Résultats de recherche

La recherche en didactique de la chimie constitue un champ d’étude relativement récent à l’Université de Namur. Rattachée à l’Institut de recherche IRDENa, l’URDC vise à comprendre les processus didactiques en jeu lors des situations d’enseignement-apprentissage impliquant des contenus à enseigner en chimie. Ces recherches contribuent ainsi tant à la construction de savoirs d’avant-garde dans le domaine qu’à l’élaboration de nouveaux dispositifs de formation et de pédagogies innovantes.

Membre du centre de recherche NAMEDIC associé à l’Institut NARILIS, le CBS développe activement des projets de recherche en chimie médicinale. Les activités du laboratoire reposent sur une collaboration étroite avec d'autres groupes (inter)nationaux. Les efforts des membres du CBS peuvent être regroupés en 3 axes de recherche principaux : l'étude structurelle des systèmes hôte-invité et des cocristaux (pharmaceutiques)la cristallographie des protéines et la conception de médicaments à base de structure. 

L'Unité de recherche en biologie des micro-organismes (URBM) étudie les micro-organismes (principalement des bactéries) à tous les niveaux d'intégration (du cellulaire au moléculaire) et leur relation avec les hôtes eucaryotes.

Consanguinity refers to the offspring produced from the union of two closely related individuals who share at least one common ancestor (Temaj et al. 2022). Some communities have high rates of consanguineous marriages, especially in the Middle East, where consanguinity rates of first-cousin marriages vary in Gulf countries from 20 to 50 % (Ben-Omran et al. 2020). This high rate of consanguineous marriages is due to cultural, geographical, historical, financial, political, or religious reasons (Temaj et al. 2022) (Ben-Omran et al. 2020).Consanguinity increases the chance/risk/probability to be homozygous for rare mutations in the general population (Temaj et al. 2022). These mutations can cause recessive autosomal pathologies that may be extremely rare known as rare diseases (Temaj et al. 2022). In many Middle Eastern populations, consanguineous relationships are very common, providing geneticists with a valuable source for discovering "new" genes and identifying their functions (Ben-Omran et al. 2020). Identifying these genes can help carry out diagnostic and predictive tests (genetic counseling) in affected families (Ben-Omran et al. 2020; Temaj et al. 2022). In some cases, understanding the pathophysiological mechanisms involved in diseases can also lead to new therapeutic strategies (Salzberg 2018).In recent years, the development of Next Generation Sequencing (NGS) technologies has led to a faster identification of genes involved in rare diseases (Lal et al. 2016). Sequencing the entire genome (Whole Genome Sequencing, WGS) or the exome (Whole Exome sequencing, WES) can be achieved quickly and inexpensively (Salzberg 2018).Rare diseases are Mendelian monogenic diseases, that result from specific pathogenic variants in single genes, called germline mutations. These mutations occurring in the coding or the non-coding regions in the gene, can be inherited in dominant, recessive, or X-linked transmission modes within a family (Tukker et al. 2021). Coding sequences, known as exons, directly encode the amino acid sequence of proteins essential for various cellular functions, including enzymatic reactions, cell signaling, and structural support. Pathogenic variants within coding sequences can lead to significant disruptions and alterations in the protein structure, function, and stability (Li et al. 2013).  However non-coding sequences that represents around 98% of the entire human genome, include introns, enhancers, promotors, and regulatory elements that regulate genes’ expression. The presence of a pathogenic variant in one of these regions can alter mRNA processing and gene expression and disrupt the delicate balance of gene regulation. REFERENCEWhile coding regions, constitutes around 1 to 2% of the entire genome, , the precise functions of non-coding regions are still unraveled (Moyon et al. 2022).Our project has two main objectives.A) Firstly, to identify the pathogenic variant responsible for a syndromic neurodevelopmental disorder (NDD) in a young boy from a consanguineous Lebanese family. This step was achieved in 2020 and our results were published in Clinical Genetics. Indeed, a homozygous stop gain mutation in the BOD1 gene (p.R151*) was identified and was shown to be involved in the disease observed in this family. BOD1 is a crucial protein that inhibits the PP2A-B56 phosphatase at the kinetochore, which regulates the recruitment of various proteins (such as PLK1: Polo like Kinase 1 ) to ensure proper chromosome orientation during mitosis (Porter et al. 2013). Additionally, BOD1 is a part of a cytosolic variant of the SET1B/COMPASS complex, which affects the expression of genes related to fatty acid metabolism (Wang et al. 2017). Studies in Drosophila have shown that BOD1 depletion in neurons causes synapse morphological abnormalities and learning defects (Esmaeeli-Nieh et al. 2016). Moreover, BOD1 was described to be responsible for ataxic-like behaviors in mice with conditional in what tissue? Knock-Out (KO) of exon 2 of this gene in the lobes IV-V of the cerebellum  (Liu et al. 2022). On another note, a homozygous nonsense mutation in BOD1 gene (p.R112*) was identified in two related Iranian females, who were diagnosed with moderate form of ID (Intellectual Disability) and primary/secondary amenorrhea (Esmaeeli-Nieh et al. 2016).B) Secondly, we aimed to study the effect of the p.R151* mutation in BOD1 gene on protein expression. To achieve this, we used the CRISPR-Cas9 genome editing technique to create a knock-in (KI) of the mutation in HEK293T cells. We then analyzed the effect of this mutation on the expression of Bod1 protein using Western blot technique. Furthermore, we wanted to investigate the physiological and developmental function of the BOD1 gene. For this purpose, we have generated a conditional knock-out cKO mouse model.

