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Genome wide distribution of G-quadruplexes and their impact on gene expression in malaria parasites
E. Gazanion, L. Lacroix, P. Alberti, P. Gurung, S. Wein, M. Cheng, JL. Mergny, AR. Gomes, JJ. Lopez-Rubio,
Jazyk angličtina Země Spojené státy americké
Typ dokumentu časopisecké články, práce podpořená grantem
NLK
Directory of Open Access Journals
od 2005
Free Medical Journals
od 2005
Public Library of Science (PLoS)
od 2005-07-01
PubMed Central
od 2005
Europe PubMed Central
od 2005
ProQuest Central
od 2005-07-01
Open Access Digital Library
od 2005-07-01
Open Access Digital Library
od 2005-01-01
Open Access Digital Library
od 2005-01-01
Medline Complete (EBSCOhost)
od 2005-07-01
Health & Medicine (ProQuest)
od 2005-07-01
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od 2005
- MeSH
- aminochinoliny farmakologie MeSH
- G-kvadruplexy * MeSH
- genom účinky léků MeSH
- kyseliny pikolinové farmakologie MeSH
- lidé MeSH
- malárie farmakoterapie genetika parazitologie MeSH
- nukleotidové motivy genetika MeSH
- Plasmodium falciparum genetika patogenita MeSH
- promotorové oblasti (genetika) genetika MeSH
- regulace genové exprese účinky léků MeSH
- ribozomy účinky léků genetika MeSH
- zvířata MeSH
- Check Tag
- lidé MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
Mechanisms of transcriptional control in malaria parasites are still not fully understood. The positioning patterns of G-quadruplex (G4) DNA motifs in the parasite's AT-rich genome, especially within the var gene family which encodes virulence factors, and in the vicinity of recombination hotspots, points towards a possible regulatory role of G4 in gene expression and genome stability. Here, we carried out the most comprehensive genome-wide survey, to date, of G4s in the Plasmodium falciparum genome using G4Hunter, which identifies G4 forming sequences (G4FS) considering their G-richness and G-skewness. We show an enrichment of G4FS in nucleosome-depleted regions and in the first exon of var genes, a pattern that is conserved within the closely related Laverania Plasmodium parasites. Under G4-stabilizing conditions, i.e., following treatment with pyridostatin (a high affinity G4 ligand), we show that a bona fide G4 found in the non-coding strand of var promoters modulates reporter gene expression. Furthermore, transcriptional profiling of pyridostatin-treated parasites, shows large scale perturbations, with deregulation affecting for instance the ApiAP2 family of transcription factors and genes involved in ribosome biogenesis. Overall, our study highlights G4s as important DNA secondary structures with a role in Plasmodium gene expression regulation, sub-telomeric recombination and var gene biology.
ARNA Laboratory IECB CNRS UMR5320 INSERM U1212 Bordeaux University Pessac France
IBENS Ecole Normale Supérieure CNRS Inserm PSL Research University Paris France
Laboratory of Pathogen Host Interactions UMR5235 CNRS Montpellier University Montpellier France
MIVEGEC UMR IRD 224 CNRS 5290 Montpellier University Montpellier France
Citace poskytuje Crossref.org
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