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In early September, the University of Namur hosted the first Main-Group Elements Reactivity Conference (MG-ERC). Over 100 researchers from 12 countries and 32 institutions gathered around Professor Guillaume Berionni. An event hailed as "one of the best chemistry conferences" by its prestigious guests.

A team of American researchers, with the help of Frédérik De Laender, professor in the Department of Biology at UNamur, has just published in the prestigious journal Nature. Their study describes how changing stream temperatures and human introductions of fish can alter river biodiversity in the USA.

Initiated in 1969 by Pullmann and Del Re, the congress is an annual meeting to promote collaboration and friendship between Latin-speaking theoretical chemists. In its early years, European researchers were the main contributors. Subsequently, the Latin American community has made a major contribution, with the emergence of teams whose international reputation now extends far beyond our own community.We are delighted to be holding this meeting at the University of Namur, 55 years after the first CHITEL was organised in Paris, France. We are sure that this 2024 edition will once again be an opportunity to take advantage of the good humour and dynamism of Latin to encourage, develop and strengthen scientific exchanges.We look forward to welcoming you at the University of Namur,The CHITEL 2024 Local Organising Committee. Website

EMBO Courses and Workshops are selected for their excellent scientific quality and timelines, provision of good networking activities for all participants and speaker gender diversity (at least 40% of speakers must be from the underrepresented gender). Organisers are encouraged to implement measures to make the meeting environmentally more sustainable.Upon registration - More info and registration on the EMBO website.

On Thursday May 30, for our last Chill&Sciences of the season, Candy Sonvaux and Alexis Coyette, mathematics researchers, invite you to discover the mathematics where the movements of the planets and the spread of viruses intertwine until they impact our society.Chill&Science: enriching encountersWith nearly 20 years' experience of scientific cafés, the Confluent des Savoirs has set up a new concept of scientific encounters. The Chill&Sciences are a unique opportunity for the public to come and discuss and ask questions of experts on research topics related to current affairs and citizen issues.Come and enjoy the unique, relaxed atmosphere of Quai22. Researchers and experts from the seven faculties of the University of Namur will present their research and discuss with you over a drink (or two, but never without exaggeration).In practiceThe meetings are open to everyone aged 16 and over. Evenings are limited to around 20 people to ensure a relaxed atmosphere and to facilitate discussions. Meetings take place if a minimum of 10 people are registered. Except in exceptional circumstances, meetings take place every 2 months at the University of Namur's cultural space, Quai22, located at n°22 Rue du Séminaire.Tarif Participation in a Chill&Sciences costs 5€. A discounted annual pass is available. Please note: preferential rate for students (discount code: PromoCDS).The booking fee includes a drink* (soft or beer), a snack (chips and cookies) and management fees linked to the organization Unless cancelled by us, bookings are non-refundable. (*additional drinks will be available upon electronic payment.)

Title of the dissertation: Ion implantation in Low-E coatings Low-emissivity (Low-E) coating technology revolutionizes glass applications for windows, offering high optical transparency while reducing heat transfer. They consist of a silver-based thin film deposited on a glass panel by physical vapor deposition. However, these coatings are fragile and must be placed inside a double-glazing cavity where an inert gas resides. Otherwise, they can be easily degraded by bad atmospheric conditions.The thesis approach is to combine low-E technology with a post-treatment of ion implantation. The research question driving this thesis is: how does ion implantation enhance the durability of low-E coatings containing silver?The experiments conducted during the thesis show that implantation indeed increases the coating resistance while having a small impact on its color. However, the treatment degrades the thermal insulation properties. Hence, a series of hypotheses are formulated based on the literature to explain and control this behavior.A deeper investigation shows that implantation impacts the silver nanostructure. First by dewetting the film which allows reorganization into larger crystallites, second by forcing silver mixing at its interface through ballistic ejections. These two phenomena increase the toughness of the silver interface by interlocking effects. However, dewetting has also been linked to thermal insulation properties degradation. Nonetheless, it was shown that using light gas implantation limits the destructive effect (dewetting) while still inducing good durability (due to interface mixing).. Jury Prof. Julien COLAUX (UNamur), presidentProf. Stéphane LUCAS (UNamur), promoter and secretaryDr Amory JACQUES (Service Public de Wallonie)Dr Philippe ROQUINY (AGC Glass Europe)Prof. Rony SNYDERS (University of Mons)

