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Biology subjects

Harun, S.

Publications and source records attributed to Harun, S..

2 recordsLinked to original sources

Integrative Transcriptomic and Network Analysis Reveals Small Open Reading Frames as Regulators of DNA Methylation-Linked Pathogenicity and Adaptability in Leptospira interrogans

Small open reading frames (sORFs) are increasingly recognized as crucial regulators in bacterial gene expression, yet their biological roles remain largely unexplored in pathogenic species. Here, we investigated the genome-wide regulatory landscape of sORFs in Leptospira interrogans serovar Manilae strain UP-MMC-NIID-LP using RNA-seq-based transcriptomic profiling integrated with weighted gene co-expression network analysis (WGCNA) following targeted disruption of lomA, a gene mediating 4-methylcytosine (4mC) DNA modification. Loss of 4mC was associated with broad transcriptional dysregulation and phenotypic impairments, including reduced motility, adhesion, and virulence. Analysis of 363 predicted sORFs identified 39 with significant differential expression (FDR < 0.05, |log2FC| [&ge;] 1) across wild-type, mutant, and complemented strains. Gene co-expression networks constructed using WGCNA and interrogated with Cytoscape tools (MCODE, CytoHubba, ClueGO) revealed ten differentially expressed sORFs (FDR-adjusted p < 0.05); eight upregulated and two downregulated, across the three pairwise comparisons of wild-type, mutant, and complemented strains. These sORFs were enriched in pathways related to flagellar assembly, DNA recombination, and transcriptional regulation, which are core processes supporting genome stability and adaptive stress responses. Several previously uncharacterized sORFs occupied hub-like positions within co-expression modules, highlighting their integrative roles in metabolic and regulatory networks. To our knowledge, this represents the first genome-wide integration of methylation-driven sORF regulation in Leptospira, revealing small proteins as central mediators that link epigenetic control with bacterial pathogenicity and adaptability. These findings provide a foundation for future antimicrobial and synthetic biology strategies targeting sORF-mediated regulation. ImportanceSmall open reading frames (sORFs) are emerging as important regulators of bacterial gene expression, yet their roles in pathogenic species remain largely unexplored. This study provides the first genome-wide framework linking methylation-driven sORF regulation to virulence and adaptive processes in Leptospira interrogans. We identify previously uncharacterized sORFs occupying central positions in regulatory networks, connecting epigenetic control to motility, adhesion, and stress adaptation. Understanding these mechanisms in a neglected tropical disease pathogen has implications for improving public health and informs future antimicrobial and synthetic biology strategies.

bioinformatics↗

Cellular and biophysical barriers to lipid nanoparticle mediated delivery of RNA to the cytosol

Lipid nanoparticle (LNP) formulation was the first approved delivery strategy for liver-targeted siRNA delivery and currently represent the most advanced platform for delivery of therapeutic mRNA in clinical use, after the approval of mRNA-based vaccines against the SARS-CoV-2 coronavirus. Still, poor efficiency of LNPs to promote cytosolic delivery of both mRNA and siRNA after internalization by target cells limits their potency and thus clinical application as RNA delivery vehicles - especially in extrahepatic tissues and tumors. It is still unclear how endosomal escape of LNP-delivered RNA cargo occurs, and why only a minute proportion of all therapeutic molecules reach the cytoplasm. Here, we explored the intracellular sorting, integrity and endosomal escape of both mRNA and siRNA loaded LNPs to characterize the nature of RNA release from endosomal compartments and pinpoint current bottlenecks. Using live-cell imaging and super-resolution microscopy of LNPs with fluorescently labeled RNA payload, we identify multiple distinct steps of substantial inefficiency in the cytosolic delivery of nucleic acid cargoes. We demonstrate that membrane damages marked by recruitment of galectins are conducive to cytosolic RNA delivery, while membrane perturbations recruiting the ESCRT machinery do not permit endosomal escape. By quantitative single-vesicle analysis, we show that only a small fraction of the nucleic acid cargo contained in the endosome is released to the cytosol upon LNP-triggered membrane damage detected by galectins. Unexpectedly, we also observe that only a subset of damaged endosomes contain RNA payload. Through FRET and super-resolution microscopy, using LNPs formulated with both fluorescently labeled ionizable lipid (MC3-BODIPY) and RNA, we find that RNA cargo and ionizable lipid segregate during endosomal sorting - both within single endosomes and to different endosomal compartments. Finally, we visualize localized MC3-BODIPY enrichment in endosomal membranes and membrane damage in direct proximity to siRNA-LNPs tethered to the luminal vesicle membrane. Taken together, this work has identified multiple mechanistically distinct barriers limiting intracellular RNA delivery by LNPs.

bioengineering↗