Applications of synthetic oligoribonucleotide analogues in studies of RNA structure and function

1994 ◽  
Vol 106 (5) ◽  
pp. 1003-1022
Author(s):  
Jane A. Grasby ◽  
Clare E. Pritchard ◽  
Michael J. Gait
2014 ◽  
Vol 15 (7) ◽  
pp. 469-479 ◽  
Author(s):  
Stefanie A. Mortimer ◽  
Mary Anne Kidwell ◽  
Jennifer A. Doudna

2019 ◽  
Vol 14 (9) ◽  
pp. 866-873 ◽  
Author(s):  
Joseph D. Yesselman ◽  
Daniel Eiler ◽  
Erik D. Carlson ◽  
Michael R. Gotrik ◽  
Anne E. d’Aquino ◽  
...  

ACS Omega ◽  
2019 ◽  
Vol 4 (1) ◽  
pp. 699-709 ◽  
Author(s):  
Antarip Halder ◽  
Saurabh Vemuri ◽  
Rohit Roy ◽  
Jayanth Katuri ◽  
Dhananjay Bhattacharyya ◽  
...  

2017 ◽  
Vol 46 (4) ◽  
pp. 1052-1079 ◽  
Author(s):  
Anouk S. Lubbe ◽  
Wiktor Szymanski ◽  
Ben L. Feringa

A critical overview is given of recent applications of molecular photoswitches to modulate DNA and RNA structure and function.


2012 ◽  
pp. 23-51 ◽  
Author(s):  
Namhee Kim ◽  
Katherine Niccole Fuhr ◽  
Tamar Schlick

2020 ◽  
Author(s):  
Jennifer Frommer ◽  
Sabine Müller

Synthesis of site-specifically modified oligonucleotides has become a major tool for RNA structure and function studies. Reporter groups or specific functional entities are required to be attached at a pre-defined site of the oligomer.  An attractive strategy is the incorporation of suitably functionalized building blocks that allow post-synthetic conjugation of the desired moiety. A C8-alkynyl modified adenosine derivative was synthesized, reviving an old synthetic pathway for iodination of purine nucleobases. Silylation of the C8-alkynyl modified adenosine revealed unexpected selectivity of the two secondary sugar hydroxyl groups, with the 3'-O-isomer being preferentially formed. Optimization of the protection scheme lead to a new and economic route to the desired C8-alkynylated building block and its incorporation in RNA.


F1000Research ◽  
2018 ◽  
Vol 7 ◽  
pp. 1824 ◽  
Author(s):  
Brigitte Schönberger ◽  
Christoph Schaal ◽  
Richard Schäfer ◽  
Björn Voß

Tight regulation of cellular processes is key to the development of complex organisms but also vital for simpler ones. During evolution, different regulatory systems have emerged, among them RNA-based regulation that is carried out mainly by intramolecular and intermolecular RNA–RNA interactions. However, methods for the transcriptome-wide detection of these interactions were long unavailable. Recently, three publications described high-throughput methods to directly detect RNA duplexes in living cells. This promises to enable in-depth studies of RNA-based regulation and will narrow the gaps in our understanding of RNA structure and function. In this review, we highlight the benefits of these methods and their commonalities and differences and, in particular, point to methodological shortcomings that hamper their wider application. We conclude by presenting ideas for how to overcome these problems and commenting on the prospects we see in this area of research.


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