Characterization of trehalase from Acyrthosiphon pisum for the design of new insecticides SummaryAphids are major pests in agriculture, causing direct damage to plants and acting as vectors for phytopathogenic viruses. Conventional insecticides are widely used to control them, but their toxicity and efficacy pose problems in terms of the environment, human health and the emergence of resistance to these compounds. New alternatives are therefore needed, such as biological control using predators or parasitoids. However, these methods are not always economically viable on a large scale. As part of this thesis, another approach is being explored which involves developing new insecticides targeting the biochemical functions of aphids.The project aims to discover new inhibitors of trehalase, an enzyme essential for insect energy metabolism. Inhibition of this enzyme could disrupt vital insect functions without affecting mammals. This research involved several stages: the purification and complete characterization of trehalase from Acyrthosiphon pisum (the model for this study), the in vivo, in vitro and in silico analysis of commercial inhibitors on this enzyme, before moving on to the search for new inhibitors. Two points of integrated insect management were explored, biological and chemical control.The biological side saw the study of a strain of Streptomyces naturally producing trehalase-inhibiting metabolites, notably validamycin A, a molecule recognized in the literature as one of the best inhibitors, but not applicable as an insecticide. Other molecules appear to have interesting features, but we have not been able to isolate and characterize them.The chemical side has enabled us to create a pharmacophore hypothesis based on experimental results on molecules obtained by virtual screening. Although these molecules are not usable as insecticides as they stand, this hypothesis provides a better understanding of trehalase inhibitors in general and can be used to refine future analyses. JuryProf. Jean-Yves MATROULE (UNamur), presidentDr Catherine MICHAUX (UNamur), promoter and secretaryProf. Frédéric FRANCIS (ULiège), co-promoterProf. André MATAGNE (ULiège)Dr Rudy CAPARROS (ULiège)Dr Morgan HANS (Biocidal)

Thesis subject Use of BioID within mitochondria: examples with the study of human mitochondrial co-translational import process and with the identification of MPV17 function Summary This thesis was divided into two different parts dedicated to the study of a mitochondrial process and of a mitochondrial protein using a proximity labelling assay called BioID. The first project was dedicated to the study of a poorly characterized process, the mitochondrial co-translational import. In this process, translation is coupled to the translocation of the mitochondrial proteins, alleviating the energy cost typically associated with the post-translational import relying on chaperone systems. However, the mechanisms are still unclear with only few actors identified but none that have been described in mammals yet. We thus profiled endogenously the TOM20 proxisome using BioID. Despite the enrichment of RNA binding proteins in the TOM20 proxisome, we could not demonstrate a role for a selected candidate, LARP4, in the mitochondrial co-translational import process. Nonetheless, additional uses of this BioID cell line were highlighted such as the monitoring of protein entry inside mitochondria and a potential application in the prediction of mitochondrial protein half-life.The second project was dedicated to the study of MPV17, a protein of the inner mitochondrial membrane whose gene is associated with mitochondrial DNA depletion syndrome. However, the exact molecular function of the protein is still unclear. The approach used in this project was to identify the interacting partners of MPV17, using BioID, to get additional clues about the protein function. In this project we demonstrated an interaction of MPV17 with the MICOS complex but the KO of MPV17 didn't impact mitochondria ultrastructure. However, the depletion of MPV17 protein led to increased mitochondria-derived vesicle formation. Therefore, we investigated a potential degradation of the mtDNA as the cause of the mtDNA depletion observed in MPV17 KO cells but, despite a higher mitophagy level in KO cells, the blockade of the lysosomal activity didn't prevent the depletion. Additional in silico analyses suggested a channel activity of MPV17 further supported by its direct interaction with the Cyclophilin D, a protein of the mitochondrial permeability transition pore. Interestingly, MPV17 KO cells also display higher level of mitochondrial calcium which would be related to the degradation of the mtDNA since the blockade of mitochondrial calcium entry prevents the depletion. We thus propose a role of MPV17 as a potential new member of the mitochondrial permeability transition pore whereas in the absence of the protein, the build-up of calcium inside the mitochondria would lead to the observed mtDNA degradation. Jury Prof. Benoît MUYLKENS (UNamur), ChairmanProf. Patsy RENARD (UNamur), Promoter and SecretaryProf. Thierry ARNOULD (UNamur), Co-PromoterProf. Dr. David PLA-MARTIN (Heinrich Heine University Düsseldorf, Germany)Dr. Timothy WAI (Institut Pasteur Paris, France)Prof. David PLA-MARTIN (Heinrich Heine University Düsseldorf, Germany)Dr. Timothy WAI (Institut Pasteur de Paris, France)Prof. Guy LENAERS (Université d'Angers, France)Prof. Sven EYCKERMAN (Universiteit Gent)

