Divergent distributions of inverted repeats and G-quadruplex forming sequences in Saccharomyces cerevisiae
Language English Country United States Media print-electronic
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
31706022
DOI
10.1016/j.ygeno.2019.11.002
PII: S0888-7543(19)30526-9
Knihovny.cz E-resources
- Keywords
- G-quadruplex, Inverted repeat, Saccharomyces cerevisiae,
- MeSH
- Centromere genetics MeSH
- DNA, Fungal chemistry genetics MeSH
- G-Quadruplexes * MeSH
- Genome, Fungal MeSH
- Inverted Repeat Sequences * MeSH
- RNA, Ribosomal genetics MeSH
- Saccharomyces cerevisiae MeSH
- Telomere genetics MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- DNA, Fungal MeSH
- RNA, Ribosomal MeSH
The importance of DNA structure in the regulation of basic cellular processes is an emerging field of research. Among local non-B DNA structures, inverted repeat (IR) sequences that form cruciforms and G-rich sequences that form G-quadruplexes (G4) are found in all prokaryotic and eukaryotic organisms and are targets for regulatory proteins. We analyzed IRs and G4 sequences in the genome of the most important biotechnology microorganism, S. cerevisiae. IR and G4-prone sequences are enriched in specific genomic locations and differ markedly between mitochondrial and nuclear DNA. While G4s are overrepresented in telomeres and regions surrounding tRNAs, IRs are most enriched in centromeres, rDNA, replication origins and surrounding tRNAs. Mitochondrial DNA is enriched in both IR and G4-prone sequences relative to the nuclear genome. This extensive analysis of local DNA structures adds to the emerging picture of their importance in genome maintenance, DNA replication and transcription of subsets of genes.
References provided by Crossref.org
Variability of Inverted Repeats in All Available Genomes of Bacteria
Interaction of Proteins with Inverted Repeats and Cruciform Structures in Nucleic Acids
Analysis of putative quadruplex-forming sequences in fungal genomes: novel antifungal targets?