scholarly journals Probing the Folding Dynamics of Human Telomeric G-Quadruplex with Single-Molecule FRET

2016 ◽  
Vol 110 (3) ◽  
pp. 406a
Author(s):  
Mikayel Aznauryan ◽  
Siri Søndergaard ◽  
Sofie Noer ◽  
Birgit Schiøtt ◽  
Victoria Birkedal
2015 ◽  
Vol 44 (1) ◽  
pp. 464-471 ◽  
Author(s):  
Sofie L. Noer ◽  
Søren Preus ◽  
Daniel Gudnason ◽  
Mikayel Aznauryan ◽  
Jean-Louis Mergny ◽  
...  

2012 ◽  
Vol 51 (24) ◽  
pp. 5876-5879 ◽  
Author(s):  
Martin Hengesbach ◽  
Nak-Kyoon Kim ◽  
Juli Feigon ◽  
Michael D. Stone

2020 ◽  
Vol 295 (16) ◽  
pp. 5461-5469 ◽  
Author(s):  
Wen-Qiang Wu ◽  
Ming-Li Zhang ◽  
Chun-Peng Song

Telomeres are specific nucleoprotein structures that are located at the ends of linear eukaryotic chromosomes and play crucial roles in genomic stability. Telomere DNA consists of simple repeats of a short G-rich sequence: TTAGGG in mammals and TTTAGGG in most plants. In recent years, the mammalian telomeric G-rich repeats have been shown to form G-quadruplex (G4) structures, which are crucial for modulating telomere functions. Surprisingly, even though plant telomeres are essential for plant growth, development, and environmental adaptions, only few reports exist on plant telomeric G4 DNA (pTG4). Here, using bulk and single-molecule assays, including CD spectroscopy, and single-molecule FRET approaches, we comprehensively characterized the structure and dynamics of a typical plant telomeric sequence, d[GGG(TTTAGGG)3]. We found that this sequence can fold into mixed G4s in potassium, including parallel and antiparallel structures. We also directly detected intermediate dynamic transitions, including G-hairpin, parallel G-triplex, and antiparallel G-triplex structures. Moreover, we observed that pTG4 is unfolded by the AtRecQ2 helicase but not by AtRecQ3. The results of our work shed light on our understanding about the existence, topological structures, stability, intermediates, unwinding, and functions of pTG4.


2012 ◽  
Vol 124 (24) ◽  
pp. 5978-5981 ◽  
Author(s):  
Martin Hengesbach ◽  
Nak-Kyoon Kim ◽  
Juli Feigon ◽  
Michael D. Stone

2020 ◽  
Author(s):  
Hamza Balci ◽  
Viktorija Globyte ◽  
Chirlmin Joo

ABSTRACTClustered Regularly Interspaced Palindromic Repeats (CRISPR) and CRISPR-associated (Cas) proteins, particularly Cas9, have provided unprecedented control on targeting and editing specific DNA sequences. If the target sequences are prone to folding into non-canonical secondary structures, such as G-quadruplex (GQ), the conformational states and activity of CRISPR-Cas9 complex would be influenced, but the impact has not been assessed. Using single molecule FRET, we investigated structural characteristics of the complex formed by CRISPR-Cas9 and target DNA, which contains a potentially GQ forming sequence (PQS) in either the target or the non-target strand (TS or NTS). We observed different conformational states and dynamics depending on the stability of the GQ and the position of PQS. When PQS was in NTS, we observed evidence for GQ formation for both weak and stable GQs. This is consistent with R-loop formation between TS and crRNA releasing NTS from Watson-Crick pairing and facilitating secondary structure formation in it. When PQS was in TS, R-loop formation was adequate to maintain a weak GQ in the unfolded state but not a GQ with moderate or high stability. The observed structural heterogeneity within the target dsDNA and the R-loop strongly depended on whether the PQS was in TS or NTS. We propose these variations in the complex structures to have functional implications for Cas9 activity.


2017 ◽  
Vol 292 (3) ◽  
pp. 483-498 ◽  
Author(s):  
Parastoo Maleki ◽  
Jagat B. Budhathoki ◽  
William A. Roy ◽  
Hamza Balci

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