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Medaglia-Mata, A.

Publications and source records attributed to Medaglia-Mata, A..

3 recordsLinked to original sources

Nanoplastic-mediated non-B DNA mutagenicity

Plastic-derived materials have become persistent ecological contaminants since their industrial introduction in the mid-20th century. In that context, nanoplastics (NPs) have been discussed as an emerging, ubiquitous plastic-derived pollutant with unique physicochemical properties. Their increased surface-to-volume ratio enhances their adsorption, reactivity, and cellular penetration, driving distinct ecotoxicological behaviours when compared to larger plastic particles. In this study, we identify direct NP-induced DNA mutagenesis in Salmonella enterica. Using a combination of biochemical and biophysical studies, as well as mutagenicity assays, we show that functionalized and non-functionalized NPs induce mutations, depending on the energy state of the bacteria and the NP surface chemistry, by disrupting base-stacking and base-pairing - an intrinsic property of all DNA. Whole-genome analysis revealed that exposure to NPs alters the mutational spectrum and mutation frequency, while circular dichroism spectroscopy demonstrated NP-induced helical flipping from B- to non-B DNA conformations. These motifs preferentially adopt Z-like or A/B-hybrid structures associated with localized mutagenesis through DNA destabilization. Our combined data reveal that NP-mediated mutagenesis is based on surface chemistry and DNA topology, linking surface chemistry on nanoplastics to genomic instability in vivo. The proposed mechanism redefines the current perspective on nanoplastic toxicity shifting it from an indirect stress to direct macromolecular interactions. This mechanism provides a molecular framework for understanding how NPs could impose mutation bias, environmental selection pressure, and potential genomic risk across biological systems.

microbiology↗

Editing-independent effects of Adar in Drosophila melanogaster

Vertebrate ADAR RNA editing enzymes prevent cellular dsRNA from aberrantly activating antiviral dsRNA sensors. ADARs inhibit antiviral sensor activation by deaminating selected adenosines to inosines in dsRNA and by engaging in inhibitory protein interactions with sensors on dsRNA. ADARs interact with Dicers and, in the Drosophila Adar5G1 null mutant Dicer 2 acts as the antiviral dsRNA sensor mediating aberrant innate immune induction. We overexpressed active Adar isoforms or a catalytically-inactive Adar E374A protein from UAS-Adar constructs under the control of a temperature-regulated Act5Cts-GAL4 driver. Overexpression of the edited AdarG isoform or AdarEA cause larval lethality with aberrant innate immune induction. Some escaper pupae are formed with head eversion defects. AdarS overexpression is also lethal with no progeny pupae. Ecdysone signaling gene and innate immune gene expression are aberrantly elevated in the AdarG overexpressing pupae. RNAi knockdown of Ecdysone Receptor A (EcR A) or increasing expression of HP1 partially rescue AdarG overexpression defects and normalize gene expression in progeny flies, indicating that aberrant epigenetic silencing is also involved. The structure of an ADAR2 dimer on dsRNA shows the the glycine in AdarG is suitably positioned for Adar contacts with other proteins on dsRNA.

developmental biology↗

Long-term high temperatures affect seed maturation and seed coat integrity in Brassica napus

Temperatures above the optimum growth threshold affect seed development, accelerating embryo development and producing seeds with ruptured seed coats. However, the underlying mechanisms of this effect remain unclear. To investigate temperature-induced seed coat rupture, we used a multidisciplinary approach combining detailed phenotyping, transcriptomics, histology, immunolabelling, cell wall profiling and nanoindentation-based mechanics of the seed coat in oilseed rape (Brassica napus). Our data reveal that high temperatures accelerate embryo growth, resulting in larger embryos without a compensatory increase in overall seed size. This rapid embryo expansion may exert elevated mechanical stress on the seed coat cells, significantly thinning the seed coat layers. Concurrently, prolonged exposure to high temperatures drives premature biochemical maturation of the seed coat, characterized by accumulation of demethylesterified pectin. Nanoindentation analysis demonstrated that these changes may have compromised the structural integrity of seed coat cell walls. Ultimately, the weakened seed coat may not withstand the internal tension imposed by the fast-growing embryo, leading to seed coat rupture and reduced seed quality. Our work on seed maturation and the mechanism of heat-induced seed coat rupture provides valuable insights for future research into breeding thermotolerant Brassica napus, crucial in the context of a changing climate. HIGHLIGHTSO_LIGrowth of Brassica napus under long-term high temperatures accelerated embryo growth and led to seed coat rupture in approximately half of the seeds. C_LIO_LIPathways linked to cell wall modification were found to be significantly differentially regulated at high temperatures, accompanied by increased pectin demethylesterification in the seed coat. C_LIO_LIA lower reduced modulus and hardness indicate that the surface of HT seeds is mechanically more compliant and softer. Together with the reduced thickness of the seed coat layers, such a seed coat, as a whole structure, is mechanically weaker and less able to resist deformation imposed by embryo growth, resulting in seed coat rupture. C_LI

plant biology↗