The detailed structure of tandem G·A mismatched base-pair motifs in RNA duplexes is context dependent

1997 ◽  
Vol 271 (1) ◽  
pp. 147-158 ◽  
Author(s):  
Hans A. Heus ◽  
Sybren S. Wijmenga ◽  
Hans Hoppe ◽  
Cornelis W. Hilbers
2003 ◽  
Vol 3 (1) ◽  
pp. 131-132 ◽  
Author(s):  
A. Kobori ◽  
H. Suda ◽  
K. Nakatani ◽  
I. Saito

2017 ◽  
Author(s):  
Andrew Dittmore ◽  
Sumitabha Brahmachari ◽  
Yasuhara Takagi ◽  
John F. Marko ◽  
Keir C. Neuman

We present a method of detecting sequence defects by supercoiling DNA with magnetic tweezers. The method is sensitive to a single mismatched base pair in a DNA sequence of several thousand base pairs. We systematically compare DNA molecules with 0 to 16 adjacent mismatches at 1 M monovalent salt and 3.5 pN force and show that, under these conditions, a single plectoneme forms and is stably pinned at the defect. We use these measurements to estimate the energy and degree of end-loop kinking at defects. From this, we calculate the relative probability of plectoneme pinning at the mismatch under physiologically relevant conditions. Based on this estimate, we propose that DNA supercoiling could contribute to mismatch and damage sensing in vivo.


2018 ◽  
Vol 32 (11-12) ◽  
pp. 806-821 ◽  
Author(s):  
Riki Terui ◽  
Koji Nagao ◽  
Yoshitaka Kawasoe ◽  
Kanae Taki ◽  
Torahiko L. Higashi ◽  
...  

2010 ◽  
Vol 16 (44) ◽  
pp. 13218-13225 ◽  
Author(s):  
Hidetaka Torigoe ◽  
Akira Ono ◽  
Tetsuo Kozasa

Biochemistry ◽  
1999 ◽  
Vol 38 (27) ◽  
pp. 8635-8646 ◽  
Author(s):  
Sherry L. Painter ◽  
Irene S. Zegar ◽  
Pamela J. Tamura ◽  
Susanna Bluhm ◽  
Constance M. Harris ◽  
...  

2010 ◽  
Vol 20 (4) ◽  
pp. 199-206 ◽  
Author(s):  
Malgorzata Sierant ◽  
Julia Kazmierczak-Baranska ◽  
Alina Paduszynska ◽  
Milena Sobczak ◽  
Aleksandra Pietkiewicz ◽  
...  

Symmetry ◽  
2020 ◽  
Vol 12 (5) ◽  
pp. 737
Author(s):  
Udo Heinemann ◽  
Yvette Roske

In nature and in the test tube, nucleic acids occur in many different forms. Apart from single-stranded, coiled molecules, DNA and RNA prefer to form helical arrangements, in which the bases are stacked to shield their hydrophobic surfaces and expose their polar edges. Focusing on double helices, we describe the crucial role played by symmetry in shaping DNA and RNA structure. The base pairs in nucleic-acid double helices display rotational pseudo-symmetry. In the Watson–Crick base pairs found in naturally occurring DNA and RNA duplexes, the symmetry axis lies in the base-pair plane, giving rise to two different helical grooves. In contrast, anti-Watson–Crick base pairs have a dyad axis perpendicular to the base-pair plane and identical grooves. In combination with the base-pair symmetry, the syn/anti conformation of paired nucleotides determines the parallel or antiparallel strand orientation of double helices. DNA and RNA duplexes in nature are exclusively antiparallel. Watson–Crick base-paired DNA or RNA helices display either right-handed or left-handed helical (pseudo-) symmetry. Genomic DNA is usually in the right-handed B-form, and RNA double helices adopt the right-handed A-conformation. Finally, there is a higher level of helical symmetry in superhelical DNA in which B-form double strands are intertwined in a right- or left-handed sense.


Molecules ◽  
2020 ◽  
Vol 25 (4) ◽  
pp. 769 ◽  
Author(s):  
Kenji Takagi ◽  
Tenko Hayashi ◽  
Shinjiro Sawada ◽  
Miku Okazaki ◽  
Sakiko Hori ◽  
...  

During the treatment of viral or bacterial infections, it is important to evaluate any resistance to the therapeutic agents used. An amino acid substitution arising from a single base mutation in a particular gene often causes drug resistance in pathogens. Therefore, molecular tools that discriminate a single base mismatch in the target sequence are required for achieving therapeutic success. Here, we synthesized peptide nucleic acids (PNAs) derivatized with tolane via an amide linkage at the N-terminus and succeeded in improving the sequence specificity, even with a mismatched base pair located near the terminal region of the duplex. We assessed the sequence specificities of the tolane-PNAs for single-strand DNA and RNA by UV-melting temperature analysis, thermodynamic analysis, an in silico conformational search, and a gel mobility shift assay. As a result, all of the PNA-tolane derivatives stabilized duplex formation to the matched target sequence without inducing mismatch target binding. Among the different PNA-tolane derivatives, PNA that was modified with a naphthyl-type tolane could efficiently discriminate a mismatched base pair and be utilized for the detection of resistance to neuraminidase inhibitors of the influenza A/H1N1 virus. Therefore, our molecular tool can be used to discriminate single nucleotide polymorphisms that are related to drug resistance in pathogens.


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