Biology subjects

Olivier, N.

Publications and source records attributed to Olivier, N..

4 recordsLinked to original sources

bioRxiv2026

Multi-foci replication domains in Haloferax volcanii visualised by super-resolution microscopy

The archaeon Haloferax volcanii is a unique model organism to investigate replication dynamics and dissect the interplay between multiple origins, alternative replication pathways, and polyploidy. The combination of variable chromosome copy number and asynchronous replication across the cell population gives rise to pronounced phenotypic heterogeneity, further increasing system complexity. To investigate these mechanisms, we implemented (spt-)PALM and STORM microscopy to probe replication dynamics in different cell lines and growth conditions. We established the first STORM-based super-resolution imaging approach of a protein in Haloferax volcanii. Altogether, our results support a model in which each H. volcanii cell replicates a constant fraction of its chromosome copies, irrespective of total ploidy. Consequently, cells with a higher number of chromosomes exhibit proportionally more replication forks, resulting in pronounced ploidy heterogeneity across the population. Moreover, we show that replication foci are not randomly distributed but cluster into discrete Replication Domains containing multiple active sites. This organization persists across different growth conditions and is independent of canonical replication origins, as demonstrated in a strain lacking all four origins. Our findings suggest that replication coordination in H. volcanii is governed by spatial architecture rather than origin-dependent initiation, providing new insights into the evolutionary diversity of replication control mechanisms.

microbiology↗

bioRxiv2024

G-quadruplexes in Haloferax volcanii

Archaea, a domain of microorganisms found in diverse environments including the human microbiome, represent the closest known prokaryotic relatives of eukaryotes. This phylogenetic proximity positions them as a relevant model for investigating the evolutionary origins of nucleic acid secondary structures such as G-quadruplexes (G4s), which play regulatory roles in transcription and replication. Although G4s have been extensively studied in eukaryotes, their presence and function in archaea remain poorly characterized. In this study, a genome-wide analysis of the halophilic archaeon Haloferax volcanii identified over 5, 800 potential G4-forming sequences. Biophysical validation confirmed that many of these sequences adopt stable G4 conformations in vitro. Using G4-specific detection tools and super-resolution microscopy, G4 structures were visualized in vivo in both DNA and RNA across multiple growth phases. Comparable findings were observed in the thermophilic archaeon Thermococcus barophilus. Functional analysis using helicase-deficient H. volcanii strains further identified candidate enzymes involved in G4 resolution. These results establish H. volcanii as a tractable archaeal model for G4 biology.

molecular biology↗

bioRxiv2022

Spatial modeling of telomere intra-nuclear distribution reveals non-random organization that varies during cell cycle and depends on LAP2 and BAF

Genome organization within the 3D nuclear volume influences major biological processes but is completely lost during mitosis, which represents a major challenge to maintain cellular identity and cell fate. To restore a functional G1 nucleus for the next cell cycle, it is imperative to reestablish genome organization during post-mitotic nuclear assembly. Importantly, the configuration of linear chromosomes has been shown to directly impact spatial genome architecture. Both centromeres and telomeres are known to associate with nuclear structures, such as the nuclear envelope, and support chromatin distribution. Here, using high-resolution 3D imaging combined with 3D spatial statistics and modeling, we showed that telomeres generally followed a regular distribution compared to what is expected under a random organization. While the preferential localization of telomeres at nuclear periphery was restricted to early G1, we found a strong clustering of centromeres in addition to their predominant peripheral localization at all cell cycle stages. We then conducted a targeted screen using MadID to identify the molecular pathways driving or maintaining telomere anchoring to the nuclear envelope. Among these factors, we could show that LAP2 transiently localizes to telomeres in anaphase, at a stage where LAP2 initiates the reformation of the nuclear envelope. Moreover, co-depletion of LAP proteins and their partner BAF impacted telomere redistribution in the next interphase. There results suggest that in addition to their crucial role in genome protection, telomeres also participate in reshaping functional G1 nuclei after mitosis.

cell biology↗

bioRxiv2022

An Optimized Buffer for Repeatable Multicolor STORM

STORM microscopy is one of the most popular method of super-resolution microscopy, due to moderate requirements on the optical setup, and high achievable resolution. However, since its inception more than 15 years ago, protocols have barely evolved, and despite some recent progress, multicolor imaging can still be complex without the right equipment. We decided to optimize the buffer composition to improve the blinking of the most popular red dye CF-568 while maintaining good performance for far-red fluorophores such as Alexa-647 using the concentration of three chemicals and the pH as 4 optimization parameters. We developed a simple, cheap and stable buffer, that can be stored several weeks and frozen for longer term storage that allow high quality 3-color STORM imaging. O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=184 SRC="FIGDIR/small/491818v2_ufig1.gif" ALT="Figure 1"> View larger version (136K): org.highwire.dtl.DTLVardef@375943org.highwire.dtl.DTLVardef@1c57e71org.highwire.dtl.DTLVardef@f05fe3org.highwire.dtl.DTLVardef@1274e4f_HPS_FORMAT_FIGEXP M_FIG C_FIG

biophysics↗