2025
Asymmetric distribution of G-quadruplex forming sequences in genomes of retroviruses
KLEDUS, Filip; Michaela DOBROVOLNA; Jean-Louis MERGNY and Václav BRÁZDABasic information
Original name
Asymmetric distribution of G-quadruplex forming sequences in genomes of retroviruses
Authors
KLEDUS, Filip (203 Czech Republic, belonging to the institution); Michaela DOBROVOLNA (203 Czech Republic); Jean-Louis MERGNY (250 France) and Václav BRÁZDA (203 Czech Republic, guarantor)
Edition
Nature Scientific Reports, BERLIN, NATURE PORTFOLIO, 2025, 2045-2322
Other information
Language
English
Type of outcome
Article in a journal
Field of Study
10608 Biochemistry and molecular biology
Country of publisher
Germany
Confidentiality degree
is not subject to a state or trade secret
References:
Impact factor
Impact factor: 3.800 in 2023
Organization unit
Faculty of Science
UT WoS
001390050200002
EID Scopus
2-s2.0-85213943520
Keywords in English
G-quadruplex; Retroviral genome; Bioinformatics; Persistent infection; G4Hunter
Tags
Tags
International impact, Reviewed
Changed: 27/2/2025 10:28, Mgr. Marie Novosadová Šípková, DiS.
Abstract
V originále
Retroviruses are among the most extensively studied viral families, both historically and in contemporary research. They are primarily investigated in the fields of viral oncogenesis, reverse transcription mechanisms, and other infection-specific aspects. These include the integration of endogenous retroviruses (ERVs) into host genomes, a process widely utilized in genetic engineering, and the ongoing search for HIV/AIDS treatment. G-quadruplexes (G4) have emerged as potential therapeutic targets in antiviral therapy and have been identified in important regulatory regions of viral genomes. In this study, we examine the presence of potential G-quadruplex-forming sequences (PQS) across all currently available unique retroviral genomes. Given that these retroviral genomes typically consist of single-stranded RNA (ssRNA) molecules, we also investigated whether the localization of PQSs is strand-dependent. This is particularly relevant since antisense transcripts have been detected in HIV, and ERV integration into the host genome involves reverse transcription from genomic positive strand ssRNA to double-stranded DNA (dsDNA), implicating both strands in this process. We show that in most mammalian retroviruses, including human retroviruses, PQSs are significantly more prevalent on the negative (antisense) strand, with some notable exceptions such as HIV-1. In sharp contrast, avian retroviruses exhibit a higher prevalence of PQSs on the positive (sense) strand.