Abstract
DNA can form several secondary structures besides the classic double helix: one that has received much attention in recent years is the G-quadruplex (G4). This is a stable four-stranded structure formed by the stacking of quartets of guanine bases. Recent work has convincingly shown that G4s can form in vivo as well as in vitro and can affect both replication and transcription of DNA. They also play important roles at G-rich telomeres. Now, a spate of exciting reports has begun to reveal roles for G4 structures in virulence processes in several important microbial pathogens of humans. Interestingly, these come from a range of kingdoms—bacteria and protozoa as well as viruses—and all facilitate immune evasion in different ways. In particular, roles for G4s have been posited in the antigenic variation systems of bacteria and protozoa, as well as in the silencing of at least two major human viruses, human immunodeficiency virus (HIV) and Epstein-Barr virus (EBV). Although antigenic variation and the silencing of latent viruses are quite distinct from one another, both are routes to immune evasion and the maintenance of chronic infections. Thus, highly disparate pathogens can use G4 motifs to control DNA/RNA dynamics in ways that are relevant to common virulence phenotypes. This review explores the evidence for G4 biology in such processes across a range of important human pathogens.
Highlights
The conformation of glycosidic bonds of guanine bases in G-tetrads, the cations present and the number of stacked G-tetrads further contribute to the myriad of topologies found amongst G4s [3,4,5,6]
Intramolecular G4s form from short runs of guanine bases separated by short runs of other bases
Several experimental techniques can determine whether the biophysical features of a synthetic putative quadruplex sequences (PQS)-containing oligonucleotide are consistent with G4 structure formation
Summary
Recent work has convincingly shown that G4s can form in vivo as well as in vitro and can affect both replication and transcription of DNA They play important roles at G-rich telomeres. The conformation of glycosidic bonds of guanine bases in G-tetrads, the cations present and the number of stacked G-tetrads further contribute to the myriad of topologies found amongst G4s [3,4,5,6] Predictive algorithms, such as G4P Calculator [7] and QuadParser [8], have been developed to identify putative quadruplex sequences (PQS) within nucleic acid sequences.
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