Jury Prof. Benoît MUYLKENS (URVI, Université de Namur), PresidentProf. Carine MICHIELS (URBC, Université de Namur), SecretaryProf. Xavier DE BOLLE (URBC, Université de Namur)Prof. René REZSOHAZY (LIBST, Université catholique de Louvain)Prof. Florian STEINER (Dept. of Molecular and Cellular Biology, Université de Genève)Prof. Germano CECERE (Department of developmental and Stem Cell Biology, Institut Pasteur) Summary In animals, germ cells are often distinguished from somatic lineages at the earliest stages of embryogenesis. In some organisms, germ blastomeres appear to enter a state of transcriptional quiescence. For example, in the worm Caenorhabditis elegans, transcription is activated in somatic blastomeres as early as the 4-cell stage, whereas it is not initiated in germline blastomeres until the 100-cell stage. This transcriptional repression in germ blastomeres has been attributed to the PIE-1 protein, specifically localized in these cells from the first embryonic division. PIE-1 is thought to inhibit the activity of CDK-9, a cyclin-dependent kinase previously considered essential for the phosphorylation of serine 2 (CTD-Ser2) of the C-terminal domain (CTD) of RNA polymerase II and for transcription elongation. However, recent studies, showing that embryogenesis proceeds normally in a mutant strain expressing a CTD in which serines 2 is replaced by an alanine (CTD-S2A) and identifying CDK-12 as the main kinase phosphorylating CTD-Ser2, call this model into question.To study the transcriptome of germline blastomeres in the worm C. elegans, an approach combining cell sorting and RNA sequencing (RNA-seq) was developed. Pilot analyses validated this method on a wild-type strain, enabling its use on a strain in which PIE-1 can be specifically degraded using the Auxin-Inducible Degron (AID) system. This made it possible to examine the effect of PIE-1 depletion on the transcriptome of germline blastomeres revealing that in its absence, germline blastomeres adopt a transcriptional profile close to that of somatic blastomeres, confirming the fundamental role of PIE-1 in preserving germline identity during embryogenesis. In parallel, the fission yeast Schizosaccharomyces pombe was used to analyze the consequences of PIE-1 expression in a heterologous organism. The results showed that PIE-1 by localizing near transcription termination sites induces further transcription by RNA polymerase II beyond the termination site, leading to transcription of intergenic regions. These observations led to the hypothesis that in C. elegans,within germinal blastomeres, PIE-1 might regulate alternative polyadenylation in 3' untranslated regions, producing longer RNA isoforms susceptible to degradation. In the absence of PIE-1, shorter isoforms could be generated, allowing accumulation of somatic transcripts and potentially degradation of maternal mRNAs via somatic protein translation. Although further investigations are required in C. elegans to validate this hypothesis, it provides an innovative conceptual framework for understanding the role of PIE-1, independent of CTD-Ser2 phosphorylation.

Jury Prof. Marielle BOONEN (UNamur), presidentProf. Henri-François RENARD (UNamur), secretaryProf. Claire HIVROZ (PSL University)Prof. Michel GHISLAIN (UCLouvain)Prof. Pierre VAN DER BRUGGEN (UCLouvain)Prof. Ludger JOHANNES (PSL University)Prof. Pierre MORSOMME (UCLouvain) Summary Clathrin-independent endocytosis (CIE) mediates the cellular uptake of endogenous and exogenous cargoes, including bacterial toxins and viruses. Endophilin A3-mediated endocytosis is a specific CIE mechanism that differs from fast endophilin-mediated endocytosis (FEME), with ALCAM and L1CAM being the first confirmed Endophilin A3-specific cargoes. Here, we report ICAM1 as a new Endophilin A3-dependent endocytic cargo. ALCAM and ICAM1 are important components of immune synapses (IS), which are polarized structures formed between immune cells and target cells, such as cancer cells. These molecules transduce essential co-stimulatory signals to T cells to help their effective activation and proliferation. We find that both ALCAM and ICAM1 serve as cargoes for retromer-dependent retrograde transport to the trans-Golgi network (TGN) in cancer cells. Interestingly, disrupting Endophilin A3-mediated endocytosis or retromer-dependent retrograde transport machinery impairs activation of autologous cytotoxic CD8 T cells, possibly by affecting the polarized redistribution of immune synapse components at the plasma membrane. Altogether, our findings demonstrate that CIE and retrograde transport are key pathways in cancer cells that promote the activation of cytotoxic CD8 T cells.