La question omniprésente des scientifiques (et de tout être humain) est l'existence d'une planète semblable à la nôtre, permettant le développement de la vie. Les scientifiques ont introduit le concept d'habitabilité pour caractériser les conditions dans lesquelles une forme de vie basée sur le carbone pourrait apparaître, survivre et évoluer. Ce concept est basé sur des contraintes issues de différentes disciplines : de l'insolation, la chaleur interne, l'atmosphère, les périodes caractéristiques nécessaires au démarrage du processus de vie, à la forme de l'orbite et sa stabilité (dynamique), qui dépend aussi de sa rotation (spin), de la présence de résonances entre les fréquences actives et doit inclure d'éventuelles dissipations (marées, frottements).

"Au cœur des mécanismes de réponse et de régulation cellulaires"L'Unité de Recherche en Biologie Cellulaire (URBC) comprend 40 chercheurs et techniciens qui étudient dans 5 domaines différents. Les recherches sont consacrées à la compréhension des mécanismes de réponse cellulaire dans les situations normales et pathologiques.  Elle développe également des recherches plus appliquées associées au développement de la protéomique et des nanotechnologies.

Un projet Interreg France-Wallonie-Vlaanderen sur la qualité de l'air intérieur (QAI).

Jury Prof. Nathalie BURNAY (UNamur), présidenteProf. Sabine HENRY (UNamur), secrétaireDr. Florence DE LONGUEVILLE (UNamur)Prof. Nathalie MONDAIN (Université d’Ottawa)Prof. Etienne PIGUET (Université de Neuchâtel)Prof. Sane TIDIANE (Université Assane Seck/Ziguinchor) Abstract Recent attention to environmental change has highlighted its impact on rural communities, particularly in Africa, where household-level adaptations play a crucial role in larger societal responses. Current research often overlooks these small-scale, everyday adaptations and how they evolve over time, limiting our understanding of rural communities' dynamic responses to environmental changes. This study focused on households living in rural West Africa, more specifically in the region of Saint-Louis in Senegal. To capture the complexity of the household adaptation journeys, the structured timeline mapping methodology was developed, which consists of completing timelines during interviews. Timelines were collected from 39 individuals in 17 households to explore how families perceive and adapt to environmental shifts. In addition, this research reflected on the added value and necessity of interviewing multiple household members to capture diverse lived experiences and ensure a comprehensive household-level perspective.Analysis of the data categorized the adaptation journeys into four typological groups reflecting different sensitivities and adaptive capacities: (1) diversified adjusters, (2) system maintainers, (3) environmental independence strivers, and (4) opportunity-driven adapters. All groups have differentiated responses to similar environmental changes, with differences in the temporality of the response, differences in the types of adaptations, and differences in the amount and diversity of adaptations. These differences result in resilience that evolves unevenly over time. Understanding these varied adaptation pathways lead to formulate policy recommendations aimed at improving adaptive capacity, resilience, and sustainable livelihoods.

Depuis son inauguration en 2019, l’observatoire astronomique de l’UNamur a déployé un programme pédagogique et de médiation scientifique ouvert à toutes et à tous, avec l’ambition de faire découvrir les sciences par le prisme de l’observation des merveilles du ciel. 5 ans plus tard, le pari est réussi ! La petite équipe qui anime les lieux multiplie les collaborations et les activités proposées aux étudiantes et aux étudiants, aux écoles et au grand public. Cet automne, l’Observatoire astronomique célébrera l’empreinte durable qu’il a construite dans les yeux et les cœurs de son public en fêtant son 5e anniversaire. Une occasion de rassembler la communauté qui s’est développée autour de ses projets passés, présents et futurs ! Au programme 11H-16H : Visites de l’observatoireUNamur – Faculté des sciences12H-18H : Possibilité de visiter de l’exposition Stellar ScapeLe Pavillon de la Citadelle de Namur18H30 : Séance académique et réceptionUNamur – Faculté des sciences (S01)Inscriptions demandées via billetweb :

JuryProf. DE BOLLE Xavier (UNamur), PresidentProf. VINCENT Stéphane (UNamur), SecretaryProf. BOLTJE Thomas (Radboud University)Prof. GUIANVARC’H Dominique (Paris-Saclay University)Prof. WOUTERS Johan (UNamur)AbstractMannose is a carbohydrate that we can naturally find in some bacterial cell envelope, more precisely in lipopolysaccharide core. To explore the metabolic route of this natural sugar: Metabolic Gylcoengineering (MGE) has been employed for studying biomolecules in living systems. We aim to chemically modify the cell surfaces to install unnatural monosaccharides that are metabolically transformed and incorporated by microorganisms. The metabolic incorporation into glycans pathway can be visualized by biorthogonal click reactions with fluorescent reporters that can bind to unnatural carbohydrates. In this project, the strategy is to synthesize several mannose derivatives to target the metabolic route of D-mannose and explore the glycosylation pathway in Gram-negative bacteria.On top of that, another application is to apply this clickable mannose as an interesting building block to synthesize nucleotide sugar for antibodies (Ab) functionalization. Indeed, antibody-drug conjugates (ADC) constitute a new emerging class of highly potent pharmaceutical drugs, especially in cancer therapy. The aim is to perform regioselective modification in antibody’s subunit containing glycan chains from GDP-mannose derivative. This latter must be synthesized and tested as unnatural mannose donors for glycosyltransferase that catalyzes the transfer of sugar moiety to mannose acceptor in specific site of the antibody.