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Smialkovska, V.

Publications and source records attributed to Smialkovska, V..

3 recordsLinked to original sources

Capture-(Hi)C analysis with PostChicago: Integrative metaprofiling and quantitative comparison of chromatin interactions

Functionally linking enhancers to gene promoters at high resolution often entails analysis of 3C datasets, including viewpoint-based methods such as Capture-(Hi)C. Quantitative comparison across samples and experiments, together with visualization and integration of promoter interactions with other datasets are of critical importance. While existing statistical tools identify significant interactions and quantify underlying signal, systematically comparing the shape and extent of this signal across large sets of intervals remains challenging. Moreover, experimental artefacts, such as inefficient crosslinking, can affect downstream interpretation, but are difficult to detect systematically. Here we introduce PostChicago, an R/Bioconductor package that fills this gap. Building upon the widely used interaction-calling package Chicago, PostChicago provides a complete workflow for quality control, visualization, integration and quantitative analysis of promoter interactions between multiple samples, including annotation and quantification of genomic regions based on external datasets. PostChicago extends visual quantitative comparisons beyond individual viewpoints by computing normalized metaprofiles around large sets of intervals that visualize the distribution of interaction signal, enabling comparison between narrow and broad interaction patterns. We further demonstrate how PostChicago can identify experimental crosslinking artefacts. Together, PostChicago enables integrative, shape-sensitive analysis and quality control of promoter Capture-(Hi)C datasets at a scale that would otherwise require extensive custom scripting.

bioinformatics↗

Developmentally programmed loss of long-range Polycomb interactions is regulated by cohesin

Distal regulatory elements (DREs), such as enhancers, can regulate genes across megabase-long distances, presumably via coming into close spatial proximity. The establishment of new transcriptional programmes during cell type transitions is associated with widespread rewiring of the spatial organisation of the genome, including gain and loss of chromatin interactions. Extensive effort has been invested into understanding how chromatin interactions are formed during development, yet the mechanisms underlying their developmental loss remain largely unclear. By leveraging chromatin accessibility-assisted footprinting, acute protein degradation and chromatin conformation capture, we show that loss of promoter interactions cannot be explained by reduced binding of sequence-specific transcription factors (TFs). Instead, we identify a subset of interactions that depend on cohesin for programmed developmental disruption. These sites are characterized by high Polycomb enrichment and TF occupancy and engage in strong long-range interactions that undergo extensive differentiation-dependent rewiring. Preventing interaction loss by acute cohesin degradation results in the preferential downregulation of associated genes. Together, these results suggest that cohesin indirectly regulates developmental loss of Polycomb interactions by enabling the acquisition of other potentially regulatory contacts in a process that may shape transcriptional programs during cell type transitions.

genomics↗

Anti-phase clustering of regulatory factors shapes gene bursting

Stem cell self-renewal relies on finely tuned transcriptional oscillations of pluripotency genes, yet the sequence by which transcription factors (TFs) govern "on" and "off" states remains unclear. Here, we integrate trimodal single-molecule imaging - SOX2 mobility, Nanog locus diffusion, and real-time Nanog mRNA synthesis using the STREAMING-tag reporter - to visualise endogenous regulatory dynamics in living cells. We identify two SOX2 binding modes linked to transcriptional priming and termination and show coordinated temporal activity of SOX2, OCT4, BRD4, and MED22 at the Nanog locus. Live-cell and fixed-cell measurements reveal that local RNA fluctuations modulate SOX2 visiting-frequency rates. During the active elongation, high nascent enhancer and mRNA levels transiently sequester SOX2 through non-specific interactions, reducing its effective repetitive rebinding and limiting interference with elongating polymerase. After transcript release, declining RNA density permits SOX2 re-engagement, with high-visiting frequency with longer residency and increased locus mobility. These dynamics reveal RNA-dependent feedback that alternately buffers and primes transcriptional re-initiation.

molecular biology↗