Abstract

Irradiation of G-quadruplex forming human telomeric DNA with ultraviolet B (UVB) light results in the formation of anti cyclobutane pyrimidine dimers (CPDs) between loop 1 and loop 3 in the presence of potassium ions but not sodium ions. This was unexpected because the sequences involved favor the nonphotoreactive hybrid conformations in K+ solution, whereas a potentially photoreactive basket conformation is favored in Na+ solution. To account for these contradictory results, it was proposed that the loops are too far apart in the basket conformation in Na+ solution but close enough in a two G-tetrad basket-like form 3 conformation that can form in K+ solution. In the current study, Na+ was still found to inhibit anti CPD formation in sequences designed to stabilize the form 3 conformation. Furthermore, anti CPD formation in K+ solution was slower for the sequence previously shown to exist primarily in the proposed photoreactive form 3 conformation than the sequence shown to exist primarily in a nonphotoreactive hybrid conformation. These results suggest that the form 3 conformation is not the principal photoreactive conformation, and that G-quadruplexes in K+ solution are dynamic and able to access photoreactive conformations more easily than in Na+ solution.

Highlights

  • Telomeres are the capping structures at the ends of each chromosome that are responsible for protecting DNA against gene erosion during cellular division and act as a cellular marker for apoptosis when the sequence has been shortened to a critical length [1]

  • To elucidate the structure–activity relationships of UVinduced anti cyclobutane pyrimidine dimers (CPDs) formation in human telomeric G-quadruplexes, we first focused on Tel26

  • The first goal of this study was to see whether the yield of the trans,anti CPD was enhanced in the NF3 sequence and whether anti CPD formation could be further enhanced by sequence modifications to Tel26 and NF3 (Figure 2) that would stabilize a 4-nt loop 1 basket structure with three G-tetrads in both Na+ and K+ solutions

Read more

Summary

Introduction

Telomeres are the capping structures at the ends of each chromosome that are responsible for protecting DNA against gene erosion during cellular division and act as a cellular marker for apoptosis when the sequence has been shortened to a critical length [1]. The displaced oligomeric TTAGGG strand is bound by a sixprotein shelterin complex composed of the telomere repeat binding factors TRF1, TRF2 and protection of telomere protein POT1, along with accessory proteins RAP1, TPP1 and TIN2a [2,3] These proteins serve to protect the otherwise single-stranded telomeric DNA from degradation. The sequence d[AAAGGG(TTAGGG)3AA], (Tel26), which initially forms a mixture of hybrid-1 and hybrid-2 structures in the presence of K+, converts primarily to the hybrid-1 conformer [10,11] Another unique G-quadruplex structure, form 3, has been discovered for d[GGG(TTAGGG)3T], (NF3), in K+ solution that forms a basket-type structure that contains only two G quartets instead of three [12].

Objectives
Results
Conclusion
Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.