The concept that G-quadruplex (G4) structures can form within DNA or RNA in vitro has been long known and extensively discussed. In recent years, accumulating evidences imply that G-quadruplex structures form in vivo. Initially, inefficient regulation of G-quadruplex structures was mainly associated with genome instability. However, due to the location of G-quadruplex motifs and their evolutionary conservation, different cellular functions of these structures have been postulated (e.g. in telomere maintenance, DNA replication, transcription, and translation). Regardless of their function, efficient and controlled formation and unwinding are very important, because ‘mis’-regulated G-quadruplex structures are detrimental for a given process, causing genome instability and diseases. Several helicases have been shown to target and regulate specific G-quadruplex structures. This mini-review focuses on the biological consequences of G4 disruption by different helicases in vivo.
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Cover Image
Cover Image
The Holliday junction. The structure of the Holliday junction is highly variable, being adaptable to its biological function in recombination and to applications in biomolecular engineering. This image shows the how the junction extends from simple schematics to crystal structures as DNA only and in protein complexes. In addition, the junction has been exploited as an element in the design of 2-D and 3-D lattices in crystal engineering and more complex images and shapes through DNA origami. In this issue of Biochemical Society Transactions, P. Shing Ho reviews some interesting recent research on the Holliday junction; for details see pages 1149–1158.
G-quadruplex unwinding helicases and their function in vivo
Markus Sauer, Katrin Paeschke; G-quadruplex unwinding helicases and their function in vivo. Biochem Soc Trans 15 October 2017; 45 (5): 1173–1182. doi: https://doi.org/10.1042/BST20170097
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