scholarly journals New 3D graphical representation for RNA structure analysis and its application in the pre-miRNA identification of plants

RSC Advances ◽  
2018 ◽  
Vol 8 (54) ◽  
pp. 30833-30841 ◽  
Author(s):  
Xiangzheng Fu ◽  
Bo Liao ◽  
Wen Zhu ◽  
Lijun Cai

MicroRNAs (miRNAs) are a family of short non-coding RNAs that play significant roles as post-transcriptional regulators.

PLoS ONE ◽  
2016 ◽  
Vol 11 (5) ◽  
pp. e0152238 ◽  
Author(s):  
Yi Zhang ◽  
Haiyun Huang ◽  
Xiaoqing Dong ◽  
Yiliang Fang ◽  
Kejing Wang ◽  
...  

Methods ◽  
2020 ◽  
Vol 183 ◽  
pp. 68-75 ◽  
Author(s):  
Phillip Tomezsko ◽  
Harish Swaminathan ◽  
Silvi Rouskin

Author(s):  
José M. Andrade ◽  
Ricardo F. dos Santos ◽  
Cecília M. Arraiano

2018 ◽  
Vol 48 (5) ◽  
pp. 1915-1927 ◽  
Author(s):  
Fariha Kanwal ◽  
Ting Chen ◽  
Yunlon Zhang ◽  
Altaf Simair ◽  
Cai Rujie ◽  
...  

Background/Aims: RNA elements such as catalytic RNA, riboswitch, microRNA, and long non coding RNA (lncRNA) play central roles in many cellular processes. Studying diverse RNA functions require large quantities of RNA for precise structure analysis. Current RNA structure and function studies can benefit from improved RNA quantity and quality, simpler separation procedure and enhanced accuracy of structural analysis. Methods: Here we present an optimized protocol for analyzing the structure of any RNA, including in vitro transcription, size-exclusion chromatography (SEC) based denaturing purification and improved secondary structure analysis by chemical probing. Results: We observed that higher Mg2+, nucleoside triphosphate (NTP) concentrations and longer reaction duration can improve the RNA yield from in vitro transcription, specifically for longer and more complicated constructs. Our improved SEC-based denaturing RNA purification effectively halved the experiment duration and labor without introducing any contaminant. Finally, this study increased the accuracy and signal-to-noise ratio (SNR) of selective 2′-hydroxyl acylation analyzed by primer extension (SHAPE) chemical probing for analyzing RNA structure. Conclusion: Part or all of our modified method can improve almost any RNA-related study from protein-RNA interaction analysis to crystallography.


2017 ◽  
Vol 46 (1) ◽  
pp. 11-21 ◽  
Author(s):  
David Mellis ◽  
Andrea Caporali

MicroRNAs (miRNAs) are small non-coding RNAs of ∼22 nucleotides, which have increasingly been recognized as potent post-transcriptional regulators of gene expression. MiRNA targeting is defined by the complementarities between positions 2–8 of miRNA 5′-end with generally the 3′-untranslated region of target mRNAs (messenger RNAs). The capacity of miRNAs to simultaneously inhibit many different mRNAs allows for an amplification of biological responses. Hence, miRNAs are extremely attractive targets for therapeutic regulation in several diseases, including cardiovascular. Novel approaches are emerging to identify the miRNA functions in cardiovascular biology processes and to improve miRNA delivery in the heart and vasculature. In the present study, we provide an overview of current studies of miRNA functions in cardiovascular cells by the use of high-content screening. We also discuss the challenge to achieve a safe and targeted delivery of miRNA therapeutics in cardiovascular cells.


2013 ◽  
Vol 32 (21) ◽  
pp. 2804-2818 ◽  
Author(s):  
Maria Anokhina ◽  
Sergey Bessonov ◽  
Zhichao Miao ◽  
Eric Westhof ◽  
Klaus Hartmuth ◽  
...  

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