

结论

总体而言,我们对在人类miRNA前体、高表达人类RNA和来自其他生物体的RNA中发现的基序进行了广泛的调查。有趣的是,在人类miRNA加工位点鉴定出了独特的基序,与这些基序结合可能会抑制miRNA的成熟,从而抑制其功能。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1a09/4772329/c05e95e61430/12859_2016_960_Fig1_HTML.jpg

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