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Biology subjects

Szczesniak, M.

Publications and source records attributed to Szczesniak, M..

3 recordsLinked to original sources

Cajal bodies shape the nuclear transcriptome, intron retention and transcripts redistribution in Arabidopsis roots under hypoxia

Cajal bodies (CBs) are nuclear condensates known for their role in sn- and snoRNA maturation in animal, but their function in plant stress responses remains poorly understood. We compared wild-type (WT) Arabidopsis thaliana with the CB-lacking ncb-1 mutant during hypoxia and reoxygenation, focusing on nuclear retention of transcripts. In both genotypes, hypoxia caused nuclear accumulation of poly(A+) RNA and extensive reprogramming of gene expression. However, the transcriptional response, including induction of hypoxia-responsive genes, was considerably weaker in ncb-1, both during stress and recovery. In nuclear RNA, introns with low (intron retention index, IRX < 10%) and high (IRX > 50%) retention showed opposite, genotype-dependent dynamics. During hypoxia, efficiently spliced introns (IRX < 10%) accounted for over 70% of introns detected in nuclear RNA. Relative to normoxia, this proportion increased two- to threefold in WT but only moderately in the mutant. Together with poly(A+) RNA accumulation, this suggests that largely spliced transcripts, including those of genes involved in protein transport and ribosome biogenesis, are held in the nucleus during stress. Conversely, strongly retained introns, often terminal and located in genes related to hypoxia and other abiotic stresses, were most abundant in WT nuclear RNA under normoxia. Their proportion dropped sharply during hypoxia, and much less so in ncb-1. This indicate that WT plants maintain a nuclear reserve of incompletely spliced stress-related transcripts that are processed upon stress. The mutant also showed reduced interaction between U2 snRNA and U2B'', which leads to splicing defects. Our results indicate that CBs regulate which transcripts are held in the nucleus and how they are processed, contributing to plant tolerance of oxygen deprivation and recovery.

cell biology↗

Time-resolved transcriptomic mapping reveals conserved stress programs and metabolic rewiring in Escherichia coli under antimicrobial photodynamic and blue light exposure.

Antimicrobial photodynamic inactivation (aPDI) and antimicrobial blue light (aBL) are emerging, resistance-agnostic strategies for controlling bacterial pathogens, yet their systems-level impact on prokaryotic physiology remains incompletely understood. Here, we used time-resolved global transcriptomics to define how Escherichia coli reprograms gene expression in response to diverse photodynamic stresses. E. coli K-12 BW25113 was exposed to five phototreatments differing in photosensitizer chemistry and light wavelength, including rose bengal, TMPyP, new methylene blue, aBL alone, and aBL combined with 5-aminolevulinic acid, and transcriptional responses were profiled after short (30 min) and prolonged (7-8 h) exposure. Short-term phototreatments triggered rapid and extensive transcriptional remodeling, affecting up to [~]58% of the genes and dominated by conserved stress programs including oxidative defense, sulfur metabolism, and a broad downshift in biosynthesis and energy generation. In contrast, prolonged exposure elicited more restrained but highly treatment-specific adaptive responses, characterized by suppression of core energy metabolism, including oxidative phosphorylation and the tricarboxylic acid cycle, coupled with activation of alternative catabolic pathways. Together, these findings reveal a common acute stress architecture across photodynamic modalities followed by divergent long-term adaptive trajectories, providing a systems-level framework for understanding bacterial responses to light-based antimicrobials and informing the rational optimization of photodynamic therapies. O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=66 SRC="FIGDIR/small/703343v1_ufig1.gif" ALT="Figure 1"> View larger version (22K): org.highwire.dtl.DTLVardef@a990a1org.highwire.dtl.DTLVardef@5670bcorg.highwire.dtl.DTLVardef@1035840org.highwire.dtl.DTLVardef@96ff67_HPS_FORMAT_FIGEXP M_FIG C_FIG

genomics↗

FUS controls the processing of snoRNAs into smaller RNA fragments that can regulate gene expression

FUS is a multifunctional protein involved in many steps of RNA metabolism, including transcription, splicing, miRNA processing and replication-dependent histone gene expression. In this paper, we show for the first time that FUS binds and negatively regulates the levels of a subset of snoRNAs in cells. Scanning of available human small RNA databases revealed the existence of smaller RNA fragments that can be processed from FUS-dependent snoRNAs. Therefore, we suggest that FUS mediates the biogenesis of snoRNA-derived small RNAs, called sdRNAs. Further in silico approaches enabled us to predict putative targets of selected FUS-dependent sdRNAs. Our results indicate that sdRNAs may bind to different regions of target mRNAs as well as to noncoding transcripts and influence the posttranscriptional level or translation of these targets. SIGNIFICANCE STATEMENTRNA metabolism is orchestrated by a complex network of RNA-protein interactions and involves various classes of RNA molecules. Small nucleolar RNAs (snoRNAs) are commonly considered essential components of the ribosome biogenesis pathway. However, recent studies have revealed that snoRNAs can also be fragmented into small entities called snoRNA-derived RNAs (sdRNAs), which have been linked to multiple cancer types and thus may serve as next-generation prognostic or diagnostic biomarkers. In this paper, a multifunctional protein, FUS, was shown to be involved in the biogenesis of snoRNA-derived fragments. Furthermore, we combined bioinformatic analyses with complementary experimental approaches to elucidate the role of FUS-dependent sdRNAs in gene expression regulation. Our findings reveal the considerable regulatory potential of this new class of small noncoding RNAs.

molecular biology↗