Faculty Opinions recommendation of Chemical interrogation of mismatches in DNA-DNA and DNA-RNA duplexes under nonstringent conditions by selective 2'-amine acylation.

Author(s):  
Jim Maher
Keyword(s):  
2021 ◽  
Vol 7 (17) ◽  
pp. eabf6106
Author(s):  
Weiwei He ◽  
Yen-Lin Chen ◽  
Lois Pollack ◽  
Serdal Kirmizialtin

Double-stranded DNA (dsDNA) and RNA (dsRNA) helices display an unusual structural diversity. Some structural variations are linked to sequence and may serve as signaling units for protein-binding partners. Therefore, elucidating the mechanisms and factors that modulate these variations is of fundamental importance. While the structural diversity of dsDNA has been extensively studied, similar studies have not been performed for dsRNA. Because of the increasing awareness of RNA’s diverse biological roles, such studies are timely and increasingly important. We integrate solution x-ray scattering at wide angles (WAXS) with all-atom molecular dynamics simulations to explore the conformational ensemble of duplex topologies for different sequences and salt conditions. These tightly coordinated studies identify robust correlations between features in the WAXS profiles and duplex geometry and enable atomic-level insights into the structural diversity of DNA and RNA duplexes. Notably, dsRNA displays a marked sensitivity to the valence and identity of its associated cations.


2020 ◽  
Vol 0 (0) ◽  
Author(s):  
Pascal Donsbach ◽  
Dagmar Klostermeier

Abstract RNA helicases are a ubiquitous class of enzymes involved in virtually all processes of RNA metabolism, from transcription, mRNA splicing and export, mRNA translation and RNA transport to RNA degradation. Although ATP-dependent unwinding of RNA duplexes is their hallmark reaction, not all helicases catalyze unwinding in vitro, and some in vivo functions do not depend on duplex unwinding. RNA helicases are divided into different families that share a common helicase core with a set of helicase signature motives. The core provides the active site for ATP hydrolysis, a binding site for the non-sequence-specific interactions with RNA, and in many cases a basal unwinding activity. Its activity is often regulated by flanking domains, by interaction partners, or by self-association. In this review, we summarize the regulatory mechanisms that modulate the activities of the helicase core. Case studies on selected helicases with functions in translation, splicing, and RNA sensing illustrate the various modes and layers of regulation in time and space that harness the helicase core for a wide spectrum of cellular tasks.


2013 ◽  
Vol 639 (8-9) ◽  
pp. 1655-1660 ◽  
Author(s):  
Christopher Polonyi ◽  
Ingrid Albertsson ◽  
Mariana S. Damian ◽  
Sofi K. C. Elmroth
Keyword(s):  

2013 ◽  
Vol 49 (85) ◽  
pp. 9983 ◽  
Author(s):  
Yusuke Sato ◽  
Yu Toriyabe ◽  
Seiichi Nishizawa ◽  
Norio Teramae

2016 ◽  
pp. gkw1307 ◽  
Author(s):  
Fusheng Shen ◽  
Zhipu Luo ◽  
Hehua Liu ◽  
Rui Wang ◽  
Shenglong Zhang ◽  
...  

2018 ◽  
Vol 46 (22) ◽  
pp. 12099-12108 ◽  
Author(s):  
Daniel J Wright ◽  
Christopher R Force ◽  
Brent M Znosko
Keyword(s):  

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