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As with all new fields of discovery, work on the biological role of G-quadruplexes (GQs) has produced a number of results that at first glance are quite baffling, sometimes because they do not fit well together, but mostly because they are different from commonly held expectations. Like other classes of flipons, those that form G-quadruplexes have a repeat sequence motif that enables the fold. The canonical DNA motif (GN)G, where N is any nucleotide and G is guanine, is a feature that is under active selection in avian and mammalian genomes. The involvement of G-flipons in genome maintenance traces back to the invertebrate and to ancient DNA repair pathways. The role of GQs in transcription is supported by the observation that yeast Rap1 protein binds both B-DNA, in a sequence-specific manner, and GQs, in a structure-specific manner, through the same helix. Other sequence-specific transcription factors (TFs) also engage both conformations to actuate cellular transactions. Noncoding RNAs can also modulate GQ formation in a sequence-specific manner and engage the same cellular machinery as localized by TFs, linking the ancient RNA world with the modern protein world. The coevolution of noncoding RNAs and sequence-specific proteins is supported by studies of early embryonic development, where the transient formation of G-quadruplexes coordinates the epigenetic specification of cell fate.
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http://dx.doi.org/10.3390/ijms251910299 | DOI Listing |
Nature
September 2025
Division of Genetics, Department of Medicine, Brigham and Women's Hospital and Harvard Medical School, Boston, MA, USA.
Transcription factors (TFs) regulate gene expression by interacting with DNA in a sequence-specific manner. High-throughput in vitro technologies, such as protein-binding microarrays and HT-SELEX (high-throughput systematic evolution of ligands by exponential enrichment), have revealed the DNA-binding specificities of hundreds of TFs. However, they have limited ability to reliably identify lower-affinity DNA binding sites, which are increasingly recognized as important for precise spatiotemporal control of gene expression.
View Article and Find Full Text PDFMethods Mol Biol
August 2025
Department of Computational Biology and Medical Sciences, Graduate School of Frontier Sciences, The University of Tokyo, Chiba, Japan.
RNA interference (RNAi) is a mechanism for regulating gene expression through small interfering RNAs (siRNAs), double-stranded RNA molecules approximately 20-23 nucleotides in length. The RNAi holds significant therapeutic potential for suppressing disease-related genes in a sequence-specific manner. Most commercially available siRNAs are extensively chemically modified to enhance stability or reduce immunogenicity.
View Article and Find Full Text PDFPlant Cell Environ
August 2025
State Key Laboratory of Crop Stress Resistance and High-Efficiency Production, College of Plant Protection, Northwest A&F University, Yangling, Shaanxi, China.
Genetic robustness refers to the ability of organisms to maintain normal phenotypes in the face of genetic variation, such as gene deletion. In plant pathogenic fungi, RNA-dependent RNA polymerases (RdRPs) play a crucial role in RNA interference (RNAi) signalling amplification in plant-pathogen interactions. However, the genetic robustness of RdRP-mediated fungal virulence and the molecular mechanisms regulating robustness remain elusive.
View Article and Find Full Text PDFIntegr Environ Assess Manag
August 2025
GreenLight Biosciences, 9 Laboratory Drive, Suite 300, Durham, NC 27709, USA.
Double-stranded RNA (dsRNA)-based biopesticides are a promising new method of pest management. These biopesticides leverage the endogenous RNA interference (RNAi) pathway to selectively regulate expression of key genes involved in growth and development in pests, providing the potential to minimize harmful environmental effects by highly specific targeting. As dsRNA-based biopesticides are presented for regulatory review, evaluating potential off-target effects on Non-Target Organisms (NTOs) in a manner that may be unique to this novel sequence-specific mode of action (MoA) is crucial.
View Article and Find Full Text PDFFront Mol Biosci
July 2025
Klaus Tschira Institute for Integrative Computational Cardiology, Department of Internal Medicine III, University Hospital Heidelberg, Heidelberg, Germany.
Nanopore direct RNA-sequencing is the first commercialized method to sequence native RNA directly, thus preserving RNA modifications. With the current technology, sequencing is initiated from the 3'end. While for relatively short polyadenylated RNAs, full coverage is obtained, the 5'end of many long RNAs is not sufficiently covered resulting in a substantial 3'bias.
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